Project acronym ACTIVE_ADAPTIVE
Project Active and Adaptive: Reconfigurable Active Colloids with Internal Feedback and Communication Schemes
Researcher (PI) Lucio ISA
Host Institution (HI) EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH
Country Switzerland
Call Details Consolidator Grant (CoG), PE3, ERC-2020-COG
Summary The vision of creating autonomous materials constituted of microscale motile units promises to disrupt a broad range of technologies but is still far beyond our reach. Inspired by nature, these materials are active, i.e. they convert available energy into functions, and adaptive, i.e. they respond to stimuli by reconfiguring via internal feedback and signalling schemes. In order to progress, we need to rethink the way in which we design, fabricate and control synthetic active units, aka active colloids or artificial microswimmers.
I propose an innovative approach that combines colloidal synthesis, assembly and actuation with nanofabrication and the implementation of feedback to realize a new class of active colloids. Borrowing ideas from soft-robotic systems, we aim to realize and study “cyber-free” artificial microswimmers, which, in addition to on-board energy conversion, present internal degrees of freedom allowing for sensing, feedback and communication pathways ultimately to be regulated without external intervention. In particular, we will: 1) Numerically and experimentally implement feedback schemes to regulate single-particle motility and collective behaviour based on control theory. 2) Use a unique combination of capillary assembly and two-photon nanolithography to create shape-shifting active colloids that autonomously regulate their motility based on stimuli orthogonal to their propulsion schemes. 3) Create “transmitting” and “receiving” active colloids, sending and sensing chemical signals (pH changes), to regulate their motility.
By introducing strong coupling between particles, and with stimuli beyond classical colloidal interactions, this proposal will enable a forward leap in the study of the emergent physics of active systems, as required to realize the vision of autonomous materials and microscale devices.
Summary
The vision of creating autonomous materials constituted of microscale motile units promises to disrupt a broad range of technologies but is still far beyond our reach. Inspired by nature, these materials are active, i.e. they convert available energy into functions, and adaptive, i.e. they respond to stimuli by reconfiguring via internal feedback and signalling schemes. In order to progress, we need to rethink the way in which we design, fabricate and control synthetic active units, aka active colloids or artificial microswimmers.
I propose an innovative approach that combines colloidal synthesis, assembly and actuation with nanofabrication and the implementation of feedback to realize a new class of active colloids. Borrowing ideas from soft-robotic systems, we aim to realize and study “cyber-free” artificial microswimmers, which, in addition to on-board energy conversion, present internal degrees of freedom allowing for sensing, feedback and communication pathways ultimately to be regulated without external intervention. In particular, we will: 1) Numerically and experimentally implement feedback schemes to regulate single-particle motility and collective behaviour based on control theory. 2) Use a unique combination of capillary assembly and two-photon nanolithography to create shape-shifting active colloids that autonomously regulate their motility based on stimuli orthogonal to their propulsion schemes. 3) Create “transmitting” and “receiving” active colloids, sending and sensing chemical signals (pH changes), to regulate their motility.
By introducing strong coupling between particles, and with stimuli beyond classical colloidal interactions, this proposal will enable a forward leap in the study of the emergent physics of active systems, as required to realize the vision of autonomous materials and microscale devices.
Max ERC Funding
1 997 718 €
Duration
Start date: 2021-05-01, End date: 2026-04-30
Project acronym AHH-OMICS
Project Understanding collective mechanisms of cell fate regulation using single-cell genomics
Researcher (PI) Steffen Rulands
Host Institution (HI) MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Country Germany
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary Biological systems rely on an influx of energy to build and maintain complex spatio-temporal structures. A striking example of this is the self-organisation of cells into tissues, which relies on an interplay of molecular programs and tissue-level feedback. The mechanistic basis underlying these processes is poorly understood. The recent advent of single-cell sequencing technologies for the first time gives the opportunity to probe these processes with unprecedented molecular resolution in vivo. Biological function, however, relies on collective processes on the cellular scale which emerge from many interactions on the microscopic scale. But what can we learn about such collective processes from detailed empirical information on the molecular scale? Concepts from non-equilibrium statistical physics provide a powerful framework to understand collective processes underlying the self-organisation of cells. In the proposed research endeavour, we will combine the possibilities of novel single-cell technologies with methods from non-equilibrium statistical physics to understand collective processes regulating cellular behaviour. Using this conceptually new approach, we will 1) unveil collective epigenetic processes during differentiation, reprogramming and ageing, 2) determine how the interplay between different layers of regulation leads to the emergence of mesoscopic spatio-temporal structures in vivo, and 3) understand universal fluctuations in gene expression to unveil mechanistic principles of cellular decisions. Our theoretical work will be challenged by single-cell sequencing experiments performed by our collaborators. We will overcome important conceptual limitations in an emerging technology in biology and pioneer the application of methods from non-equilibrium statistical physics to single-cell genomics. At the same time, we take an interdisciplinary approach to tackle questions at the frontier of non-equilibrium physics.
Summary
Biological systems rely on an influx of energy to build and maintain complex spatio-temporal structures. A striking example of this is the self-organisation of cells into tissues, which relies on an interplay of molecular programs and tissue-level feedback. The mechanistic basis underlying these processes is poorly understood. The recent advent of single-cell sequencing technologies for the first time gives the opportunity to probe these processes with unprecedented molecular resolution in vivo. Biological function, however, relies on collective processes on the cellular scale which emerge from many interactions on the microscopic scale. But what can we learn about such collective processes from detailed empirical information on the molecular scale? Concepts from non-equilibrium statistical physics provide a powerful framework to understand collective processes underlying the self-organisation of cells. In the proposed research endeavour, we will combine the possibilities of novel single-cell technologies with methods from non-equilibrium statistical physics to understand collective processes regulating cellular behaviour. Using this conceptually new approach, we will 1) unveil collective epigenetic processes during differentiation, reprogramming and ageing, 2) determine how the interplay between different layers of regulation leads to the emergence of mesoscopic spatio-temporal structures in vivo, and 3) understand universal fluctuations in gene expression to unveil mechanistic principles of cellular decisions. Our theoretical work will be challenged by single-cell sequencing experiments performed by our collaborators. We will overcome important conceptual limitations in an emerging technology in biology and pioneer the application of methods from non-equilibrium statistical physics to single-cell genomics. At the same time, we take an interdisciplinary approach to tackle questions at the frontier of non-equilibrium physics.
Max ERC Funding
1 489 500 €
Duration
Start date: 2021-01-01, End date: 2025-12-31
Project acronym AQE2D
Project Atomic Quantum Emitters in 2D Frameworks
Researcher (PI) Bruno Schuler
Host Institution (HI) EIDGENOSSISCHE MATERIALPRUFUNGS- UND FORSCHUNGSANSTALT
Country Switzerland
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary The ability to create and control connected quantum states established the advent of quantum information technologies (Q-IT). Manipulation of the electron spin associated with colour centres in solid state crystals is one of the pillar technologies that could eventually push Q-IT beyond cryogenic environments. Exploitation of the full potential of these atomic qubit systems is, however, hampered by two key challenges: the lack of atomistic insights into their properties, and the ability to place them with the required fidelity and atomic spatial precision.
Here I propose to converge recent breakthrough developments in the synthetic control of two-dimensional (2D) materials and ultra-fast, single-atom resolving probes to overcome these challenges. Specifically, I will develop a platform for electro-optically addressable spin qubits (Atomic Quantum Emitters, AQEs) in 2D materials based on atomic dopants in transition metal dichalcogenide (TMD) monolayers and molecular spin systems in 2D covalent organic frameworks (2D-COFs). These systems will provide an ideal platform to generate AQEs by chemical design, to control the mesoscopic environment averting variability between emitters, to achieve atomically precise spatial placement, to identify and eliminate decoherence channels, and to develop high-fidelity scalable pumping schemes.
The proposed construction of a spin-polarized ultrafast THz scanning probe microscope with optical detection capabilities will enable the direct correlation of structural, electronic, magnetic, and optical properties of individual AQEs with simultaneous atomic spatial resolution and picosecond time resolution. This will open new frontiers in the spatio-temporal characterization and control of solid-state AQE systems.
The atomically precise engineering of 2D quantum materials and unprecedented microscopic insights into AQEs bear transformative potential for the field of quantum sensing, communication and information processing.
Summary
The ability to create and control connected quantum states established the advent of quantum information technologies (Q-IT). Manipulation of the electron spin associated with colour centres in solid state crystals is one of the pillar technologies that could eventually push Q-IT beyond cryogenic environments. Exploitation of the full potential of these atomic qubit systems is, however, hampered by two key challenges: the lack of atomistic insights into their properties, and the ability to place them with the required fidelity and atomic spatial precision.
Here I propose to converge recent breakthrough developments in the synthetic control of two-dimensional (2D) materials and ultra-fast, single-atom resolving probes to overcome these challenges. Specifically, I will develop a platform for electro-optically addressable spin qubits (Atomic Quantum Emitters, AQEs) in 2D materials based on atomic dopants in transition metal dichalcogenide (TMD) monolayers and molecular spin systems in 2D covalent organic frameworks (2D-COFs). These systems will provide an ideal platform to generate AQEs by chemical design, to control the mesoscopic environment averting variability between emitters, to achieve atomically precise spatial placement, to identify and eliminate decoherence channels, and to develop high-fidelity scalable pumping schemes.
The proposed construction of a spin-polarized ultrafast THz scanning probe microscope with optical detection capabilities will enable the direct correlation of structural, electronic, magnetic, and optical properties of individual AQEs with simultaneous atomic spatial resolution and picosecond time resolution. This will open new frontiers in the spatio-temporal characterization and control of solid-state AQE systems.
The atomically precise engineering of 2D quantum materials and unprecedented microscopic insights into AQEs bear transformative potential for the field of quantum sensing, communication and information processing.
Max ERC Funding
2 139 400 €
Duration
Start date: 2021-10-01, End date: 2026-09-30
Project acronym CoherentGlasses
Project A coherent view of Glasses: How coherent x-rays can elucidate the complex dynamics of glasses
Researcher (PI) Beatrice RUTA
Host Institution (HI) CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
Country France
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary "Glasses are mysterious materials. Fundamental blocks in many natural and technological processes, still, their properties keep puzzling a large community of scientists nowadays. Following different experimental routes, materials as diverse as colloidal suspensions, emulsions and viscous liquids can be driven in an out-of-equilibrium state, where they solidify under conditions that still remain unknown. This process, traditionally called glass transition, leads to many intriguing phenomena as the emergence of multiple relaxations processes, dynamical heterogeneities, crossovers between distinct amorphous states, and uncommon mechanisms of particle motions.
Within the large family of disordered systems, structural glasses play a key role being often considered as archetypes of out-of-equilibrium materials. Despite decades of studies, a microscopic theory of glasses is still missing due to the difficulty to probe their atomic motion with experiments and simulations.
Few years ago, I used coherent x-rays to perform the first worldwide experiments probing the atomic motion of glasses. My works reported on a surprising glassy dynamic reminiscent of an anomalous stress-driven particle motion observed in some soft systems. Due to severe technical constraints, the studies performed so far were limited to the external, tiny portion of the huge ""iceberg” of dynamical features occurring at the atomic level, whose comprehension would enable substantial advances in the frontiers of knowledge.
Thanks to the new possibilities offered by coherent x-rays, now is the right time to unveil the atomic dance of glasses in all its complexity with the CoherentGlasses project. Following four challenging experimental Research Objectives, we will provide a coherent picture of the microscopic dynamic and structural features accounting for the above discussed fascinating phenomena in glass-formers.
A successful project keeps the promise to boost our knowledge on out-of-equilibrium material."
Summary
"Glasses are mysterious materials. Fundamental blocks in many natural and technological processes, still, their properties keep puzzling a large community of scientists nowadays. Following different experimental routes, materials as diverse as colloidal suspensions, emulsions and viscous liquids can be driven in an out-of-equilibrium state, where they solidify under conditions that still remain unknown. This process, traditionally called glass transition, leads to many intriguing phenomena as the emergence of multiple relaxations processes, dynamical heterogeneities, crossovers between distinct amorphous states, and uncommon mechanisms of particle motions.
Within the large family of disordered systems, structural glasses play a key role being often considered as archetypes of out-of-equilibrium materials. Despite decades of studies, a microscopic theory of glasses is still missing due to the difficulty to probe their atomic motion with experiments and simulations.
Few years ago, I used coherent x-rays to perform the first worldwide experiments probing the atomic motion of glasses. My works reported on a surprising glassy dynamic reminiscent of an anomalous stress-driven particle motion observed in some soft systems. Due to severe technical constraints, the studies performed so far were limited to the external, tiny portion of the huge ""iceberg” of dynamical features occurring at the atomic level, whose comprehension would enable substantial advances in the frontiers of knowledge.
Thanks to the new possibilities offered by coherent x-rays, now is the right time to unveil the atomic dance of glasses in all its complexity with the CoherentGlasses project. Following four challenging experimental Research Objectives, we will provide a coherent picture of the microscopic dynamic and structural features accounting for the above discussed fascinating phenomena in glass-formers.
A successful project keeps the promise to boost our knowledge on out-of-equilibrium material."
Max ERC Funding
1 486 931 €
Duration
Start date: 2021-03-01, End date: 2026-02-28
Project acronym CoulENGINE
Project Coulomb Engineering of Quantum States in Matter
Researcher (PI) Alexey Chernikov
Host Institution (HI) UNIVERSITAET REGENSBURG
Country Germany
Call Details Consolidator Grant (CoG), PE3, ERC-2020-COG
Summary Key phenomena in condensed matter are determined by the properties of the electronic states, strongly motivating the development of strategies for their artificial design. In semiconducting solids, heavily studied from fundamental and technological perspectives, electronic structures are currently defined using strong perturbations of the materials such as tuning the chemical composition, changing the geometry, or applying external fields. Traditional concepts, however, inherently rely on modifying single-particle properties of individual electrons, while the influence of many-particle interactions has been largely neglected in the context of bandstructure engineering so far. In addition, conventional methods start to approach intrinsic barriers in today’s technology, driving an intense search for fundamentally novel concepts.
Here, I propose to explore an alternative pathway to design and manipulate electronic states in matter that is exclusively based on many-particle interactions between electronic excitations mediated by Coulomb forces. These are exceptionally strong in two-dimensional (2D) semiconductors with a major impact on the energies of the electronic states, and are highly sensitive to the dielectric surroundings. Using layered heterostructures I intend to show how the dielectric environment of a 2D semiconductor can be tuned on ultrafast timescales by pulsed optical injection to manipulate electronic states via proximity screening. Similarly, external screening will be used to study how the geometry of proximate objects can be imprinted on the electronic structure of a 2D layer, creating dielectrically defined zero-, one-, and two-dimensional potentials in one unified system. Ultimately, the realization of rapidly tunable electronic quantum states through dielectric environment will offer novel, versatile experimental platforms for fundamental many-body physics research and establish a new approach for electronic structure engineering on the nanoscale.
Summary
Key phenomena in condensed matter are determined by the properties of the electronic states, strongly motivating the development of strategies for their artificial design. In semiconducting solids, heavily studied from fundamental and technological perspectives, electronic structures are currently defined using strong perturbations of the materials such as tuning the chemical composition, changing the geometry, or applying external fields. Traditional concepts, however, inherently rely on modifying single-particle properties of individual electrons, while the influence of many-particle interactions has been largely neglected in the context of bandstructure engineering so far. In addition, conventional methods start to approach intrinsic barriers in today’s technology, driving an intense search for fundamentally novel concepts.
Here, I propose to explore an alternative pathway to design and manipulate electronic states in matter that is exclusively based on many-particle interactions between electronic excitations mediated by Coulomb forces. These are exceptionally strong in two-dimensional (2D) semiconductors with a major impact on the energies of the electronic states, and are highly sensitive to the dielectric surroundings. Using layered heterostructures I intend to show how the dielectric environment of a 2D semiconductor can be tuned on ultrafast timescales by pulsed optical injection to manipulate electronic states via proximity screening. Similarly, external screening will be used to study how the geometry of proximate objects can be imprinted on the electronic structure of a 2D layer, creating dielectrically defined zero-, one-, and two-dimensional potentials in one unified system. Ultimately, the realization of rapidly tunable electronic quantum states through dielectric environment will offer novel, versatile experimental platforms for fundamental many-body physics research and establish a new approach for electronic structure engineering on the nanoscale.
Max ERC Funding
1 999 627 €
Duration
Start date: 2021-07-01, End date: 2026-06-30
Project acronym DeQ
Project Quantifying electron-electron forces at the atomic scale
Researcher (PI) Nadine HAUPTMANN
Host Institution (HI) STICHTING KATHOLIEKE UNIVERSITEIT
Country Netherlands
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary Quantum phases of matter in novel 2D materials host fascinating correlated electron properties, such as unconventional superconductivity, novel insulating phases and exotic magnetic order. These phenomena are a hotbed of new forms of energy-efficient technologies, which require fundamental understanding and exploration of these material classes. Since the beginning, scientists have been struggling with the puzzling lack of consistent predictability of such materials, leading predominantly to serendipitous discoveries. The key ingredient driving these exotic quantum phases are electron-electron interactions, so-called correlations. These correlations between the electrons play a prominent role in their movement, and often result into atomic-scale charge and spin order, and are amplified in 2D materials compared to their 3D counterparts. Owing to the 2D nature, a new state-of-the-art methodology is needed to elucidate the electronic and magnetic properties in correlated 2D quantum materials. DeQ investigates the role of electron correlations and their interplay with structural and spin degrees of freedom at the single-atom level in insulating quantum phases of novel 2D materials. To accomplish this aim, my innovative strategy is to quantify atomic-scale charge and spin order at transitions between different quantum phases in three classes of hallmark 2D materials: twisted bilayers, correlated quasi-2D compounds, and 2D magnetic materials. My novel approach is based on creating a new state of the art in atomic imaging and spectroscopy, the JAQ setup. The development of JAQ will enable us to precisely tune relevant parameters, like electric and magnetic fields, in the highest-quality materials available. The outcome of DeQ will be groundbreaking for predicting electron correlations in novel quantum phases in 2D materials, which that are a hotbed of innovative forms of energy-efficient technologies.
Summary
Quantum phases of matter in novel 2D materials host fascinating correlated electron properties, such as unconventional superconductivity, novel insulating phases and exotic magnetic order. These phenomena are a hotbed of new forms of energy-efficient technologies, which require fundamental understanding and exploration of these material classes. Since the beginning, scientists have been struggling with the puzzling lack of consistent predictability of such materials, leading predominantly to serendipitous discoveries. The key ingredient driving these exotic quantum phases are electron-electron interactions, so-called correlations. These correlations between the electrons play a prominent role in their movement, and often result into atomic-scale charge and spin order, and are amplified in 2D materials compared to their 3D counterparts. Owing to the 2D nature, a new state-of-the-art methodology is needed to elucidate the electronic and magnetic properties in correlated 2D quantum materials. DeQ investigates the role of electron correlations and their interplay with structural and spin degrees of freedom at the single-atom level in insulating quantum phases of novel 2D materials. To accomplish this aim, my innovative strategy is to quantify atomic-scale charge and spin order at transitions between different quantum phases in three classes of hallmark 2D materials: twisted bilayers, correlated quasi-2D compounds, and 2D magnetic materials. My novel approach is based on creating a new state of the art in atomic imaging and spectroscopy, the JAQ setup. The development of JAQ will enable us to precisely tune relevant parameters, like electric and magnetic fields, in the highest-quality materials available. The outcome of DeQ will be groundbreaking for predicting electron correlations in novel quantum phases in 2D materials, which that are a hotbed of innovative forms of energy-efficient technologies.
Max ERC Funding
1 912 095 €
Duration
Start date: 2021-01-01, End date: 2025-12-31
Project acronym DynaQuanta
Project Nonequilibrium Terahertz Dynamics of Interacting Quantum Spins: from Novel Driven States towards Coherent Controls
Researcher (PI) Zhe Wang
Host Institution (HI) TECHNISCHE UNIVERSITAT DORTMUND
Country Germany
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary The study of non-equilibrium dynamics of magnetic degrees of freedom has shown remarkable progress over the past two decades. This is in particular true concerning the understanding of ultrafast magnetization dynamics in classical magnets. In contrast, the field of non-equilibrium spin dynamics of many-body quantum magnetic systems is still in its infancy. Despite a number of ground-breaking recent theoretical proposals, experimental studies in this direction are truly scarce and this research field is a largely unexplored territory.
Here I propose to study non-equilibrium dynamics in a number of well-selected quantum spin systems, utilizing a novel and powerful experimental technique – time-resolved terahertz spectroscopy under extreme conditions. By carrying out the here proposed program of non-equilibrium and nonlinear studies on low-dimensional and/or frustrated quantum magnets, I aim to explore and reveal novel physics and the governing fundamental principles for the non-equilibrium quantum spin dynamics. Firstly, I aim to realize novel quantum phenomena and quantum effects, which are difficult to be detected in the equilibrium state, such as complex many-body bound states. Secondly, I will explore novel characteristics for exotic quantum states like quantum spin liquids and quantum critical phases in the nonlinear response regime, by driving the quantum disordered states far from equilibrium. Thirdly, I aim to tune and control the non-equilibrium and nonlinear response of the quantum spin states either by the terahertz electromagnetic fields directly or via coupling to other degrees of freedom, such as phonons. Gaining momentum from the on-going intensive theoretical studies and based on my previous work in the field of quantum spin systems, I anticipate a productive, impactful, and successful research project exploring the new physics offered by non-equilibrium quantum spin systems.
Summary
The study of non-equilibrium dynamics of magnetic degrees of freedom has shown remarkable progress over the past two decades. This is in particular true concerning the understanding of ultrafast magnetization dynamics in classical magnets. In contrast, the field of non-equilibrium spin dynamics of many-body quantum magnetic systems is still in its infancy. Despite a number of ground-breaking recent theoretical proposals, experimental studies in this direction are truly scarce and this research field is a largely unexplored territory.
Here I propose to study non-equilibrium dynamics in a number of well-selected quantum spin systems, utilizing a novel and powerful experimental technique – time-resolved terahertz spectroscopy under extreme conditions. By carrying out the here proposed program of non-equilibrium and nonlinear studies on low-dimensional and/or frustrated quantum magnets, I aim to explore and reveal novel physics and the governing fundamental principles for the non-equilibrium quantum spin dynamics. Firstly, I aim to realize novel quantum phenomena and quantum effects, which are difficult to be detected in the equilibrium state, such as complex many-body bound states. Secondly, I will explore novel characteristics for exotic quantum states like quantum spin liquids and quantum critical phases in the nonlinear response regime, by driving the quantum disordered states far from equilibrium. Thirdly, I aim to tune and control the non-equilibrium and nonlinear response of the quantum spin states either by the terahertz electromagnetic fields directly or via coupling to other degrees of freedom, such as phonons. Gaining momentum from the on-going intensive theoretical studies and based on my previous work in the field of quantum spin systems, I anticipate a productive, impactful, and successful research project exploring the new physics offered by non-equilibrium quantum spin systems.
Max ERC Funding
1 840 898 €
Duration
Start date: 2021-07-01, End date: 2026-06-30
Project acronym FERMIcQED
Project Manipulating single fermions with light in cQED architectures
Researcher (PI) Landry, Beranger Bretheau
Host Institution (HI) ECOLE POLYTECHNIQUE
Country France
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary FERMIcQED aims at interfacing novel quantum materials with microwave light at the level of the single photon and fermion. To achieve this ambitious goal, I plan to use low-dimensional quantum conductors – such as carbon nanotubes or semiconducting nanowires – combined with state-of-the-art architectures and techniques of circuit Quantum Electrodynamics. The idea consists in isolating an individual fermionic degree of freedom within a hybrid Josephson junction – a quantum dot connected to two superconductors. Due to the superconducting proximity effect, entangled electron-hole states – called the Andreev bound states – form in the quantum dot and depend on the superconducting phase difference. By enclosing the hybrid Josephson junction inside a superconducting photonic cavity, one can couple these fermionic states to microwave light and probe their quantum properties in a well-controlled environment.
Specifically, FERMIcQED will tackle three key experiments. First, we will detect the spin degree of freedom of the Andreev bound states and manipulate it coherently as a superconducting spin qubit. We will demonstrate strong coupling with cavity photons, which will enable quantum logic operations and long-range qubit interactions. Second, we will operate the hybrid Josephson junction in the topological regime in order to observe and manipulate Majorana fermions, thus implementing a topological qubit. At last, we will probe the joint entangled dynamics of bosonic and fermionic modes that coexist in hybrid Josephson junctions and simulate the spin-boson problem.
Summary
FERMIcQED aims at interfacing novel quantum materials with microwave light at the level of the single photon and fermion. To achieve this ambitious goal, I plan to use low-dimensional quantum conductors – such as carbon nanotubes or semiconducting nanowires – combined with state-of-the-art architectures and techniques of circuit Quantum Electrodynamics. The idea consists in isolating an individual fermionic degree of freedom within a hybrid Josephson junction – a quantum dot connected to two superconductors. Due to the superconducting proximity effect, entangled electron-hole states – called the Andreev bound states – form in the quantum dot and depend on the superconducting phase difference. By enclosing the hybrid Josephson junction inside a superconducting photonic cavity, one can couple these fermionic states to microwave light and probe their quantum properties in a well-controlled environment.
Specifically, FERMIcQED will tackle three key experiments. First, we will detect the spin degree of freedom of the Andreev bound states and manipulate it coherently as a superconducting spin qubit. We will demonstrate strong coupling with cavity photons, which will enable quantum logic operations and long-range qubit interactions. Second, we will operate the hybrid Josephson junction in the topological regime in order to observe and manipulate Majorana fermions, thus implementing a topological qubit. At last, we will probe the joint entangled dynamics of bosonic and fermionic modes that coexist in hybrid Josephson junctions and simulate the spin-boson problem.
Max ERC Funding
1 499 133 €
Duration
Start date: 2021-09-01, End date: 2026-08-31
Project acronym FlowMem
Project Flow network morphology as memory map: Principles of fluid flow driven dynamic memory in living tubular networks
Researcher (PI) Karen Alim
Host Institution (HI) TECHNISCHE UNIVERSITAET MUENCHEN
Country Germany
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary Fluid flows through tubular networks are crucial for life as they are the dominant means of substance and signal transport. In living networks – across organisms as disparate as animals and fungi, alterations of flows drive dynamic adaptation of tube diameters which in turn alters transport performance. In effect, local transient stimuli that affect flows are memorized as long-lived alterations to tube diameters across the network. I aim to identify the physical principles behind fluid flows driving dynamic memory storage in network morphology. I will thereby uncover how to control network morphology and performance by applied flow-altering stimuli, which promises significant advances in important challenges of the future: treatment of vascular diseases and tumour development, encoding complex behaviour in soft robotics and self-optimizing porous media.
The dynamic nature of flows and networks’ complex morphologies requires a combined experimental and theoretical approach to address: What are the physical mechanisms of how flows in living tubular networks can encode and store information about stimuli? How do memories impact network performance? As experimental model system I choose the slime mould Physarum polycephalum. It is ideally suited as a starting point, as it reduces the problem in its complexity to just a tubular network. This model allows me to follow with unprecedented level of detail how stimuli transiently perturb network-wide flows – flows that subsequently drive long-term changes in network morphology. Theoretical models will verify mechanisms and allow investigation of impact on network function. Identified principles of dynamic memory formation will be applied to study consequences of mini-stroke stimuli and possible treatment in brain microvasculature and to design self-optimizing porous media. I will develop general principles advancing physics and biology with far-reaching implications in medicine and engineering.
Summary
Fluid flows through tubular networks are crucial for life as they are the dominant means of substance and signal transport. In living networks – across organisms as disparate as animals and fungi, alterations of flows drive dynamic adaptation of tube diameters which in turn alters transport performance. In effect, local transient stimuli that affect flows are memorized as long-lived alterations to tube diameters across the network. I aim to identify the physical principles behind fluid flows driving dynamic memory storage in network morphology. I will thereby uncover how to control network morphology and performance by applied flow-altering stimuli, which promises significant advances in important challenges of the future: treatment of vascular diseases and tumour development, encoding complex behaviour in soft robotics and self-optimizing porous media.
The dynamic nature of flows and networks’ complex morphologies requires a combined experimental and theoretical approach to address: What are the physical mechanisms of how flows in living tubular networks can encode and store information about stimuli? How do memories impact network performance? As experimental model system I choose the slime mould Physarum polycephalum. It is ideally suited as a starting point, as it reduces the problem in its complexity to just a tubular network. This model allows me to follow with unprecedented level of detail how stimuli transiently perturb network-wide flows – flows that subsequently drive long-term changes in network morphology. Theoretical models will verify mechanisms and allow investigation of impact on network function. Identified principles of dynamic memory formation will be applied to study consequences of mini-stroke stimuli and possible treatment in brain microvasculature and to design self-optimizing porous media. I will develop general principles advancing physics and biology with far-reaching implications in medicine and engineering.
Max ERC Funding
1 499 905 €
Duration
Start date: 2021-10-01, End date: 2026-09-30
Project acronym FuelledLife
Project Selection and Regulation of Compartments by Fuel-driven Phase Separation
Researcher (PI) Christoph Weber
Host Institution (HI) LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN
Country Germany
Call Details Starting Grant (StG), PE3, ERC-2020-STG
Summary Living cells rely on the compartmentalisation of thousands of different molecules and their chemical reactions. Remarkably, many of such compartments form by phase separation of heteropolymers controlled by sequence-specific interactions and fuel that drives reactions away from equilibrium. If we knew how such polymers with sequence-specific interactions evolve and compartmentalise in fuel-driven multi-component mixtures, we would better understand the role of phase separation in living cells and how synthetic or prebiotic cells emerge.
I aim to study how fuel-driven phase separation can drive the selection and replication of hetero-polymers with sequence-specific interactions, the control of their chemical reactions and the emergence and selection of different compartments. My team and I will develop a theory for phase separation and chemical reactions in multi-component mixtures driven away from equilibrium by irreversible, fuel-driven reactions. This theory will provide a link between phenomena on the compartment scale and coarse-grained properties of sequences. First, we will use this theory to study how compartments control biochemical reactions, and how this control is determined by sequence. Second, we will investigate how sequences are selected, replicated and evolve under cyclic, non-equilibrium conditions. Third, we will use our theory to unravel how fuel-driven chemical reactions regulate formation and division of compartments, and affect selection of different compartments within a population. Our theoretical studies will elucidate the physical mechanisms and conditions which will be experimentally scrutinised by our collaborators.
Our results will let us understand how living cells regulate phase separation, like the formation of stress granules by selecting RNA. Moreover, our results will elucidate the role of phase separation for the emergence of life by determining the prerequisites of a protocell to divide, replicate and undergo selection.
Summary
Living cells rely on the compartmentalisation of thousands of different molecules and their chemical reactions. Remarkably, many of such compartments form by phase separation of heteropolymers controlled by sequence-specific interactions and fuel that drives reactions away from equilibrium. If we knew how such polymers with sequence-specific interactions evolve and compartmentalise in fuel-driven multi-component mixtures, we would better understand the role of phase separation in living cells and how synthetic or prebiotic cells emerge.
I aim to study how fuel-driven phase separation can drive the selection and replication of hetero-polymers with sequence-specific interactions, the control of their chemical reactions and the emergence and selection of different compartments. My team and I will develop a theory for phase separation and chemical reactions in multi-component mixtures driven away from equilibrium by irreversible, fuel-driven reactions. This theory will provide a link between phenomena on the compartment scale and coarse-grained properties of sequences. First, we will use this theory to study how compartments control biochemical reactions, and how this control is determined by sequence. Second, we will investigate how sequences are selected, replicated and evolve under cyclic, non-equilibrium conditions. Third, we will use our theory to unravel how fuel-driven chemical reactions regulate formation and division of compartments, and affect selection of different compartments within a population. Our theoretical studies will elucidate the physical mechanisms and conditions which will be experimentally scrutinised by our collaborators.
Our results will let us understand how living cells regulate phase separation, like the formation of stress granules by selecting RNA. Moreover, our results will elucidate the role of phase separation for the emergence of life by determining the prerequisites of a protocell to divide, replicate and undergo selection.
Max ERC Funding
1 498 852 €
Duration
Start date: 2021-06-01, End date: 2026-05-31