Project acronym ACOPS
Project Advanced Coherent Ultrafast Laser Pulse Stacking
Researcher (PI) Jens Limpert
Host Institution (HI) FRIEDRICH-SCHILLER-UNIVERSITAT JENA
Country Germany
Call Details Consolidator Grant (CoG), PE2, ERC-2013-CoG
Summary "An important driver of scientific progress has always been the envisioning of applications far beyond existing technological capabilities. Such thinking creates new challenges for physicists, driven by the groundbreaking nature of the anticipated application. In the case of laser physics, one of these applications is laser wake-field particle acceleration and possible future uses thereof, such as in collider experiments, or for medical applications such as cancer treatment. To accelerate electrons and positrons to TeV-energies, a laser architecture is required that allows for the combination of high efficiency, Petawatt peak powers, and Megawatt average powers. Developing such a laser system would be a challenging task that might take decades of aggressive research, development, and, most important, revolutionary approaches and innovative ideas.
The goal of the ACOPS project is to develop a compact, efficient, scalable, and cost-effective high-average and high-peak power ultra-short pulse laser concept.
The proposed approach to this goal relies on the spatially and temporally separated amplification of ultrashort laser pulses in waveguide structures, followed by coherent combination into a single train of pulses with increased average power and pulse energy. This combination can be realized through the coherent addition of the output beams of spatially separated amplifiers, combined with the pulse stacking of temporally separated pulses in passive enhancement cavities, employing a fast-switching element as cavity dumper.
Therefore, the three main tasks are the development of kW-class high-repetition-rate driving lasers, the investigation of non-steady state pulse enhancement in passive cavities, and the development of a suitable dumping element.
If successful, the proposed concept would undoubtedly provide a tool that would allow researchers to surpass the current limits in high-field physics and accelerator science."
Summary
"An important driver of scientific progress has always been the envisioning of applications far beyond existing technological capabilities. Such thinking creates new challenges for physicists, driven by the groundbreaking nature of the anticipated application. In the case of laser physics, one of these applications is laser wake-field particle acceleration and possible future uses thereof, such as in collider experiments, or for medical applications such as cancer treatment. To accelerate electrons and positrons to TeV-energies, a laser architecture is required that allows for the combination of high efficiency, Petawatt peak powers, and Megawatt average powers. Developing such a laser system would be a challenging task that might take decades of aggressive research, development, and, most important, revolutionary approaches and innovative ideas.
The goal of the ACOPS project is to develop a compact, efficient, scalable, and cost-effective high-average and high-peak power ultra-short pulse laser concept.
The proposed approach to this goal relies on the spatially and temporally separated amplification of ultrashort laser pulses in waveguide structures, followed by coherent combination into a single train of pulses with increased average power and pulse energy. This combination can be realized through the coherent addition of the output beams of spatially separated amplifiers, combined with the pulse stacking of temporally separated pulses in passive enhancement cavities, employing a fast-switching element as cavity dumper.
Therefore, the three main tasks are the development of kW-class high-repetition-rate driving lasers, the investigation of non-steady state pulse enhancement in passive cavities, and the development of a suitable dumping element.
If successful, the proposed concept would undoubtedly provide a tool that would allow researchers to surpass the current limits in high-field physics and accelerator science."
Max ERC Funding
1 881 040 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym ASTONISH
Project Atomic-scale STudies Of the Nature of and conditions for Inducing Superconductivity at High-temperatures
Researcher (PI) Roland Martin Wiesendanger
Host Institution (HI) UNIVERSITAET HAMBURG
Country Germany
Call Details Advanced Grant (AdG), PE3, ERC-2013-ADG
Summary "One of the greatest challenges these days in condensed matter physics is the fundamental understanding of the mechanisms leading to high-Tc superconductivity and ultimately, as a result of that, the discovery of a material system exhibiting a superconducting state with a transition temperature Tc above room temperature. While several different classes of high-Tc materials have been discovered in the past decades, including the well-known CuO-based superconductors (cuprates) or the more recently discovered class of Fe-based superconductors (pnictides), the mechanisms behind high-Tc superconductivity remain controversial. Up to date, no theory exists which would allow for a rational design of a superconducting material with a transition temperature above room temperature. On the other hand, experiments on rather complex material systems often suffer from material imperfections or from a lack of tunability of materials’ properties within a wide range. Our experimental studies within this project therefore will focus on model-type systems which can be prepared and thoroughly characterized with atomic level precision. The growth of the model-type samples will be controlled vertically one atomic layer at a time and laterally by making use of single-atom manipulation techniques. Atomic-scale characterization at low energy-scales will be performed by low-temperature spin-resolved elastic and inelastic scanning tunnelling microscopy (STM) and spectroscopy (STS) as well as by non-contact atomic force microscopy and spectroscopy based techniques. Transport experiments will be conducted by a four-probe STM setup under well-defined ultra-high vacuum conditions. By having access to the electronic and spin, as well as to the vibrational degrees of freedom down to the atomic level, we hope to be able to identify the nature of and the conditions for inducing superconductivity at high temperatures, which could ultimately lead a knowledge-based design of high-Tc superconductors."
Summary
"One of the greatest challenges these days in condensed matter physics is the fundamental understanding of the mechanisms leading to high-Tc superconductivity and ultimately, as a result of that, the discovery of a material system exhibiting a superconducting state with a transition temperature Tc above room temperature. While several different classes of high-Tc materials have been discovered in the past decades, including the well-known CuO-based superconductors (cuprates) or the more recently discovered class of Fe-based superconductors (pnictides), the mechanisms behind high-Tc superconductivity remain controversial. Up to date, no theory exists which would allow for a rational design of a superconducting material with a transition temperature above room temperature. On the other hand, experiments on rather complex material systems often suffer from material imperfections or from a lack of tunability of materials’ properties within a wide range. Our experimental studies within this project therefore will focus on model-type systems which can be prepared and thoroughly characterized with atomic level precision. The growth of the model-type samples will be controlled vertically one atomic layer at a time and laterally by making use of single-atom manipulation techniques. Atomic-scale characterization at low energy-scales will be performed by low-temperature spin-resolved elastic and inelastic scanning tunnelling microscopy (STM) and spectroscopy (STS) as well as by non-contact atomic force microscopy and spectroscopy based techniques. Transport experiments will be conducted by a four-probe STM setup under well-defined ultra-high vacuum conditions. By having access to the electronic and spin, as well as to the vibrational degrees of freedom down to the atomic level, we hope to be able to identify the nature of and the conditions for inducing superconductivity at high temperatures, which could ultimately lead a knowledge-based design of high-Tc superconductors."
Max ERC Funding
2 170 696 €
Duration
Start date: 2014-01-01, End date: 2018-12-31
Project acronym CellInspired
Project Mechanotransduction mediating cell adhesion - towards cell-inspired adaptive materials
Researcher (PI) Christine Johanna Maria Selhuber-Unkel
Host Institution (HI) CHRISTIAN-ALBRECHTS-UNIVERSITAET ZU KIEL
Country Germany
Call Details Starting Grant (StG), PE3, ERC-2013-StG
Summary Adhesion is a key event for eukaryotic cells to establish contact with the extracellular matrix and other cells. It allows cells to quickly adapt to mechanical changes in their environment by either adhesion reinforcement or release. Understanding and mimicking the interplay between adhesion reinforcement and release could result in novel cell-inspired adaptive materials. In order to ultimately be able to transfer functional principles of cell adhesion to a next generation of biomimetic materials, we will elucidate the biophysics of cell adhesion in response to external force. We have already obtained important results that have provided new insights into cell adhesion. For example, we have found that the nanoscale spacing of adhesion sites controls cell adhesion reinforcement. With the project proposed here I want to advance our understanding of cell adhesion by generating a comprehensive model of mechanotransduction-mediated cell adhesion. Therefore, my group will develop new force measurement methods based on atomic force microscopy and 2D force sensor arrays that allow for a systematic investigation of key parameters in the cell adhesion system, including the concept of cellular mechanosensing. My hypothesis is that there is a transition between adhesion reinforcement and release as a function of external mechanical stress, stress history, and the biofunctionalization of the adhesive surface. Transferring our biophysical knowledge into materials science promises new materials with a dynamic adaptive mechanical and adhesion response. This transfer of biological concepts into cell-inspired materials will follow the construction principles of cells: the proposed material will be based on polymer fibers that are reversibly cross-linked and reinforce adhesion upon mechanical stress. The ultimate goal of the proposed project is to develop an intelligent polymer material with an adaptive adhesive and mechanical response similar to that found in living cells.
Summary
Adhesion is a key event for eukaryotic cells to establish contact with the extracellular matrix and other cells. It allows cells to quickly adapt to mechanical changes in their environment by either adhesion reinforcement or release. Understanding and mimicking the interplay between adhesion reinforcement and release could result in novel cell-inspired adaptive materials. In order to ultimately be able to transfer functional principles of cell adhesion to a next generation of biomimetic materials, we will elucidate the biophysics of cell adhesion in response to external force. We have already obtained important results that have provided new insights into cell adhesion. For example, we have found that the nanoscale spacing of adhesion sites controls cell adhesion reinforcement. With the project proposed here I want to advance our understanding of cell adhesion by generating a comprehensive model of mechanotransduction-mediated cell adhesion. Therefore, my group will develop new force measurement methods based on atomic force microscopy and 2D force sensor arrays that allow for a systematic investigation of key parameters in the cell adhesion system, including the concept of cellular mechanosensing. My hypothesis is that there is a transition between adhesion reinforcement and release as a function of external mechanical stress, stress history, and the biofunctionalization of the adhesive surface. Transferring our biophysical knowledge into materials science promises new materials with a dynamic adaptive mechanical and adhesion response. This transfer of biological concepts into cell-inspired materials will follow the construction principles of cells: the proposed material will be based on polymer fibers that are reversibly cross-linked and reinforce adhesion upon mechanical stress. The ultimate goal of the proposed project is to develop an intelligent polymer material with an adaptive adhesive and mechanical response similar to that found in living cells.
Max ERC Funding
1 467 483 €
Duration
Start date: 2013-09-01, End date: 2018-08-31
Project acronym CellMechanoControl
Project The physical basis of cellular mechanochemical
control circuits
Researcher (PI) Christoph Friedrich Schmidt
Host Institution (HI) GEORG-AUGUST-UNIVERSITAT GOTTINGEN STIFTUNG OFFENTLICHEN RECHTS
Country Germany
Call Details Advanced Grant (AdG), PE3, ERC-2013-ADG
Summary Biological cells possess a chemical “sense of smell” and a physical “sense of touch”. Structure, dynamics, development, differentiation and even apoptosis of cells are guided by physical stimuli feeding into a regulatory network integrating biochemical and mechanical signals. Cells are equipped with both, force-generating structures, and stress sensors including force-sensitive structural proteins or mechanosensitive ion channels. Pathways from force sensing to structural and transcriptional controls are not yet understood.
The goal of the proposed interdisciplinary project is to quantitatively establish such pathways, connecting the statistical physics and the mechanics to the biochemistry. We will measure and model the complex non-equilibrium mechanical structures in cells, and we will study how external and cell-generated forces activate sensory processes that (i) act (back) on the morphology of the cell structures, and (ii) lead to cell-fate decisions, such as differentiation. The most prominent stress-bearing and -generating structures in cells are actin/myosin based, and the most prominent mechanoactive and -sensitive cell types are fibroblasts in connective tissue and myocytes in muscle. We will first focus on actin/myosin bundles in fibroblasts and in sarcomeres in developing heart muscle cells. We will observe cells under the influence of exactly controlled external stresses. Forces on suspended single cells or cell clusters will be exerted by laser trapping and sensitively detected by laser interferometry. We furthermore will monitor mechanically triggered transcriptional regulation by detecting mRNA in the nucleus of mouse stem cells differentiating to cardiomyocytes. We will develop fluorescent mRNA sensors that can be imaged in cells, based on near-IR fluorescent single-walled carbon nanotubes.
Understanding mechanical cell regulation has far-ranging relevance for fundamental cell biophysics, developmental biology and for human health.
Summary
Biological cells possess a chemical “sense of smell” and a physical “sense of touch”. Structure, dynamics, development, differentiation and even apoptosis of cells are guided by physical stimuli feeding into a regulatory network integrating biochemical and mechanical signals. Cells are equipped with both, force-generating structures, and stress sensors including force-sensitive structural proteins or mechanosensitive ion channels. Pathways from force sensing to structural and transcriptional controls are not yet understood.
The goal of the proposed interdisciplinary project is to quantitatively establish such pathways, connecting the statistical physics and the mechanics to the biochemistry. We will measure and model the complex non-equilibrium mechanical structures in cells, and we will study how external and cell-generated forces activate sensory processes that (i) act (back) on the morphology of the cell structures, and (ii) lead to cell-fate decisions, such as differentiation. The most prominent stress-bearing and -generating structures in cells are actin/myosin based, and the most prominent mechanoactive and -sensitive cell types are fibroblasts in connective tissue and myocytes in muscle. We will first focus on actin/myosin bundles in fibroblasts and in sarcomeres in developing heart muscle cells. We will observe cells under the influence of exactly controlled external stresses. Forces on suspended single cells or cell clusters will be exerted by laser trapping and sensitively detected by laser interferometry. We furthermore will monitor mechanically triggered transcriptional regulation by detecting mRNA in the nucleus of mouse stem cells differentiating to cardiomyocytes. We will develop fluorescent mRNA sensors that can be imaged in cells, based on near-IR fluorescent single-walled carbon nanotubes.
Understanding mechanical cell regulation has far-ranging relevance for fundamental cell biophysics, developmental biology and for human health.
Max ERC Funding
2 425 200 €
Duration
Start date: 2014-06-01, End date: 2019-05-31
Project acronym EXQUISITE
Project External Quantum Control of Photonic Semiconductor Nanostructures
Researcher (PI) Stephan Erich Reitzenstein
Host Institution (HI) TECHNISCHE UNIVERSITAT BERLIN
Country Germany
Call Details Consolidator Grant (CoG), PE3, ERC-2013-CoG
Summary In this project, we will control photonic nanostructures by external feedback, optical injection and synchronization. This will allow us to study nonlinear dynamics in quantum systems and to externally manipulate and stabilize light-matter interaction in the regime of quantum electrodynamics (cQED). We will experimentally and theoretically address a) optical injection and feedback control of quantum dot (QD)–microlasers, b) quantum control cQED systems via delayed single photon feedback, and c) mutually coupled and synchronized chaotic microcavity systems. In a) we will advance the concepts of time-delayed coupling in standard semiconductor laser diodes to few photon states, where quantum fluctuations contribute to or even dominate over the usual classical dynamics. Feedback-coupling in microlasers will allow us to explore the limits of a classical description of chaotic laser dynamics via the Lang-Kobayashi rate equations and to develop an advanced model taking cQED- and QD-specific effects into account. This subject will be complemented by the study of optical injection of coherent light and non-classical light into microlasers to influence and study mode-locking, chaos and stimulated emission down to the quantum level. Single photon feedback in b) will be applied to stabilize coherent coupling of light and matter and to act against decoherence which constitutes a major bottleneck for application of semiconductor nanostructures in quantum information technology. In c) the mutual coupling of microlasers will be used to study synchronization of chaotic quantum devices at the single photon limit and to explore the underlying physics of isochronal synchronization. Our work will have important impact at an interdisciplinary level on the development of nonlinear dynamical systems towards the quantum limit and the understanding of fundamental light-matter interaction in the presence of time delayed single photon feedback.
Summary
In this project, we will control photonic nanostructures by external feedback, optical injection and synchronization. This will allow us to study nonlinear dynamics in quantum systems and to externally manipulate and stabilize light-matter interaction in the regime of quantum electrodynamics (cQED). We will experimentally and theoretically address a) optical injection and feedback control of quantum dot (QD)–microlasers, b) quantum control cQED systems via delayed single photon feedback, and c) mutually coupled and synchronized chaotic microcavity systems. In a) we will advance the concepts of time-delayed coupling in standard semiconductor laser diodes to few photon states, where quantum fluctuations contribute to or even dominate over the usual classical dynamics. Feedback-coupling in microlasers will allow us to explore the limits of a classical description of chaotic laser dynamics via the Lang-Kobayashi rate equations and to develop an advanced model taking cQED- and QD-specific effects into account. This subject will be complemented by the study of optical injection of coherent light and non-classical light into microlasers to influence and study mode-locking, chaos and stimulated emission down to the quantum level. Single photon feedback in b) will be applied to stabilize coherent coupling of light and matter and to act against decoherence which constitutes a major bottleneck for application of semiconductor nanostructures in quantum information technology. In c) the mutual coupling of microlasers will be used to study synchronization of chaotic quantum devices at the single photon limit and to explore the underlying physics of isochronal synchronization. Our work will have important impact at an interdisciplinary level on the development of nonlinear dynamical systems towards the quantum limit and the understanding of fundamental light-matter interaction in the presence of time delayed single photon feedback.
Max ERC Funding
1 999 800 €
Duration
Start date: 2014-04-01, End date: 2019-03-31
Project acronym MassQ
Project Massive-Object Quantum Physics
Researcher (PI) Roman Schnabel
Host Institution (HI) UNIVERSITAET HAMBURG
Country Germany
Call Details Advanced Grant (AdG), PE2, ERC-2013-ADG
Summary The world of quantum physics is usually associated with the microscopic cosmos of atoms and photons. In principle, but so far without any demonstration, even heavy objects can exhibit the distinguished properties of quantum world particles. In 1935, Einstein, Podolsky and Rosen (EPR) challenged a particular prediction of quantum theory saying that two particles can exist in a so-called entangled state in which the two particles do not have individually defined (‘local’) positions and momenta. Most interestingly, the existence of entangled states was subsequently fully confirmed in experiments with photons and atoms.
The new project MassQ aims to test and to confirm quantum theory in the macroscopic world of massive, human-world sized objects by realizing an EPR entanglement experiment with heavy mirrors. Two kg-sized mirrors will be cooled to low temperature and their centre of mass motion driven by radiation pressure of intense laser light in such a way that the mirrors will lose their individually defined positions and momenta. As a result, their joint motion will form a unified massive quantum object.
This project will realize a fundamental test of quantum theory in the so far unexplored regime of human-world sized objects. Recent advances in gravitational wave detector research and in opto-mechanics make this project feasible. The vision of this project points even further into the future. This project aims to lay the basis for a completely new class of physics experiments. Mirrors with kilogram masses have a proper gravitational field and cause a space-time curvature in their vicinity. This way, in principle, the dynamics of two heavy entangled mirrors need to be described not only by quantum theory but also by general relativity. Today it is completely unclear what the results of such a new class of physics experiments will be. Undoubtedly, they are important to illuminate the deep connection between the two most successful theories in physics.
Summary
The world of quantum physics is usually associated with the microscopic cosmos of atoms and photons. In principle, but so far without any demonstration, even heavy objects can exhibit the distinguished properties of quantum world particles. In 1935, Einstein, Podolsky and Rosen (EPR) challenged a particular prediction of quantum theory saying that two particles can exist in a so-called entangled state in which the two particles do not have individually defined (‘local’) positions and momenta. Most interestingly, the existence of entangled states was subsequently fully confirmed in experiments with photons and atoms.
The new project MassQ aims to test and to confirm quantum theory in the macroscopic world of massive, human-world sized objects by realizing an EPR entanglement experiment with heavy mirrors. Two kg-sized mirrors will be cooled to low temperature and their centre of mass motion driven by radiation pressure of intense laser light in such a way that the mirrors will lose their individually defined positions and momenta. As a result, their joint motion will form a unified massive quantum object.
This project will realize a fundamental test of quantum theory in the so far unexplored regime of human-world sized objects. Recent advances in gravitational wave detector research and in opto-mechanics make this project feasible. The vision of this project points even further into the future. This project aims to lay the basis for a completely new class of physics experiments. Mirrors with kilogram masses have a proper gravitational field and cause a space-time curvature in their vicinity. This way, in principle, the dynamics of two heavy entangled mirrors need to be described not only by quantum theory but also by general relativity. Today it is completely unclear what the results of such a new class of physics experiments will be. Undoubtedly, they are important to illuminate the deep connection between the two most successful theories in physics.
Max ERC Funding
1 566 210 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym MEMBRANESACT
Project Biological Membranes in Action: A Unified Approach
to Complexation, Scaffolding and Active Transport
Researcher (PI) Ana-Suncana Barisic Smith
Host Institution (HI) FRIEDRICH-ALEXANDER-UNIVERSITAET ERLANGEN-NUERNBERG
Country Germany
Call Details Starting Grant (StG), PE3, ERC-2013-StG
Summary In recent breakthrough publications, the effect of fluctuations on the affinity of membrane-confined molecules has been evaluated, and a quantitative model for the time evolution of small adhesion domains has been developed under my leadership. Now I propose to bring my research to a new level by tackling the problem of active and passive organisation of proteins into macromolecular structures on fluctuating fluid membranes, using a physicist’s approach across established disciplinary boundaries.
The formation and transport of supramolecular complexes in membranes is ubiquitous to nearly all functions of biological cells. Today, there is a variety of experiments suggesting that macromolecular complexes act as scaffolds for free proteins, overall yielding obstructed diffusion, counterbalanced by active transport by molecular motors. However, an integrative view connecting complexation and transport is largely missing. Furthermore, the effects of membrane mediated interactions and (non)-thermal fluctuations were so far overlooked. Gaining a quantitative insight into these processes is key to understanding the fundamental functioning of cells.
Together with my carefully selected team, I will address these intrinsically biological problems, by means of theoretical physics. Phenomena such as active and anomalous transport, as well as complexation are also currently subject to intense research in the statistical and soft matter physics communities. In this context, the aim of this proposal is to bridge the divide between the two worlds and significantly contribute to both physics and the life sciences by developing general principles that can be applied to processes in cells. Resolving these issues is of fundamental importance since it would identify how interactions on the cell surface arise, and may translate directly into pharmaceutical applications.
Summary
In recent breakthrough publications, the effect of fluctuations on the affinity of membrane-confined molecules has been evaluated, and a quantitative model for the time evolution of small adhesion domains has been developed under my leadership. Now I propose to bring my research to a new level by tackling the problem of active and passive organisation of proteins into macromolecular structures on fluctuating fluid membranes, using a physicist’s approach across established disciplinary boundaries.
The formation and transport of supramolecular complexes in membranes is ubiquitous to nearly all functions of biological cells. Today, there is a variety of experiments suggesting that macromolecular complexes act as scaffolds for free proteins, overall yielding obstructed diffusion, counterbalanced by active transport by molecular motors. However, an integrative view connecting complexation and transport is largely missing. Furthermore, the effects of membrane mediated interactions and (non)-thermal fluctuations were so far overlooked. Gaining a quantitative insight into these processes is key to understanding the fundamental functioning of cells.
Together with my carefully selected team, I will address these intrinsically biological problems, by means of theoretical physics. Phenomena such as active and anomalous transport, as well as complexation are also currently subject to intense research in the statistical and soft matter physics communities. In this context, the aim of this proposal is to bridge the divide between the two worlds and significantly contribute to both physics and the life sciences by developing general principles that can be applied to processes in cells. Resolving these issues is of fundamental importance since it would identify how interactions on the cell surface arise, and may translate directly into pharmaceutical applications.
Max ERC Funding
1 500 000 €
Duration
Start date: 2013-10-01, End date: 2019-09-30
Project acronym MesoFermi
Project Mesoscopic Fermi Gases
Researcher (PI) Henning Moritz
Host Institution (HI) UNIVERSITAET HAMBURG
Country Germany
Call Details Starting Grant (StG), PE2, ERC-2013-StG
Summary This proposal brings together the fields of ultracold Fermi gases and of mesoscopic systems. Starting with a two-dimensional (2D) Fermi gas, we will imprint small-scale potential structures onto the atoms. Thus, a mesoscopic system embedded in a 2D reservoir is produced.
Specifically, we will imprint optical dipole potentials varying on a micrometre scale onto a 2D gas of 6Li atoms. Due to the widely different energy scales, the entropy of the atoms in the mesoscopic structures will be massively reduced as compared to the reservoir atoms. The atoms in the mesoscopic structures will be characterised by an innovative detection scheme with single atom sensitivity. The combination of mesoscopic potentials, single atom detection and entropy reduction will put us in a unique position to access new regimes of many-body physics.
First, we will investigate a mesoscopic realisation of the 2D Hubbard model. Beyond the study of the fermionic Mott insulating phase and its excitations, the possibility to study staggered Hubbard models and create domain structures is a very attractive prospect. Most importantly, the massive entropy reduction inherent to the mesoscopic approach will enable us to observe antiferromagnetic ordering, the major milestone central to further progress in the field.
Going beyond periodic structures, we will focus on the direct creation of mesoscopic model systems. In a bottom-up approach, we will realise a plaquette consisting of 2x2 sites, the essential building block for models of d-wave superconductivity. The creation of 1D structures with local defects will open the possibility to study phenomena such as spin-charge separation, Friedel oscillations and the rectification of atomic transport. Finally, the physics of open quantum systems will become accessible when studying the interaction between mesoscopic system and reservoir. In conclusion, I believe that the proposed research programme will bring a new level of functionality to the field.
Summary
This proposal brings together the fields of ultracold Fermi gases and of mesoscopic systems. Starting with a two-dimensional (2D) Fermi gas, we will imprint small-scale potential structures onto the atoms. Thus, a mesoscopic system embedded in a 2D reservoir is produced.
Specifically, we will imprint optical dipole potentials varying on a micrometre scale onto a 2D gas of 6Li atoms. Due to the widely different energy scales, the entropy of the atoms in the mesoscopic structures will be massively reduced as compared to the reservoir atoms. The atoms in the mesoscopic structures will be characterised by an innovative detection scheme with single atom sensitivity. The combination of mesoscopic potentials, single atom detection and entropy reduction will put us in a unique position to access new regimes of many-body physics.
First, we will investigate a mesoscopic realisation of the 2D Hubbard model. Beyond the study of the fermionic Mott insulating phase and its excitations, the possibility to study staggered Hubbard models and create domain structures is a very attractive prospect. Most importantly, the massive entropy reduction inherent to the mesoscopic approach will enable us to observe antiferromagnetic ordering, the major milestone central to further progress in the field.
Going beyond periodic structures, we will focus on the direct creation of mesoscopic model systems. In a bottom-up approach, we will realise a plaquette consisting of 2x2 sites, the essential building block for models of d-wave superconductivity. The creation of 1D structures with local defects will open the possibility to study phenomena such as spin-charge separation, Friedel oscillations and the rectification of atomic transport. Finally, the physics of open quantum systems will become accessible when studying the interaction between mesoscopic system and reservoir. In conclusion, I believe that the proposed research programme will bring a new level of functionality to the field.
Max ERC Funding
1 236 060 €
Duration
Start date: 2013-10-01, End date: 2018-09-30
Project acronym MOLPROCOMP
Project From Structure Property to Structure Process Property Relations in Soft Matter – a Computational Physics Approach
Researcher (PI) Kurt Kremer
Host Institution (HI) Klinik Max Planck Institut für Psychiatrie
Country Germany
Call Details Advanced Grant (AdG), PE3, ERC-2013-ADG
Summary "From cell biology to polymer photovoltaics, (self-)assembly processes that give rise to morphology and functionality result from non-equilibrium processes, which are driven by both, external forces, such as flow due to pressure gradients, inserting energy, or manipulation on a local molecular level, or internal forces, such as relaxation into a state of lower free energy. The resulting material is arrested in a metastable state. Most previous work has focused on the relationship between structure and properties, while insight into the guiding principles governing the formation of a (new) material, has been lacking. However, a comprehensive molecular level understanding of non-equilibrium assembly would allow for control and manipulation of material processes and their resulting properties. This lag of knowledge can be traced to the formidable challenge in obtaining a molecular picture of non-equilibrium assembly. Non-equilibrium processes have been studied extensively on a macroscopic level by non-equilibrium thermodynamics. We take a novel route approaching the challenge from a molecular point of view. Recent advances in experimental, but especially computational modeling, now allow to follow (supra-) molecular structural evolution across the range of length and time scales necessary to comprehend, and ultimately control and manipulate macroscopic functional properties of soft matter at the molecular level. Soft matter is particularly suited for that approach, as it is “slow” and easy to manipulate. We take the computational physics route, based on simulations on different levels of resolution (all atom, coarse grained, continuum) in combination with recent multiscale and adaptive resolution techniques. This work will initiate the way towards a paradigm change from conventional Structure Property Relations (SPR) to molecularly based Structure Process Property Relations (SPPR)."
Summary
"From cell biology to polymer photovoltaics, (self-)assembly processes that give rise to morphology and functionality result from non-equilibrium processes, which are driven by both, external forces, such as flow due to pressure gradients, inserting energy, or manipulation on a local molecular level, or internal forces, such as relaxation into a state of lower free energy. The resulting material is arrested in a metastable state. Most previous work has focused on the relationship between structure and properties, while insight into the guiding principles governing the formation of a (new) material, has been lacking. However, a comprehensive molecular level understanding of non-equilibrium assembly would allow for control and manipulation of material processes and their resulting properties. This lag of knowledge can be traced to the formidable challenge in obtaining a molecular picture of non-equilibrium assembly. Non-equilibrium processes have been studied extensively on a macroscopic level by non-equilibrium thermodynamics. We take a novel route approaching the challenge from a molecular point of view. Recent advances in experimental, but especially computational modeling, now allow to follow (supra-) molecular structural evolution across the range of length and time scales necessary to comprehend, and ultimately control and manipulate macroscopic functional properties of soft matter at the molecular level. Soft matter is particularly suited for that approach, as it is “slow” and easy to manipulate. We take the computational physics route, based on simulations on different levels of resolution (all atom, coarse grained, continuum) in combination with recent multiscale and adaptive resolution techniques. This work will initiate the way towards a paradigm change from conventional Structure Property Relations (SPR) to molecularly based Structure Process Property Relations (SPPR)."
Max ERC Funding
2 025 000 €
Duration
Start date: 2014-02-01, End date: 2019-01-31
Project acronym NanoSpin
Project Nanoscale spin interactions and dynamics on superconducting surfaces
Researcher (PI) Katharina Jennifer Franke
Host Institution (HI) FREIE UNIVERSITAET BERLIN
Country Germany
Call Details Consolidator Grant (CoG), PE3, ERC-2013-CoG
Summary The latest concepts for quantum computing and data storage envision the use of single spins, which can be addressed and manipulated reliably. One of the main limitations towards this challenging goal is the ultra-short lifetime of excited spin states due to the interaction with the contacting leads. Another limitation is that coherence between individual spins is quickly lost. Already the measurement process for resolving coherent electron-spin interactions at the single atom level is highly challenging and has not been achieved so far.
Within our proposal, we will construct a low-temperature scanning tunneling microscope with a radio-frequency current detection system and a microwave source close to the tip. With this unique machine, we will be able to carry out state-of-the-art STM experiments combined with atomic-scale precision of measuring electron-spin resonance signals. With the approach of measuring in the frequency domain, we increase our energy resolution beyond the thermal energy level broadening into the µeV range and can thus investigate magnetic coupling, hyperfine interactions and spin coherence properties, which are not accessible in conventional STM experiments. We will also be able to probe the timescales of spin-lattice and spin-spin relaxations by pump-probe excitation schemes.
We will use this machine for resolving magnetic properties of single atoms and atomic-size nanostructures on superconducting substrates. These substrates exhibit two peculiarities, which are of crucial importance for quantum information processing. The spin lifetimes are orders of magnitudes larger than on normal metal surfaces. Furthermore, the long coherence length of Cooper pairs mediates coherent coupling of the spin states of paramagnetic atoms. We will manipulate the spin states by the intrinsic Josephson current as well as with external microwave radiation. Our model systems on superconductors will provide crucial steps towards quantum spin processing.
Summary
The latest concepts for quantum computing and data storage envision the use of single spins, which can be addressed and manipulated reliably. One of the main limitations towards this challenging goal is the ultra-short lifetime of excited spin states due to the interaction with the contacting leads. Another limitation is that coherence between individual spins is quickly lost. Already the measurement process for resolving coherent electron-spin interactions at the single atom level is highly challenging and has not been achieved so far.
Within our proposal, we will construct a low-temperature scanning tunneling microscope with a radio-frequency current detection system and a microwave source close to the tip. With this unique machine, we will be able to carry out state-of-the-art STM experiments combined with atomic-scale precision of measuring electron-spin resonance signals. With the approach of measuring in the frequency domain, we increase our energy resolution beyond the thermal energy level broadening into the µeV range and can thus investigate magnetic coupling, hyperfine interactions and spin coherence properties, which are not accessible in conventional STM experiments. We will also be able to probe the timescales of spin-lattice and spin-spin relaxations by pump-probe excitation schemes.
We will use this machine for resolving magnetic properties of single atoms and atomic-size nanostructures on superconducting substrates. These substrates exhibit two peculiarities, which are of crucial importance for quantum information processing. The spin lifetimes are orders of magnitudes larger than on normal metal surfaces. Furthermore, the long coherence length of Cooper pairs mediates coherent coupling of the spin states of paramagnetic atoms. We will manipulate the spin states by the intrinsic Josephson current as well as with external microwave radiation. Our model systems on superconductors will provide crucial steps towards quantum spin processing.
Max ERC Funding
1 999 469 €
Duration
Start date: 2014-05-01, End date: 2019-04-30