Project acronym ALPAM
Project Atomic-Level Physics of Advanced Materials
Researcher (PI) Börje Johansson
Host Institution (HI) KUNGLIGA TEKNISKA HOEGSKOLAN
Call Details Advanced Grant (AdG), PE5, ERC-2008-AdG
Summary Most of the technological materials have been developed by very expensive and cumbersome trial and error methods. On the other hand, computer based theoretical design of advanced materials is an area where rapid and extensive developments are taking place. Within my group new theoretical tools have now been established which are extremely well suited to the study of complex materials. In this approach basic quantum mechanical theories are used to describe fundamental properties of alloys and compounds. The utilization of such calculations to investigate possible optimizations of certain key properties represents a major departure from the traditional design philosophy. The purpose of my project is to build up a new competence in the field of computer-aided simulations of advanced materials. The main goal will be to achieve a deep understanding of the behaviour of complex metallic systems under equilibrium and non-equilibrium conditions at the atomic level by studying their electronic, magnetic and atomic structure using the most modern and advanced computational methods. This will enable us to establish a set of materials parameters and composition-structure-property relations that are needed for materials optimization.
The research will be focused on fundamental technological properties related to defects in advanced metallic alloys (high-performance steels, superalloys, and refractory, energy related and geochemical materials) and alloy phases (solid solutions, intermetallic compounds), which will be studied by means of parameter free atomistic simulations combined with continuum modelling. As a first example, we will study the Fe-Cr system, which is of great interest to industry as well as in connection to nuclear waste. The Fe-Cr-Ni system will form another large group of materials under the aegis of this project. Special emphasis will also be placed on those Fe-alloys which exist under extreme conditions and are possible candidates for the Earth core.
Summary
Most of the technological materials have been developed by very expensive and cumbersome trial and error methods. On the other hand, computer based theoretical design of advanced materials is an area where rapid and extensive developments are taking place. Within my group new theoretical tools have now been established which are extremely well suited to the study of complex materials. In this approach basic quantum mechanical theories are used to describe fundamental properties of alloys and compounds. The utilization of such calculations to investigate possible optimizations of certain key properties represents a major departure from the traditional design philosophy. The purpose of my project is to build up a new competence in the field of computer-aided simulations of advanced materials. The main goal will be to achieve a deep understanding of the behaviour of complex metallic systems under equilibrium and non-equilibrium conditions at the atomic level by studying their electronic, magnetic and atomic structure using the most modern and advanced computational methods. This will enable us to establish a set of materials parameters and composition-structure-property relations that are needed for materials optimization.
The research will be focused on fundamental technological properties related to defects in advanced metallic alloys (high-performance steels, superalloys, and refractory, energy related and geochemical materials) and alloy phases (solid solutions, intermetallic compounds), which will be studied by means of parameter free atomistic simulations combined with continuum modelling. As a first example, we will study the Fe-Cr system, which is of great interest to industry as well as in connection to nuclear waste. The Fe-Cr-Ni system will form another large group of materials under the aegis of this project. Special emphasis will also be placed on those Fe-alloys which exist under extreme conditions and are possible candidates for the Earth core.
Max ERC Funding
2 000 000 €
Duration
Start date: 2009-03-01, End date: 2014-02-28
Project acronym ASTROGEOBIOSPHERE
Project An astronomical perspective on Earth's geological record and evolution of life
Researcher (PI) Birger Schmitz
Host Institution (HI) LUNDS UNIVERSITET
Call Details Advanced Grant (AdG), PE10, ERC-2011-ADG_20110209
Summary "This project will develop the use of relict, extraterrestrial minerals in Archean to Cenozoic slowly formed sediments as tracers of events in the solar system and cosmos, and to decipher the possible relation between such events and evolution of life and environmental change on Earth. There has been consensus that it would not be possible to reconstruct variations in the flux of different types of meteorites to Earth through the ages. Meteorite falls are rare and meteorites weather and decay rapidly on the Earth surface. However, the last years we have developed the first realistic approach to circumvent these problems. Almost all meteorite types contain a small fraction of spinel minerals that survives weathering and can be recovered from large samples of condensed sediments of any age. Inside the spinels we can locate by synchrotron-light X-ray tomography 1-30 micron sized inclusions of most of the other minerals that made up the original meteorite. With cutting-edge frontier microanalyses such as Ne-21 (solar wind, galactic rays), oxygen isotopes (meteorite group and type) and cosmic ray tracks (supernova densities) we will be able to unravel from the geological record fundamental new information about the solar system at specific times through the past 3.8 Gyr. Variations in flux and types of meteorites may reflect solar-system and galaxy gravity disturbances as well as the sequence of disruptions of the parent bodies for meteorite types known and not yet known. Cosmic-ray tracks in spinels may identify the galactic year (230 Myr) in the geological record. For the first time it will be possible to systematically relate major global biotic and tectonic events, changes in sea-level, climate and asteroid and comet impacts to what happened in the larger astronomical realm. In essence, the project is a robust approach to establish a pioneer ""astrostratigraphy"" for Earth's geological record, complementing existing bio-, chemo-, and magnetostratigraphies."
Summary
"This project will develop the use of relict, extraterrestrial minerals in Archean to Cenozoic slowly formed sediments as tracers of events in the solar system and cosmos, and to decipher the possible relation between such events and evolution of life and environmental change on Earth. There has been consensus that it would not be possible to reconstruct variations in the flux of different types of meteorites to Earth through the ages. Meteorite falls are rare and meteorites weather and decay rapidly on the Earth surface. However, the last years we have developed the first realistic approach to circumvent these problems. Almost all meteorite types contain a small fraction of spinel minerals that survives weathering and can be recovered from large samples of condensed sediments of any age. Inside the spinels we can locate by synchrotron-light X-ray tomography 1-30 micron sized inclusions of most of the other minerals that made up the original meteorite. With cutting-edge frontier microanalyses such as Ne-21 (solar wind, galactic rays), oxygen isotopes (meteorite group and type) and cosmic ray tracks (supernova densities) we will be able to unravel from the geological record fundamental new information about the solar system at specific times through the past 3.8 Gyr. Variations in flux and types of meteorites may reflect solar-system and galaxy gravity disturbances as well as the sequence of disruptions of the parent bodies for meteorite types known and not yet known. Cosmic-ray tracks in spinels may identify the galactic year (230 Myr) in the geological record. For the first time it will be possible to systematically relate major global biotic and tectonic events, changes in sea-level, climate and asteroid and comet impacts to what happened in the larger astronomical realm. In essence, the project is a robust approach to establish a pioneer ""astrostratigraphy"" for Earth's geological record, complementing existing bio-, chemo-, and magnetostratigraphies."
Max ERC Funding
1 950 000 €
Duration
Start date: 2012-04-01, End date: 2017-03-31
Project acronym ATM-GTP
Project Atmospheric Gas-to-Particle conversion
Researcher (PI) Markku KULMALA
Host Institution (HI) HELSINGIN YLIOPISTO
Call Details Advanced Grant (AdG), PE10, ERC-2016-ADG
Summary Atmospheric Gas-to-Particle conversion (ATM-GTP) is a 5-year project focusing on one of the most critical atmospheric processes relevant to global climate and air quality: the first steps of atmospheric aerosol particle formation and growth. The project will concentrate on the currently lacking environmentally-specific knowledge about the interacting, non-linear, physical and chemical atmospheric processes associated with nano-scale gas-to-particle conversion (GTP). The main scientific objective of ATM-GTP is to create a deep understanding on atmospheric GTP taking place at the sub-5 nm size range, particularly in heavily-polluted Chinese mega cities like Beijing and in pristine environments like Siberia and Nordic high-latitude regions. We also aim to find out how nano-GTM is associated with air quality-climate interactions and feedbacks. We are interested in quantifying the effect of nano-GTP on the COBACC (Continental Biosphere-Aerosol-Cloud-Climate) feedback loop that is important in Arctic and boreal regions. Our approach enables to point out the effective reduction mechanisms of the secondary air pollution by a factor of 5-10 and to make reliable estimates of the global and regional aerosol loads, including anthropogenic and biogenic contributions to these loads. We can estimate the future role of Northern Hemispheric biosphere in reducing the global radiative forcing via the quantified feedbacks. The project is carried out by the world-leading scientist in atmospheric aerosol science, being also one of the founders of terrestrial ecosystem meteorology, together with his research team. The project uses novel infrastructures including SMEAR (Stations Measuring Ecosystem Atmospheric Relations) stations, related modelling platforms and regional data from Russia and China. The work will be carried out in synergy with several national, Nordic and EU research-innovation projects: Finnish Center of Excellence-ATM, Nordic CoE-CRAICC and EU-FP7-BACCHUS.
Summary
Atmospheric Gas-to-Particle conversion (ATM-GTP) is a 5-year project focusing on one of the most critical atmospheric processes relevant to global climate and air quality: the first steps of atmospheric aerosol particle formation and growth. The project will concentrate on the currently lacking environmentally-specific knowledge about the interacting, non-linear, physical and chemical atmospheric processes associated with nano-scale gas-to-particle conversion (GTP). The main scientific objective of ATM-GTP is to create a deep understanding on atmospheric GTP taking place at the sub-5 nm size range, particularly in heavily-polluted Chinese mega cities like Beijing and in pristine environments like Siberia and Nordic high-latitude regions. We also aim to find out how nano-GTM is associated with air quality-climate interactions and feedbacks. We are interested in quantifying the effect of nano-GTP on the COBACC (Continental Biosphere-Aerosol-Cloud-Climate) feedback loop that is important in Arctic and boreal regions. Our approach enables to point out the effective reduction mechanisms of the secondary air pollution by a factor of 5-10 and to make reliable estimates of the global and regional aerosol loads, including anthropogenic and biogenic contributions to these loads. We can estimate the future role of Northern Hemispheric biosphere in reducing the global radiative forcing via the quantified feedbacks. The project is carried out by the world-leading scientist in atmospheric aerosol science, being also one of the founders of terrestrial ecosystem meteorology, together with his research team. The project uses novel infrastructures including SMEAR (Stations Measuring Ecosystem Atmospheric Relations) stations, related modelling platforms and regional data from Russia and China. The work will be carried out in synergy with several national, Nordic and EU research-innovation projects: Finnish Center of Excellence-ATM, Nordic CoE-CRAICC and EU-FP7-BACCHUS.
Max ERC Funding
2 500 000 €
Duration
Start date: 2017-06-01, End date: 2022-05-31
Project acronym ATMNUCLE
Project Atmospheric nucleation: from molecular to global scale
Researcher (PI) Markku Tapio Kulmala
Host Institution (HI) HELSINGIN YLIOPISTO
Call Details Advanced Grant (AdG), PE10, ERC-2008-AdG
Summary Atmospheric aerosol particles and trace gases affect the quality of our life in many ways (e.g. health effects, changes in climate and hydrological cycle). Trace gases and atmospheric aerosols are tightly connected via physical, chemical, meteorological and biological processes occurring in the atmosphere and at the atmosphere-biosphere interface. One important phenomenon is atmospheric aerosol formation, which involves the production of nanometer-size particles by nucleation and their growth to detectable sizes. The main scientific objectives of this project are 1) to quantify the mechanisms responsible for atmospheric new particle formation and 2) to find out how important this process is for the behaviour of the global aerosol system and, ultimately, for the whole climate system. Our scientific plan is designed as a research chain that aims to advance our understanding of climate and air quality through a series of connected activities. We start from molecular simulations and laboratory measurements to understand nucleation and aerosol thermodynamic processes. We measure nanoparticles and atmospheric clusters at 15-20 sites all around the world using state of the art instrumentation and study feedbacks and interactions between climate and biosphere. With these atmospheric boundary layer studies we form a link to regional-scale processes and further to global-scale phenomena. In order to be able to simulate global climate and air quality, the most recent progress on this chain of processes must be compiled, integrated and implemented in Climate Change and Air Quality numerical models via novel parameterizations.
Summary
Atmospheric aerosol particles and trace gases affect the quality of our life in many ways (e.g. health effects, changes in climate and hydrological cycle). Trace gases and atmospheric aerosols are tightly connected via physical, chemical, meteorological and biological processes occurring in the atmosphere and at the atmosphere-biosphere interface. One important phenomenon is atmospheric aerosol formation, which involves the production of nanometer-size particles by nucleation and their growth to detectable sizes. The main scientific objectives of this project are 1) to quantify the mechanisms responsible for atmospheric new particle formation and 2) to find out how important this process is for the behaviour of the global aerosol system and, ultimately, for the whole climate system. Our scientific plan is designed as a research chain that aims to advance our understanding of climate and air quality through a series of connected activities. We start from molecular simulations and laboratory measurements to understand nucleation and aerosol thermodynamic processes. We measure nanoparticles and atmospheric clusters at 15-20 sites all around the world using state of the art instrumentation and study feedbacks and interactions between climate and biosphere. With these atmospheric boundary layer studies we form a link to regional-scale processes and further to global-scale phenomena. In order to be able to simulate global climate and air quality, the most recent progress on this chain of processes must be compiled, integrated and implemented in Climate Change and Air Quality numerical models via novel parameterizations.
Max ERC Funding
2 000 000 €
Duration
Start date: 2009-01-01, End date: 2013-12-31
Project acronym ATMOGAIN
Project Atmospheric Gas-Aerosol Interface:
From Fundamental Theory to Global Effects
Researcher (PI) Ilona Anniina Riipinen
Host Institution (HI) STOCKHOLMS UNIVERSITET
Call Details Starting Grant (StG), PE10, ERC-2011-StG_20101014
Summary Atmospheric aerosol particles are a major player in the earth system: they impact the climate by scattering and absorbing solar radiation, as well as regulating the properties of clouds. On regional scales aerosol particles are among the main pollutants deteriorating air quality. Capturing the impact of aerosols is one of the main challenges in understanding the driving forces behind changing climate and air quality.
Atmospheric aerosol numbers are governed by the ultrafine (< 100 nm in diameter) particles. Most of these particles have been formed from atmospheric vapours, and their fate and impacts are governed by the mass transport processes between the gas and particulate phases. These transport processes are currently poorly understood. Correct representation of the aerosol growth/shrinkage by condensation/evaporation of atmospheric vapours is thus a prerequisite for capturing the evolution and impacts of aerosols.
I propose to start a research group that will address the major current unknowns in atmospheric ultrafine particle growth and evaporation. First, we will develop a unified theoretical framework to describe the mass accommodation processes at aerosol surfaces, aiming to resolve the current ambiguity with respect to the uptake of atmospheric vapours by aerosols. Second, we will study the condensational properties of selected organic compounds and their mixtures. Organic compounds are known to contribute significantly to atmospheric aerosol growth, but the properties that govern their condensation, such as saturation vapour pressures and activities, are largely unknown. Third, we aim to resolve the gas and particulate phase processes that govern the growth of realistic atmospheric aerosol. Fourth, we will parameterize ultrafine aerosol growth, implement the parameterizations to chemical transport models, and quantify the impact of these condensation and evaporation processes on global and regional aerosol budgets.
Summary
Atmospheric aerosol particles are a major player in the earth system: they impact the climate by scattering and absorbing solar radiation, as well as regulating the properties of clouds. On regional scales aerosol particles are among the main pollutants deteriorating air quality. Capturing the impact of aerosols is one of the main challenges in understanding the driving forces behind changing climate and air quality.
Atmospheric aerosol numbers are governed by the ultrafine (< 100 nm in diameter) particles. Most of these particles have been formed from atmospheric vapours, and their fate and impacts are governed by the mass transport processes between the gas and particulate phases. These transport processes are currently poorly understood. Correct representation of the aerosol growth/shrinkage by condensation/evaporation of atmospheric vapours is thus a prerequisite for capturing the evolution and impacts of aerosols.
I propose to start a research group that will address the major current unknowns in atmospheric ultrafine particle growth and evaporation. First, we will develop a unified theoretical framework to describe the mass accommodation processes at aerosol surfaces, aiming to resolve the current ambiguity with respect to the uptake of atmospheric vapours by aerosols. Second, we will study the condensational properties of selected organic compounds and their mixtures. Organic compounds are known to contribute significantly to atmospheric aerosol growth, but the properties that govern their condensation, such as saturation vapour pressures and activities, are largely unknown. Third, we aim to resolve the gas and particulate phase processes that govern the growth of realistic atmospheric aerosol. Fourth, we will parameterize ultrafine aerosol growth, implement the parameterizations to chemical transport models, and quantify the impact of these condensation and evaporation processes on global and regional aerosol budgets.
Max ERC Funding
1 498 099 €
Duration
Start date: 2011-09-01, End date: 2016-08-31
Project acronym CC-TOP
Project Cryosphere-Carbon on Top of the Earth (CC-Top):Decreasing Uncertainties of Thawing Permafrost and Collapsing Methane Hydrates in the Arctic
Researcher (PI) Örjan GUSTAFSSON
Host Institution (HI) STOCKHOLMS UNIVERSITET
Call Details Advanced Grant (AdG), PE10, ERC-2015-AdG
Summary The enormous quantities of frozen carbon in the Arctic, held in shallow soils and sediments, act as “capacitors” of the global carbon system. Thawing permafrost (PF) and collapsing methane hydrates are top candidates to cause a net transfer of carbon from land/ocean to the atmosphere this century, yet uncertainties abound.
Our program targets the East Siberian Arctic Ocean (ESAO), the World’s largest shelf sea, as it holds 80% of coastal PF, 80% of subsea PF and 75% of shallow hydrates. Our initial findings (e.g., Science, 2010; Nature, 2012; PNAS; 2013; Nature Geoscience, 2013, 2014) are challenging earlier notions by showing complexities in terrestrial PF-Carbon remobilization and extensive venting of methane from subsea PF/hydrates. The objective of the CC-Top Program is to transform descriptive and data-lean pictures into quantitative understanding of the CC system, to pin down the present and predict future releases from these “Sleeping Giants” of the global carbon system.
The CC-Top program combines unique Arctic field capacities with powerful molecular-isotopic characterization of PF-carbon/methane to break through on:
The “awakening” of terrestrial PF-C pools: CC-Top will employ great pan-arctic rivers as natural integrators and by probing the δ13C/Δ14C and molecular fingerprints, apportion release fluxes of different PF-C pools.
The ESAO subsea cryosphere/methane: CC-Top will use recent spatially-extensive observations, deep sediment cores and gap-filling expeditions to (i) estimate distribution of subsea PF and hydrates; (ii) establish thermal state (thawing rate) of subsea PF-C; (iii) apportion sources of releasing methane btw subsea-PF, shallow hydrates vs seepage from the deep petroleum megapool using source-diagnostic triple-isotope fingerprinting.
Arctic Ocean slope hydrates: CC-Top will investigate sites (discovered by us 2008-2014) of collapsed hydrates venting methane, to characterize geospatial distribution and causes of destabilization.
Summary
The enormous quantities of frozen carbon in the Arctic, held in shallow soils and sediments, act as “capacitors” of the global carbon system. Thawing permafrost (PF) and collapsing methane hydrates are top candidates to cause a net transfer of carbon from land/ocean to the atmosphere this century, yet uncertainties abound.
Our program targets the East Siberian Arctic Ocean (ESAO), the World’s largest shelf sea, as it holds 80% of coastal PF, 80% of subsea PF and 75% of shallow hydrates. Our initial findings (e.g., Science, 2010; Nature, 2012; PNAS; 2013; Nature Geoscience, 2013, 2014) are challenging earlier notions by showing complexities in terrestrial PF-Carbon remobilization and extensive venting of methane from subsea PF/hydrates. The objective of the CC-Top Program is to transform descriptive and data-lean pictures into quantitative understanding of the CC system, to pin down the present and predict future releases from these “Sleeping Giants” of the global carbon system.
The CC-Top program combines unique Arctic field capacities with powerful molecular-isotopic characterization of PF-carbon/methane to break through on:
The “awakening” of terrestrial PF-C pools: CC-Top will employ great pan-arctic rivers as natural integrators and by probing the δ13C/Δ14C and molecular fingerprints, apportion release fluxes of different PF-C pools.
The ESAO subsea cryosphere/methane: CC-Top will use recent spatially-extensive observations, deep sediment cores and gap-filling expeditions to (i) estimate distribution of subsea PF and hydrates; (ii) establish thermal state (thawing rate) of subsea PF-C; (iii) apportion sources of releasing methane btw subsea-PF, shallow hydrates vs seepage from the deep petroleum megapool using source-diagnostic triple-isotope fingerprinting.
Arctic Ocean slope hydrates: CC-Top will investigate sites (discovered by us 2008-2014) of collapsed hydrates venting methane, to characterize geospatial distribution and causes of destabilization.
Max ERC Funding
2 499 756 €
Duration
Start date: 2016-11-01, End date: 2021-10-31
Project acronym COALA
Project Comprehensive molecular characterization of secondary organic aerosol formation in the atmosphere
Researcher (PI) Mikael Ehn
Host Institution (HI) HELSINGIN YLIOPISTO
Call Details Starting Grant (StG), PE10, ERC-2014-STG
Summary Key words: Atmospheric secondary organic aerosol, chemical ionization mass spectrometry
The increase in anthropogenic atmospheric aerosol since the industrial revolution has considerably mitigated the global warming caused by concurrent anthropogenic greenhouse gas emissions. However, the uncertainty in the magnitude of the aerosol climate influence is larger than that of any other man-made climate-perturbing component.
Secondary organic aerosol (SOA) is one of the most prominent aerosol types, yet a detailed mechanistic understanding of its formation process is still lacking. We recently presented the ground-breaking discovery of a new important compound group in our publication in Nature: a prompt and abundant source of extremely low-volatility organic compounds (ELVOC), able to explain the majority of the SOA formed from important atmospheric precursors.
Quantifying the atmospheric role of ELVOCs requires further focused studies and I will start a research group with the main task of providing a comprehensive, quantitative and mechanistic understanding of the formation and evolution of SOA. Our recent discovery of an important missing component of SOA highlights the need for comprehensive chemical characterization of both the gas and particle phase composition.
This project will use state-of-the-art chemical ionization mass spectrometry (CIMS), which was critical also in the detection of the ELVOCs. We will extend the applicability of CIMS techniques and conduct innovative experiments in both laboratory and field settings using a novel suite of instrumentation to achieve the goals set out in this project.
We will provide unprecedented insights into the compounds and mechanisms producing SOA, helping to decrease the uncertainties in assessing the magnitude of aerosol effects on climate. Anthropogenic SOA contributes strongly to air quality deterioration as well and therefore our results will find direct applicability also in this extremely important field.
Summary
Key words: Atmospheric secondary organic aerosol, chemical ionization mass spectrometry
The increase in anthropogenic atmospheric aerosol since the industrial revolution has considerably mitigated the global warming caused by concurrent anthropogenic greenhouse gas emissions. However, the uncertainty in the magnitude of the aerosol climate influence is larger than that of any other man-made climate-perturbing component.
Secondary organic aerosol (SOA) is one of the most prominent aerosol types, yet a detailed mechanistic understanding of its formation process is still lacking. We recently presented the ground-breaking discovery of a new important compound group in our publication in Nature: a prompt and abundant source of extremely low-volatility organic compounds (ELVOC), able to explain the majority of the SOA formed from important atmospheric precursors.
Quantifying the atmospheric role of ELVOCs requires further focused studies and I will start a research group with the main task of providing a comprehensive, quantitative and mechanistic understanding of the formation and evolution of SOA. Our recent discovery of an important missing component of SOA highlights the need for comprehensive chemical characterization of both the gas and particle phase composition.
This project will use state-of-the-art chemical ionization mass spectrometry (CIMS), which was critical also in the detection of the ELVOCs. We will extend the applicability of CIMS techniques and conduct innovative experiments in both laboratory and field settings using a novel suite of instrumentation to achieve the goals set out in this project.
We will provide unprecedented insights into the compounds and mechanisms producing SOA, helping to decrease the uncertainties in assessing the magnitude of aerosol effects on climate. Anthropogenic SOA contributes strongly to air quality deterioration as well and therefore our results will find direct applicability also in this extremely important field.
Max ERC Funding
1 892 221 €
Duration
Start date: 2015-03-01, End date: 2020-02-29
Project acronym DAMOCLES
Project Simulating Non-Equilibrium Dynamics of Atmospheric Multicomponent Clusters
Researcher (PI) Hanna Vehkamäki
Host Institution (HI) HELSINGIN YLIOPISTO
Call Details Advanced Grant (AdG), PE10, ERC-2015-AdG
Summary Atmospheric aerosol particles play a key role in regulating the climate, and particulate matter is responsible for most of the 7 million deaths per year attributed to air pollution. Lack of understanding of aerosol processes, especially the formation of ice crystals and secondary particles from condensable trace gases, hampers the development of air quality modelling, and remains one of the major uncertainties in predicting climate.
The purpose of this project is to achieve a comprehensive understanding of atmospheric nanocluster and ice crystal formation based on fundamental physico-chemical principles. We will use a wide palette of theoretical methods including quantum chemistry, reaction kinetics, continuum solvent models, molecular dynamics, Monte Carlo simulations, Markov chain Monte Carlo methods, computational fluid dynamics, cluster kinetic and thermodynamic models. We will study non-equilibrium effects and kinetic barriers in atmospheric clustering, and use these to build cluster distribution models with genuine predictive capacity.
Chemical ionization mass spectrometers can, unlike any other instruments, detect the elemental composition of many of the smallest clusters at ambient low concentrations. However, the charging process and the environment inside the instrument change the composition of the clusters in hitherto unquantifiable ways. We will solve this problem by building an accurate model for the fate of clusters inside mass spectrometers, which will vastly improve the amount and quality of information that can be extracted from mass spectrometric measurements in atmospheric science and elsewhere.
DAMOCLES will produce reliable and consistent models for secondary aerosol and ice particle formation and growth. This will lead to improved predictions of aerosol concentrations and size distributions, leading to improved air quality forecasting, more accurate estimates of aerosol indirect climate forcing and other aerosol-cloud-climate interactions.
Summary
Atmospheric aerosol particles play a key role in regulating the climate, and particulate matter is responsible for most of the 7 million deaths per year attributed to air pollution. Lack of understanding of aerosol processes, especially the formation of ice crystals and secondary particles from condensable trace gases, hampers the development of air quality modelling, and remains one of the major uncertainties in predicting climate.
The purpose of this project is to achieve a comprehensive understanding of atmospheric nanocluster and ice crystal formation based on fundamental physico-chemical principles. We will use a wide palette of theoretical methods including quantum chemistry, reaction kinetics, continuum solvent models, molecular dynamics, Monte Carlo simulations, Markov chain Monte Carlo methods, computational fluid dynamics, cluster kinetic and thermodynamic models. We will study non-equilibrium effects and kinetic barriers in atmospheric clustering, and use these to build cluster distribution models with genuine predictive capacity.
Chemical ionization mass spectrometers can, unlike any other instruments, detect the elemental composition of many of the smallest clusters at ambient low concentrations. However, the charging process and the environment inside the instrument change the composition of the clusters in hitherto unquantifiable ways. We will solve this problem by building an accurate model for the fate of clusters inside mass spectrometers, which will vastly improve the amount and quality of information that can be extracted from mass spectrometric measurements in atmospheric science and elsewhere.
DAMOCLES will produce reliable and consistent models for secondary aerosol and ice particle formation and growth. This will lead to improved predictions of aerosol concentrations and size distributions, leading to improved air quality forecasting, more accurate estimates of aerosol indirect climate forcing and other aerosol-cloud-climate interactions.
Max ERC Funding
2 390 450 €
Duration
Start date: 2016-06-01, End date: 2021-05-31
Project acronym DEVOCEAN
Project Impact of diatom evolution on the oceans
Researcher (PI) Daniel CONLEY
Host Institution (HI) LUNDS UNIVERSITET
Call Details Advanced Grant (AdG), PE10, ERC-2018-ADG
Summary Motivated by a series of recent discoveries, DEVOCEAN will provide the first comprehensive evaluation of the emergence of diatoms and their impact on the global biogeochemical cycle of silica, carbon and other nutrients that regulate ocean productivity and ultimately climate. I propose that the proliferation of phytoplankton that occurred after the Permian-Triassic extinction, in particular the diatoms, fundamentally influenced oceanic environments through the enhancement of carbon export to depth as part of the biological pump. Although molecular clocks suggest that diatoms evolved over 200 Ma ago, this result has been largely ignored because of the lack of diatoms in the geologic fossil record with most studies therefore focused on diversification during the Cenozoic where abundant diatom fossils are found. Much of the older fossil evidence has likely been destroyed by dissolution during diagenesis, subducted or is concealed deep within the Earth under many layers of rock. DEVOCEAN will provide evidence on diatom evolution and speciation in the geological record by examining formations representing locations in which diatoms are likely to have accumulated in ocean sediments. We will generate robust estimates of the timing and magnitude of dissolved Si drawdown following the origin of diatoms using the isotopic silicon composition of fossil sponge spicules and radiolarians. The project will also provide fundamental new insights into the timing of dissolved Si drawdown and other key events, which reorganized the distribution of carbon and nutrients in seawater, changing energy flows and productivity in the biological communities of the ancient oceans.
Summary
Motivated by a series of recent discoveries, DEVOCEAN will provide the first comprehensive evaluation of the emergence of diatoms and their impact on the global biogeochemical cycle of silica, carbon and other nutrients that regulate ocean productivity and ultimately climate. I propose that the proliferation of phytoplankton that occurred after the Permian-Triassic extinction, in particular the diatoms, fundamentally influenced oceanic environments through the enhancement of carbon export to depth as part of the biological pump. Although molecular clocks suggest that diatoms evolved over 200 Ma ago, this result has been largely ignored because of the lack of diatoms in the geologic fossil record with most studies therefore focused on diversification during the Cenozoic where abundant diatom fossils are found. Much of the older fossil evidence has likely been destroyed by dissolution during diagenesis, subducted or is concealed deep within the Earth under many layers of rock. DEVOCEAN will provide evidence on diatom evolution and speciation in the geological record by examining formations representing locations in which diatoms are likely to have accumulated in ocean sediments. We will generate robust estimates of the timing and magnitude of dissolved Si drawdown following the origin of diatoms using the isotopic silicon composition of fossil sponge spicules and radiolarians. The project will also provide fundamental new insights into the timing of dissolved Si drawdown and other key events, which reorganized the distribution of carbon and nutrients in seawater, changing energy flows and productivity in the biological communities of the ancient oceans.
Max ERC Funding
2 500 000 €
Duration
Start date: 2019-10-01, End date: 2024-09-30
Project acronym DRIVEN
Project Field driven materials for functions, dissipation, and mimicking Pavlovian adaptation
Researcher (PI) Olli Ikkala
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Call Details Advanced Grant (AdG), PE5, ERC-2016-ADG
Summary During the recent years, biological materials have extensively inspired materials scientists towards new properties, e.g., for composites, photonics, and wetting. The future grand challenge is to mimic biological active materials towards new properties that commonly have not been connected with man-made materials. Due to the biological complexity, conceptually new approaches are needed in materials science. In the project DRIVEN, field-driven dissipative out-of-equilibrium self-assemblies are developed in the colloidal and molecular scale. In the proposal, instead of using chemical fuels to drive dissipative self-assemblies, which is ubiquitous in Nature, imposed fields are here used to drive the system out-of-equilibrium towards new assemblies and functions. The project show steps with growing risks towards highly ambitious new materials mimicking aspects from active biological materials.
Summary
During the recent years, biological materials have extensively inspired materials scientists towards new properties, e.g., for composites, photonics, and wetting. The future grand challenge is to mimic biological active materials towards new properties that commonly have not been connected with man-made materials. Due to the biological complexity, conceptually new approaches are needed in materials science. In the project DRIVEN, field-driven dissipative out-of-equilibrium self-assemblies are developed in the colloidal and molecular scale. In the proposal, instead of using chemical fuels to drive dissipative self-assemblies, which is ubiquitous in Nature, imposed fields are here used to drive the system out-of-equilibrium towards new assemblies and functions. The project show steps with growing risks towards highly ambitious new materials mimicking aspects from active biological materials.
Max ERC Funding
2 499 999 €
Duration
Start date: 2017-10-01, End date: 2022-09-30
Project acronym e-NeuroPharma
Project Electronic Neuropharmacology
Researcher (PI) Rolf Magnus BERGGREN
Host Institution (HI) LINKOPINGS UNIVERSITET
Call Details Advanced Grant (AdG), PE5, ERC-2018-ADG
Summary As the population ages, neurodegenerative diseases (ND) will have a devastating impact on individuals and society. Despite enormous research efforts there is still no cure for these diseases, only care! The origin of ND is hugely complex, spanning from the molecular level to systemic processes, causing malfunctioning of signalling in the central nervous system (CNS). This signalling includes the coupled processing of biochemical and electrical signals, however current approaches for symptomatic- and disease modifying treatments are all based on biochemical approaches, alone.
Organic bioelectronics has arisen as a promising technology providing signal translation, as sensors and modulators, across the biology-technology interface; especially, it has proven unique in neuronal applications. There is great opportunity with organic bioelectronics since it can complement biochemical pharmacology to enable a twinned electric-biochemical therapy for ND and neurological disorders. However, this technology is traditionally manufactured on stand-alone substrates. Even though organic bioelectronics has been manufactured on flexible and soft carriers in the past, current technology consume space and volume, that when applied to CNS, rule out close proximity and amalgamation between the bioelectronics technology and CNS components – features that are needed in order to reach high therapeutic efficacy.
e-NeuroPharma includes development of innovative organic bioelectronics, that can be in-vivo-manufactured within the brain. The overall aim is to evaluate and develop electrodes, delivery devices and sensors that enable a twinned biochemical-electric therapy approach to combat ND and other neurological disorders. e-NeuroPharma will focus on the development of materials that can cross the blood-brain-barrier, that self-organize and -polymerize along CNS components, and that record and regulate relevant electrical, electrochemical and physical parameters relevant to ND and disorders
Summary
As the population ages, neurodegenerative diseases (ND) will have a devastating impact on individuals and society. Despite enormous research efforts there is still no cure for these diseases, only care! The origin of ND is hugely complex, spanning from the molecular level to systemic processes, causing malfunctioning of signalling in the central nervous system (CNS). This signalling includes the coupled processing of biochemical and electrical signals, however current approaches for symptomatic- and disease modifying treatments are all based on biochemical approaches, alone.
Organic bioelectronics has arisen as a promising technology providing signal translation, as sensors and modulators, across the biology-technology interface; especially, it has proven unique in neuronal applications. There is great opportunity with organic bioelectronics since it can complement biochemical pharmacology to enable a twinned electric-biochemical therapy for ND and neurological disorders. However, this technology is traditionally manufactured on stand-alone substrates. Even though organic bioelectronics has been manufactured on flexible and soft carriers in the past, current technology consume space and volume, that when applied to CNS, rule out close proximity and amalgamation between the bioelectronics technology and CNS components – features that are needed in order to reach high therapeutic efficacy.
e-NeuroPharma includes development of innovative organic bioelectronics, that can be in-vivo-manufactured within the brain. The overall aim is to evaluate and develop electrodes, delivery devices and sensors that enable a twinned biochemical-electric therapy approach to combat ND and other neurological disorders. e-NeuroPharma will focus on the development of materials that can cross the blood-brain-barrier, that self-organize and -polymerize along CNS components, and that record and regulate relevant electrical, electrochemical and physical parameters relevant to ND and disorders
Max ERC Funding
3 237 335 €
Duration
Start date: 2019-09-01, End date: 2024-08-31
Project acronym ECLAIR
Project Emulation of subgrid-scale aerosol-cloud interactions in climate models: towards a realistic representation of aerosol indirect effect
Researcher (PI) Sari Hannele Korhonen
Host Institution (HI) ILMATIETEEN LAITOS
Call Details Consolidator Grant (CoG), PE10, ERC-2014-CoG
Summary I propose to develop an innovative interdisciplinary model framework to refine the estimate of aerosol indirect effect (i.e. influence of atmospheric aerosol particles on cloud properties), which remains the single largest uncertainty in the current drivers of climate change.
A major reason for this uncertainty is that current climate models are unable to resolve the spatial scales for aerosol-cloud interactions. We will resolve this scale problem by using statistical emulation to build computationally fast surrogate models (i.e. emulators) that can reproduce the effective output of a detailed high-resolution cloud-resolving model. By incorporating these emulators into a state-of-the-science climate model, we will for the first time achieve the accuracy of a limited-area high-resolution model on a global scale with negligible computational cost.
The main scientific outcome of the project will be a highly refined and physically sound estimate of the aerosol indirect effect that enables more accurate projections of future climate change, and thus has high societal relevance. In addition, the developed emulators will help to quantify how the remaining uncertainties in aerosol properties propagate to predictions of aerosol indirect effect. This information will be used, together with an extensive set of remote sensing, in-situ and laboratory data from our collaborators, to improve the process-level understanding of aerosol-cloud interactions.
The comprehensive uncertainty analyses performed during this project will be highly valuable for future research efforts as they point to processes and interactions that most urgently need to be experimentally constrained. Furthermore, our pioneering model framework that incorporates emulators to represent subgrid- scale processes will open up completely new research opportunities also in other fields that deal with heterogeneous spatial scales.
Summary
I propose to develop an innovative interdisciplinary model framework to refine the estimate of aerosol indirect effect (i.e. influence of atmospheric aerosol particles on cloud properties), which remains the single largest uncertainty in the current drivers of climate change.
A major reason for this uncertainty is that current climate models are unable to resolve the spatial scales for aerosol-cloud interactions. We will resolve this scale problem by using statistical emulation to build computationally fast surrogate models (i.e. emulators) that can reproduce the effective output of a detailed high-resolution cloud-resolving model. By incorporating these emulators into a state-of-the-science climate model, we will for the first time achieve the accuracy of a limited-area high-resolution model on a global scale with negligible computational cost.
The main scientific outcome of the project will be a highly refined and physically sound estimate of the aerosol indirect effect that enables more accurate projections of future climate change, and thus has high societal relevance. In addition, the developed emulators will help to quantify how the remaining uncertainties in aerosol properties propagate to predictions of aerosol indirect effect. This information will be used, together with an extensive set of remote sensing, in-situ and laboratory data from our collaborators, to improve the process-level understanding of aerosol-cloud interactions.
The comprehensive uncertainty analyses performed during this project will be highly valuable for future research efforts as they point to processes and interactions that most urgently need to be experimentally constrained. Furthermore, our pioneering model framework that incorporates emulators to represent subgrid- scale processes will open up completely new research opportunities also in other fields that deal with heterogeneous spatial scales.
Max ERC Funding
1 999 511 €
Duration
Start date: 2015-09-01, End date: 2020-08-31
Project acronym ECOHERB
Project Drivers and impacts of invertebrate herbivores across forest ecosystems globally.
Researcher (PI) Daniel Metcalfe
Host Institution (HI) LUNDS UNIVERSITET
Call Details Consolidator Grant (CoG), PE10, ERC-2015-CoG
Summary Forests slow global climate change by absorbing atmospheric carbon dioxide but this ecosystem service is limited by soil nutrients. Herbivores potentially alter soil nutrients in a range of ways, but these have mostly only been recorded for large mammals. By comparison, the impacts of the abundant invertebrates in forests have largely been ignored and are not included in current models used to generate the climate predictions so vital for designing governmental policies
The proposed project will use a pioneering new interdisciplinary approach to provide the most complete picture yet available of the rates, underlying drivers and ultimate impacts of key nutrient inputs from invertebrate herbivores across forest ecosystems worldwide. Specifically, we will:
(1) Establish a network of herbivory monitoring stations across all major forest types, and across key environmental gradients (temperature, rainfall, ecosystem development).
(2) Perform laboratory experiments to examine the effects of herbivore excreta on soil processes under different temperature and moisture conditions.
(3) Integrate this information into a cutting-edge ecosystem model, to generate more accurate predictions of forest carbon sequestration under future climate change.
The network established will form the foundation for a unique long-term global monitoring effort which we intend to continue long after the current funding time scale. This work represents a powerful blend of several disciplines harnessing an array of cutting edge tools to provide fundamentally novel insights into an area of direct and urgent importance for the society.
Summary
Forests slow global climate change by absorbing atmospheric carbon dioxide but this ecosystem service is limited by soil nutrients. Herbivores potentially alter soil nutrients in a range of ways, but these have mostly only been recorded for large mammals. By comparison, the impacts of the abundant invertebrates in forests have largely been ignored and are not included in current models used to generate the climate predictions so vital for designing governmental policies
The proposed project will use a pioneering new interdisciplinary approach to provide the most complete picture yet available of the rates, underlying drivers and ultimate impacts of key nutrient inputs from invertebrate herbivores across forest ecosystems worldwide. Specifically, we will:
(1) Establish a network of herbivory monitoring stations across all major forest types, and across key environmental gradients (temperature, rainfall, ecosystem development).
(2) Perform laboratory experiments to examine the effects of herbivore excreta on soil processes under different temperature and moisture conditions.
(3) Integrate this information into a cutting-edge ecosystem model, to generate more accurate predictions of forest carbon sequestration under future climate change.
The network established will form the foundation for a unique long-term global monitoring effort which we intend to continue long after the current funding time scale. This work represents a powerful blend of several disciplines harnessing an array of cutting edge tools to provide fundamentally novel insights into an area of direct and urgent importance for the society.
Max ERC Funding
1 750 000 €
Duration
Start date: 2016-03-01, End date: 2021-02-28
Project acronym FUN POLYSTORE
Project FUNctionalized POLYmer electrolytes for energy STORagE
Researcher (PI) Daniel BRANDELL
Host Institution (HI) UPPSALA UNIVERSITET
Call Details Consolidator Grant (CoG), PE5, ERC-2017-COG
Summary Besides the need for large-scale implementation of renewable energy sources, there is an equivalent need for new energy storage solutions. This is not least true for the transport sector, where electric vehicles are expanding rapidly. The rich flora of battery chemistries – today crowned by the Li-ion battery – is likewise expected to expand in upcoming years. Novel types of batteries, “post-lithium ion”, will challenge the Li-ion chemistries by advantages in cost, sustainability, elemental abundance or energy density. This requires significant improvements of the materials, not least regarding the electrolyte. The conventional liquid battery electrolytes pose a problem already for the mature Li-ion chemistries due to safety and cost, but are particularly destructive for future battery types such as Li-metal, organic electrodes, Li-S, Li-O2, Na- or Mg-batteries, where rapid degradation and loss of material are associated with incompatibilities with the electrolytes. In this context, solid state polymer electrolytes (SPEs) could provide a considerable improvement.
The field of solid polymer electrolytes (SPEs) is dominated by polyethers, particularly poly(ethylene oxide) (PEO). This application regards moving out of the established PEO-paradigm and exploring alternative polymer hosts for SPEs, primarily polycarbonates and polyesters. These ‘alternative’ polymers are comparatively easy to work with synthetically, and their possible functionalization is straightforward. The work aims at exploring functionalized alternative polymer host for mechanically robust block-copolymer systems, for alternative cation chemistries (Na, Mg, etc.), for extremely high and low electrochemical potentials, and for unstable and easily dissolved electrode materials (sulfur, organic). Moreover, since the ion transport processes in the host materials are fundamentally different from polyethers, there is a need for investigating the conduction mechanisms using simulations.
Summary
Besides the need for large-scale implementation of renewable energy sources, there is an equivalent need for new energy storage solutions. This is not least true for the transport sector, where electric vehicles are expanding rapidly. The rich flora of battery chemistries – today crowned by the Li-ion battery – is likewise expected to expand in upcoming years. Novel types of batteries, “post-lithium ion”, will challenge the Li-ion chemistries by advantages in cost, sustainability, elemental abundance or energy density. This requires significant improvements of the materials, not least regarding the electrolyte. The conventional liquid battery electrolytes pose a problem already for the mature Li-ion chemistries due to safety and cost, but are particularly destructive for future battery types such as Li-metal, organic electrodes, Li-S, Li-O2, Na- or Mg-batteries, where rapid degradation and loss of material are associated with incompatibilities with the electrolytes. In this context, solid state polymer electrolytes (SPEs) could provide a considerable improvement.
The field of solid polymer electrolytes (SPEs) is dominated by polyethers, particularly poly(ethylene oxide) (PEO). This application regards moving out of the established PEO-paradigm and exploring alternative polymer hosts for SPEs, primarily polycarbonates and polyesters. These ‘alternative’ polymers are comparatively easy to work with synthetically, and their possible functionalization is straightforward. The work aims at exploring functionalized alternative polymer host for mechanically robust block-copolymer systems, for alternative cation chemistries (Na, Mg, etc.), for extremely high and low electrochemical potentials, and for unstable and easily dissolved electrode materials (sulfur, organic). Moreover, since the ion transport processes in the host materials are fundamentally different from polyethers, there is a need for investigating the conduction mechanisms using simulations.
Max ERC Funding
1 950 732 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym FUNMAT
Project Self-Organized Nanostructuring in Functional Thin Film Materials
Researcher (PI) Lars Hultman
Host Institution (HI) LINKOPINGS UNIVERSITET
Call Details Advanced Grant (AdG), PE5, ERC-2008-AdG
Summary I aim to achieve a fundamental understanding of the atomistic kinetic pathways responsible for nanostructure formation and to explore the concept of self-organization by thermodynamic segregation in functional ceramics. Model systems are advanced ceramic thin films, which will be studied under two defining cases: 1) deposition of supersaturated solid solutions or nanocomposites by magnetron sputtering (epitaxy) and arc evaporation. 2) post-deposition annealing (ageing) of as-synthesized material. Thin film ceramics are terra incognita for compositions in the miscibility gap. The field is exciting since both surface and in-depth decomposition can take place in the alloys. The methodology is based on combined growth experiments, characterization, and ab initio calculations to identify and describe systems with a large miscibility gap. A hot topic is to elucidate the bonding nature of the cubic-SiNx interfacial phase, discovered by us in TiN/Si3N4 with impact for superhard nanocomposites. I have also pioneered studies of self-organization by spinodal decomposition in TiAlN alloy films (age hardening). Here, the details of metastable c-AlN nm domain formation are unknown and the systems HfAlN and ZrAlN are predicted to be even more promising. Other model systems are III-nitrides (band gap engineering), semiconductor/insulator oxides (interface conductivity) and carbides (tribology). The proposed research is exploratory and has the potential of explaining outstanding phenomena (Gibbs-Thomson effect, strain, and spinodal decomposition) as well as discovering new phases, for which my group has a track-record, backed-up by state-of-the-art in situ techniques. One can envision a new class of super-hard all-crystalline ceramic nanocomposites with relevance for a large number of research areas where elevated temperature is of concern, significant in impact for areas as diverse as microelectronics and cutting tools as well as mechanical and optical components.
Summary
I aim to achieve a fundamental understanding of the atomistic kinetic pathways responsible for nanostructure formation and to explore the concept of self-organization by thermodynamic segregation in functional ceramics. Model systems are advanced ceramic thin films, which will be studied under two defining cases: 1) deposition of supersaturated solid solutions or nanocomposites by magnetron sputtering (epitaxy) and arc evaporation. 2) post-deposition annealing (ageing) of as-synthesized material. Thin film ceramics are terra incognita for compositions in the miscibility gap. The field is exciting since both surface and in-depth decomposition can take place in the alloys. The methodology is based on combined growth experiments, characterization, and ab initio calculations to identify and describe systems with a large miscibility gap. A hot topic is to elucidate the bonding nature of the cubic-SiNx interfacial phase, discovered by us in TiN/Si3N4 with impact for superhard nanocomposites. I have also pioneered studies of self-organization by spinodal decomposition in TiAlN alloy films (age hardening). Here, the details of metastable c-AlN nm domain formation are unknown and the systems HfAlN and ZrAlN are predicted to be even more promising. Other model systems are III-nitrides (band gap engineering), semiconductor/insulator oxides (interface conductivity) and carbides (tribology). The proposed research is exploratory and has the potential of explaining outstanding phenomena (Gibbs-Thomson effect, strain, and spinodal decomposition) as well as discovering new phases, for which my group has a track-record, backed-up by state-of-the-art in situ techniques. One can envision a new class of super-hard all-crystalline ceramic nanocomposites with relevance for a large number of research areas where elevated temperature is of concern, significant in impact for areas as diverse as microelectronics and cutting tools as well as mechanical and optical components.
Max ERC Funding
2 292 000 €
Duration
Start date: 2008-12-01, End date: 2013-11-30
Project acronym GASPARCON
Project Molecular steps of gas-to-particle conversion: From oxidation to precursors, clusters and secondary aerosol particles.
Researcher (PI) Mikko SIPILÄ
Host Institution (HI) HELSINGIN YLIOPISTO
Call Details Starting Grant (StG), PE10, ERC-2016-STG
Summary Atmospheric aerosol particles impact Earth’s climate, by directly scattering sunlight and indirectly by affecting cloud properties. The largest uncertainties in climate change projections are associated with the atmospheric aerosol system that has been altered by anthropogenic activities. A major source of that uncertainty involves the formation of secondary particles and cloud condensation nuclei from natural and anthropogenic emissions of volatile compounds. This research challenge persists despite significant efforts within recent decades.
I will build a research group that aims to resolve the atmospheric oxidation processes that convert volatile trace gases to particle precursor vapours, clusters and new aerosol particles. We will create novel measurement techniques and utilize the tremendous potential of mass spectrometry for detection of i) particle precursor vapours ii) oxidants, both conventional but also recently discovered stabilized Criegee intermediates, and, most importantly, iii) newly formed clusters. These methods and instrumentation will be applied for resolving the initial steps of new particle formation on molecular level from oxidation to clusters and stable aerosol particles. To reach these goals, targeted laboratory and field experiments together with long term field measurements will be performed employing the state-of-the-art instrumentation developed.
Principal outcomes of this project include i) new experimental methods and techniques vital for atmospheric research and a deep understanding of ii) oxidation pathways producing aerosol particle precursors, iii) the initial molecular steps of new particle formation and iv) mechanisms of growth of freshly formed clusters toward larger sizes, particularly in the crucial size range of a few nanometers. The conceptual understanding obtained during this project will open multiple new research horizons from oxidation chemistry to Earth system modeling.
Summary
Atmospheric aerosol particles impact Earth’s climate, by directly scattering sunlight and indirectly by affecting cloud properties. The largest uncertainties in climate change projections are associated with the atmospheric aerosol system that has been altered by anthropogenic activities. A major source of that uncertainty involves the formation of secondary particles and cloud condensation nuclei from natural and anthropogenic emissions of volatile compounds. This research challenge persists despite significant efforts within recent decades.
I will build a research group that aims to resolve the atmospheric oxidation processes that convert volatile trace gases to particle precursor vapours, clusters and new aerosol particles. We will create novel measurement techniques and utilize the tremendous potential of mass spectrometry for detection of i) particle precursor vapours ii) oxidants, both conventional but also recently discovered stabilized Criegee intermediates, and, most importantly, iii) newly formed clusters. These methods and instrumentation will be applied for resolving the initial steps of new particle formation on molecular level from oxidation to clusters and stable aerosol particles. To reach these goals, targeted laboratory and field experiments together with long term field measurements will be performed employing the state-of-the-art instrumentation developed.
Principal outcomes of this project include i) new experimental methods and techniques vital for atmospheric research and a deep understanding of ii) oxidation pathways producing aerosol particle precursors, iii) the initial molecular steps of new particle formation and iv) mechanisms of growth of freshly formed clusters toward larger sizes, particularly in the crucial size range of a few nanometers. The conceptual understanding obtained during this project will open multiple new research horizons from oxidation chemistry to Earth system modeling.
Max ERC Funding
1 953 790 €
Duration
Start date: 2017-02-01, End date: 2022-01-31
Project acronym GLOBALVISION
Project Global Optimization Methods in Computer Vision, Pattern Recognition and Medical Imaging
Researcher (PI) Fredrik Kahl
Host Institution (HI) LUNDS UNIVERSITET
Call Details Starting Grant (StG), PE5, ERC-2007-StG
Summary Computer vision concerns itself with understanding the real world through the analysis of images. Typical problems are object recognition, medical image segmentation, geometric reconstruction problems and navigation of autonomous vehicles. Such problems often lead to complicated optimization problems with a mixture of discrete and continuous variables, or even infinite dimensional variables in terms of curves and surfaces. Today, state-of-the-art in solving these problems generally relies on heuristic methods that generate only local optima of various qualities. During the last few years, work by the applicant, co-workers, and others has opened new possibilities. This research project builds on this. We will in this project focus on developing new global optimization methods for computing high-quality solutions for a broad class of problems. A guiding principle will be to relax the original, complicated problem to an approximate, simpler one to which globally optimal solutions can more easily be computed. Technically, this relaxed problem often is convex. A crucial point in this approach is to estimate the quality of the exact solution of the approximate problem compared to the (unknown) global optimum of the original problem. Preliminary results have been well received by the research community and we now wish to extend this work to more difficult and more general problem settings, resulting in thorough re-examination of algorithms used widely in different and trans-disciplinary fields. This project is to be considered as a basic research project with relevance to industry. The expected outcome is new knowledge spread to a wide community through scientific papers published at international journals and conferences as well as publicly available software.
Summary
Computer vision concerns itself with understanding the real world through the analysis of images. Typical problems are object recognition, medical image segmentation, geometric reconstruction problems and navigation of autonomous vehicles. Such problems often lead to complicated optimization problems with a mixture of discrete and continuous variables, or even infinite dimensional variables in terms of curves and surfaces. Today, state-of-the-art in solving these problems generally relies on heuristic methods that generate only local optima of various qualities. During the last few years, work by the applicant, co-workers, and others has opened new possibilities. This research project builds on this. We will in this project focus on developing new global optimization methods for computing high-quality solutions for a broad class of problems. A guiding principle will be to relax the original, complicated problem to an approximate, simpler one to which globally optimal solutions can more easily be computed. Technically, this relaxed problem often is convex. A crucial point in this approach is to estimate the quality of the exact solution of the approximate problem compared to the (unknown) global optimum of the original problem. Preliminary results have been well received by the research community and we now wish to extend this work to more difficult and more general problem settings, resulting in thorough re-examination of algorithms used widely in different and trans-disciplinary fields. This project is to be considered as a basic research project with relevance to industry. The expected outcome is new knowledge spread to a wide community through scientific papers published at international journals and conferences as well as publicly available software.
Max ERC Funding
1 440 000 €
Duration
Start date: 2008-07-01, End date: 2013-06-30
Project acronym GRINDOOR
Project Green Nanotechnology for the Indoor Environment
Researcher (PI) Claes-Göran Sture Granqvist
Host Institution (HI) UPPSALA UNIVERSITET
Call Details Advanced Grant (AdG), PE5, ERC-2010-AdG_20100224
Summary The GRINDOOR project aims at developing and implementing new materials that enable huge energy savings in buildings and improve the quality of the indoor environment. About 40% of the primary energy, and 70% of the electricity, is used in buildings, and therefore the outcome of this project can have an impact on the long-term energy demand in the EU and the World. It is a highly focused study on new nanomaterials based on some transition metal oxides, which are used for four interrelated applications related to indoor lighting and indoor air: (i) electrochromic coatings are integrated in devices and used in “smart windows” to regulate the inflow of visible light and solar energy in order to minimize air condition and create indoor comfort, (ii) thermochromic nanoparticulate coatings are used on windows to provide large temperature-dependent control of the inflow of infrared solar radiation (in stand-alone cases as well as in conjunction with electrochromics), (iii) oxide-based gas sensors are used to measure indoor air quality especially with regard to formaldehyde, and (iv) photocatalytic coatings are used for indoor air cleaning. The investigated materials have many things in common and a joint and focused study, such as the one proposed here, will generate important new knowledge that can be transferred between the various sub-projects. The new oxide materials are prepared by advanced reactive gas deposition—using unique equipment—and high-pressure reactive dc magnetron sputtering. The materials are characterized and investigated by a wide range of state-of-the-art techniques.
Summary
The GRINDOOR project aims at developing and implementing new materials that enable huge energy savings in buildings and improve the quality of the indoor environment. About 40% of the primary energy, and 70% of the electricity, is used in buildings, and therefore the outcome of this project can have an impact on the long-term energy demand in the EU and the World. It is a highly focused study on new nanomaterials based on some transition metal oxides, which are used for four interrelated applications related to indoor lighting and indoor air: (i) electrochromic coatings are integrated in devices and used in “smart windows” to regulate the inflow of visible light and solar energy in order to minimize air condition and create indoor comfort, (ii) thermochromic nanoparticulate coatings are used on windows to provide large temperature-dependent control of the inflow of infrared solar radiation (in stand-alone cases as well as in conjunction with electrochromics), (iii) oxide-based gas sensors are used to measure indoor air quality especially with regard to formaldehyde, and (iv) photocatalytic coatings are used for indoor air cleaning. The investigated materials have many things in common and a joint and focused study, such as the one proposed here, will generate important new knowledge that can be transferred between the various sub-projects. The new oxide materials are prepared by advanced reactive gas deposition—using unique equipment—and high-pressure reactive dc magnetron sputtering. The materials are characterized and investigated by a wide range of state-of-the-art techniques.
Max ERC Funding
2 328 726 €
Duration
Start date: 2011-06-01, End date: 2016-05-31
Project acronym highECS
Project Reining in the upper bound on Earth’s Climate Sensitivities
Researcher (PI) Thorsten MAURITSEN
Host Institution (HI) STOCKHOLMS UNIVERSITET
Call Details Consolidator Grant (CoG), PE10, ERC-2017-COG
Summary One of the greatest recent advances in climate science is that it is now beyond reasonable doubt that human activity is warming the Earth. The next natural question is by how much the Earth will warm for a given emission – a quantity that will be essential to regulating global warming. Yet, the likely range of 1.5-4.5 K for equilibrium climate sensitivity (ECS) for a doubling of the atmospheric CO2 concentration has not been reduced for decades. In particular the risk of ECS being high is concerning, but also represents a scientifically intriguing challenge.
In this project I will conduct unconventional and innovative research designed to limit the upper bound of ECS: I will confront leading hypotheses of extreme cloud feedbacks – the primary potential source of a high ECS – with observations from the full instrumental- and satellite records, and proxies from warm- and cold past climates. I will investigate how ocean- and atmospheric circulations impact cloud feedbacks, and seek the limits for how much past greenhouse warming could have been masked by aerosol cooling.
The highECS project builds on my developments of climate modeling, diagnostics and statistical methods, the strengths of the host institution and developments in national and international projects. The effort is timely in that the World Climate Research Programme (WCRP) has identified uncertainty in ECS as one of the grand challenges of climate science, while the capacity to observe ongoing climate change, key cloud processes, extracting new proxy evidence of past change and computing power is greater than ever before.
If successful in my objective of reining in the upper bound on climate sensitivity this will be a major breakthrough upon a nearly 40-year scientific deadlock and reduce the risk of catastrophic climate change – if not, it will indicate that extreme policy measures may be needed to curb future global warming. Either way, the economic value of knowing is tremendous.
Summary
One of the greatest recent advances in climate science is that it is now beyond reasonable doubt that human activity is warming the Earth. The next natural question is by how much the Earth will warm for a given emission – a quantity that will be essential to regulating global warming. Yet, the likely range of 1.5-4.5 K for equilibrium climate sensitivity (ECS) for a doubling of the atmospheric CO2 concentration has not been reduced for decades. In particular the risk of ECS being high is concerning, but also represents a scientifically intriguing challenge.
In this project I will conduct unconventional and innovative research designed to limit the upper bound of ECS: I will confront leading hypotheses of extreme cloud feedbacks – the primary potential source of a high ECS – with observations from the full instrumental- and satellite records, and proxies from warm- and cold past climates. I will investigate how ocean- and atmospheric circulations impact cloud feedbacks, and seek the limits for how much past greenhouse warming could have been masked by aerosol cooling.
The highECS project builds on my developments of climate modeling, diagnostics and statistical methods, the strengths of the host institution and developments in national and international projects. The effort is timely in that the World Climate Research Programme (WCRP) has identified uncertainty in ECS as one of the grand challenges of climate science, while the capacity to observe ongoing climate change, key cloud processes, extracting new proxy evidence of past change and computing power is greater than ever before.
If successful in my objective of reining in the upper bound on climate sensitivity this will be a major breakthrough upon a nearly 40-year scientific deadlock and reduce the risk of catastrophic climate change – if not, it will indicate that extreme policy measures may be needed to curb future global warming. Either way, the economic value of knowing is tremendous.
Max ERC Funding
1 998 654 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym HYDROCARB
Project Towards a new understanding of carbon processing in freshwaters: methane emission hot spots and carbon burial
Researcher (PI) Sebastian Sobek
Host Institution (HI) UPPSALA UNIVERSITET
Call Details Starting Grant (StG), PE10, ERC-2013-StG
Summary In spite of their small areal extent, inland waters play a vital role in the carbon cycle of the continents, as they emit significant amounts of the greenhouse gases (GHG) carbon dioxide (CO2) and methane (CH4) to the atmosphere, and simultaneously bury more organic carbon (OC) in their sediments than the entire ocean. Particularly in tropical hydropower reservoirs, GHG emissions can be large, mainly owing to high CH4 emission. Moreover, the number of tropical hydropower reservoirs will continue to increase dramatically, due to an urgent need for economic growth and a vast unused hydropower potential in many tropical countries. However, the current understanding of the magnitude of GHG emission, and of the processes regulating it, is insufficient. Here I propose a research program on tropical reservoirs in Brazil that takes advantage of recent developments in both concepts and methodologies to provide unique evaluations of GHG emission and OC burial in tropical reservoirs. In particular, I will test the following hypotheses: 1) Current estimates of reservoir CH4 emission are at least one order of magnitude too low, since they have completely missed the recently discovered existence of gas bubble emission hot spots; 2) The burial of land-derived OC in reservoir sediments offsets a significant share of the GHG emissions; and 3) The sustained, long-term CH4 emission from reservoirs is to a large degree fuelled by primary production of new OC within the reservoir, and may therefore be reduced by management of nutrient supply. The new understanding and the cross-disciplinary methodological approach will constitute a major advance to aquatic science in general, and have strong impacts on the understanding of other aquatic systems at other latitudes as well. In addition, the results will be merged into an existing reservoir GHG risk assessment tool to improve planning, design, management and judgment of hydropower reservoirs.
Summary
In spite of their small areal extent, inland waters play a vital role in the carbon cycle of the continents, as they emit significant amounts of the greenhouse gases (GHG) carbon dioxide (CO2) and methane (CH4) to the atmosphere, and simultaneously bury more organic carbon (OC) in their sediments than the entire ocean. Particularly in tropical hydropower reservoirs, GHG emissions can be large, mainly owing to high CH4 emission. Moreover, the number of tropical hydropower reservoirs will continue to increase dramatically, due to an urgent need for economic growth and a vast unused hydropower potential in many tropical countries. However, the current understanding of the magnitude of GHG emission, and of the processes regulating it, is insufficient. Here I propose a research program on tropical reservoirs in Brazil that takes advantage of recent developments in both concepts and methodologies to provide unique evaluations of GHG emission and OC burial in tropical reservoirs. In particular, I will test the following hypotheses: 1) Current estimates of reservoir CH4 emission are at least one order of magnitude too low, since they have completely missed the recently discovered existence of gas bubble emission hot spots; 2) The burial of land-derived OC in reservoir sediments offsets a significant share of the GHG emissions; and 3) The sustained, long-term CH4 emission from reservoirs is to a large degree fuelled by primary production of new OC within the reservoir, and may therefore be reduced by management of nutrient supply. The new understanding and the cross-disciplinary methodological approach will constitute a major advance to aquatic science in general, and have strong impacts on the understanding of other aquatic systems at other latitudes as well. In addition, the results will be merged into an existing reservoir GHG risk assessment tool to improve planning, design, management and judgment of hydropower reservoirs.
Max ERC Funding
1 798 227 €
Duration
Start date: 2013-09-01, End date: 2019-08-31
Project acronym ISOBOREAL
Project Towards Understanding the Impact of Climate Change on Eurasian Boreal Forests: a Novel Stable Isotope Approach
Researcher (PI) Katja Teresa RINNE-GARMSTON
Host Institution (HI) LUONNONVARAKESKUS
Call Details Starting Grant (StG), PE10, ERC-2017-STG
Summary The vast boreal forests play a critical role in the carbon cycle. As a consequence of increasing temperature and atmospheric CO2, forest growth and subsequently carbon sequestration may be strongly affected. It is thus crucial to understand and predict the consequences of climate change on these ecosystems. Stable isotope analysis of tree rings represents a versatile archive where the effects of environmental changes are recorded. The main goal of the project is to obtain a better understanding of δ13C and δ18O in tree rings that can be used to infer the response of forests to climate change. The goal is achieved by a detailed analysis of the incorporation and fractionation of isotopes in trees using four novel methods: (1) We will measure compound-specific δ13C and δ18O of leaf sugars and (2) combine these with intra-annual δ13C and δ18O analysis of tree rings. The approaches are enabled by methodological developments made by me and ISOBOREAL collaborators (Rinne et al. 2012, Lehmann et al. 2016, Loader et al. in prep.). Our aim is to determine δ13C and δ18O dynamics of individual sugars in response to climatic and physiological factors, and to define how these signals are altered before being stored in tree rings. The improved mechanistic understanding will be applied on tree ring isotope chronologies to infer the response of the studied forests to climate change. (3) The fact that δ18O in tree rings is a mixture of source and leaf water signals is a major problem for its application on climate studies. To solve this we aim to separate the two signals using position-specific δ18O analysis on tree ring cellulose for the first time, which we will achieve by developing novel methods. (4) We will for the first time link the climate signal both in leaf sugars and annual rings with measured ecosystem exchange of greenhouse gases CO2 and H2O using eddy-covariance techniques.
Summary
The vast boreal forests play a critical role in the carbon cycle. As a consequence of increasing temperature and atmospheric CO2, forest growth and subsequently carbon sequestration may be strongly affected. It is thus crucial to understand and predict the consequences of climate change on these ecosystems. Stable isotope analysis of tree rings represents a versatile archive where the effects of environmental changes are recorded. The main goal of the project is to obtain a better understanding of δ13C and δ18O in tree rings that can be used to infer the response of forests to climate change. The goal is achieved by a detailed analysis of the incorporation and fractionation of isotopes in trees using four novel methods: (1) We will measure compound-specific δ13C and δ18O of leaf sugars and (2) combine these with intra-annual δ13C and δ18O analysis of tree rings. The approaches are enabled by methodological developments made by me and ISOBOREAL collaborators (Rinne et al. 2012, Lehmann et al. 2016, Loader et al. in prep.). Our aim is to determine δ13C and δ18O dynamics of individual sugars in response to climatic and physiological factors, and to define how these signals are altered before being stored in tree rings. The improved mechanistic understanding will be applied on tree ring isotope chronologies to infer the response of the studied forests to climate change. (3) The fact that δ18O in tree rings is a mixture of source and leaf water signals is a major problem for its application on climate studies. To solve this we aim to separate the two signals using position-specific δ18O analysis on tree ring cellulose for the first time, which we will achieve by developing novel methods. (4) We will for the first time link the climate signal both in leaf sugars and annual rings with measured ecosystem exchange of greenhouse gases CO2 and H2O using eddy-covariance techniques.
Max ERC Funding
1 814 610 €
Duration
Start date: 2018-01-01, End date: 2022-12-31
Project acronym LAYERENG-HYBMAT
Project Molecular-Layer-Engineered Inorganic-Organic Hybrid Materials
Researcher (PI) Maarit Johanna Karppinen
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Call Details Advanced Grant (AdG), PE5, ERC-2013-ADG
Summary "On-demand-designed and precision-synthesized multicomponent or hybrid materials with unorthodox combinations of properties are potential keys to fascinating next-generation devices. At the same time there is a strong scientific desire to create a comprehensive repertory of basic understanding, design strategies and experimental tools to construct such outstanding smart materials from different building blocks and to shape them into sophisticated hierarchical architectures.
In LAYERENG-HYBMAT I propose a fundamentally new category of nanocomposite materials, that is, layer-by-layer grown coherent inorganic-organic hybrid materials where the cohesion between the layers is based on covalent bonding. Such materials are – once carefully designed and fabricated – able to display in a single material a tailored combination of properties of conventional inorganics and organics, and even beyond. The core hypothesis is that such intimately fused outstanding hybrids are materialized in a simple but extremely elegant manner by mimicking the state-of-the-art thin-film technology, i.e. ALD (atomic layer deposition), originally developed for purely inorganic thin films. The proposed method combines ALD and MLD (molecular layer deposition) cycles and enables the layer-by-layer deposition of coherent inorganic-organic thin films and coatings through sequential self-limiting gas-surface reactions with high precision for the composition and polymer-chain dispersity. With additional nanostructuring capacity these materials have the potential to open up new horizons in electronics, photonics, thermoelectrics, diagnostics, packaging, etc.
The project builds on my long experience in frontier new-material research on other types of multilayered materials and successful proof-of-the-concept ALD/MLD experiments, and addresses all the fundamental aspects of new-material design, modelling, precision synthesis, property tailoring and function characterization."
Summary
"On-demand-designed and precision-synthesized multicomponent or hybrid materials with unorthodox combinations of properties are potential keys to fascinating next-generation devices. At the same time there is a strong scientific desire to create a comprehensive repertory of basic understanding, design strategies and experimental tools to construct such outstanding smart materials from different building blocks and to shape them into sophisticated hierarchical architectures.
In LAYERENG-HYBMAT I propose a fundamentally new category of nanocomposite materials, that is, layer-by-layer grown coherent inorganic-organic hybrid materials where the cohesion between the layers is based on covalent bonding. Such materials are – once carefully designed and fabricated – able to display in a single material a tailored combination of properties of conventional inorganics and organics, and even beyond. The core hypothesis is that such intimately fused outstanding hybrids are materialized in a simple but extremely elegant manner by mimicking the state-of-the-art thin-film technology, i.e. ALD (atomic layer deposition), originally developed for purely inorganic thin films. The proposed method combines ALD and MLD (molecular layer deposition) cycles and enables the layer-by-layer deposition of coherent inorganic-organic thin films and coatings through sequential self-limiting gas-surface reactions with high precision for the composition and polymer-chain dispersity. With additional nanostructuring capacity these materials have the potential to open up new horizons in electronics, photonics, thermoelectrics, diagnostics, packaging, etc.
The project builds on my long experience in frontier new-material research on other types of multilayered materials and successful proof-of-the-concept ALD/MLD experiments, and addresses all the fundamental aspects of new-material design, modelling, precision synthesis, property tailoring and function characterization."
Max ERC Funding
2 358 102 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym MEMETRE
Project From processes to modelling of methane emissions from trees
Researcher (PI) Mari PIHLATIE
Host Institution (HI) HELSINGIN YLIOPISTO
Call Details Starting Grant (StG), PE10, ERC-2017-STG
Summary Atmospheric concentration of the strong greenhouse gas methane (CH4) is rising with an increased annual growth rate. Biosphere has an important role in the global CH4 budget, but high uncertainties remain in the strength of its different sink and source components. Among the natural sources, the contribution of vegetation to the global CH4 budget is the least well understood. Role of trees to the CH4 budget of forest ecosystems has long been overlooked due to the perception that trees do not play a role in the CH4 dynamics. Methanogenic Archaea were long considered as the sole CH4 producing organisms, while new findings of aerobic CH4 production in terrestrial vegetation and in fungi show our incomplete understanding of the CH4 cycling processes. Enclosure measurements from trees reveal that trees can emit CH4 and may substantially contribute to the net CH4 exchange of forests.
The main aim of MEMETRE project is to raise the process-based understanding of CH4 exchange in boreal and temperate forests to the level where we can construct a sound process model for the soil-tree-atmosphere CH4 exchange. We will achieve this by novel laboratory and field experiment focusing on newly identified processes, quantifying CH4 fluxes, seasonal and daily variability and drivers of CH4 at leaf-level, tree and ecosystem level. We use novel CH4 flux measurement techniques to identify the roles of fungal and methanogenic production and transport mechanisms to the CH4 emission from trees, and we synthesize the experimental work to build a process model including CH4 exchange processes within trees and the soil, transport of CH4 between the soil and the trees, and transport of CH4 within the trees. The project will revolutionize our understanding of CH4 flux dynamics in forest ecosystems. It will significantly narrow down the high uncertainties in boreal and temperate forests for their contribution to the global CH4 budget.
Summary
Atmospheric concentration of the strong greenhouse gas methane (CH4) is rising with an increased annual growth rate. Biosphere has an important role in the global CH4 budget, but high uncertainties remain in the strength of its different sink and source components. Among the natural sources, the contribution of vegetation to the global CH4 budget is the least well understood. Role of trees to the CH4 budget of forest ecosystems has long been overlooked due to the perception that trees do not play a role in the CH4 dynamics. Methanogenic Archaea were long considered as the sole CH4 producing organisms, while new findings of aerobic CH4 production in terrestrial vegetation and in fungi show our incomplete understanding of the CH4 cycling processes. Enclosure measurements from trees reveal that trees can emit CH4 and may substantially contribute to the net CH4 exchange of forests.
The main aim of MEMETRE project is to raise the process-based understanding of CH4 exchange in boreal and temperate forests to the level where we can construct a sound process model for the soil-tree-atmosphere CH4 exchange. We will achieve this by novel laboratory and field experiment focusing on newly identified processes, quantifying CH4 fluxes, seasonal and daily variability and drivers of CH4 at leaf-level, tree and ecosystem level. We use novel CH4 flux measurement techniques to identify the roles of fungal and methanogenic production and transport mechanisms to the CH4 emission from trees, and we synthesize the experimental work to build a process model including CH4 exchange processes within trees and the soil, transport of CH4 between the soil and the trees, and transport of CH4 within the trees. The project will revolutionize our understanding of CH4 flux dynamics in forest ecosystems. It will significantly narrow down the high uncertainties in boreal and temperate forests for their contribution to the global CH4 budget.
Max ERC Funding
1 908 652 €
Duration
Start date: 2018-02-01, End date: 2023-01-31
Project acronym METLAKE
Project Predicting future methane fluxes from Northern lakes
Researcher (PI) DAVID TORBJORN EMANUEL BASTVIKEN
Host Institution (HI) LINKOPINGS UNIVERSITET
Call Details Consolidator Grant (CoG), PE10, ERC-2016-COG
Summary The new global temperature goal calls for reliable quantification of present and future greenhouse gas (GHG) emissions, including climate feedbacks. Non-CO2 GHGs, with methane (CH4) being the most important, represent a large but highly uncertain component in global GHG budget. Lakes are among the largest natural sources of CH4 but our understanding of lake CH4 fluxes is rudimentary. Lake emissions are not yet routinely monitored, and coherent, spatially representative, long-term datasets are rare which hamper accurate flux estimates and predictions.
METLAKE aims to improve our ability to quantify and predict lake CH4 emissions. Major goals include: (1) the development of robust validated predictive models suitable for use at the lake rich northern latitudes where large climate changes are anticipated in the near future, (2) the testing of the idea that appropriate consideration of spatiotemporal scaling can greatly facilitate generation of accurate yet simple predictive models, (3) to reveal and quantify detailed flux regulation patterns including spatiotemporal interactions and response times to environmental change, and (4) to pioneer novel use of sensor networks and near ground remote sensing with a new hyperspectral CH4 camera suitable for large-scale high resolution CH4 measurements.
Extensive field work based on optimized state-of-the-art approaches will generate multi-scale and multi-system data, supplemented by experiments, and evaluated by data analyses and modelling approaches targeting effects of scaling on model performance.
Altogether, METLAKE will advance our understanding of one of the largest natural CH4 sources, and provide us with systematic tools to predict future lake emissions. Such quantification of feedbacks on natural GHG emissions is required to move beyond state-of-the-art regarding global GHG budgets and to estimate the mitigation efforts needed to reach global climate goals.
Summary
The new global temperature goal calls for reliable quantification of present and future greenhouse gas (GHG) emissions, including climate feedbacks. Non-CO2 GHGs, with methane (CH4) being the most important, represent a large but highly uncertain component in global GHG budget. Lakes are among the largest natural sources of CH4 but our understanding of lake CH4 fluxes is rudimentary. Lake emissions are not yet routinely monitored, and coherent, spatially representative, long-term datasets are rare which hamper accurate flux estimates and predictions.
METLAKE aims to improve our ability to quantify and predict lake CH4 emissions. Major goals include: (1) the development of robust validated predictive models suitable for use at the lake rich northern latitudes where large climate changes are anticipated in the near future, (2) the testing of the idea that appropriate consideration of spatiotemporal scaling can greatly facilitate generation of accurate yet simple predictive models, (3) to reveal and quantify detailed flux regulation patterns including spatiotemporal interactions and response times to environmental change, and (4) to pioneer novel use of sensor networks and near ground remote sensing with a new hyperspectral CH4 camera suitable for large-scale high resolution CH4 measurements.
Extensive field work based on optimized state-of-the-art approaches will generate multi-scale and multi-system data, supplemented by experiments, and evaluated by data analyses and modelling approaches targeting effects of scaling on model performance.
Altogether, METLAKE will advance our understanding of one of the largest natural CH4 sources, and provide us with systematic tools to predict future lake emissions. Such quantification of feedbacks on natural GHG emissions is required to move beyond state-of-the-art regarding global GHG budgets and to estimate the mitigation efforts needed to reach global climate goals.
Max ERC Funding
2 000 000 €
Duration
Start date: 2017-04-01, End date: 2022-03-31
Project acronym MIMEFUN
Project Biomimetics for Functions and Responses
Researcher (PI) Olli Tapio Ikkala
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Call Details Advanced Grant (AdG), PE5, ERC-2011-ADG_20110209
Summary Energy efficiency and sustainability encourage to develop lightweight materials with excellent mechanical properties, combining also additional functionalities and responses. Therein nature allows inspiration, as e.g. pearl of nacre and silk show extraordinary mechanical properties due to their aligned self-assemblies. However, biological complexity poses great challenges and in biomimetics selected features are mimicked using simpler concepts. Previously artificial nacre has been mimicked by multilayer and sequential techniques and ice-templating. However, concepts for aligned spontaneous self-assemblies are called for scalability. We will develop toughened nacre-inspired materials by templating functionalized polymers on colloidal sheets in suspension, followed by self-assembly by solvent removal. Similarly, we will develop silk-mimetic materials using aligned organic fibrous reinforcements in soft dissipative matrix. Nanofibrillated cellulose will be wet-spun using extrusion into coagulant bath, followed by post drawing, drying and functionalization to allow silk-like fibers with high mechanical properties. In another route, cellulose rod-like whiskers will be decorated with soft functional polymers allowing energy dissipation, followed by alignment and interlinking to mimick silk-assemblies. The colloidal routes allow also new functionalities by using functional polymers, e.g. electroactive and conjugated polymers and nanoparticles. Importantly, redox-active polymers are bound on the colloidal sheets. Incorporating in a planar electrochemical cell with flexible electrodes, electrochemical switching of stiffness is obtained using a small voltage, as the intercolloidal interaction is controlled by the charge state of the redox-active layers. This would allow a new class of material, eg. to interface users and devices. In summary, we present a colloidal self-assembly platform for biomimetic materials with exciting mechanical, functional, and switching properties.
Summary
Energy efficiency and sustainability encourage to develop lightweight materials with excellent mechanical properties, combining also additional functionalities and responses. Therein nature allows inspiration, as e.g. pearl of nacre and silk show extraordinary mechanical properties due to their aligned self-assemblies. However, biological complexity poses great challenges and in biomimetics selected features are mimicked using simpler concepts. Previously artificial nacre has been mimicked by multilayer and sequential techniques and ice-templating. However, concepts for aligned spontaneous self-assemblies are called for scalability. We will develop toughened nacre-inspired materials by templating functionalized polymers on colloidal sheets in suspension, followed by self-assembly by solvent removal. Similarly, we will develop silk-mimetic materials using aligned organic fibrous reinforcements in soft dissipative matrix. Nanofibrillated cellulose will be wet-spun using extrusion into coagulant bath, followed by post drawing, drying and functionalization to allow silk-like fibers with high mechanical properties. In another route, cellulose rod-like whiskers will be decorated with soft functional polymers allowing energy dissipation, followed by alignment and interlinking to mimick silk-assemblies. The colloidal routes allow also new functionalities by using functional polymers, e.g. electroactive and conjugated polymers and nanoparticles. Importantly, redox-active polymers are bound on the colloidal sheets. Incorporating in a planar electrochemical cell with flexible electrodes, electrochemical switching of stiffness is obtained using a small voltage, as the intercolloidal interaction is controlled by the charge state of the redox-active layers. This would allow a new class of material, eg. to interface users and devices. In summary, we present a colloidal self-assembly platform for biomimetic materials with exciting mechanical, functional, and switching properties.
Max ERC Funding
2 296 320 €
Duration
Start date: 2012-04-01, End date: 2017-03-31
Project acronym MOFcat
Project Fundamental and Applied Science on Molecular Redox-Catalysts of Energy Relevance in Metal-Organic Frameworks
Researcher (PI) Sascha Ott
Host Institution (HI) UPPSALA UNIVERSITET
Call Details Consolidator Grant (CoG), PE5, ERC-2015-CoG
Summary Organometallic redox-catalysts of energy relevance, i.e. water and hydrogen oxidation, and proton and carbon dioxide reduction catalysts, will be incorporated into metal-organic frameworks (MOFs). Immobilization and spatial organization of the molecular catalysts will stabilize their molecular integrity and ensure longevity and recyclability of the resulting MOFcats. The organized environment provided by the MOF will enable the control of conformational flexibility, diffusion, charge transport, and higher coordination sphere effects that play crucial roles in enzymes, but cannot be addressed in homogenous solution and are thus largely unexplored. The effect that the MOF environment has on catalysis will be directly probed electrochemically in MOFcats that are immobilized or grown on electrode surfaces. In combination with spectroscopic techniques in spectroelectrochemical cells, intermediates in the catalytic cycles will be detected and characterized. Kinetic information of the individual steps in the catalytic cycles will be obtained in MOFs that contain both a molecular photosensitizer (PS) and a molecular catalyst (PS-MOFcats). The envisaged systems will allow light-induced electron transfer processes to generate reduced or oxidized catalyst states the reactivity of which will be studied with high time resolution by transient UV/Vis and IR spectroscopy. The acquired fundamental mechanistic knowledge is far beyond the current state-of-the-art in MOF chemistry and catalysis, and will be used to prepare MOFcat-based electrodes that function at highest possible rates and lowest overpotentials. PS-MOFcats will be grown on flat semiconductor surfaces, and explored as a novel concept to photoanode and -cathode designs for dye-sensitized solar fuel devices (DSSFDs). The design is particularly appealing as it accommodates high PS concentrations for efficient light-harvesting, while providing potent catalysts close to the solvent interface.
Summary
Organometallic redox-catalysts of energy relevance, i.e. water and hydrogen oxidation, and proton and carbon dioxide reduction catalysts, will be incorporated into metal-organic frameworks (MOFs). Immobilization and spatial organization of the molecular catalysts will stabilize their molecular integrity and ensure longevity and recyclability of the resulting MOFcats. The organized environment provided by the MOF will enable the control of conformational flexibility, diffusion, charge transport, and higher coordination sphere effects that play crucial roles in enzymes, but cannot be addressed in homogenous solution and are thus largely unexplored. The effect that the MOF environment has on catalysis will be directly probed electrochemically in MOFcats that are immobilized or grown on electrode surfaces. In combination with spectroscopic techniques in spectroelectrochemical cells, intermediates in the catalytic cycles will be detected and characterized. Kinetic information of the individual steps in the catalytic cycles will be obtained in MOFs that contain both a molecular photosensitizer (PS) and a molecular catalyst (PS-MOFcats). The envisaged systems will allow light-induced electron transfer processes to generate reduced or oxidized catalyst states the reactivity of which will be studied with high time resolution by transient UV/Vis and IR spectroscopy. The acquired fundamental mechanistic knowledge is far beyond the current state-of-the-art in MOF chemistry and catalysis, and will be used to prepare MOFcat-based electrodes that function at highest possible rates and lowest overpotentials. PS-MOFcats will be grown on flat semiconductor surfaces, and explored as a novel concept to photoanode and -cathode designs for dye-sensitized solar fuel devices (DSSFDs). The design is particularly appealing as it accommodates high PS concentrations for efficient light-harvesting, while providing potent catalysts close to the solvent interface.
Max ERC Funding
1 968 750 €
Duration
Start date: 2017-01-01, End date: 2021-12-31
Project acronym NanoPokers
Project Deciphering cell heterogeneity in tumors using arrays of nanowires to controllably poke single cells in longitudinal studies
Researcher (PI) Christelle Nathalie Prinz
Host Institution (HI) LUNDS UNIVERSITET
Call Details Consolidator Grant (CoG), PE5, ERC-2015-CoG
Summary Cancer is responsible for 20% of all deaths in Europe. Current cancer research is based on cell ensemble measurements or on snapshot studies of individual cells. However, cancer is a systemic disease, involving many cells that interact and evolve over time in a complex manner, which cell ensemble studies and snapshot studies cannot grasp. It is therefore crucial to investigate cancer at the single cell level and in longitudinal studies (over time). Despite the recent developments in micro- and nanotechnologies, combined with live cell imaging, today, there is no method available that meets the crucial need for global monitoring of individual cell responses to stimuli/perturbation in real-time.
This project addresses this crucial need by combining super resolution live-cell imaging and the development of sensors, as well as injection devices based on vertical nanowire arrays. The devices will penetrate multiple single cells in a fully controlled manner, with minimal invasiveness.
The objectives of the project are:
1) To develop nanowire based-tools in order to gain controlled and reliable access to the cell interior with minimal invasiveness.
2) Developing mRNA sensing and biomolecule injection capabilities based on nanowires.
3) Performing longitudinal single cell studies in tumours, including monitoring gene expression in real time, under controlled cell perturbation.
By enabling global, long term monitoring of individual tumour cells submitted to controlled stimuli, the project will open up new horizons in Biology and in Medical Research. It will enable ground-breaking discoveries in understanding the complexity of molecular events underlying the disease. This cross-disciplinary project will lead to paradigm-shifting research, which will enable the development of optimal treatment strategies. This will be applicable, not only for cancer, but also for a broad range of diseases, such as diabetes and neurodegenerative diseases.
Summary
Cancer is responsible for 20% of all deaths in Europe. Current cancer research is based on cell ensemble measurements or on snapshot studies of individual cells. However, cancer is a systemic disease, involving many cells that interact and evolve over time in a complex manner, which cell ensemble studies and snapshot studies cannot grasp. It is therefore crucial to investigate cancer at the single cell level and in longitudinal studies (over time). Despite the recent developments in micro- and nanotechnologies, combined with live cell imaging, today, there is no method available that meets the crucial need for global monitoring of individual cell responses to stimuli/perturbation in real-time.
This project addresses this crucial need by combining super resolution live-cell imaging and the development of sensors, as well as injection devices based on vertical nanowire arrays. The devices will penetrate multiple single cells in a fully controlled manner, with minimal invasiveness.
The objectives of the project are:
1) To develop nanowire based-tools in order to gain controlled and reliable access to the cell interior with minimal invasiveness.
2) Developing mRNA sensing and biomolecule injection capabilities based on nanowires.
3) Performing longitudinal single cell studies in tumours, including monitoring gene expression in real time, under controlled cell perturbation.
By enabling global, long term monitoring of individual tumour cells submitted to controlled stimuli, the project will open up new horizons in Biology and in Medical Research. It will enable ground-breaking discoveries in understanding the complexity of molecular events underlying the disease. This cross-disciplinary project will lead to paradigm-shifting research, which will enable the development of optimal treatment strategies. This will be applicable, not only for cancer, but also for a broad range of diseases, such as diabetes and neurodegenerative diseases.
Max ERC Funding
2 621 251 €
Duration
Start date: 2016-09-01, End date: 2021-08-31
Project acronym NAPOLI
Project Nanoporous Asymmetric Poly(Ionic Liquid) Membrane
Researcher (PI) Jiayin Yuan
Host Institution (HI) STOCKHOLMS UNIVERSITET
Call Details Starting Grant (StG), PE5, ERC-2014-STG
Summary Nanoporous polymer membranes (NPMs) play a crucial, irreplaceable role in fundamental research and industrial usage, including separation, filtration, water treatment and sustainable environment. The vast majority of advances concentrate on neutral or weakly charged polymers, such as the ongoing interest on self-assembled block copolymer NPMs. There is an urgent need to process polyelectrolytes into NPMs that critically combine a high charge density with nanoporous morphology. Additionally, engineering structural asymmetry/gradient simultaneously in the membrane is equally beneficial, as it would improve membrane performance by building up compartmentalized functionalities. For example, a gradient in pore size forms high pressure resistance coupled with improved selectivity. Nevertheless, developing such highly charged, nanoporous and gradient membranes has remained a challenge, owing to the water solubility and ionic nature of conventional polyelectrolytes, poorly processable into nanoporous state via common routes.
Recently, my group first reported an easy-to-perform production of nanoporous polyelectrolyte membranes. Building on this important but rather preliminary advance, I propose to develop the next generation of NPMs, nanoporous asymmetric poly(ionic liquid) membranes (NAPOLIs). The aim is to produce NAPOLIs bearing diverse gradients, understand the unique transport behavior, improve the membrane stability/sustainability/applicability, and finally apply them in the active fields of energy and environment. Both the currently established route and the newly proposed ones will be employed for the membrane fabrication.
This proposal is inherently interdisciplinary, as it must combine polymer chemistry/engineering, physical chemistry, membrane/materials science, and nanoscience for its success. This research will fundamentally advance nanoporous membrane design for a wide scope of applications and reveal unique physical processes in an asymmetric context.
Summary
Nanoporous polymer membranes (NPMs) play a crucial, irreplaceable role in fundamental research and industrial usage, including separation, filtration, water treatment and sustainable environment. The vast majority of advances concentrate on neutral or weakly charged polymers, such as the ongoing interest on self-assembled block copolymer NPMs. There is an urgent need to process polyelectrolytes into NPMs that critically combine a high charge density with nanoporous morphology. Additionally, engineering structural asymmetry/gradient simultaneously in the membrane is equally beneficial, as it would improve membrane performance by building up compartmentalized functionalities. For example, a gradient in pore size forms high pressure resistance coupled with improved selectivity. Nevertheless, developing such highly charged, nanoporous and gradient membranes has remained a challenge, owing to the water solubility and ionic nature of conventional polyelectrolytes, poorly processable into nanoporous state via common routes.
Recently, my group first reported an easy-to-perform production of nanoporous polyelectrolyte membranes. Building on this important but rather preliminary advance, I propose to develop the next generation of NPMs, nanoporous asymmetric poly(ionic liquid) membranes (NAPOLIs). The aim is to produce NAPOLIs bearing diverse gradients, understand the unique transport behavior, improve the membrane stability/sustainability/applicability, and finally apply them in the active fields of energy and environment. Both the currently established route and the newly proposed ones will be employed for the membrane fabrication.
This proposal is inherently interdisciplinary, as it must combine polymer chemistry/engineering, physical chemistry, membrane/materials science, and nanoscience for its success. This research will fundamentally advance nanoporous membrane design for a wide scope of applications and reveal unique physical processes in an asymmetric context.
Max ERC Funding
1 500 000 €
Duration
Start date: 2015-03-01, End date: 2021-01-31
Project acronym NEWIRES
Project Next Generation Semiconductor Nanowires
Researcher (PI) Kimberly Thelander
Host Institution (HI) LUNDS UNIVERSITET
Call Details Starting Grant (StG), PE5, ERC-2013-StG
Summary Semiconductor nanowires composed of III-V materials have enormous potential to add new functionality to electronics and optical applications. However, integration of these promising structures into applications is severely limited by the current near-universal reliance on gold nanoparticles as seeds for nanowire fabrication. Although highly controlled fabrication is achieved, this metal is entirely incompatible with the Si-based electronics industry. It also presents limitations for the extension of nanowire research towards novel materials not existing in bulk. To date, exploration of alternatives has been limited to selective-area and self-seeded processes, both of which have major limitations in terms of size and morphology control, potential to combine materials, and crystal structure tuning. There is also very little understanding of precisely why gold has proven so successful for nanowire growth, and which alternatives may yield comparable or better results. The aim of this project will be to explore alternative nanoparticle seed materials to go beyond the use of gold in III-V nanowire fabrication. This will be achieved using a unique and recently developed capability for aerosol-phase fabrication of highly controlled nanoparticles directly integrated with conventional nanowire fabrication equipment. The primary goal will be to deepen the understanding of the nanowire fabrication process, and the specific advantages (and limitations) of gold as a seed material, in order to develop and optimize alternatives. The use of a wide variety of seed particle materials in nanowire fabrication will greatly broaden the variety of novel structures that can be fabricated. The results will also transform the nanowire fabrication research field, in order to develop important connections between nanowire research and the semiconductor industry, and to greatly improve the viability of nanowire integration into future devices.
Summary
Semiconductor nanowires composed of III-V materials have enormous potential to add new functionality to electronics and optical applications. However, integration of these promising structures into applications is severely limited by the current near-universal reliance on gold nanoparticles as seeds for nanowire fabrication. Although highly controlled fabrication is achieved, this metal is entirely incompatible with the Si-based electronics industry. It also presents limitations for the extension of nanowire research towards novel materials not existing in bulk. To date, exploration of alternatives has been limited to selective-area and self-seeded processes, both of which have major limitations in terms of size and morphology control, potential to combine materials, and crystal structure tuning. There is also very little understanding of precisely why gold has proven so successful for nanowire growth, and which alternatives may yield comparable or better results. The aim of this project will be to explore alternative nanoparticle seed materials to go beyond the use of gold in III-V nanowire fabrication. This will be achieved using a unique and recently developed capability for aerosol-phase fabrication of highly controlled nanoparticles directly integrated with conventional nanowire fabrication equipment. The primary goal will be to deepen the understanding of the nanowire fabrication process, and the specific advantages (and limitations) of gold as a seed material, in order to develop and optimize alternatives. The use of a wide variety of seed particle materials in nanowire fabrication will greatly broaden the variety of novel structures that can be fabricated. The results will also transform the nanowire fabrication research field, in order to develop important connections between nanowire research and the semiconductor industry, and to greatly improve the viability of nanowire integration into future devices.
Max ERC Funding
1 496 246 €
Duration
Start date: 2013-09-01, End date: 2018-08-31
Project acronym NINA
Project Nitride-based nanostructured novel thermoelectric thin-film materials
Researcher (PI) Per Daniel Eklund
Host Institution (HI) LINKOPINGS UNIVERSITET
Call Details Starting Grant (StG), PE5, ERC-2013-StG
Summary My recent discovery of the anomalously high thermoelectric power factor of ScN thin films demonstrates that unexpected thermoelectric materials can be found among the early transition-metal and rare-earth nitrides. Corroborated by first-principles calculations, we have well-founded hypotheses that these properties stem from nitrogen vacancies, dopants, and alloying, which introduce controllable sharp features with a large slope at the Fermi level, causing a drastically increased Seebeck coefficient. In-depth fundamental studies are needed to enable property tuning and materials design in these systems, to timely exploit my discovery and break new ground.
The project concerns fundamental, primarily experimental, studies on scandium nitride-based and related single-phase and nanostructured films. The overall goal is to understand the complex correlations between electronic, thermal and thermoelectric properties and structural features such as layering, orientation, epitaxy, dopants and lattice defects. Ab initio calculations of band structures, mixing thermodynamics, and properties are integrated with the experimental activities. Novel mechanisms are proposed for drastic reduction of the thermal conductivity with retained high power factor. This will be realized by intentionally introduced secondary phases and artificial nanolaminates; the layering causing discontinuities in the phonon distribution and thus reducing thermal conductivity.
My expertise in thin-film processing and advanced materials characterization places me in a unique position to pursue this novel high-gain approach to thermoelectrics, and an ERC starting grant will be essential in achieving critical mass and consolidating an internationally leading research platform. The scientific impact and vision is in pioneering an understanding of a novel class of thermoelectric materials with potential for thermoelectric devices for widespread use in environmentally friendly energy applications.
Summary
My recent discovery of the anomalously high thermoelectric power factor of ScN thin films demonstrates that unexpected thermoelectric materials can be found among the early transition-metal and rare-earth nitrides. Corroborated by first-principles calculations, we have well-founded hypotheses that these properties stem from nitrogen vacancies, dopants, and alloying, which introduce controllable sharp features with a large slope at the Fermi level, causing a drastically increased Seebeck coefficient. In-depth fundamental studies are needed to enable property tuning and materials design in these systems, to timely exploit my discovery and break new ground.
The project concerns fundamental, primarily experimental, studies on scandium nitride-based and related single-phase and nanostructured films. The overall goal is to understand the complex correlations between electronic, thermal and thermoelectric properties and structural features such as layering, orientation, epitaxy, dopants and lattice defects. Ab initio calculations of band structures, mixing thermodynamics, and properties are integrated with the experimental activities. Novel mechanisms are proposed for drastic reduction of the thermal conductivity with retained high power factor. This will be realized by intentionally introduced secondary phases and artificial nanolaminates; the layering causing discontinuities in the phonon distribution and thus reducing thermal conductivity.
My expertise in thin-film processing and advanced materials characterization places me in a unique position to pursue this novel high-gain approach to thermoelectrics, and an ERC starting grant will be essential in achieving critical mass and consolidating an internationally leading research platform. The scientific impact and vision is in pioneering an understanding of a novel class of thermoelectric materials with potential for thermoelectric devices for widespread use in environmentally friendly energy applications.
Max ERC Funding
1 499 976 €
Duration
Start date: 2013-10-01, End date: 2018-09-30
Project acronym OXLEET
Project Oxidation via low-energy electron transfer. Development of green oxidation methodology via a biomimetic approach
Researcher (PI) Jan Erling Bäckvall
Host Institution (HI) STOCKHOLMS UNIVERSITET
Call Details Advanced Grant (AdG), PE5, ERC-2009-AdG
Summary Oxidation reactions are of fundamental importance in Nature and are key transformation in organic synthesis. There is currently a need from society to replace waste-producing expensive oxidants by environmentally benign oxidants in industrial oxidation reactions. The aim with the proposed research is to develop novel green oxidation methodology that also involves hydrogen transfer reactions. In the oxidation reactions the goal is to use molecular oxygen (air) or hydrogen peroxide as the oxidants. In the present project new catalytic oxidations via low-energy electron transfer will be developed. The catalytic reactions obtained can be used for racemization of alcohols and amines and for oxygen- and hydrogen peroxide-driven oxidations of various substrates. Examples of some reactions that will be studied are oxidative palladium-catalyzed C-C bond formation and metal-catalyzed C-H oxidation including dehydrogenation reactions with iron and ruthenium. Coupled catalytic systems where electron transfer mediators (ETMs) facilitate electron transfer from the reduced catalyst to molecular oxygen (hydrogen peroxide) will be studied. Highly efficient reoxidation systems will be designed by covalently linking two electron transfer mediators (ETMs). The intramolecular electron transfer in these hybrid ETM catalysts will significantly increase the rate of oxidation reactions. The research will lead to development of more efficient reoxidation systems based on molecular oxygen and hydrogen peroxide, as well as more versatile racemization catalysts for alcohols and amines.
Summary
Oxidation reactions are of fundamental importance in Nature and are key transformation in organic synthesis. There is currently a need from society to replace waste-producing expensive oxidants by environmentally benign oxidants in industrial oxidation reactions. The aim with the proposed research is to develop novel green oxidation methodology that also involves hydrogen transfer reactions. In the oxidation reactions the goal is to use molecular oxygen (air) or hydrogen peroxide as the oxidants. In the present project new catalytic oxidations via low-energy electron transfer will be developed. The catalytic reactions obtained can be used for racemization of alcohols and amines and for oxygen- and hydrogen peroxide-driven oxidations of various substrates. Examples of some reactions that will be studied are oxidative palladium-catalyzed C-C bond formation and metal-catalyzed C-H oxidation including dehydrogenation reactions with iron and ruthenium. Coupled catalytic systems where electron transfer mediators (ETMs) facilitate electron transfer from the reduced catalyst to molecular oxygen (hydrogen peroxide) will be studied. Highly efficient reoxidation systems will be designed by covalently linking two electron transfer mediators (ETMs). The intramolecular electron transfer in these hybrid ETM catalysts will significantly increase the rate of oxidation reactions. The research will lead to development of more efficient reoxidation systems based on molecular oxygen and hydrogen peroxide, as well as more versatile racemization catalysts for alcohols and amines.
Max ERC Funding
1 722 000 €
Duration
Start date: 2010-01-01, End date: 2015-12-31
Project acronym PBL-PMES
Project Atmospheric planetary boundary layers: physics, modelling and role in Earth system
Researcher (PI) Sergej Zilitinkevich
Host Institution (HI) ILMATIETEEN LAITOS
Call Details Advanced Grant (AdG), PE10, ERC-2008-AdG
Summary This project aims to systematically revise the planetary-boundary-layer (PBL) physics accounting for the non-local effects of coherent structures (long-lived large eddies especially pronounced in convective PBLs and internal waves in stable PBLs). It focuses on the key physical problems related to the role of PBLs in the Earth system as the atmosphere-land/ocean/biosphere coupling modules: the resistance and heat/mass transfer laws determining the near-surface turbulent fluxes, the entrainment laws determining the fluxes at the PBL outer boundary, the PBL depth equations, and turbulence closures. In this project the first round of revision will be completed, the advanced concepts/models will be empirically validated and employed to develop new PBL parameterization for use in meteorological modelling and analyses of the climate and Earth systems. The new parameterizations and closures will be implemented in state-of-the-art numerical weather prediction, climate, meso-scale and air-pollution models; evaluated through case studies and statistical analyses of the quality of forecasts/simulations; and applied to a range of environmental problems. By this means the project will contribute to better modelling of extreme weather events, heavy air pollution episodes, and fine features of climate change. The new physical concepts and models will be included in the university course and new textbook on PBL physics. This project summarises and further extends our last-decade works in the PBL physics: discovery and the theory of the new PBL types of essentially non-local nature: long-lived stable and conventionally neutral ; quantification of the basic effects of coherent eddies in the shear-free convective PBLs including the non-local heat-transfer law; physical solution to the turbulence cut off problem in the closure models for stable stratification; and discovery of the stability dependences of the roughness length and displacement height.
Summary
This project aims to systematically revise the planetary-boundary-layer (PBL) physics accounting for the non-local effects of coherent structures (long-lived large eddies especially pronounced in convective PBLs and internal waves in stable PBLs). It focuses on the key physical problems related to the role of PBLs in the Earth system as the atmosphere-land/ocean/biosphere coupling modules: the resistance and heat/mass transfer laws determining the near-surface turbulent fluxes, the entrainment laws determining the fluxes at the PBL outer boundary, the PBL depth equations, and turbulence closures. In this project the first round of revision will be completed, the advanced concepts/models will be empirically validated and employed to develop new PBL parameterization for use in meteorological modelling and analyses of the climate and Earth systems. The new parameterizations and closures will be implemented in state-of-the-art numerical weather prediction, climate, meso-scale and air-pollution models; evaluated through case studies and statistical analyses of the quality of forecasts/simulations; and applied to a range of environmental problems. By this means the project will contribute to better modelling of extreme weather events, heavy air pollution episodes, and fine features of climate change. The new physical concepts and models will be included in the university course and new textbook on PBL physics. This project summarises and further extends our last-decade works in the PBL physics: discovery and the theory of the new PBL types of essentially non-local nature: long-lived stable and conventionally neutral ; quantification of the basic effects of coherent eddies in the shear-free convective PBLs including the non-local heat-transfer law; physical solution to the turbulence cut off problem in the closure models for stable stratification; and discovery of the stability dependences of the roughness length and displacement height.
Max ERC Funding
2 390 000 €
Duration
Start date: 2009-01-01, End date: 2013-12-31
Project acronym PHDVIRTA
Project Physically-based Virtual Acoustics
Researcher (PI) Kalle Tapio Lokki
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Call Details Starting Grant (StG), PE5, ERC-2007-StG
Summary The objective of the project is to find new methods for quality evaluation and modeling of room acoustics. Room acoustics has been studied over 100 years, but, e.g., the relation between objective attributes and subjective measures is not fully understood yet. This project will develop novel methods to simulate and auralize sound propagation in rooms, in particular in concert halls. The research is divided into three main topics. First, authentic auralization with physically-based room acoustics modeling methods will be studied. The recently introduced acoustic radiance transfer method is developed further to handle complex reflections from surfaces as well as diffraction. The second research topic is quality evaluation of concert hall acoustics. Novel algorithms will be developed for spatial sound analysis of a large impulse response database. Live recordings will be analyzed to find new objective quality measures. Quality assessments will also be performed subjectively with sensory evaluation methods borrowed from food industry. The third topic is related to augmented reality audio technology, which reveals the potential and richness of emerging technologies, giving a scenario of the possible future personalized mobile audio communications. The results of the project will be widely applicable in the academia, but also in every day life of people all over the world. The new knowledge in room acoustics will help to build acoustically better concert halls and public places such as libraries, shopping malls, etc. The augmented reality audio applications will help and enrich communication between humans. The concert hall acoustics research has great potential to find novel objective and subjective quality metrics. They also help in creation of authentic auralization, which will be one of the main tools for consultants in design, and in particular when explaining design results to architects, clients, and public audience.
Summary
The objective of the project is to find new methods for quality evaluation and modeling of room acoustics. Room acoustics has been studied over 100 years, but, e.g., the relation between objective attributes and subjective measures is not fully understood yet. This project will develop novel methods to simulate and auralize sound propagation in rooms, in particular in concert halls. The research is divided into three main topics. First, authentic auralization with physically-based room acoustics modeling methods will be studied. The recently introduced acoustic radiance transfer method is developed further to handle complex reflections from surfaces as well as diffraction. The second research topic is quality evaluation of concert hall acoustics. Novel algorithms will be developed for spatial sound analysis of a large impulse response database. Live recordings will be analyzed to find new objective quality measures. Quality assessments will also be performed subjectively with sensory evaluation methods borrowed from food industry. The third topic is related to augmented reality audio technology, which reveals the potential and richness of emerging technologies, giving a scenario of the possible future personalized mobile audio communications. The results of the project will be widely applicable in the academia, but also in every day life of people all over the world. The new knowledge in room acoustics will help to build acoustically better concert halls and public places such as libraries, shopping malls, etc. The augmented reality audio applications will help and enrich communication between humans. The concert hall acoustics research has great potential to find novel objective and subjective quality metrics. They also help in creation of authentic auralization, which will be one of the main tools for consultants in design, and in particular when explaining design results to architects, clients, and public audience.
Max ERC Funding
880 224 €
Duration
Start date: 2008-07-01, End date: 2013-06-30
Project acronym QAPPA
Project Quantifying the atmospheric implications of the solid phase and phase transitions of secondary organic aerosols
Researcher (PI) Annele Kirsi Katriina Virtanen
Host Institution (HI) ITA-SUOMEN YLIOPISTO
Call Details Starting Grant (StG), PE10, ERC-2013-StG
Summary In our ground-breaking paper published in Nature we showed, that the atmospheric Secondary Organic Aerosol (SOA) particles formed in boreal forest can be amorphous solid in their physical phase. Our result has already re-directed the SOA related research. In the several follow-up studies, it has been shown that SOA particles generated in the laboratory chamber from different pre-cursors and in various conditions are amorphous solid.
My ultimate task is to quantify the atmospheric implications of the phase state of SOA particles. Solid phase of the particles implies surface-confined chemistry and kinetic vapour uptake limitations because mass transport (diffusion) of reactants within the aerosol particle bulk becomes the rate limiting step. The diffusivity of the molecules in particle bulk depends on the viscosity of the SOA material. Hence, it would be a scientific break-through, if the kinetic limitations or the viscosity of the SOA particles could be estimated since these factors are a key to quantify the atmospheric implications of amorphous solid phase of the particles.
To achieve the final goal of the research, measurement method development is needed as currently there is no method to quantify the viscosity of the SOA particles, or to study the kinetic limitations and surface-confined chemistry caused by the solid phase of nanometer sized SOA particles. The methodology that will be developed in the proposed study, aims ambitiously to quantify the essential factors affecting the atmospheric processes of the SOA particles. The developed methodology will be use in extensive measurement campaigns performed both in SOA chambers and in atmospheric measurement sites in Europe and in US maximising the global significance of the results gained in this study.
The project enables two scientific breakthroughs: 1) the new methodology applicable in the field of nanoparticle research and 2) the quantified atmospheric implications of the amorphous solid phase of particles.
Summary
In our ground-breaking paper published in Nature we showed, that the atmospheric Secondary Organic Aerosol (SOA) particles formed in boreal forest can be amorphous solid in their physical phase. Our result has already re-directed the SOA related research. In the several follow-up studies, it has been shown that SOA particles generated in the laboratory chamber from different pre-cursors and in various conditions are amorphous solid.
My ultimate task is to quantify the atmospheric implications of the phase state of SOA particles. Solid phase of the particles implies surface-confined chemistry and kinetic vapour uptake limitations because mass transport (diffusion) of reactants within the aerosol particle bulk becomes the rate limiting step. The diffusivity of the molecules in particle bulk depends on the viscosity of the SOA material. Hence, it would be a scientific break-through, if the kinetic limitations or the viscosity of the SOA particles could be estimated since these factors are a key to quantify the atmospheric implications of amorphous solid phase of the particles.
To achieve the final goal of the research, measurement method development is needed as currently there is no method to quantify the viscosity of the SOA particles, or to study the kinetic limitations and surface-confined chemistry caused by the solid phase of nanometer sized SOA particles. The methodology that will be developed in the proposed study, aims ambitiously to quantify the essential factors affecting the atmospheric processes of the SOA particles. The developed methodology will be use in extensive measurement campaigns performed both in SOA chambers and in atmospheric measurement sites in Europe and in US maximising the global significance of the results gained in this study.
The project enables two scientific breakthroughs: 1) the new methodology applicable in the field of nanoparticle research and 2) the quantified atmospheric implications of the amorphous solid phase of particles.
Max ERC Funding
1 499 612 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym SHINING
Project Stable and High-Efficiency Perovskite Light-Emitting Diodes
Researcher (PI) Feng GAO
Host Institution (HI) LINKOPINGS UNIVERSITET
Call Details Starting Grant (StG), PE5, ERC-2016-STG
Summary Light-emitting diodes (LEDs), which emit light by a solid-state process called electroluminescence, are considered as the most promising energy-efficient technology for future lighting and display. It has been demonstrated that optimal use of LEDs could significantly reduce the world’s electricity use for lighting from 20% to 4%. However, current LED technologies typically rely on expensive high-vacuum manufacturing processes, hampering their widespread applications. Therefore, it is highly desirable to develop low-cost LEDs based on solution-processed semiconductors.
A superstar in the family of solution-processed semiconductors is metal halide perovskites, which have shown great success in photovoltaic applications during the past few years. The same perovskites can also been applied in LEDs. Despite being at an early stage of development with associated challenges, metal halide perovskites provide great promise as a new generation of materials for low-cost LEDs.
This project aims to develop high-efficiency and stable perovskite LEDs based on solution-processed perovskites. Two different classes of low-dimensional perovskites will be investigated independently. These new perovskites materials will then be coupled with novel interface engineering to fabricate perovskite LEDs with the performance beyond the state of the art. At the core of the research is the synthesis of new perovskite nanostructures, combined with advanced spectroscopic characterization and device development. This project combines recent advances in perovskite optoelectronics and low-dimensional materials to create a new paradigm for perovskite LEDs. This research will also lead to the development of new perovskites materials which will serve future advances in photovoltaics, transistors, lasers, etc.
Summary
Light-emitting diodes (LEDs), which emit light by a solid-state process called electroluminescence, are considered as the most promising energy-efficient technology for future lighting and display. It has been demonstrated that optimal use of LEDs could significantly reduce the world’s electricity use for lighting from 20% to 4%. However, current LED technologies typically rely on expensive high-vacuum manufacturing processes, hampering their widespread applications. Therefore, it is highly desirable to develop low-cost LEDs based on solution-processed semiconductors.
A superstar in the family of solution-processed semiconductors is metal halide perovskites, which have shown great success in photovoltaic applications during the past few years. The same perovskites can also been applied in LEDs. Despite being at an early stage of development with associated challenges, metal halide perovskites provide great promise as a new generation of materials for low-cost LEDs.
This project aims to develop high-efficiency and stable perovskite LEDs based on solution-processed perovskites. Two different classes of low-dimensional perovskites will be investigated independently. These new perovskites materials will then be coupled with novel interface engineering to fabricate perovskite LEDs with the performance beyond the state of the art. At the core of the research is the synthesis of new perovskite nanostructures, combined with advanced spectroscopic characterization and device development. This project combines recent advances in perovskite optoelectronics and low-dimensional materials to create a new paradigm for perovskite LEDs. This research will also lead to the development of new perovskites materials which will serve future advances in photovoltaics, transistors, lasers, etc.
Max ERC Funding
1 499 759 €
Duration
Start date: 2017-03-01, End date: 2022-02-28
Project acronym SIMONE
Project Single Molecule Nano Electronics (SIMONE)
Researcher (PI) Kasper Moth-Poulsen
Host Institution (HI) CHALMERS TEKNISKA HOEGSKOLA AB
Call Details Starting Grant (StG), PE5, ERC-2013-StG
Summary "The development of micro fabrication and field effect transistors are key enabling technologies for todays information society. It is hard to imagine superfast and omnipresent electronic devices, information technology, the Internet and mobile communication technologies without access to continuously cheaper and miniaturized microprocessors. The giant leaps in performance of microprocessors from the first personal computing machines to todays mobile devices are to a large extent realized via miniaturization of the active components. The ultimate limit of miniaturization of electronic components is the realization of single molecule electronics. Due to fundamental physical limitations, single molecule resolution cannot be achieved using classical top-down lithographic techniques. At the same time, existing surface functionalization schemes do not provide any means of placing a single molecule with high precision at a specific location on a nanostructure. This project has the ambitious goal of establishing the first method ever allowing for self-assembly of multiple single molecule devices in a parallel way and thereby provide the first method ever allowing for multiple individual single molecule components to operate together in the same device.
The impact of the technology platforms described herein goes vastly beyond the field of single molecule electronics and utilization in ultra-sensitive plasmonic biosensors with a digital single molecule response will be explored in parallel with the main roadmaps of the project."
Summary
"The development of micro fabrication and field effect transistors are key enabling technologies for todays information society. It is hard to imagine superfast and omnipresent electronic devices, information technology, the Internet and mobile communication technologies without access to continuously cheaper and miniaturized microprocessors. The giant leaps in performance of microprocessors from the first personal computing machines to todays mobile devices are to a large extent realized via miniaturization of the active components. The ultimate limit of miniaturization of electronic components is the realization of single molecule electronics. Due to fundamental physical limitations, single molecule resolution cannot be achieved using classical top-down lithographic techniques. At the same time, existing surface functionalization schemes do not provide any means of placing a single molecule with high precision at a specific location on a nanostructure. This project has the ambitious goal of establishing the first method ever allowing for self-assembly of multiple single molecule devices in a parallel way and thereby provide the first method ever allowing for multiple individual single molecule components to operate together in the same device.
The impact of the technology platforms described herein goes vastly beyond the field of single molecule electronics and utilization in ultra-sensitive plasmonic biosensors with a digital single molecule response will be explored in parallel with the main roadmaps of the project."
Max ERC Funding
1 500 000 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym single-C
Project Automatized Catalysis and Single-Carbon Insertion
Researcher (PI) Abraham MENDOZA VALDERREY
Host Institution (HI) STOCKHOLMS UNIVERSITET
Call Details Starting Grant (StG), PE5, ERC-2016-STG
Summary This project is aimed at accelerating the synthesis of important organic molecules through key enabling technologies towards automatized catalysis and single-carbon insertion reactions. Transferring the simplest carbon units to organic molecules has the potential to change the way we approach synthesis planning through new asymmetric skeletal homologations and rearrangements of simple raw materials, for which only long workarounds exist now. These methods can reduce to half the manipulations required to access relevant medicines, organocatalysts, ligands, bio-molecular tools and photovoltaic devices. They target unreactive functions to introduce fundamental one-carbon units (CO or C) that are present in virtually any organic compound. New powerful reagents that resemble these basic single-carbon units in excited electronic configurations are to be developed for this purpose. The new catalytic methods needed are based on the solid grounds of carbene-transfer reactions and the recent advances of my group in the development of new homogeneous catalysts. Moreover, a new catalyst platform will be developed to complement our existing portfolio for success in the challenging processes targeted in this proposal. We aim to pioneer a fully automatized workflow for research in catalysis that devoid the synthesis of organic ligands replacing them by combinatorial assemblies built in situ from un-structured simple molecules. The new reactions arising from these new catalysts and reagents will expedite the valorization of raw materials (such as carbonyls, olefins and hydrocarbons) into important chiral molecules in a single transformation. This bold aim is a priority of the European Commission for the coming years as it will save time, protect the environment and reduce cost at once. Thus, these innovative technologies have the potential of transforming the research workflow in homogeneous catalysis and the logics of retrosynthesis of organic molecules at a fundamental level.
Summary
This project is aimed at accelerating the synthesis of important organic molecules through key enabling technologies towards automatized catalysis and single-carbon insertion reactions. Transferring the simplest carbon units to organic molecules has the potential to change the way we approach synthesis planning through new asymmetric skeletal homologations and rearrangements of simple raw materials, for which only long workarounds exist now. These methods can reduce to half the manipulations required to access relevant medicines, organocatalysts, ligands, bio-molecular tools and photovoltaic devices. They target unreactive functions to introduce fundamental one-carbon units (CO or C) that are present in virtually any organic compound. New powerful reagents that resemble these basic single-carbon units in excited electronic configurations are to be developed for this purpose. The new catalytic methods needed are based on the solid grounds of carbene-transfer reactions and the recent advances of my group in the development of new homogeneous catalysts. Moreover, a new catalyst platform will be developed to complement our existing portfolio for success in the challenging processes targeted in this proposal. We aim to pioneer a fully automatized workflow for research in catalysis that devoid the synthesis of organic ligands replacing them by combinatorial assemblies built in situ from un-structured simple molecules. The new reactions arising from these new catalysts and reagents will expedite the valorization of raw materials (such as carbonyls, olefins and hydrocarbons) into important chiral molecules in a single transformation. This bold aim is a priority of the European Commission for the coming years as it will save time, protect the environment and reduce cost at once. Thus, these innovative technologies have the potential of transforming the research workflow in homogeneous catalysis and the logics of retrosynthesis of organic molecules at a fundamental level.
Max ERC Funding
1 487 245 €
Duration
Start date: 2017-04-01, End date: 2022-03-31
Project acronym SMAC-MC
Project Small Molecule Activation by Main-Group Compounds
Researcher (PI) Heikki Markus Tuononen
Host Institution (HI) JYVASKYLAN YLIOPISTO
Call Details Consolidator Grant (CoG), PE5, ERC-2017-COG
Summary Many basic chemical processes involve the activation of small unreactive molecules, such as hydrogen, nitrogen, ammonia, water and carbon dioxide, by transition-metal-based catalysts or by enzymes. This proposal focusses on the interesting and recently observed possibility to perform similar transformations with main-group compounds that consist entirely of cheap earth-abundant elements. The proposed research is split into four work packages of which the first investigates the mechanisms by which different main-group singlet diradicaloids activate small molecules and how their reactivity correlates with their radical character. The second work package focusses on small molecule activation using main-group metalloid clusters, a new emerging field that we have recently pioneered, and compares the reactivity determined for main-group species with that known for related transition-metal clusters. Investigations in the third work package concentrate on the electrochemical reduction of carbon dioxide and on the possibility to lower the required overpotential with frustrated Lewis pairs that readily form adducts with small molecules. The fourth work package revolves around activating small molecules by diborenes and, in particular, observing novel reactivity in situ, that is, before the reactive diborene is trapped with a suitable Lewis base. Considered as a whole, the planned initiatives will enable significant breakthroughs in the design of novel main-group element based compounds for the activation of small molecules. The research is not only of fundamental scientific importance but also of potential practical value as many main-group systems, such as frustrated Lewis pairs, are currently being examined as novel catalysts. An ERC consolidator grant would significantly strengthen my position in this interesting subfield of inorganic chemistry and give my research group practical means to continue performing cutting-edge research.
Summary
Many basic chemical processes involve the activation of small unreactive molecules, such as hydrogen, nitrogen, ammonia, water and carbon dioxide, by transition-metal-based catalysts or by enzymes. This proposal focusses on the interesting and recently observed possibility to perform similar transformations with main-group compounds that consist entirely of cheap earth-abundant elements. The proposed research is split into four work packages of which the first investigates the mechanisms by which different main-group singlet diradicaloids activate small molecules and how their reactivity correlates with their radical character. The second work package focusses on small molecule activation using main-group metalloid clusters, a new emerging field that we have recently pioneered, and compares the reactivity determined for main-group species with that known for related transition-metal clusters. Investigations in the third work package concentrate on the electrochemical reduction of carbon dioxide and on the possibility to lower the required overpotential with frustrated Lewis pairs that readily form adducts with small molecules. The fourth work package revolves around activating small molecules by diborenes and, in particular, observing novel reactivity in situ, that is, before the reactive diborene is trapped with a suitable Lewis base. Considered as a whole, the planned initiatives will enable significant breakthroughs in the design of novel main-group element based compounds for the activation of small molecules. The research is not only of fundamental scientific importance but also of potential practical value as many main-group systems, such as frustrated Lewis pairs, are currently being examined as novel catalysts. An ERC consolidator grant would significantly strengthen my position in this interesting subfield of inorganic chemistry and give my research group practical means to continue performing cutting-edge research.
Max ERC Funding
1 424 190 €
Duration
Start date: 2018-07-01, End date: 2023-06-30
Project acronym SURFACE
Project The unexplored world of aerosol surfaces and their impacts.
Researcher (PI) Nonne PRISLE
Host Institution (HI) OULUN YLIOPISTO
Call Details Starting Grant (StG), PE10, ERC-2016-STG
Summary We are changing the composition of Earth’s atmosphere, with profound consequences for the environment and our wellbeing. Tiny aerosol particles are globally responsible for much of the health effects and mortality related to air pollution and play key roles in regulating Earth’s climate via their critical influence on both radiation balance and cloud formation. Every single cloud droplet has been nucleated on the surface of an aerosol particle. Aerosols and droplets provide the media for condensed-phase chemistry in the atmosphere, but large gaps remain in our understanding of their formation, transformations, and climate interactions. Surface properties may play crucial roles in these processes, but currently next to nothing is known about the surfaces of atmospheric aerosols and cloud droplets and their impacts are almost entirely unconstrained. My recent work strongly suggests that such surfaces are significantly different from their associated bulk material and that these unique properties can impact aerosol processes all the way to the global scale. Very few surface-specific properties are currently considered when evaluating aerosol effects on atmospheric chemistry and global climate. Novel developments of cutting-edge computational and experimental methods, in particular synchrotron-based photoelectron spectroscopy, now for the first time makes direct molecular-level characterizations of atmospheric surfaces feasible. This project will demonstrate and quantify potential surface impacts in the atmosphere, by first directly characterizing realistic atmospheric surfaces, and then trace fingerprints of specific surface properties in a hierarchy of experimental and modelled aerosol processes and atmospheric effects. Successful demonstrations of unique aerosol surface fingerprints will constitute truly novel insights into a currently uncharted area of the atmospheric system and identify an entirely new frontier in aerosol research and atmospheric science.
Summary
We are changing the composition of Earth’s atmosphere, with profound consequences for the environment and our wellbeing. Tiny aerosol particles are globally responsible for much of the health effects and mortality related to air pollution and play key roles in regulating Earth’s climate via their critical influence on both radiation balance and cloud formation. Every single cloud droplet has been nucleated on the surface of an aerosol particle. Aerosols and droplets provide the media for condensed-phase chemistry in the atmosphere, but large gaps remain in our understanding of their formation, transformations, and climate interactions. Surface properties may play crucial roles in these processes, but currently next to nothing is known about the surfaces of atmospheric aerosols and cloud droplets and their impacts are almost entirely unconstrained. My recent work strongly suggests that such surfaces are significantly different from their associated bulk material and that these unique properties can impact aerosol processes all the way to the global scale. Very few surface-specific properties are currently considered when evaluating aerosol effects on atmospheric chemistry and global climate. Novel developments of cutting-edge computational and experimental methods, in particular synchrotron-based photoelectron spectroscopy, now for the first time makes direct molecular-level characterizations of atmospheric surfaces feasible. This project will demonstrate and quantify potential surface impacts in the atmosphere, by first directly characterizing realistic atmospheric surfaces, and then trace fingerprints of specific surface properties in a hierarchy of experimental and modelled aerosol processes and atmospheric effects. Successful demonstrations of unique aerosol surface fingerprints will constitute truly novel insights into a currently uncharted area of the atmospheric system and identify an entirely new frontier in aerosol research and atmospheric science.
Max ERC Funding
1 499 626 €
Duration
Start date: 2017-03-01, End date: 2022-02-28
Project acronym ThermoTex
Project Woven and 3D-Printed Thermoelectric Textiles
Researcher (PI) Christian Müller
Host Institution (HI) CHALMERS TEKNISKA HOEGSKOLA AB
Call Details Starting Grant (StG), PE5, ERC-2014-STG
Summary Imagine a world, in which countless embedded microelectronic components continuously monitor our health and allow us to seamlessly interact with our digital environment. One particularly promising platform for the realisation of this concept is based on wearable electronic textiles. In order for this technology to become truly pervasive, a myriad of devices will have to operate autonomously over an extended period of time without the need for additional maintenance, repair or battery replacement. The goal of this research programme is to realise textile-based thermoelectric generators that without additional cost can power built-in electronics by harvesting one of the most ubiquitous energy sources available to us: our body heat.
Current thermoelectric technologies rely on toxic inorganic materials that are both expensive to produce and fragile by design, which renders them unsuitable especially for wearable applications. Instead, in this programme we will use polymer semiconductors and nanocomposites. Initially, we will focus on the preparation of materials with a thermoelectric performance significantly beyond the state-of-the-art. Then, we will exploit the ease of shaping polymers into light-weight and flexible articles such as fibres, yarns and fabrics. We will explore both, traditional weaving methods as well as emerging 3D-printing techniques, in order to realise low-cost thermoelectric textiles.
Finally, within the scope of this programme we will demonstrate the ability of prototype thermoelectric textiles to harvest a small fraction of the wearer’s body heat under realistic conditions. We will achieve this through integration into clothing to power off-the-shelf sensors for health care and security applications. Eventually, it can be anticipated that the here interrogated thermoelectric design paradigms will be of significant benefit to the European textile and health care sector as well as society in general.
Summary
Imagine a world, in which countless embedded microelectronic components continuously monitor our health and allow us to seamlessly interact with our digital environment. One particularly promising platform for the realisation of this concept is based on wearable electronic textiles. In order for this technology to become truly pervasive, a myriad of devices will have to operate autonomously over an extended period of time without the need for additional maintenance, repair or battery replacement. The goal of this research programme is to realise textile-based thermoelectric generators that without additional cost can power built-in electronics by harvesting one of the most ubiquitous energy sources available to us: our body heat.
Current thermoelectric technologies rely on toxic inorganic materials that are both expensive to produce and fragile by design, which renders them unsuitable especially for wearable applications. Instead, in this programme we will use polymer semiconductors and nanocomposites. Initially, we will focus on the preparation of materials with a thermoelectric performance significantly beyond the state-of-the-art. Then, we will exploit the ease of shaping polymers into light-weight and flexible articles such as fibres, yarns and fabrics. We will explore both, traditional weaving methods as well as emerging 3D-printing techniques, in order to realise low-cost thermoelectric textiles.
Finally, within the scope of this programme we will demonstrate the ability of prototype thermoelectric textiles to harvest a small fraction of the wearer’s body heat under realistic conditions. We will achieve this through integration into clothing to power off-the-shelf sensors for health care and security applications. Eventually, it can be anticipated that the here interrogated thermoelectric design paradigms will be of significant benefit to the European textile and health care sector as well as society in general.
Max ERC Funding
1 500 000 €
Duration
Start date: 2015-06-01, End date: 2020-05-31