Project acronym SCALMS
Project Engineering of Supported Catalytically Active Liquid Metal Solutions
Researcher (PI) Peter WASSERSCHEID
Host Institution (HI) FRIEDRICH-ALEXANDER-UNIVERSITAET ERLANGEN NUERNBERG
Call Details Advanced Grant (AdG), PE8, ERC-2017-ADG
Summary This project deals with a disruptive innovation for engineering heterogeneous catalysts. Materials technologies that promise improved catalytic performance are of utmost interest for a more sustainable chemical industry. Very recently, the applicant and his collaborators have introduced a new paradigm in heterogeneous catalysis, namely the use of Supported Catalytically Active Liquid Metal Solutions (SCALMS) (Nature Chemistry, 2017, DOI:10.1038/nchem.2822). The first account of this new class of catalytic materials demonstrated remarkable reactivity of liquid mixtures of gallium and palladium supported on porous glass, outperforming commercial catalysts in the dehydrogenation of butane with unprecedented high resistance against coke formation.
The project aims at developing these seminal findings into a general methodology for technical heterogeneous catalysis. The applicant and his team are convinced that SCALMS represent a step-change toward catalytic materials with a higher degree of surface uniformity, structural definition, reactivity and robustness. We are fascinated by the fact that the catalytic reaction in SCALMS does not proceed at the surface of solid metal nanoparticles (with their unavoidable irregularities on technical-scale production) but presumably at homogeneously distributed metal atoms in a highly dynamic liquid metal surface. From this fundamental difference, drastically altered electronic and steric properties are expected and may lead to outstanding catalytic performance. To leverage the full potential of this approach, we aim to explore all relevant effects of interface formation, reactant adsorption, and surface reactivity by a combination of synthetic, analytic, reaction engineering and material processing methodologies. We will focus on selected base and precious metals in liquid Ga supported on porous supports and aim to study these materials for alkane dehydrogenation and alkene conversion reactions.
Summary
This project deals with a disruptive innovation for engineering heterogeneous catalysts. Materials technologies that promise improved catalytic performance are of utmost interest for a more sustainable chemical industry. Very recently, the applicant and his collaborators have introduced a new paradigm in heterogeneous catalysis, namely the use of Supported Catalytically Active Liquid Metal Solutions (SCALMS) (Nature Chemistry, 2017, DOI:10.1038/nchem.2822). The first account of this new class of catalytic materials demonstrated remarkable reactivity of liquid mixtures of gallium and palladium supported on porous glass, outperforming commercial catalysts in the dehydrogenation of butane with unprecedented high resistance against coke formation.
The project aims at developing these seminal findings into a general methodology for technical heterogeneous catalysis. The applicant and his team are convinced that SCALMS represent a step-change toward catalytic materials with a higher degree of surface uniformity, structural definition, reactivity and robustness. We are fascinated by the fact that the catalytic reaction in SCALMS does not proceed at the surface of solid metal nanoparticles (with their unavoidable irregularities on technical-scale production) but presumably at homogeneously distributed metal atoms in a highly dynamic liquid metal surface. From this fundamental difference, drastically altered electronic and steric properties are expected and may lead to outstanding catalytic performance. To leverage the full potential of this approach, we aim to explore all relevant effects of interface formation, reactant adsorption, and surface reactivity by a combination of synthetic, analytic, reaction engineering and material processing methodologies. We will focus on selected base and precious metals in liquid Ga supported on porous supports and aim to study these materials for alkane dehydrogenation and alkene conversion reactions.
Max ERC Funding
2 493 650 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym ShapingRoughness
Project Emergence of Surface Roughness in Shaping, Finishing and Wear Processes
Researcher (PI) Pastewka Lars
Host Institution (HI) ALBERT-LUDWIGS-UNIVERSITAET FREIBURG
Call Details Starting Grant (StG), PE8, ERC-2017-STG
Summary Roughness on most natural and man-made surfaces shares a common fractal character from the atomic to the kilometer scale, but there is no agreed-upon understanding of its physical origin. Yet, roughness controls many aspects of engineered devices, such as friction, adhesion, wear and fatigue. Engineering roughness in surface finishing processes is costly and resource intensive. Eliminating finishing steps by controlling roughness in primary shaping or in subsequent wear processes could therefore revolutionize the way we manufacture, but this requires a deep understanding of the relevant processes that is presently lacking. Roughness emerges during mechanical deformation in processes such as folding, scratching or chipping that shape surfaces. Deformation occurs in the form of avalanches, individual bursts of irreversible motion of atoms. The central hypothesis of this project is that roughness is intrinsically linked to these deformation avalanches, which themselves are well-documented to be fractal objects. This hypothesis will be tested in large-scale atomic- and mesoscale simulations of plastic forming and fracture on state of the art high performance computing platforms. Results of these calculations will be used to develop process models for evolving the topography of large surface areas under the action of an external mechanical force, such as experienced in shaping, finishing or wear. In addition to these simulations, a public repository for sharing topography data will be build. This repository is the connection to experiments: It is a database of experimental topographies whose contents will be mined for features identified in simulations. Beyond the present project, this web-repository will advance sharing, visualization and analysis of topography data, and aid researchers to correlate surface topography with surface functionality and processing. Simulations and database lay the foundation for a rational design of surface functionality in manufacturing.
Summary
Roughness on most natural and man-made surfaces shares a common fractal character from the atomic to the kilometer scale, but there is no agreed-upon understanding of its physical origin. Yet, roughness controls many aspects of engineered devices, such as friction, adhesion, wear and fatigue. Engineering roughness in surface finishing processes is costly and resource intensive. Eliminating finishing steps by controlling roughness in primary shaping or in subsequent wear processes could therefore revolutionize the way we manufacture, but this requires a deep understanding of the relevant processes that is presently lacking. Roughness emerges during mechanical deformation in processes such as folding, scratching or chipping that shape surfaces. Deformation occurs in the form of avalanches, individual bursts of irreversible motion of atoms. The central hypothesis of this project is that roughness is intrinsically linked to these deformation avalanches, which themselves are well-documented to be fractal objects. This hypothesis will be tested in large-scale atomic- and mesoscale simulations of plastic forming and fracture on state of the art high performance computing platforms. Results of these calculations will be used to develop process models for evolving the topography of large surface areas under the action of an external mechanical force, such as experienced in shaping, finishing or wear. In addition to these simulations, a public repository for sharing topography data will be build. This repository is the connection to experiments: It is a database of experimental topographies whose contents will be mined for features identified in simulations. Beyond the present project, this web-repository will advance sharing, visualization and analysis of topography data, and aid researchers to correlate surface topography with surface functionality and processing. Simulations and database lay the foundation for a rational design of surface functionality in manufacturing.
Max ERC Funding
1 499 101 €
Duration
Start date: 2018-02-01, End date: 2023-01-31
Project acronym SHINE
Project Seeing hydrogen in matter
Researcher (PI) Baptiste GAULT
Host Institution (HI) MAX PLANCK INSTITUT FUR EISENFORSCHUNG GMBH
Call Details Consolidator Grant (CoG), PE8, ERC-2017-COG
Summary Observing hydrogen (H) in matter is a formidable challenge. Despite being ubiquitous in nature, it is elusive to scientific scrutiny like no other element. It is often portrayed as either a blessing or a curse. Certainly, it is a prime candidate for producing low-carbon emission power. But no less important is the effect of hydrogen embrittlement which has resulted in many catastrophic failures of engineering alloys. In aid of this, SHINE will realise multiple ambitions. It will facilitate the direct imaging and quantification of H atoms in candidate metallic alloys and metal-organic frameworks for gaseous storage, allow the discovery of new solid-state hydrides with controlled release, and help the improvement of fuel cell materials for energy generation. All these applications have relevance to a ‘low-carbon-emission economy’ that humanity must develop in the 21st century. SHINE will exploit a novel and entirely unique infrastructure, designed and currently implemented in the PI’s group. It will directly provide three-dimensional hydrogen mapping at the near-atomic scale. By connecting and relating this fundamental knowledge and observed physical properties, we will enable unprecedented precision in the prediction of material behaviour and so resolve to unlock control over the behaviour of hydrogen in such materials. Atom probe tomography will be the principal method of a correlative microscopy and spectroscopy approach to investigate materials where precise knowledge of the distribution of H is crucial. Informed by experimental data, modelling and simulations will provide a mechanistic understanding of the behaviour of H in materials. Novel hardware and data-treatment approaches will be developed to maximise data quality and provide new insights of the behaviour of H in the complex and dynamic microstructures of engineering materials, thereby allowing us to devise manufacturing strategies to enhance their performance and durability.
Summary
Observing hydrogen (H) in matter is a formidable challenge. Despite being ubiquitous in nature, it is elusive to scientific scrutiny like no other element. It is often portrayed as either a blessing or a curse. Certainly, it is a prime candidate for producing low-carbon emission power. But no less important is the effect of hydrogen embrittlement which has resulted in many catastrophic failures of engineering alloys. In aid of this, SHINE will realise multiple ambitions. It will facilitate the direct imaging and quantification of H atoms in candidate metallic alloys and metal-organic frameworks for gaseous storage, allow the discovery of new solid-state hydrides with controlled release, and help the improvement of fuel cell materials for energy generation. All these applications have relevance to a ‘low-carbon-emission economy’ that humanity must develop in the 21st century. SHINE will exploit a novel and entirely unique infrastructure, designed and currently implemented in the PI’s group. It will directly provide three-dimensional hydrogen mapping at the near-atomic scale. By connecting and relating this fundamental knowledge and observed physical properties, we will enable unprecedented precision in the prediction of material behaviour and so resolve to unlock control over the behaviour of hydrogen in such materials. Atom probe tomography will be the principal method of a correlative microscopy and spectroscopy approach to investigate materials where precise knowledge of the distribution of H is crucial. Informed by experimental data, modelling and simulations will provide a mechanistic understanding of the behaviour of H in materials. Novel hardware and data-treatment approaches will be developed to maximise data quality and provide new insights of the behaviour of H in the complex and dynamic microstructures of engineering materials, thereby allowing us to devise manufacturing strategies to enhance their performance and durability.
Max ERC Funding
2 000 000 €
Duration
Start date: 2018-02-01, End date: 2023-01-31
Project acronym SPAGAD
Project Speech Acts in Grammar and Discourse
Researcher (PI) Manfred KRIFKA
Host Institution (HI) GEISTESWISSENSCHAFTLICHE ZENTREN BERLIN EV
Call Details Advanced Grant (AdG), SH4, ERC-2017-ADG
Summary The SPAGAD project will investigate speech acts, the basic linguistic units with communicative function. It is made possible by recent breakthroughs in our understanding of speech acts as devices to change the world by establishing new commitments and constrain the future development of a conversation.
The project will propose a formal model for speech acts. In the light of this model it will investigate the role of speech acts in three areas. It will elucidate their role in grammar in typologically diverse languages: how they are expressed by morphological, syntactic and prosodic means, how expressions like adverbials and clause-embedding verbs can operate on them, and how they can be integrated in a formal model of the syntax/semantics interface. It will investigate speech acts in discourse: how they are used to enrich the common ground, how they can be employed to negotiate conflicts in the development of conversation, how questions, contrastive topics and discourse particles are devices that restrict the development a discourse can take, and how the choice of one speech act out of set of alternatives creates pragmatic effects like bias in questions or politeness in commands. And it will explore speech acts in communication: What are the societal norms of different speech acts, like the prohibition against asserting falsehoods, which strategies can increase or decrease the commitments of speakers, how does the context influence the type of commitments, how do social groups within one language community differ, what are the difference across language communities, how are the societal norms that come with speech acts acquired?
The SPAGAD project will have a major impact on linguistic semantics and pragmatics; it will reconceive them by a model theory based on commitments, rather than truth. Due to the pivotal role of speech acts, it will offer new perspectives for syntax, discourse studies, psycholinguistics, sociolinguistics and the philosophy of language.
Summary
The SPAGAD project will investigate speech acts, the basic linguistic units with communicative function. It is made possible by recent breakthroughs in our understanding of speech acts as devices to change the world by establishing new commitments and constrain the future development of a conversation.
The project will propose a formal model for speech acts. In the light of this model it will investigate the role of speech acts in three areas. It will elucidate their role in grammar in typologically diverse languages: how they are expressed by morphological, syntactic and prosodic means, how expressions like adverbials and clause-embedding verbs can operate on them, and how they can be integrated in a formal model of the syntax/semantics interface. It will investigate speech acts in discourse: how they are used to enrich the common ground, how they can be employed to negotiate conflicts in the development of conversation, how questions, contrastive topics and discourse particles are devices that restrict the development a discourse can take, and how the choice of one speech act out of set of alternatives creates pragmatic effects like bias in questions or politeness in commands. And it will explore speech acts in communication: What are the societal norms of different speech acts, like the prohibition against asserting falsehoods, which strategies can increase or decrease the commitments of speakers, how does the context influence the type of commitments, how do social groups within one language community differ, what are the difference across language communities, how are the societal norms that come with speech acts acquired?
The SPAGAD project will have a major impact on linguistic semantics and pragmatics; it will reconceive them by a model theory based on commitments, rather than truth. Due to the pivotal role of speech acts, it will offer new perspectives for syntax, discourse studies, psycholinguistics, sociolinguistics and the philosophy of language.
Max ERC Funding
2 499 945 €
Duration
Start date: 2019-01-01, End date: 2023-12-31
Project acronym SUGARCODING
Project The neuroenergetics of memory consolidation – hybrid PET/MR imaging of the default mode network
Researcher (PI) Valentin RIEDL
Host Institution (HI) KLINIKUM RECHTS DER ISAR DER TECHNISCHEN UNIVERSITAT MUNCHEN
Call Details Starting Grant (StG), SH4, ERC-2017-STG
Summary Since its discovery more than a decade ago, the most studied network in the human brain remains a paradox. The default mode network (DMN) is most active during the resting state and deactivates once subjects engage in goal directed behavior. Although reported in hundreds of studies using functional magnetic resonance imaging (fMRI), the function of the DMN is still unknown. I hypothesize that memories are consolidated in the DMN during resting state, a process that is interrupted once we engage in cognitive processing. This hypothesis is based on two complementary and recent findings. First, brain regions involved in encoding of novel or retrieval of consolidated memories strongly resemble regions of the DMN. Second, the DMN consumes most glucose during resting state as revealed by positron emission tomography (PET). Importantly, energy in the brain is mainly dedicated to neuronal signaling and synaptic plasticity related to memory consolidation.
To test my hypothesis, I will use hybrid PET/MR imaging to simultaneously study fMRI activity and energy metabolism of the DMN during episodic memory processing. Integrating this novel imaging approach with my recently developed brain connectivity methods, I will (i) identify the metabolic baseline of fMRI-deactivations in the DMN, (ii) track the metabolic demand and directional connectivity in the DMN during memory consolidation, and (iii) evaluate non-invasive brain stimulation as a therapeutic option to modulate memory consolidation. The DMN is massively disturbed in psychiatric disorders such as Alzheimer’s disease, anxiety and affective disorders. SUGARCODING aims at uncovering memory consolidation as a universal function of the DMN that seems to critically orchestrate the human mind and its pathological deviations.
...
Summary
Since its discovery more than a decade ago, the most studied network in the human brain remains a paradox. The default mode network (DMN) is most active during the resting state and deactivates once subjects engage in goal directed behavior. Although reported in hundreds of studies using functional magnetic resonance imaging (fMRI), the function of the DMN is still unknown. I hypothesize that memories are consolidated in the DMN during resting state, a process that is interrupted once we engage in cognitive processing. This hypothesis is based on two complementary and recent findings. First, brain regions involved in encoding of novel or retrieval of consolidated memories strongly resemble regions of the DMN. Second, the DMN consumes most glucose during resting state as revealed by positron emission tomography (PET). Importantly, energy in the brain is mainly dedicated to neuronal signaling and synaptic plasticity related to memory consolidation.
To test my hypothesis, I will use hybrid PET/MR imaging to simultaneously study fMRI activity and energy metabolism of the DMN during episodic memory processing. Integrating this novel imaging approach with my recently developed brain connectivity methods, I will (i) identify the metabolic baseline of fMRI-deactivations in the DMN, (ii) track the metabolic demand and directional connectivity in the DMN during memory consolidation, and (iii) evaluate non-invasive brain stimulation as a therapeutic option to modulate memory consolidation. The DMN is massively disturbed in psychiatric disorders such as Alzheimer’s disease, anxiety and affective disorders. SUGARCODING aims at uncovering memory consolidation as a universal function of the DMN that seems to critically orchestrate the human mind and its pathological deviations.
...
Max ERC Funding
1 499 404 €
Duration
Start date: 2018-07-01, End date: 2023-06-30
Project acronym TissueLymphoContexts
Project Tissue-resident Lymphocytes: Development and Function in “real-life” Contexts
Researcher (PI) Georg GASTEIGER
Host Institution (HI) JULIUS-MAXIMILIANS-UNIVERSITAT WURZBURG
Call Details Starting Grant (StG), LS6, ERC-2017-STG
Summary Most anatomical compartments, including mucosal barrier surfaces, solid organs and vascular spaces host different types of tissue-resident lymphocytes providing local networks for immune surveillance and front-line defense to microbial invasion. In addition to immediate effector functions, tissue-resident lymphocytes orchestrate and regulate inflammatory responses, and contribute to tissue homeostasis, repair and barrier function. Understanding the generation and function of tissue-resident lymphocytes is therefore expected to reveal targets for improving vaccination and immunotherapy. Barrier tissues of free-living mice and men, but not those of laboratory mice kept under specific pathogen free conditions, are continuously exposed to an array of antigenically complex pathogens, microbial symbionts and environmental factors, which dramatically alter the abundance, composition and basal activation state of local pools of tissue-resident cells. Therefore, we propose to study the development, functions and cellular interactions of tissue-resident lymphocytes in experimental models that mirror “real-life” contexts. First, we will investigate how polyclonal pools of tissue-resident memory CD8+ T cells (TRMs) are established during infection with antigenically complex pathogens. Second, we will restore physiologic exposure to specific pathogens and induce alterations of local microbiota in SPF mice, in order to investigate the induction, function and local interactions of tissue-resident lymphocytes in physiologic tissue environments. In addition, we will explore targeted microbial exposure as a „vaccination“ strategy to induce „non-canonical“ tissue-resident cells in the lung in order to improve protection against infections with multi-resistant bacteria representing major clinical problems in hospitalized patients. In summary, we will investigate fundamental mechanisms of tissue immunity and vaccination in contexts relevant for human physiology and disease.
Summary
Most anatomical compartments, including mucosal barrier surfaces, solid organs and vascular spaces host different types of tissue-resident lymphocytes providing local networks for immune surveillance and front-line defense to microbial invasion. In addition to immediate effector functions, tissue-resident lymphocytes orchestrate and regulate inflammatory responses, and contribute to tissue homeostasis, repair and barrier function. Understanding the generation and function of tissue-resident lymphocytes is therefore expected to reveal targets for improving vaccination and immunotherapy. Barrier tissues of free-living mice and men, but not those of laboratory mice kept under specific pathogen free conditions, are continuously exposed to an array of antigenically complex pathogens, microbial symbionts and environmental factors, which dramatically alter the abundance, composition and basal activation state of local pools of tissue-resident cells. Therefore, we propose to study the development, functions and cellular interactions of tissue-resident lymphocytes in experimental models that mirror “real-life” contexts. First, we will investigate how polyclonal pools of tissue-resident memory CD8+ T cells (TRMs) are established during infection with antigenically complex pathogens. Second, we will restore physiologic exposure to specific pathogens and induce alterations of local microbiota in SPF mice, in order to investigate the induction, function and local interactions of tissue-resident lymphocytes in physiologic tissue environments. In addition, we will explore targeted microbial exposure as a „vaccination“ strategy to induce „non-canonical“ tissue-resident cells in the lung in order to improve protection against infections with multi-resistant bacteria representing major clinical problems in hospitalized patients. In summary, we will investigate fundamental mechanisms of tissue immunity and vaccination in contexts relevant for human physiology and disease.
Max ERC Funding
1 498 750 €
Duration
Start date: 2018-03-01, End date: 2023-02-28
Project acronym ToCCaTa
Project Tailoring the functional Capacity of Cytotoxic T cells for future Therapies
Researcher (PI) Dietmar ZEHN
Host Institution (HI) TECHNISCHE UNIVERSITAET MUENCHEN
Call Details Consolidator Grant (CoG), LS6, ERC-2017-COG
Summary Cytotoxic T cells have enormous potential for prophylactic and therapeutic interventions against problematic acute or chronic infections and against malignant tumors. A major obstacle to utilizing them effectively is our limited understanding of the molecular foundation that is necessary for CD8 T cells to fulfil their pleiotropic functions. Equally important is to find solutions supporting the robust and safe induction of large numbers of pathogen- or tumor-specific T cells and strategies for customized generation of T cells equipped with a functional capacity that are optimized to the often contrasting needs of particular diseases. For instance, anti-tumor immunity requires large numbers of highly activated effector T cells, while resting memory cells with high proliferative potential in combination with tissue-resident memory cells are thought to enhance protection against viral infections. Similarly, the challenge in treating chronic infections and tumors is to overcome the hypo-functional “exhausted” stage of T cells, but therapeutic induction of the same mechanisms to attenuate an aggressive T cell response could be vital for treating autoimmunity or immunopathology in fulminant liver or lung infections. Thus, to develop prophylactic or interventional strategies through which qualitative aspects of T cell function can be adjusted is a current key challenge in the immunotherapy and vaccine field. We seek to promote such activities by performing research that aims to significantly augment our comprehension of how molecular particularities translate into functional diversity. By taking advantage of 1) experimental systems that specifically mimic disease relevant T cell phenotypes, 2) approaches to assess molecular diversity at single cell level, 3) effective strategies to alter gene expression, and 4) systematic and hypothesis-driven molecular screening, we anticipate the discovery of new targets to optimize immunotherapies for tumors and chronic infections.
Summary
Cytotoxic T cells have enormous potential for prophylactic and therapeutic interventions against problematic acute or chronic infections and against malignant tumors. A major obstacle to utilizing them effectively is our limited understanding of the molecular foundation that is necessary for CD8 T cells to fulfil their pleiotropic functions. Equally important is to find solutions supporting the robust and safe induction of large numbers of pathogen- or tumor-specific T cells and strategies for customized generation of T cells equipped with a functional capacity that are optimized to the often contrasting needs of particular diseases. For instance, anti-tumor immunity requires large numbers of highly activated effector T cells, while resting memory cells with high proliferative potential in combination with tissue-resident memory cells are thought to enhance protection against viral infections. Similarly, the challenge in treating chronic infections and tumors is to overcome the hypo-functional “exhausted” stage of T cells, but therapeutic induction of the same mechanisms to attenuate an aggressive T cell response could be vital for treating autoimmunity or immunopathology in fulminant liver or lung infections. Thus, to develop prophylactic or interventional strategies through which qualitative aspects of T cell function can be adjusted is a current key challenge in the immunotherapy and vaccine field. We seek to promote such activities by performing research that aims to significantly augment our comprehension of how molecular particularities translate into functional diversity. By taking advantage of 1) experimental systems that specifically mimic disease relevant T cell phenotypes, 2) approaches to assess molecular diversity at single cell level, 3) effective strategies to alter gene expression, and 4) systematic and hypothesis-driven molecular screening, we anticipate the discovery of new targets to optimize immunotherapies for tumors and chronic infections.
Max ERC Funding
1 999 850 €
Duration
Start date: 2018-10-01, End date: 2023-09-30
Project acronym TriboKey
Project Deformation Mechanisms are the Key to Understanding and Tayloring Tribological Behaviour
Researcher (PI) Christian Greiner
Host Institution (HI) KARLSRUHER INSTITUT FUER TECHNOLOGIE
Call Details Consolidator Grant (CoG), PE8, ERC-2017-COG
Summary Tribology, the science of interacting surfaces in relative motion, is crucial for many aspects of modern life. Friction and wear decisively impact the lifetime and durability of many products-from nanoelectromechanical systems to gears and engines. In the USA alone, an estimated 1E18 joules of energy could be saved each year through improved tribological practices.
During sliding of a metallic contact, a mutated surface layer forms, carries most further plastic deformation and largely determines friction and wear. The origin and evolution of this distinct subsurface layer remains elusive, since our knowledge of the elementary mechanisms promoting these changes is limited. Only this knowledge however will allow for a strategic tailoring of tribologically loaded metals.
In this project, we will elucidate these elementary mechanisms for a wide range of alloys and strain rates. We will develop ground-breaking new strategies for probing the subsurface microstructure during the tribological test itself with non-destructive testing sensors like ultrasound and eddy current, resulting in subsurface in situ tribology. The data from these sensors will be analysed online, during the tribological experiment, relying on cutting edge data science methods as they have already been applied for fatigue testing. Based on these analyses, implemented on a Field Programmable Gate Array, we will interrupt the test exactly when the dominating elementary mechanisms manifest themselves. These mechanisms will then be revealed by sophisticated electron microscopy and be visualized in deformation mechanism maps for unidirectional and reciprocating sliding. Such maps have proven very successful in other fields of materials science, e.g. creep at elevated temperatures. They are used to guide material selection and alloy development processes, yielding materials tailored for each specific tribological scenario, promising enormous savings in energy and resources, an important challenge of our time.
Summary
Tribology, the science of interacting surfaces in relative motion, is crucial for many aspects of modern life. Friction and wear decisively impact the lifetime and durability of many products-from nanoelectromechanical systems to gears and engines. In the USA alone, an estimated 1E18 joules of energy could be saved each year through improved tribological practices.
During sliding of a metallic contact, a mutated surface layer forms, carries most further plastic deformation and largely determines friction and wear. The origin and evolution of this distinct subsurface layer remains elusive, since our knowledge of the elementary mechanisms promoting these changes is limited. Only this knowledge however will allow for a strategic tailoring of tribologically loaded metals.
In this project, we will elucidate these elementary mechanisms for a wide range of alloys and strain rates. We will develop ground-breaking new strategies for probing the subsurface microstructure during the tribological test itself with non-destructive testing sensors like ultrasound and eddy current, resulting in subsurface in situ tribology. The data from these sensors will be analysed online, during the tribological experiment, relying on cutting edge data science methods as they have already been applied for fatigue testing. Based on these analyses, implemented on a Field Programmable Gate Array, we will interrupt the test exactly when the dominating elementary mechanisms manifest themselves. These mechanisms will then be revealed by sophisticated electron microscopy and be visualized in deformation mechanism maps for unidirectional and reciprocating sliding. Such maps have proven very successful in other fields of materials science, e.g. creep at elevated temperatures. They are used to guide material selection and alloy development processes, yielding materials tailored for each specific tribological scenario, promising enormous savings in energy and resources, an important challenge of our time.
Max ERC Funding
1 985 048 €
Duration
Start date: 2018-09-01, End date: 2023-08-31
Project acronym TURNTAKING
Project Taking turns: The ‘missing’ link in language evolution?
Researcher (PI) Simone PIKA
Host Institution (HI) UNIVERSITAET OSNABRUECK
Call Details Consolidator Grant (CoG), SH4, ERC-2017-COG
Summary Language — the most distinctive human trait — remains a ‘mystery’1 or even a ‘problem’2 for evolutionary theory. It is underpinned by cooperative turn-taking3, which has been implicated with highly sophisticated cognitive skills such as mindreading4. Some have claimed that this turn-taking system is uniquely human5,6, but others argue that it provides the evolutionary ‘missing link’ between animal and human communication7. This debate has been constrained by a lack of comparative data, methodological confounds that often prevent meaningful comparisons, and a lack of information on key components of social relationships8,9 that might strongly impact upon turn-taking propensities.
Objectives. TURNTAKING will quantify turn-taking production and comprehension in human children, chimpanzees, and two distantly related species — geladas and common marmosets. It will apply a powerful combination of systematic behavioral observations, eye-tracking paradigms, and established measures from Conversational Analysis3,10 and Primatology9 that allow the same type of data to be collected and analyzed in directly comparable ways across species. This will provide the first rigorous test of whether cooperative turn-taking is uniquely human, ancestral in the primate lineage, or evolved independently in different species. TURNTAKING will identify which hallmarks of human turn-taking are shared across different primate species, and which key components of relationship quality8,9 act upon turn-taking skills.
Outcomes. This project will found the field of comparative turn-taking, and provide pioneering insights into the behavioral flexibility underlying different turn-taking systems. It will go beyond the state of the art by exposing whether cooperative turn-taking is the evolutionary ‘missing link’ between our species and our inarticulate primate cousins, and whether pro-social behaviors drove its emergence.
Summary
Language — the most distinctive human trait — remains a ‘mystery’1 or even a ‘problem’2 for evolutionary theory. It is underpinned by cooperative turn-taking3, which has been implicated with highly sophisticated cognitive skills such as mindreading4. Some have claimed that this turn-taking system is uniquely human5,6, but others argue that it provides the evolutionary ‘missing link’ between animal and human communication7. This debate has been constrained by a lack of comparative data, methodological confounds that often prevent meaningful comparisons, and a lack of information on key components of social relationships8,9 that might strongly impact upon turn-taking propensities.
Objectives. TURNTAKING will quantify turn-taking production and comprehension in human children, chimpanzees, and two distantly related species — geladas and common marmosets. It will apply a powerful combination of systematic behavioral observations, eye-tracking paradigms, and established measures from Conversational Analysis3,10 and Primatology9 that allow the same type of data to be collected and analyzed in directly comparable ways across species. This will provide the first rigorous test of whether cooperative turn-taking is uniquely human, ancestral in the primate lineage, or evolved independently in different species. TURNTAKING will identify which hallmarks of human turn-taking are shared across different primate species, and which key components of relationship quality8,9 act upon turn-taking skills.
Outcomes. This project will found the field of comparative turn-taking, and provide pioneering insights into the behavioral flexibility underlying different turn-taking systems. It will go beyond the state of the art by exposing whether cooperative turn-taking is the evolutionary ‘missing link’ between our species and our inarticulate primate cousins, and whether pro-social behaviors drove its emergence.
Max ERC Funding
1 999 795 €
Duration
Start date: 2019-01-01, End date: 2023-12-31