Project acronym 3DPRINTEDOPTICS
Project 3D printed micro- and nano-optics for future integrated vision and endoscopy systems
Researcher (PI) Harald Giessen
Host Institution (HI) UNIVERSITY OF STUTTGART
Country Germany
Call Details Proof of Concept (PoC), ERC-2019-PoC
Summary Optics is abundant in today’s world. Smartphone cameras, optical sensors for autonomous driving, virtual and augmented reality, medical imaging technology, and many more areas all require tailored optical sensors. In most cases, the optical sensors are still based on classical optical systems. For instance, high-end cameras or high-quality endoscopes still utilize classical glass optics. The related markets have sizes of several tens of billion USD and grow with double digit rates.
For all applications, size is the limiting factor. There is a tremendous demand for imaging capabilities using optics at sizes below 1 mm, with the quality of classical optics, i.e., correction of aberrations, extremely high transmission, and broadband operation. Key features include also zooming, focusing, and f-number variation, as well as customized fields of view to realize foveated imaging and multi-aperture, multi-lens systems. Ideally, such optical systems provide 180° field of view with simultaneous zooming capabilities.
Here, we propose a novel type of micro-optics that is extremely flexible, can be created at demand, possesses unprecedented functionality, and delivers solutions to problems that could not be solved before.
The basic building block at the heart of our problem solution is the use of 3D printed microoptics by femtosecond direct laser writing. This method has all features to fulfil the above-mentioned requirements: It takes only a day from the idea to concept, optical design and simulation, and to manufacturing and testing, i.e., to generate a working prototype.
Our method will create a new class of optical elements, which enable the smallest microscope objective in the world on the tip of an optical fiber with unprecedented imaging accuracy and functionality, such as focusing and zooming capability.
Summary
Optics is abundant in today’s world. Smartphone cameras, optical sensors for autonomous driving, virtual and augmented reality, medical imaging technology, and many more areas all require tailored optical sensors. In most cases, the optical sensors are still based on classical optical systems. For instance, high-end cameras or high-quality endoscopes still utilize classical glass optics. The related markets have sizes of several tens of billion USD and grow with double digit rates.
For all applications, size is the limiting factor. There is a tremendous demand for imaging capabilities using optics at sizes below 1 mm, with the quality of classical optics, i.e., correction of aberrations, extremely high transmission, and broadband operation. Key features include also zooming, focusing, and f-number variation, as well as customized fields of view to realize foveated imaging and multi-aperture, multi-lens systems. Ideally, such optical systems provide 180° field of view with simultaneous zooming capabilities.
Here, we propose a novel type of micro-optics that is extremely flexible, can be created at demand, possesses unprecedented functionality, and delivers solutions to problems that could not be solved before.
The basic building block at the heart of our problem solution is the use of 3D printed microoptics by femtosecond direct laser writing. This method has all features to fulfil the above-mentioned requirements: It takes only a day from the idea to concept, optical design and simulation, and to manufacturing and testing, i.e., to generate a working prototype.
Our method will create a new class of optical elements, which enable the smallest microscope objective in the world on the tip of an optical fiber with unprecedented imaging accuracy and functionality, such as focusing and zooming capability.
Max ERC Funding
150 000 €
Duration
Start date: 2019-06-01, End date: 2020-11-30
Project acronym 3DSCAN
Project Commercialisation of novel ultra-fast 3D laser scanning technology
Researcher (PI) Robin Angus SILVER
Host Institution (HI) UNIVERSITY COLLEGE LONDON
Country United Kingdom
Call Details Proof of Concept (PoC), ERC-2019-PoC
Summary Understanding how the brain processes information is one of the unsolved grand challenges in science. Moreover, neurological disorders, which disrupt information processing, have an enormous societal and economic impact. Studying information processing in the brain requires measurements of signals as they flow through neural circuits. However, the 3D nature of brain circuits and the speed of information transfer makes it difficult for neuroscientists to measure their properties with sufficiently high spatial and temporal resolution. During the NEUROGAIN ERC project, we developed a novel type of Acousto-Optic Lens (AOL)-based high-speed 3D laser scanner. This technology enables the focusing and scanning of a laser beam at 20-40 kHz. This scanning technology can be added to existing two-photon microscopes to enable 3D imaging of neurons and circuits with unprecedented spatio-temporal resolution. Moreover, it also automatically corrects for brain movement in real-time providing sharper images. This ERC PoC will facilitate commercialization of this 3D scanning technology by providing support to explore the markets in biosciences and beyond, protect the IP and facilitate early stage manufacture and assembly of AOL 3D scanners to supply biomedical researchers.
Summary
Understanding how the brain processes information is one of the unsolved grand challenges in science. Moreover, neurological disorders, which disrupt information processing, have an enormous societal and economic impact. Studying information processing in the brain requires measurements of signals as they flow through neural circuits. However, the 3D nature of brain circuits and the speed of information transfer makes it difficult for neuroscientists to measure their properties with sufficiently high spatial and temporal resolution. During the NEUROGAIN ERC project, we developed a novel type of Acousto-Optic Lens (AOL)-based high-speed 3D laser scanner. This technology enables the focusing and scanning of a laser beam at 20-40 kHz. This scanning technology can be added to existing two-photon microscopes to enable 3D imaging of neurons and circuits with unprecedented spatio-temporal resolution. Moreover, it also automatically corrects for brain movement in real-time providing sharper images. This ERC PoC will facilitate commercialization of this 3D scanning technology by providing support to explore the markets in biosciences and beyond, protect the IP and facilitate early stage manufacture and assembly of AOL 3D scanners to supply biomedical researchers.
Max ERC Funding
150 000 €
Duration
Start date: 2019-06-01, End date: 2020-11-30
Project acronym 3DScavengers
Project Three-dimensional nanoscale design for the all-in-one solution to environmental multisource energy scavenging
Researcher (PI) Ana Isabel BORRAS MARTOS
Host Institution (HI) AGENCIA ESTATAL CONSEJO SUPERIOR DEINVESTIGACIONES CIENTIFICAS
Country Spain
Call Details Starting Grant (StG), PE8, ERC-2019-STG
Summary Imagine a technology for powering your smart devices by recovering energy from lights in your office, the random movements of your body while reading these lines or from small changes in temperature when you breathe or go out for a walk. This very technology will provide energy for wireless sensor networks monitoring the air in your city or the structural stability of buildings and large constructions remotely and sustainably, avoiding battery recharging or even replacing them. These are the challenges in micro energy harvesting from (local) ambient sources.
Kinetic, thermal and solar energies are ubiquitous at our surroundings under diverse forms, but their relatively low intensity and intermittent availability limit their potential recovery by microscale devices. These restrictions call for multi-source energy harvesters working under two principles: 1) combining different single-source harvesters in one device, or 2) using multifunctional materials capable of simultaneously converting various energy sources into electricity. In 1), efficiency per unit volume can decrease compared to the individual counterparts; in 2), materials as semiconductors, polymeric and oxide ferroelectrics and hybrid perovskites may act as multisource harvesters but huge advances are required to optimize their functionalities and sustainable fabrication at large scale.
I propose to fill the gap between these approaches offering an all-in-one solution to multisource energy scavenging, based on the nanoscale design of multifunctional three-dimensional materials. The demonstration of an industrially scalable one-reactor plasma/vacuum method will be crucial to integrate hybrid-scavenging components and to provide 3DScavengers materials with tailored microstructure-enhanced performance.
My ultimate goal is to build nanoarchitectures for simultaneous and enhanced individual scavenging applying photovoltaic, piezo- and pyro-electric effects, minimizing the environmental cost of their synthesis
Summary
Imagine a technology for powering your smart devices by recovering energy from lights in your office, the random movements of your body while reading these lines or from small changes in temperature when you breathe or go out for a walk. This very technology will provide energy for wireless sensor networks monitoring the air in your city or the structural stability of buildings and large constructions remotely and sustainably, avoiding battery recharging or even replacing them. These are the challenges in micro energy harvesting from (local) ambient sources.
Kinetic, thermal and solar energies are ubiquitous at our surroundings under diverse forms, but their relatively low intensity and intermittent availability limit their potential recovery by microscale devices. These restrictions call for multi-source energy harvesters working under two principles: 1) combining different single-source harvesters in one device, or 2) using multifunctional materials capable of simultaneously converting various energy sources into electricity. In 1), efficiency per unit volume can decrease compared to the individual counterparts; in 2), materials as semiconductors, polymeric and oxide ferroelectrics and hybrid perovskites may act as multisource harvesters but huge advances are required to optimize their functionalities and sustainable fabrication at large scale.
I propose to fill the gap between these approaches offering an all-in-one solution to multisource energy scavenging, based on the nanoscale design of multifunctional three-dimensional materials. The demonstration of an industrially scalable one-reactor plasma/vacuum method will be crucial to integrate hybrid-scavenging components and to provide 3DScavengers materials with tailored microstructure-enhanced performance.
My ultimate goal is to build nanoarchitectures for simultaneous and enhanced individual scavenging applying photovoltaic, piezo- and pyro-electric effects, minimizing the environmental cost of their synthesis
Max ERC Funding
1 498 414 €
Duration
Start date: 2020-03-01, End date: 2025-02-28
Project acronym [LC]2
Project 'Living' Colloidal Liquid Crystals
Researcher (PI) Tyler Shendruk
Host Institution (HI) THE UNIVERSITY OF EDINBURGH
Country United Kingdom
Call Details Starting Grant (StG), PE3, ERC-2019-STG
Summary We propose an unprecedented class of soft, self-assembled and self-motile micro-machines. The combined qualities of active fluids and colloidal liquid crystals can be leveraged to design intrinsically out-of- equilibrium hierarchal structures, or ‘Living’ Colloidal Liquid Crystals [LC]2. The study of colloidal interactions and self-assembly in active nematics has yet to be considered and constitutes an unexplored and inter-disciplinary application of the emerging sciences of active matter and colloidal liquid crystals. Activity will endow dynamical multi-scale colloidal structures with autonomous functionality, including self-motility, self-revolution and dynamical self-transformations, which are exactly the characteristics one would desire for a first generation of autonomous components of micro-biomechanical systems and soft micro-machines. As hybrids between biological active fluids and man-made materials, [LC]2 structures represent an early foray into ‘living’ metamaterials, in which active self-assembly of simple components produces a rich diversity of behaviours and the potential for autonomously tunable material properties, mimicking biological complexity. In particular, we hypothesize self-assembled [LC]2 dimer turbines, colloidal flagella and ant-like group retrieval. These systems represent a fundamentally innovative concept that we propose to drive nanotechnology into a new future of soft materials that biomimetically self-assemble and autonomously enact functions. It is our multiscale coarse-grained simulations and expertise in flowing active nematic fluids that generates the opportunity for this unique line of research.
Summary
We propose an unprecedented class of soft, self-assembled and self-motile micro-machines. The combined qualities of active fluids and colloidal liquid crystals can be leveraged to design intrinsically out-of- equilibrium hierarchal structures, or ‘Living’ Colloidal Liquid Crystals [LC]2. The study of colloidal interactions and self-assembly in active nematics has yet to be considered and constitutes an unexplored and inter-disciplinary application of the emerging sciences of active matter and colloidal liquid crystals. Activity will endow dynamical multi-scale colloidal structures with autonomous functionality, including self-motility, self-revolution and dynamical self-transformations, which are exactly the characteristics one would desire for a first generation of autonomous components of micro-biomechanical systems and soft micro-machines. As hybrids between biological active fluids and man-made materials, [LC]2 structures represent an early foray into ‘living’ metamaterials, in which active self-assembly of simple components produces a rich diversity of behaviours and the potential for autonomously tunable material properties, mimicking biological complexity. In particular, we hypothesize self-assembled [LC]2 dimer turbines, colloidal flagella and ant-like group retrieval. These systems represent a fundamentally innovative concept that we propose to drive nanotechnology into a new future of soft materials that biomimetically self-assemble and autonomously enact functions. It is our multiscale coarse-grained simulations and expertise in flowing active nematic fluids that generates the opportunity for this unique line of research.
Max ERC Funding
1 402 345 €
Duration
Start date: 2019-12-01, End date: 2024-11-30
Project acronym A.L.I.B.I.
Project Helping Children to Make the Best of their Transition to High School
Researcher (PI) Pol VAN LIER
Host Institution (HI) STICHTING VU
Country Netherlands
Call Details Proof of Concept (PoC), ERC-2019-PoC
Summary Poor social experiences with peers, such as peer rejection or peer victimization, and with teachers, such as receiving low support or having conflictual relations with teachers during elementary school impede children’s self- and stress-regulation. The affected self- and stress-regulation places these children at risk of developing similar troublesome relations with teachers and peers after the transition to high school.
We propose to develop a serious game named A.L.I.B.I. to help children make a successful transition from elementary school to high school. In A.L.I.B.I. children play in a virtual high school environment. The objective of A.L.I.B.I. is to uncover an alien, who is disguised as a teacher or peer. By engaging in prosocial interactions with teachers and peers, by taking the perspective of others, by learning to overthink multiple response options before acting, and by valuing long term perspectives over short term goals, children will receive clues that will help them to uncover the alien.
The advantage of A.L.I.B.I. is that through the use of a virtual school environment, it provides children a realistic yet safe environment to learn and rehearse prosocial behaviors, to prepare them for the new social environment. In addition, A.L.I.B.I. is intuitively attractive for children, through its use of game elements and presentation on a tablet computer. The proposed ERC PoC grant has the goal to (1) develop A.L.I.B.I. into a stand-alone serious game that will be ready for implementation, (2) to test the effectiveness of A.L.I.B.I., (3) to integrate A.L.I.B.I. in ongoing school transition trainings as provided by three school counseling organizations in three regions in The Netherlands, and (4) to develop a marketing strategy for broader Dutch and European implementation.
Summary
Poor social experiences with peers, such as peer rejection or peer victimization, and with teachers, such as receiving low support or having conflictual relations with teachers during elementary school impede children’s self- and stress-regulation. The affected self- and stress-regulation places these children at risk of developing similar troublesome relations with teachers and peers after the transition to high school.
We propose to develop a serious game named A.L.I.B.I. to help children make a successful transition from elementary school to high school. In A.L.I.B.I. children play in a virtual high school environment. The objective of A.L.I.B.I. is to uncover an alien, who is disguised as a teacher or peer. By engaging in prosocial interactions with teachers and peers, by taking the perspective of others, by learning to overthink multiple response options before acting, and by valuing long term perspectives over short term goals, children will receive clues that will help them to uncover the alien.
The advantage of A.L.I.B.I. is that through the use of a virtual school environment, it provides children a realistic yet safe environment to learn and rehearse prosocial behaviors, to prepare them for the new social environment. In addition, A.L.I.B.I. is intuitively attractive for children, through its use of game elements and presentation on a tablet computer. The proposed ERC PoC grant has the goal to (1) develop A.L.I.B.I. into a stand-alone serious game that will be ready for implementation, (2) to test the effectiveness of A.L.I.B.I., (3) to integrate A.L.I.B.I. in ongoing school transition trainings as provided by three school counseling organizations in three regions in The Netherlands, and (4) to develop a marketing strategy for broader Dutch and European implementation.
Max ERC Funding
150 000 €
Duration
Start date: 2020-08-01, End date: 2022-01-31
Project acronym AACCT
Project Advanced Atmospheric Carbon Capture Technology
Researcher (PI) Wolfgang SCHMITT
Host Institution (HI) THE PROVOST, FELLOWS, FOUNDATION SCHOLARS & THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY & UNDIVIDED TRINITY OF QUEEN ELIZABETH NEAR DUBLIN
Country Ireland
Call Details Proof of Concept (PoC), ERC-2019-PoC
Summary Ever increasing atmospheric CO2 concentrations and global emissions of 36 Gt/year impose unprecedented threats to the world’s ecosystem and endanger industrial human activities in their entirety. This AACCT project will establish a new advanced technology that facilitates efficient CO2 capture from air and results in a commercial, stand-alone prototype that will demonstrate its economical and ecological viability, outperforming all other emerging approaches to atmospheric CO2 capture. The technology takes advantage of unique, intrinsic micro- and macro-molecular structures of porous materials that were developed within the ERC SUPRAMOL and Science Foundation Ireland funded projects. These adsorbents reveal extraordinary affinity to CO2, are non-corrosive, non-toxic and are based on stable, cheap and abundant silica materials. The system operates in moist air whereby the CO2 recovery is facilitated at mild conditions under which the adsorbent is regenerated. These intrinsic characteristics in combination with the macro-structure of sub-millimetre pellets that enhances the ad/desorption kinetics, results in exceptionally low operational CO2 capture costs. The technology is modular and the number of capture units scales linearly with the desired CO2 quantity. It is not restricted to fixed locations or CO2 point sources and thus, can conceptionally lead to negative or net zero CO2 emissions.
The AACCT technology will provide pure CO2 that can be sold, used or transformed within established or emerging chemical processes (i.e. methanol synthesis). Initially, it is envisaged that the systems, using low-grade waste heat, will be employed in energy-intensive industrial sectors requiring air circulation and cooling devices. A very modest adaptation of the AACCT prototypes can facilitate the reduction of Ireland’s greenhouse gas emissions by >10%, thus highlighting the potential impact and scalability of the proposed technology at European and global levels.
Summary
Ever increasing atmospheric CO2 concentrations and global emissions of 36 Gt/year impose unprecedented threats to the world’s ecosystem and endanger industrial human activities in their entirety. This AACCT project will establish a new advanced technology that facilitates efficient CO2 capture from air and results in a commercial, stand-alone prototype that will demonstrate its economical and ecological viability, outperforming all other emerging approaches to atmospheric CO2 capture. The technology takes advantage of unique, intrinsic micro- and macro-molecular structures of porous materials that were developed within the ERC SUPRAMOL and Science Foundation Ireland funded projects. These adsorbents reveal extraordinary affinity to CO2, are non-corrosive, non-toxic and are based on stable, cheap and abundant silica materials. The system operates in moist air whereby the CO2 recovery is facilitated at mild conditions under which the adsorbent is regenerated. These intrinsic characteristics in combination with the macro-structure of sub-millimetre pellets that enhances the ad/desorption kinetics, results in exceptionally low operational CO2 capture costs. The technology is modular and the number of capture units scales linearly with the desired CO2 quantity. It is not restricted to fixed locations or CO2 point sources and thus, can conceptionally lead to negative or net zero CO2 emissions.
The AACCT technology will provide pure CO2 that can be sold, used or transformed within established or emerging chemical processes (i.e. methanol synthesis). Initially, it is envisaged that the systems, using low-grade waste heat, will be employed in energy-intensive industrial sectors requiring air circulation and cooling devices. A very modest adaptation of the AACCT prototypes can facilitate the reduction of Ireland’s greenhouse gas emissions by >10%, thus highlighting the potential impact and scalability of the proposed technology at European and global levels.
Max ERC Funding
150 000 €
Duration
Start date: 2019-10-01, End date: 2021-09-30
Project acronym ABIONYS
Project Artificial Enzyme Modules as Tools in a Tailor-made Biosynthesis
Researcher (PI) Jan DESKA
Host Institution (HI) AALTO KORKEAKOULUSAATIO SR
Country Finland
Call Details Consolidator Grant (CoG), PE5, ERC-2019-COG
Summary In order to tackle some of the prime societal challenges of this century, science has to urgently provide effective tools addressing the redesign of chemical value chains through the exploitation of novel, bio-based raw materials, and the discovery and implementation of more resource-efficient production platforms. Nature will inevitably play a pivotal role in the imminent transformation of industrial strategies, and the recent bioeconomy approaches can only be regarded as initial step towards a sustainable future. Operating at the interface between chemistry and life sciences, my ABIONYS will fundamentally challenge the widely held distinction separating chemical from biosynthesis, and will deliver the first proof-of-concept where abiotic reactions act as productive puzzle pieces in biosynthetic arrangements. On the basis of our previous ground-breaking discoveries on artificial enzyme functions, I will create a significantly extended toolbox of biocatalysis modules by applying protein-based interpretations of synthetically crucial but non-natural reactions i.e. transformations that are in no way biosynthetically encoded in living organisms. My research will exploit these tools in multi-enzyme cascades for the preparation of complex organic target structures, not only to highlight the great synthetic potential of these approaches, but also to lay the groundwork for in vivo implementations. Eventually, the knowledge gathered from enzyme discovery and cascade design will enable to create an unprecedented class of bioproduction systems, where the genetic incorporation of artificial enzyme functions into recombinant microbial host organisms will yield tailor-made cellular factories. Combining classical organic synthesis strategies with the power of modern biotechnology, ABIONYS is going to transform the way we synthesize complex and functional building blocks by allowing us to encode organic chemistry thinking into living production platforms.
Summary
In order to tackle some of the prime societal challenges of this century, science has to urgently provide effective tools addressing the redesign of chemical value chains through the exploitation of novel, bio-based raw materials, and the discovery and implementation of more resource-efficient production platforms. Nature will inevitably play a pivotal role in the imminent transformation of industrial strategies, and the recent bioeconomy approaches can only be regarded as initial step towards a sustainable future. Operating at the interface between chemistry and life sciences, my ABIONYS will fundamentally challenge the widely held distinction separating chemical from biosynthesis, and will deliver the first proof-of-concept where abiotic reactions act as productive puzzle pieces in biosynthetic arrangements. On the basis of our previous ground-breaking discoveries on artificial enzyme functions, I will create a significantly extended toolbox of biocatalysis modules by applying protein-based interpretations of synthetically crucial but non-natural reactions i.e. transformations that are in no way biosynthetically encoded in living organisms. My research will exploit these tools in multi-enzyme cascades for the preparation of complex organic target structures, not only to highlight the great synthetic potential of these approaches, but also to lay the groundwork for in vivo implementations. Eventually, the knowledge gathered from enzyme discovery and cascade design will enable to create an unprecedented class of bioproduction systems, where the genetic incorporation of artificial enzyme functions into recombinant microbial host organisms will yield tailor-made cellular factories. Combining classical organic synthesis strategies with the power of modern biotechnology, ABIONYS is going to transform the way we synthesize complex and functional building blocks by allowing us to encode organic chemistry thinking into living production platforms.
Max ERC Funding
1 995 707 €
Duration
Start date: 2020-11-01, End date: 2025-10-31
Project acronym ABODYFORCE
Project High Throughput Microfluidic Cell and Nanoparticle Handling by Molecular and Thermal Gradient Acoustic Focusing
Researcher (PI) Per AUGUSTSSON
Host Institution (HI) LUNDS UNIVERSITET
Country Sweden
Call Details Starting Grant (StG), PE7, ERC-2019-STG
Summary In this project we will push the limits of microscale ultrasound-based technology to gain access to diagnostically important rare constituents of blood within minutes from blood draw.
To meet the demands for shorter time from sampling to result in healthcare there is an increased interest to shift from heavy centralized lab equipment to point-of-care tests and patient self-testing. Key challenges with point-of-care equipment is to enable simultaneous measurement of many parameters at a reasonable cost and size of equipment. Therefore, microscale technologies that can take in small amounts of blood and output results within minutes are sought for. In addition, the high precision and potential for multi-stage serial processing offered by such microfluidic methods opens up for fast and automated isolation of rare cell populations, such as circulating tumor cells, and controlled high-throughput size fractionation of sub-micron biological particles, such as platelets, pathogens and extracellular vesicles.
To achieve effective and fast separation of blood components we will expose blood to acoustic radiation forces in a flow-through format. By exploiting a newly discovered acoustic body force, that stems from local variations the acoustic properties of the cell suspension, we can generate self-organizing configurations of the blood cells. We will tailor and tune the acoustic cell-organization in novel ways by time modulation of the acoustic field, by altering the acoustic properties of the fluid by solute molecules, and by exploiting a novel concept of sound interaction with thermal gradients.
The project will render new fundamental knowledge regarding the acoustic properties of single cells and an extensive theoretical framework for the response of cells in any aqueous medium, bounding geometry and sound field, potentially leading to new diagnostic methods.
Summary
In this project we will push the limits of microscale ultrasound-based technology to gain access to diagnostically important rare constituents of blood within minutes from blood draw.
To meet the demands for shorter time from sampling to result in healthcare there is an increased interest to shift from heavy centralized lab equipment to point-of-care tests and patient self-testing. Key challenges with point-of-care equipment is to enable simultaneous measurement of many parameters at a reasonable cost and size of equipment. Therefore, microscale technologies that can take in small amounts of blood and output results within minutes are sought for. In addition, the high precision and potential for multi-stage serial processing offered by such microfluidic methods opens up for fast and automated isolation of rare cell populations, such as circulating tumor cells, and controlled high-throughput size fractionation of sub-micron biological particles, such as platelets, pathogens and extracellular vesicles.
To achieve effective and fast separation of blood components we will expose blood to acoustic radiation forces in a flow-through format. By exploiting a newly discovered acoustic body force, that stems from local variations the acoustic properties of the cell suspension, we can generate self-organizing configurations of the blood cells. We will tailor and tune the acoustic cell-organization in novel ways by time modulation of the acoustic field, by altering the acoustic properties of the fluid by solute molecules, and by exploiting a novel concept of sound interaction with thermal gradients.
The project will render new fundamental knowledge regarding the acoustic properties of single cells and an extensive theoretical framework for the response of cells in any aqueous medium, bounding geometry and sound field, potentially leading to new diagnostic methods.
Max ERC Funding
1 999 720 €
Duration
Start date: 2019-11-01, End date: 2024-10-31
Project acronym ABOLED
Project Commercial feasibility of an anti-bacterial treatment
Researcher (PI) Ifor SAMUEL
Host Institution (HI) THE UNIVERSITY COURT OF THE UNIVERSITY OF ST ANDREWS
Country United Kingdom
Call Details Proof of Concept (PoC), ERC-2019-PoC
Summary Multidrug resistance of pathogenic bacteria has become a serious threat to public health. The need to develop novel technologies to combat the evolution of bacterial drug resistance is clearly a matter of public concern and urgency. The consequences of AMR include (i) reducing our ability to treat common infectious, resulting in prolonged illness and a greater risk of complications; (ii) patients remaining infectious for longer due to ineffective treatments, making them more likely to pass infections on to others; (iii) compromising advances in modern medicine (such as organ transplantation or chemotherapy) due to risk of infection; and (iv) increasing economic burden on health care systems, families, and societies. This project aims to assess the commercial viability of an alternative approach to this problem.
Summary
Multidrug resistance of pathogenic bacteria has become a serious threat to public health. The need to develop novel technologies to combat the evolution of bacterial drug resistance is clearly a matter of public concern and urgency. The consequences of AMR include (i) reducing our ability to treat common infectious, resulting in prolonged illness and a greater risk of complications; (ii) patients remaining infectious for longer due to ineffective treatments, making them more likely to pass infections on to others; (iii) compromising advances in modern medicine (such as organ transplantation or chemotherapy) due to risk of infection; and (iv) increasing economic burden on health care systems, families, and societies. This project aims to assess the commercial viability of an alternative approach to this problem.
Max ERC Funding
150 000 €
Duration
Start date: 2019-08-01, End date: 2021-07-31
Project acronym AccelOnChip
Project Attosecond physics, free electron quantum optics, photon generation and radiation biology with the accelerator on a photonic chip
Researcher (PI) Peter HOMMELHOFF
Host Institution (HI) FRIEDRICH-ALEXANDER-UNIVERSITAET ERLANGEN-NUERNBERG
Country Germany
Call Details Advanced Grant (AdG), PE2, ERC-2019-ADG
Summary Resting on our demonstration of laser-driven nanophotonics-based particle acceleration, we propose to build a miniature particle accelerator on a photonic chip, comprising high gradient acceleration and fully optical field-based electron control. The resulting electron beam has outstanding space-time properties: It is bunched on sub-femtosecond timescales, is nanometres wide and coherent. We aim at utilizing this new form of all-optical free electron control in a broad research program with five exciting objectives:
(1) Build a 5 MeV accelerator on a photonic chip in a shoebox-sized vessel,
(2) Perform ultrafast diffraction with attosecond and even zeptosecond electron pulses,
(3) Generate photons on chip at various wavelengths (IR to x-ray),
(4) Couple quantum-coherently electron wavepackets and light in multiple interaction zones, and
(5) Conduct radiobiological experiments, akin to the new FLASH radiotherapy and Microbeam cell treat-ment.
AccelOnChip will enable five science objectives potentially shifting the horizons of today’s knowledge and capabilities around ultrafast electron imaging, photon generation, (quantum) electron-light coupling, and radiotherapy dramatically. Moreover, AccelOnChip promises to democratize accelerators: the accelerator on a chip will be based on inexpensive nanofabrication technology. We foresee that every university lab can have access to particle and light sources, today only accessible at large facilities. Last, AccelOnChip will take decisive steps towards an ultracompact electron beam radiation device to be put into the tip of a catheter, a potentially disruptive radiation therapy device facilitating new treatment forms. AccelOnChip is a cross-disciplinary high risk/high return project combining and benefiting nanophotonics, accelerator science, ultra-fast physics, materials science, coherent light-matter coupling, light generation, and radiology - and is based on my group’s unique expertise acquired in recent years.
Summary
Resting on our demonstration of laser-driven nanophotonics-based particle acceleration, we propose to build a miniature particle accelerator on a photonic chip, comprising high gradient acceleration and fully optical field-based electron control. The resulting electron beam has outstanding space-time properties: It is bunched on sub-femtosecond timescales, is nanometres wide and coherent. We aim at utilizing this new form of all-optical free electron control in a broad research program with five exciting objectives:
(1) Build a 5 MeV accelerator on a photonic chip in a shoebox-sized vessel,
(2) Perform ultrafast diffraction with attosecond and even zeptosecond electron pulses,
(3) Generate photons on chip at various wavelengths (IR to x-ray),
(4) Couple quantum-coherently electron wavepackets and light in multiple interaction zones, and
(5) Conduct radiobiological experiments, akin to the new FLASH radiotherapy and Microbeam cell treat-ment.
AccelOnChip will enable five science objectives potentially shifting the horizons of today’s knowledge and capabilities around ultrafast electron imaging, photon generation, (quantum) electron-light coupling, and radiotherapy dramatically. Moreover, AccelOnChip promises to democratize accelerators: the accelerator on a chip will be based on inexpensive nanofabrication technology. We foresee that every university lab can have access to particle and light sources, today only accessible at large facilities. Last, AccelOnChip will take decisive steps towards an ultracompact electron beam radiation device to be put into the tip of a catheter, a potentially disruptive radiation therapy device facilitating new treatment forms. AccelOnChip is a cross-disciplinary high risk/high return project combining and benefiting nanophotonics, accelerator science, ultra-fast physics, materials science, coherent light-matter coupling, light generation, and radiology - and is based on my group’s unique expertise acquired in recent years.
Max ERC Funding
2 498 508 €
Duration
Start date: 2020-10-01, End date: 2025-09-30