Project acronym AMI
Project Animals Make identities. The Social Bioarchaeology of Late Mesolithic and Early Neolithic Cemeteries in North-East Europe
Researcher (PI) Kristiina MANNERMAA
Host Institution (HI) HELSINGIN YLIOPISTO
Country Finland
Call Details Consolidator Grant (CoG), SH6, ERC-2019-COG
Summary AMI aims to provide a novel interpretation of social links between humans and animals in hunter-gatherer cemeteries in North-East Europe, c. 9000–7500 years ago. AMI brings together cutting-edge developments in bioarchaeological science and the latest understanding of how people’s identities form in order to study the relationships between humans and animals. Grave materials and human remains will be studied from the viewpoint of process rather than as isolated objects, and will be interpreted through their histories.
The main objectives are
1) Synthesize the animal related bioarchaeological materials in mortuary contexts in North-East Europe,
2) Conduct a systematic multimethodological analysis of the animal-derived artefacts and to study them as actors in human social identity construction,
3) Reconstruct the individual life histories of humans, animals, and animal-derived artefacts in the cemeteries, and
4) Produce models for the reconstruction of social identities based on the data from the bioanalyses, literature, and GIS.
Various contextual, qualitative and quantitative biodata from animals and humans will be analysed and compared. Correlations and differences will be explored. Intra-site spatial analyses and data already published on cemeteries will contribute significantly to the research. Ethnographic information about recent hunter-gatherers from circumpolar regions gathered from literature will support the interpretation of the results from these analyses.
The research material derives from almost 300 burials from eight sites in North-East Europe and includes, for example, unique materials from Russia that have not previously been available for modern multidisciplinary research. The project will make a significant contribution to our understanding of how humans living in the forests of North-East Europe adapted the animals they shared their environment with into their social and ideological realities and practices.
Summary
AMI aims to provide a novel interpretation of social links between humans and animals in hunter-gatherer cemeteries in North-East Europe, c. 9000–7500 years ago. AMI brings together cutting-edge developments in bioarchaeological science and the latest understanding of how people’s identities form in order to study the relationships between humans and animals. Grave materials and human remains will be studied from the viewpoint of process rather than as isolated objects, and will be interpreted through their histories.
The main objectives are
1) Synthesize the animal related bioarchaeological materials in mortuary contexts in North-East Europe,
2) Conduct a systematic multimethodological analysis of the animal-derived artefacts and to study them as actors in human social identity construction,
3) Reconstruct the individual life histories of humans, animals, and animal-derived artefacts in the cemeteries, and
4) Produce models for the reconstruction of social identities based on the data from the bioanalyses, literature, and GIS.
Various contextual, qualitative and quantitative biodata from animals and humans will be analysed and compared. Correlations and differences will be explored. Intra-site spatial analyses and data already published on cemeteries will contribute significantly to the research. Ethnographic information about recent hunter-gatherers from circumpolar regions gathered from literature will support the interpretation of the results from these analyses.
The research material derives from almost 300 burials from eight sites in North-East Europe and includes, for example, unique materials from Russia that have not previously been available for modern multidisciplinary research. The project will make a significant contribution to our understanding of how humans living in the forests of North-East Europe adapted the animals they shared their environment with into their social and ideological realities and practices.
Max ERC Funding
1 992 839 €
Duration
Start date: 2020-04-01, End date: 2025-03-31
Project acronym CapTherPV
Project Integration of Capacitor, Thermoelectric and PhotoVoltaic thin films for efficient energy conversion and storage
Researcher (PI) Isabel Maria Das Merces Ferreira
Host Institution (HI) NOVA ID FCT - ASSOCIACAO PARA A INOVACAO E DESENVOLVIMENTO DA FCT
Country Portugal
Call Details Consolidator Grant (CoG), PE8, ERC-2014-CoG
Summary The possibility of having a unique device that converts thermal and photonics energy into electrical energy and simultaneously stores it, is something dreamed by the PI since the beginning of her research career. To achieve that goal, this project aims to gather, in a single substrate, solar cells with up-conversion nanoparticles, thermoelectrics and graphene super-capacitor, all made of thin films. These three main components will be developed separately and integrated sequentially. The innovation proposed is not limited to the integration of components, but rely in ground-breaking concepts: 1) thermoelectric elements based on thin film (TE-TF) oxides; 2) plasmonic nanoparticles for up conversion of near infrared radiation to visible emission in solar cells; 3) graphene super-capacitors; 4) integration and optimization of all components in a single CapTherPV device. This ambitious project will bring new insights at large area, low cost and flexible energy harvesting and comes from an old idea of combining energy conversion and storage that has been pursued by the PI. She started her career in amorphous silicon thin film solar cells, later she started the development of thin film batteries and more recently started a research line in thermoelectric films. If approved, this project will give financial support to consolidate the research being carried out and will give independence to the PI in terms of resources and creative think. More importantly, will facilitate the concretization of the dream that has been pursued with hard work.
Summary
The possibility of having a unique device that converts thermal and photonics energy into electrical energy and simultaneously stores it, is something dreamed by the PI since the beginning of her research career. To achieve that goal, this project aims to gather, in a single substrate, solar cells with up-conversion nanoparticles, thermoelectrics and graphene super-capacitor, all made of thin films. These three main components will be developed separately and integrated sequentially. The innovation proposed is not limited to the integration of components, but rely in ground-breaking concepts: 1) thermoelectric elements based on thin film (TE-TF) oxides; 2) plasmonic nanoparticles for up conversion of near infrared radiation to visible emission in solar cells; 3) graphene super-capacitors; 4) integration and optimization of all components in a single CapTherPV device. This ambitious project will bring new insights at large area, low cost and flexible energy harvesting and comes from an old idea of combining energy conversion and storage that has been pursued by the PI. She started her career in amorphous silicon thin film solar cells, later she started the development of thin film batteries and more recently started a research line in thermoelectric films. If approved, this project will give financial support to consolidate the research being carried out and will give independence to the PI in terms of resources and creative think. More importantly, will facilitate the concretization of the dream that has been pursued with hard work.
Max ERC Funding
1 999 375 €
Duration
Start date: 2015-07-01, End date: 2021-09-30
Project acronym CATCH
Project Cross-dimensional Activation of Two-Dimensional Semiconductors for Photocatalytic Heterojunctions
Researcher (PI) Wei CAO
Host Institution (HI) OULUN YLIOPISTO
Country Finland
Call Details Consolidator Grant (CoG), PE8, ERC-2020-COG
Summary Spacetime defines existence and evolution of materials. A key path to human’s sustainability through materials innovation can hardly circumvent materials dimensionalities. Despite numerous studies in electrically distinct 2D semiconductors, the route to engage them in high-performance photocatalysts remains elusive. Herein, CATCH proposes a cross-dimensional activation strategy of 2D semiconductors to implement practical photocatalysis. It operates electronic structures of dimensionally paradoxical 2D semiconductors and spatially limited nD (n=0-2) guests, directs charge migration processes, mass-produces advanced catalysts and elucidates time-evolved catalysis. Synergic impacts crossing 2D-nD will lead to > 95%/hour rates for pollutant removal and >20% quantum efficiencies for H2 evolution under visible light. CATCH enumerates chemical coordination and writes reaction equations with sub-nanosecond precision.
CATCH employs density functional theory optimization and data mining prediction to select most probable heterojunctional peers from hetero/homo- dimensions. Through facile but efficient wet and dry synthesis, nanostructures will be bonded to basal planes or brinks of 2D slabs. CATCH benefits in-house techniques for product characterizations and refinements and emphasizes on cutting-edge in situ studies to unveil photocatalysis at advanced photon sources. Assisted with theoretical modelling, ambient and time-evolved experiments will illustrate photocatalytic dynamics and kinetics in mixed spacetime.
CATCH unites low-dimensional materials designs by counting physical and electronic merits from spacetime confinements. It metrologically elaborates photocatalysis in an elevated 2D+nD+t, alters passages of materials combinations crossing dimensions, and directs future photocatalyst designs. Standing on cross-dimensional materials innovation and photocatalysis study, CATCH breaks the deadlock of practical photocatalysis that eventually leads to sustainability.
Summary
Spacetime defines existence and evolution of materials. A key path to human’s sustainability through materials innovation can hardly circumvent materials dimensionalities. Despite numerous studies in electrically distinct 2D semiconductors, the route to engage them in high-performance photocatalysts remains elusive. Herein, CATCH proposes a cross-dimensional activation strategy of 2D semiconductors to implement practical photocatalysis. It operates electronic structures of dimensionally paradoxical 2D semiconductors and spatially limited nD (n=0-2) guests, directs charge migration processes, mass-produces advanced catalysts and elucidates time-evolved catalysis. Synergic impacts crossing 2D-nD will lead to > 95%/hour rates for pollutant removal and >20% quantum efficiencies for H2 evolution under visible light. CATCH enumerates chemical coordination and writes reaction equations with sub-nanosecond precision.
CATCH employs density functional theory optimization and data mining prediction to select most probable heterojunctional peers from hetero/homo- dimensions. Through facile but efficient wet and dry synthesis, nanostructures will be bonded to basal planes or brinks of 2D slabs. CATCH benefits in-house techniques for product characterizations and refinements and emphasizes on cutting-edge in situ studies to unveil photocatalysis at advanced photon sources. Assisted with theoretical modelling, ambient and time-evolved experiments will illustrate photocatalytic dynamics and kinetics in mixed spacetime.
CATCH unites low-dimensional materials designs by counting physical and electronic merits from spacetime confinements. It metrologically elaborates photocatalysis in an elevated 2D+nD+t, alters passages of materials combinations crossing dimensions, and directs future photocatalyst designs. Standing on cross-dimensional materials innovation and photocatalysis study, CATCH breaks the deadlock of practical photocatalysis that eventually leads to sustainability.
Max ERC Funding
1 999 946 €
Duration
Start date: 2021-05-01, End date: 2026-04-30
Project acronym CAVITYQPD
Project Cavity quantum phonon dynamics
Researcher (PI) Mika Antero Sillanpaeae
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Country Finland
Call Details Consolidator Grant (CoG), PE3, ERC-2013-CoG
Summary "Large bodies usually follow the classical equations of motion. Deviations from this can be called
macroscopic quantum behavior. These phenomena have been experimentally verified with cavity Quantum
Electro Dynamics (QED), trapped ions, and superconducting Josephson junction systems. Recently, evidence
was obtained that also moving objects can display such behavior. These objects are micromechanical
resonators (MR), which can measure tens of microns in size and are hence quite macroscopic. The degree of
freedom is their vibrations: phonons.
I propose experimental research in order to push quantum mechanics closer to the classical world than ever
before. I will try find quantum behavior in the most classical objects, that is, slowly moving bodies. I will use
MR's, accessed via electrical resonators. Part of it will be in analogy to the previously studied macroscopic
systems, but with photons replaced by phonons. The experiments are done in a cryogenic temperature mostly
in dilution refrigerator. The work will open up new perspectives on how nature works, and can have
technological implications.
The first basic setup is the coupling of MR to microwave cavity resonators. This is a direct analogy to
optomechanics, and can be called circuit optomechanics. The goals will be phonon state transfer via a cavity
bus, construction of squeezed states and of phonon-cavity entanglement. The second setup is to boost the
optomechanical coupling with a Josephson junction system, and reach the single-phonon strong-coupling for
the first time. The third setup is the coupling of MR to a Josephson junction artificial atom. Here we will
access the MR same way as the motion of a trapped ions is coupled to their internal transitions. In this setup,
I am proposing to construct exotic quantum states of motion, and finally entangle and transfer phonons over
mm-distance via cavity-coupled qubits. I believe within the project it is possible to perform rudimentary Bell
measurement with phonons."
Summary
"Large bodies usually follow the classical equations of motion. Deviations from this can be called
macroscopic quantum behavior. These phenomena have been experimentally verified with cavity Quantum
Electro Dynamics (QED), trapped ions, and superconducting Josephson junction systems. Recently, evidence
was obtained that also moving objects can display such behavior. These objects are micromechanical
resonators (MR), which can measure tens of microns in size and are hence quite macroscopic. The degree of
freedom is their vibrations: phonons.
I propose experimental research in order to push quantum mechanics closer to the classical world than ever
before. I will try find quantum behavior in the most classical objects, that is, slowly moving bodies. I will use
MR's, accessed via electrical resonators. Part of it will be in analogy to the previously studied macroscopic
systems, but with photons replaced by phonons. The experiments are done in a cryogenic temperature mostly
in dilution refrigerator. The work will open up new perspectives on how nature works, and can have
technological implications.
The first basic setup is the coupling of MR to microwave cavity resonators. This is a direct analogy to
optomechanics, and can be called circuit optomechanics. The goals will be phonon state transfer via a cavity
bus, construction of squeezed states and of phonon-cavity entanglement. The second setup is to boost the
optomechanical coupling with a Josephson junction system, and reach the single-phonon strong-coupling for
the first time. The third setup is the coupling of MR to a Josephson junction artificial atom. Here we will
access the MR same way as the motion of a trapped ions is coupled to their internal transitions. In this setup,
I am proposing to construct exotic quantum states of motion, and finally entangle and transfer phonons over
mm-distance via cavity-coupled qubits. I believe within the project it is possible to perform rudimentary Bell
measurement with phonons."
Max ERC Funding
2 004 283 €
Duration
Start date: 2015-01-01, End date: 2019-12-31
Project acronym Des.solve
Project When solids become liquids: natural deep eutectic solvents for chemical process engineering
Researcher (PI) Ana Rita CRUZ DUARTE
Host Institution (HI) NOVA ID FCT - ASSOCIACAO PARA A INOVACAO E DESENVOLVIMENTO DA FCT
Country Portugal
Call Details Consolidator Grant (CoG), PE8, ERC-2016-COG
Summary Sugars, aminoacids or organic acids are typically solid at room temperature. Nonetheless when combined at a particular molar fraction they present a high melting point depression, becoming liquids at room temperature. These are called Natural Deep Eutectic Solvents – NADES. NADES are envisaged to play a major role on different chemical engineering processes in the future. Nonetheless, there is a significant lack of knowledge on fundamental and basic research on NADES, which is hindering their industrial applications. For this reason it is important to extend the knowledge on these systems, boosting their application development. NADES applications go beyond chemical or materials engineering and cover a wide range of fields from biocatalysis, extraction, electrochemistry, carbon dioxide capture or biomedical applications. Des.solve encompasses four major themes of research: 1 – Development of NADES and therapeutic deep eutectic solvents – THEDES; 2 – Characterization of the obtained mixtures and computer simulation of NADES/THEDES properties; 3 – Phase behaviour of binary/ternary systems NADES/THEDES + carbon dioxide and thermodynamic modelling 4 – Application development. Starting from the development of novel NADES/THEDES which, by different characterization techniques, will be deeply studied and characterized, the essential raw-materials will be produced for the subsequent research activities. The envisaged research involves modelling and molecular simulations. Des.solve will be deeply engaged in application development, particularly in extraction, biocatalysis and pharmaceutical/biomedical applications. The knowledge that will be created in this proposal is expected not only to have a major impact in the scientific community, but also in society, economy and industry.
Summary
Sugars, aminoacids or organic acids are typically solid at room temperature. Nonetheless when combined at a particular molar fraction they present a high melting point depression, becoming liquids at room temperature. These are called Natural Deep Eutectic Solvents – NADES. NADES are envisaged to play a major role on different chemical engineering processes in the future. Nonetheless, there is a significant lack of knowledge on fundamental and basic research on NADES, which is hindering their industrial applications. For this reason it is important to extend the knowledge on these systems, boosting their application development. NADES applications go beyond chemical or materials engineering and cover a wide range of fields from biocatalysis, extraction, electrochemistry, carbon dioxide capture or biomedical applications. Des.solve encompasses four major themes of research: 1 – Development of NADES and therapeutic deep eutectic solvents – THEDES; 2 – Characterization of the obtained mixtures and computer simulation of NADES/THEDES properties; 3 – Phase behaviour of binary/ternary systems NADES/THEDES + carbon dioxide and thermodynamic modelling 4 – Application development. Starting from the development of novel NADES/THEDES which, by different characterization techniques, will be deeply studied and characterized, the essential raw-materials will be produced for the subsequent research activities. The envisaged research involves modelling and molecular simulations. Des.solve will be deeply engaged in application development, particularly in extraction, biocatalysis and pharmaceutical/biomedical applications. The knowledge that will be created in this proposal is expected not only to have a major impact in the scientific community, but also in society, economy and industry.
Max ERC Funding
1 877 006 €
Duration
Start date: 2017-03-01, End date: 2022-02-28
Project acronym ECM_INK
Project Cells-self Extracellular Matrices-based Bioinks to create accurate 3D diseased skin tissue models
Researcher (PI) Alexandra Margarida PINTO MARQUES
Host Institution (HI) UNIVERSIDADE DO MINHO
Country Portugal
Call Details Consolidator Grant (CoG), PE8, ERC-2016-COG
Summary It has been recognized that growing cells within 3D structures reduces the gap between 2D in vitro cell cultures and native tissue physiology. This has been paving the way for the development of reliable 3D in vitro cell-based platforms with major impact in the reduction/elimination of animal experimentation, diseases modelling and drug development. So far, the many strategies that have been followed to bioengineer in vitro 3D human tissue models mostly rely on the random culture of cells within a 3D structure without reflecting the compositional and structural complexity of the native tissues. Recently proposed bioprinting technologies that allow accurate and high speed deposition of various cells and matrices at high resolution, have therefore great potential in the development of physiologically reliable 3D in vitro tissue models by recreating the different microenvironments/microfunctionalities found in each tissue. Nonetheless, among the components required for bioprinting, bioinks in particular have demanding requirements and much has still to be done regarding their intrinsic formulation to lead cell behaviour and support specific functionalities.
ECM_INK intends to tackle this issue by developing cells-self extracellular matrices-based bioinks to create accurate and pathophysiological relevant 3D in vitro diseased skin tissue models. The development of cell phenotype-driven bioinks will generate complex microenvironments comprising varied cell types within matrices that were specifically designed to attain a particular response from each one of those cell types. The use of cells from patients suffering from chronic, genetic and neoplastic skin diseases represents a major advantage that will be reflected in the accuracy and functionality of the respective 3D in vitro models. The ultimate confirmation of their potential will be complete after validation using animal-free approaches reinforcing the intrinsic relationship of ECM_INK with the 3Rs policy.
Summary
It has been recognized that growing cells within 3D structures reduces the gap between 2D in vitro cell cultures and native tissue physiology. This has been paving the way for the development of reliable 3D in vitro cell-based platforms with major impact in the reduction/elimination of animal experimentation, diseases modelling and drug development. So far, the many strategies that have been followed to bioengineer in vitro 3D human tissue models mostly rely on the random culture of cells within a 3D structure without reflecting the compositional and structural complexity of the native tissues. Recently proposed bioprinting technologies that allow accurate and high speed deposition of various cells and matrices at high resolution, have therefore great potential in the development of physiologically reliable 3D in vitro tissue models by recreating the different microenvironments/microfunctionalities found in each tissue. Nonetheless, among the components required for bioprinting, bioinks in particular have demanding requirements and much has still to be done regarding their intrinsic formulation to lead cell behaviour and support specific functionalities.
ECM_INK intends to tackle this issue by developing cells-self extracellular matrices-based bioinks to create accurate and pathophysiological relevant 3D in vitro diseased skin tissue models. The development of cell phenotype-driven bioinks will generate complex microenvironments comprising varied cell types within matrices that were specifically designed to attain a particular response from each one of those cell types. The use of cells from patients suffering from chronic, genetic and neoplastic skin diseases represents a major advantage that will be reflected in the accuracy and functionality of the respective 3D in vitro models. The ultimate confirmation of their potential will be complete after validation using animal-free approaches reinforcing the intrinsic relationship of ECM_INK with the 3Rs policy.
Max ERC Funding
1 998 939 €
Duration
Start date: 2017-05-01, End date: 2022-10-31
Project acronym MagTendon
Project Magnetically Assisted Tissue Engineering Technologies for Tendon Regeneration
Researcher (PI) Maria Manuela ESTIMA GOMES
Host Institution (HI) UNIVERSIDADE DO MINHO
Country Portugal
Call Details Consolidator Grant (CoG), PE8, ERC-2017-COG
Summary The poor healing ability of tendons, which play a critical role in the musculoskeletal system, as well as the limitations of currently used therapies have motivated tissue engineering (TE) strategies to develop living tendon substitutes. However, the limited knowledge on tendon development and healing processes has hindered the design of TE procedures that more closely recapitulate tendon morphogenesis. Extending beyond the state-of-the-art, MagTendon will explore conventional and innovative tools such as multimaterial 3 dimensional (3D) bioprinting to design magnetic responsive systems mimicking specific aspects of tendon tissue architecture, composition and biomechanical properties, which, combined with adequate stem cells, will render appropriate behavioural instructions to stimulate the regeneration of tendon tissue. Stem cell bioengineering approaches based on superparamagnetic nanoparticles (SPMNs), namely cell sorting, mechanoreceptors targeting and cell programming, will be used to unveil the cellular signalling pathways that trigger the tenogenic differentiation of the widely and easily obtained human adipose derived stem cells. Simultaneously, the 3D cell-laden magnetic system shall enable sophisticated 3D tissue models to unravel mechanisms behind tendon homeostasis and repair that will support the base knowledge to establish rational design criteria for the biofabrication of living tendon substitutes with the adequate signaling and structural cues to recapitulate tendon tissue developmental patterns. Therefore, the ground-breaking nature of the research proposed relies on the development of disruptive technological concepts for obtaining unique cell-laden 3D magnetically responsive systems that recapitulate key features of the native tissue and that can be further remotely modulated both in vitro and in vivo by the application of external magnetic stimuli, offering the prospect of tendon regeneration as opposed to simple tissue repair.
Summary
The poor healing ability of tendons, which play a critical role in the musculoskeletal system, as well as the limitations of currently used therapies have motivated tissue engineering (TE) strategies to develop living tendon substitutes. However, the limited knowledge on tendon development and healing processes has hindered the design of TE procedures that more closely recapitulate tendon morphogenesis. Extending beyond the state-of-the-art, MagTendon will explore conventional and innovative tools such as multimaterial 3 dimensional (3D) bioprinting to design magnetic responsive systems mimicking specific aspects of tendon tissue architecture, composition and biomechanical properties, which, combined with adequate stem cells, will render appropriate behavioural instructions to stimulate the regeneration of tendon tissue. Stem cell bioengineering approaches based on superparamagnetic nanoparticles (SPMNs), namely cell sorting, mechanoreceptors targeting and cell programming, will be used to unveil the cellular signalling pathways that trigger the tenogenic differentiation of the widely and easily obtained human adipose derived stem cells. Simultaneously, the 3D cell-laden magnetic system shall enable sophisticated 3D tissue models to unravel mechanisms behind tendon homeostasis and repair that will support the base knowledge to establish rational design criteria for the biofabrication of living tendon substitutes with the adequate signaling and structural cues to recapitulate tendon tissue developmental patterns. Therefore, the ground-breaking nature of the research proposed relies on the development of disruptive technological concepts for obtaining unique cell-laden 3D magnetically responsive systems that recapitulate key features of the native tissue and that can be further remotely modulated both in vitro and in vivo by the application of external magnetic stimuli, offering the prospect of tendon regeneration as opposed to simple tissue repair.
Max ERC Funding
1 999 854 €
Duration
Start date: 2018-05-01, End date: 2023-10-31
Project acronym PARTIFACE
Project Green Route to Wood-Derived Janus Particles for Stabilized Interfaces
Researcher (PI) Kirsi MIKKONEN
Host Institution (HI) HELSINGIN YLIOPISTO
Country Finland
Call Details Consolidator Grant (CoG), PE8, ERC-2019-COG
Summary Emulsions are elemental to many aspects of every-day life, from food to pharmaceuticals. However, today’s emulsion science faces a grand challenge in developing stabilizers with outstanding functionality in a sustainable manner. To enable society’s transformation from oil-based economy to bioeconomy, there is an urgent need to develop sophisticated biocompatible materials, such as stabilizers of food and non-food emulsions, from biomass-derived precursors through sustainable conversion routes. Current bio-based stabilizers are poorly defined and not as efficient as the synthetic ones, primarily because key technologies to construct sophisticated hierarchical structures from abundant biopolymers are lacking. I will use my expertise on wood biomass and emulsion stabilizer research to develop a novel approach for asymmetric, bi-facial “Janus” nanoparticles from two of the most abundant, but underused biopolymers: lignin and hemicelluloses. I will develop a green conversion route using enzymatic crosslinking to build a novel concept: tailored wood-based Janus particles with superior capacity to stabilize emulsion interfaces. I will further tailor the particles to control their cooling rate through reversible bond formation, which will revolutionize the materials science. To achieve this ambitious goal, it is crucial to carefully characterize the particles and formed interfaces. I will develop a novel method to characterize real emulsion systems with high precision, which existing methods cannot achieve. PARTIFACE will establish a green route to sophisticated hierarchical architectures—bi-facial Janus-particle-stabilized interfaces—and thermal control systems utilizing abundant bioresources. The project will lead to a breakthrough in colloid and interface science and contribute to more sustainable use of Earth’s resources.
Summary
Emulsions are elemental to many aspects of every-day life, from food to pharmaceuticals. However, today’s emulsion science faces a grand challenge in developing stabilizers with outstanding functionality in a sustainable manner. To enable society’s transformation from oil-based economy to bioeconomy, there is an urgent need to develop sophisticated biocompatible materials, such as stabilizers of food and non-food emulsions, from biomass-derived precursors through sustainable conversion routes. Current bio-based stabilizers are poorly defined and not as efficient as the synthetic ones, primarily because key technologies to construct sophisticated hierarchical structures from abundant biopolymers are lacking. I will use my expertise on wood biomass and emulsion stabilizer research to develop a novel approach for asymmetric, bi-facial “Janus” nanoparticles from two of the most abundant, but underused biopolymers: lignin and hemicelluloses. I will develop a green conversion route using enzymatic crosslinking to build a novel concept: tailored wood-based Janus particles with superior capacity to stabilize emulsion interfaces. I will further tailor the particles to control their cooling rate through reversible bond formation, which will revolutionize the materials science. To achieve this ambitious goal, it is crucial to carefully characterize the particles and formed interfaces. I will develop a novel method to characterize real emulsion systems with high precision, which existing methods cannot achieve. PARTIFACE will establish a green route to sophisticated hierarchical architectures—bi-facial Janus-particle-stabilized interfaces—and thermal control systems utilizing abundant bioresources. The project will lead to a breakthrough in colloid and interface science and contribute to more sustainable use of Earth’s resources.
Max ERC Funding
2 000 000 €
Duration
Start date: 2020-06-01, End date: 2025-05-31
Project acronym POLITICS
Project The politics of anti-racism in Europe and Latin America: knowledge production, decision-making and collective struggles
Researcher (PI) Silvia RODRIGUEZ MAESO
Host Institution (HI) CENTRO DE ESTUDOS SOCIAIS
Country Portugal
Call Details Consolidator Grant (CoG), SH3, ERC-2016-COG
Summary The main objective of POLITICS is to innovate knowledge on anti-racism that brings about a greater understanding of how historically rooted injustices are being challenged by institutions and grassroots movements. Considering the centrality and mutual influence of Europe and Latin America in the global processes of racial formation, POLITICS will develop an inter-disciplinary and comprehensive approach towards two core goals: (a) the analysis of processes of knowledge production about ‘race’ and (anti-)racism in the spheres of (inter)national governmental politics, State universities and grassroots movements; (b) the examination of diverse paths of denunciation and collective mobilisation against everyday racism concerning police practice and representations in the mass media.
POLITICS embraces a multilevel analysis and information-oriented selection of case-studies in three interrelated research streams: (i) Global, regional and state-sponsored political frameworks and public policies; (ii) Cultures of scholarship and the study of racism and (post)colonialism at State universities; (iii) Tackling everyday racism: processes of denunciation, political mobilisation and case-law concerning police practice, and racist representations in the media and mass media. The research challenges the shortcomings of evaluative comparisons and the selection of research contexts enables interrogating the relations between the global, national and local levels. They include the Organisation of American States, the European Union and national and local politics in Brazil, Peru, Portugal and Spain. Qualitative research and data collection engage with race critical theories, critical discourse analysis and participatory methods that consider power/knowledge at their core.
POLITICS will unravel the configuration of different notions of dignity, justice and equality resulting from anti-racist struggles and policy interventions and their significance for envisaging decolonial horizons.
Summary
The main objective of POLITICS is to innovate knowledge on anti-racism that brings about a greater understanding of how historically rooted injustices are being challenged by institutions and grassroots movements. Considering the centrality and mutual influence of Europe and Latin America in the global processes of racial formation, POLITICS will develop an inter-disciplinary and comprehensive approach towards two core goals: (a) the analysis of processes of knowledge production about ‘race’ and (anti-)racism in the spheres of (inter)national governmental politics, State universities and grassroots movements; (b) the examination of diverse paths of denunciation and collective mobilisation against everyday racism concerning police practice and representations in the mass media.
POLITICS embraces a multilevel analysis and information-oriented selection of case-studies in three interrelated research streams: (i) Global, regional and state-sponsored political frameworks and public policies; (ii) Cultures of scholarship and the study of racism and (post)colonialism at State universities; (iii) Tackling everyday racism: processes of denunciation, political mobilisation and case-law concerning police practice, and racist representations in the media and mass media. The research challenges the shortcomings of evaluative comparisons and the selection of research contexts enables interrogating the relations between the global, national and local levels. They include the Organisation of American States, the European Union and national and local politics in Brazil, Peru, Portugal and Spain. Qualitative research and data collection engage with race critical theories, critical discourse analysis and participatory methods that consider power/knowledge at their core.
POLITICS will unravel the configuration of different notions of dignity, justice and equality resulting from anti-racist struggles and policy interventions and their significance for envisaging decolonial horizons.
Max ERC Funding
1 915 381 €
Duration
Start date: 2017-09-01, End date: 2022-08-31
Project acronym QUANTOM
Project Quantitative Tomography Using Coupled Physics of Waves
Researcher (PI) Tanja TARVAINEN
Host Institution (HI) ITA-SUOMEN YLIOPISTO
Country Finland
Call Details Consolidator Grant (CoG), PE8, ERC-2020-COG
Summary Tomographic images are a valuable tool in various applications of medicine and biomedicine, industry and in security applications. Although efficient tomographic imaging techniques exist, development of new modalities that would overcome the limitations of the existing techniques are required. Overall, there is a need for development of new tomographic techniques that would provide quantitative information of unknown parameters of interest, such as tomographic images on the concentration of molecules. In particular, information on the reliability of the tomographic images is required.
The objective of the project is to develop quantitative tomographic imaging technique based on coupled physics of waves. In coupled physics imaging, contrast and resolution originating from different physical phenomena are combined. In the project, light, microwaves and ultrasound, i.e. waves, will be utilised through photoacoustic, thermoacoustic and acousto-optic effects. These techniques will be developed to produce tomographic images with an outstanding quantitative contrast in the sense of statistical information and modelling of uncertainties, combined with superior resolution and imaging depth.
Most tomographic imaging techniques are ill-posed problems that need to be approached in the framework of inverse problems. In the project, a Bayesian approach to ill-posed inverse problems, which supports the quantitative nature of the problem, will be taken. In the project, mathematical modelling and computational methods will be developed in close connection with experimental system development. The research is founded on a strong understanding of the underlying physics of coupled physics problems, knowledge on instrumentation on the related fields and experimental tomography, and state-of-the-art methods of computational inverse mathematics, that all come together in the PI’s research group.
Summary
Tomographic images are a valuable tool in various applications of medicine and biomedicine, industry and in security applications. Although efficient tomographic imaging techniques exist, development of new modalities that would overcome the limitations of the existing techniques are required. Overall, there is a need for development of new tomographic techniques that would provide quantitative information of unknown parameters of interest, such as tomographic images on the concentration of molecules. In particular, information on the reliability of the tomographic images is required.
The objective of the project is to develop quantitative tomographic imaging technique based on coupled physics of waves. In coupled physics imaging, contrast and resolution originating from different physical phenomena are combined. In the project, light, microwaves and ultrasound, i.e. waves, will be utilised through photoacoustic, thermoacoustic and acousto-optic effects. These techniques will be developed to produce tomographic images with an outstanding quantitative contrast in the sense of statistical information and modelling of uncertainties, combined with superior resolution and imaging depth.
Most tomographic imaging techniques are ill-posed problems that need to be approached in the framework of inverse problems. In the project, a Bayesian approach to ill-posed inverse problems, which supports the quantitative nature of the problem, will be taken. In the project, mathematical modelling and computational methods will be developed in close connection with experimental system development. The research is founded on a strong understanding of the underlying physics of coupled physics problems, knowledge on instrumentation on the related fields and experimental tomography, and state-of-the-art methods of computational inverse mathematics, that all come together in the PI’s research group.
Max ERC Funding
2 000 000 €
Duration
Start date: 2021-06-01, End date: 2026-05-31