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DTSTART;TZID=Europe/Paris:20260904T110000
DTEND;TZID=Europe/Paris:20260904T120000
DTSTAMP:20260828T125150Z
CREATED:20260828T125150Z
LAST-MODIFIED:20260828T125150Z
UID:10000232-1788519600-1788523200@sfp-alpes.fr
SUMMARY:Sara MATYAS​ (Ingénieur innovation)​ & Stéphanie CELIS-JUAREZ (CNRS\, Direction des Relations Territoriales\, DR11)
DESCRIPTION:La Valorisation : quels dispositifs d’accompagnement au CNRS ?\nRésumé : \nLors de ce séminaire\, les dispositifs d’accompagnement en valorisation proposés par le CNRS vous seront présentés. Une opportunité de mieux connaitre les guichets de financement mais aussi de reparler de la déclaration d’invention\, point de départ de toute démarche de valorisation. \nLes guichets Prématuration CNRS et PUI\, Programme PISE\, Programme RISE vous seront notamment présentés\, ainsi que des Programmes de financement 2027 ciblant des projets à impacts sociétaux et environnementaux. \nEnfin\, un temps d’échange avec les oratrices permettra de répondre aux questions relatives à vos projets. \n_ \n\nLes séminaires et soutenances sont ouverts à tous\, notez toutefois que l’accès au campus EPN nécessite un avis de rendez-vous. Merci de remplir ce formulaire  et de l’adresser\, plus de 48h à l’avance\, à ce contact.\nPensez à vous munir d’une pièce d’identité le jour de votre visite.
URL:https://sfp-alpes.fr/event/sara-matyas-ingenieur-innovation-stephanie-celis-juarez-cnrs-direction-des-relations-territoriales-dr11/
LOCATION:IBS – Salle des séminaires\, IBS 71 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IBS":MAILTO:ibs.seminaires@ibs.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260908T110000
DTEND;TZID=Europe/Paris:20260908T120000
DTSTAMP:20260903T153516Z
CREATED:20260903T153408Z
LAST-MODIFIED:20260903T153516Z
UID:10000238-1788865200-1788868800@sfp-alpes.fr
SUMMARY:Delphine DELACOUR (IBDM \, Marseille (France))
DESCRIPTION:Deciphering the principles of epithelial tissue organization\nRésumé : \nEpithelia constitute the primary physical barrier against external insults while simultaneously ensuring organ function. Defects in epithelial assembly or function lead to a broad spectrum of pathological conditions\, ranging from rare developmental disorders to cancer. Despite their fundamental importance\, the mechanisms by which epithelial cells coordinate individual behaviors across entire tissues to ensure spatial organization\, integrity\, and function remain poorly understood. To date\, epithelial coherence has been studied predominantly in invertebrate systems or in transformed cell lines\, limiting our understanding of its regulation in physiological mammalian contexts.\nThe intestinal epithelium represents an exceptional model to address these questions. It is one of the most rapidly renewing tissues in mammals and is continuously exposed to challenges. Its homeostasis relies on the precise balance between cell proliferation\, differentiation\, migration\, and death. However\, the cellular and developmental principles governing intestinal tissue organization and maintenance remain largely unexplored. \nThe overarching objective of this project is to elucidate how functional domains of the intestinal epithelium are established\, maintained\, and coordinated in space and time. Specifically\, the project aims to : \n1. understand the mechanisms that preserve the integrity of the proliferative compartment and determine their role in crypt formation and maintenance ;\n2. uncover epithelial connectivity and collective behavior within the differentiated compartment\, both under homeostatic conditions and in response to perturbations. \nA major strength of this project lies in its integrative and comparative strategy\, combining in vivo and in vitro murine models with human disease-relevant systems. The project brings together advanced approaches in cell and developmental biology\, tissue engineering\, histology\, molecular biology\, biophysics\, and computational modeling. This multidisciplinary framework will enable the identification of adaptive mechanisms by which epithelial cells polarize\, self-organize\, and dynamically regulate their fate in response to their environment\, with broad implications for developmental biology\, regenerative medicine\, and disease pathology. \n_ \nContact : monika.dolega@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/delphine-delacour-ibdm-marseille-france/
LOCATION:IAB – Salle de séminaire\, IAB Site Santé - Allée des Alpes\, La Tronche\, 38700\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IAB":MAILTO:appaixfl@univ-grenoble-alpes.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260908T140000
DTEND;TZID=Europe/Paris:20260908T150000
DTSTAMP:20260827T152108Z
CREATED:20260827T152108Z
LAST-MODIFIED:20260827T152108Z
UID:10000224-1788876000-1788879600@sfp-alpes.fr
SUMMARY:Paul CANFIELD (Ames Laboratory\, Iowa State University\, Ames\, Iowa 50010\, USA)
DESCRIPTION:Negotiations with Nature — What happens when a Physicist tries to be a Chemist\nRésumé : \nOver the past 30 plus years my group has made over 10\,000 solution growth attempts to grow or explore 1\,000’s of different compounds or phase spaces. Over the past decade we have been developing a variety of different algorithms for identifying and accessing poorly explored spaces\, partly with an eye toward discovering new phases\, partly with an eye toward discovering new electrical or magnetic phase transitions and ground states. In this talk I will try to address the basic research questions of\, “where should I look for new materials or physics?” and “how can I enhance my chances of discovering X\, Y\, or Z (where XYZ can be your favorite state\, structure or behavior)?”. Specific examples spanning superconductors\, quasicrystals\, heavy fermions\, fragile magnets\, topological electronic systems\, local moment magnets and a few lost puppies will be given and reviewed. \n_ \nContact : jean-pascal.brison@cea.fr
URL:https://sfp-alpes.fr/event/paul-canfield-ames-laboratory-iowa-state-university-ames-iowa-50010-usa/
LOCATION:GreenER – Amphi Bergès\, GreenER\, 21 avenue des Martyrs\, Grenoble\, 38031\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260910T143000
DTEND;TZID=Europe/Paris:20260910T153000
DTSTAMP:20260904T141514Z
CREATED:20260904T141514Z
LAST-MODIFIED:20260904T141514Z
UID:10000240-1789050600-1789054200@sfp-alpes.fr
SUMMARY:Kayla NGUYEN (Oregon University)
DESCRIPTION:Three-Dimensional Atomic Reconstruction using Electron Ptychography\nRésumé : \nElectrons play a pivotal role in stabilizing matter\, but they are also tools that can reveal the underlying physics of complex systems from high energy physics to condensed matter. Electrons can be used as imaging probes\, where properties of matter such as magnetism or topology can be observed atom-by-atom.  In this talk\, I will show how electron ptychography\, a computational phase retrieval technique\, can improve resolution beyond the numerical aperture of electromagnetic lenses and reveal atomic structures in three-dimensions.  In particular\, I use this ‘computation lens’ approach on Er: CeO2 nanocrystals and thin films with dramatically different crystallographic orientations to uncover dopants\, defects and strain with picometer precision.  Ptychography can also be extended to visualize topological magnetism in three dimensions.  Here\, I will devise an approach to image magnetic structures of centrosymmetric skyrmions grown from amorphous FeGePt; here\, internal Bloch domains with Néel caps can be reconstructed\, as predicted from micromagnetic simulations. For non-idealized emergent materials\, solving the atomic or magnetic structure in three dimensions can support results from density functional theory\, micromagnetic simulations and enable a deeper understanding of a system’s physical properties. \n_ \nContact : martien.den-hertog@neel.cnrs.fr
URL:https://sfp-alpes.fr/event/kayla-nguyen-oregon-university/
LOCATION:CNRS – Salle Erwin Bertaut (F418)\, CNRS - Institut Néel 25 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260911T110000
DTEND;TZID=Europe/Paris:20260911T120000
DTSTAMP:20260827T154120Z
CREATED:20260827T154120Z
LAST-MODIFIED:20260827T154120Z
UID:10000226-1789124400-1789128000@sfp-alpes.fr
SUMMARY:Alexander BRONSTEIN (Institute of Science & Technology\, Autriche)
DESCRIPTION:Experiment-guided generative models for protein structure and dynamics\nRésumé : \n\nProteins exist as a dynamic ensemble of multiple conformations\, and these motions are often crucial for their functions. However\, current structure prediction methods predominantly yield a single conformation\, overlooking the conformational heterogeneity revealed by diverse experimental modalities. I will present a framework for building experiment-grounded protein structure generative models that infer conformational ensembles consistent with measured experimental data. The key idea is to treat state-of-the-art protein structure predictors (e.g.\, AlphaFold3) as sequence-conditioned structural priors\, and cast ensemble modeling as posterior inference of protein structures given experimental measurements. Through extensive real-data experiments\, I will demonstrate the generality of our method to incorporate a variety of experimental measurements. In particular\, our framework uncovers previously unmodeled conformational heterogeneity from crystallographic densities\, and generates high-accuracy NMR ensembles orders of magnitude faster than the state-of-the-art and often better fitting the experimental data than the publicly deposited structures to the Protein Data Bank. I believe that this approach will unlock building predictive models that fully embrace experimentally observed conformational diversity.​\n_\n​\n\n\n\nLes séminaires et soutenances sont ouverts à tous\, notez toutefois que l’accès au campus EPN nécessite un avis de rendez-vous. Merci de remplir ce formulaire  et de l’adresser\, plus de 48h à l’avance\, à ce contact.\nPensez à vous munir d’une pièce d’identité le jour de votre visite.
URL:https://sfp-alpes.fr/event/alexander-bronstein-institute-of-science-technology-autriche/
LOCATION:IBS – Salle des séminaires\, IBS 71 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IBS":MAILTO:ibs.seminaires@ibs.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260911T110000
DTEND;TZID=Europe/Paris:20260911T120000
DTSTAMP:20260903T154443Z
CREATED:20260903T154413Z
LAST-MODIFIED:20260903T154443Z
UID:10000239-1789124400-1789128000@sfp-alpes.fr
SUMMARY:William FAUGNO (LKB)
DESCRIPTION:Topology in the Many-Body Spectrum: A Spectral Localizer Approach to Quantum Scars\nRésumé : \nTopological phases\, both single-particle and many-body\, are often formulated through momentum-space invariants\, many of which rely on the presence of a spectral gap. However\, disorder and gapless spectra can make these conventional approaches difficult to apply. The spectral localizer provides an alternative real-space framework for defining and characterizing topology in such settings. By combining the Hamiltonian with position operators\, it constructs a pseudospectrum that can identify topologically protected states while simultaneously providing a measure of their spectral stability. The spectral localizer has been successfully applied to a variety of single-particle systems\, including disordered and gapless systems. In this seminar\, I will present recent work extending the spectral localizer to many-body systems. Our construction provides a general pseudospectral framework for identifying topologically protected states throughout the many-body spectrum. We have used this framework to identify candidates for quantum many-body scarring in both an interacting chiral bosonic chain and the PXP model\, demonstrating that the approach is not tied to a particular microscopic mechanism for scarring. The many-body spectral localizer thus provides new insight into the structure and stability of these anomalous ETH-violating states\, while offering a quantitative measure of their stability. Finally\, I will discuss the implications of this framework for quantum error-correcting codes constructed from quantum many-body scar subspaces. \nContact : jeanne.colbois@neel.cnrs.fr \nLe séminaire théorie est financé par la fédération de recherche Quantalps.
URL:https://sfp-alpes.fr/event/william-faugno-lkb/
LOCATION:LPMMC – salle Roger Maynard (G421)\, CNRS - LPMMC 25 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260911T123000
DTEND;TZID=Europe/Paris:20260911T131500
DTSTAMP:20260827T150826Z
CREATED:20260827T150807Z
LAST-MODIFIED:20260827T150826Z
UID:10000222-1789129800-1789132500@sfp-alpes.fr
SUMMARY:Sandra LAVOREL (Laboratoire d’Écologie Alpine\, Grenoble)
DESCRIPTION:S’allier avec la nature pour l’adaptation au changement climatique\nRésumé : \nLes écosystèmes en bon état et leur biodiversité contribuent de multiples façons à la qualité de notre vie. Outre leur rôle dans la séquestration du carbone\, ils soutiennent l’adaptation au changement climatique par leur résilience\, la régulation des risques naturels ou le soutien du tissu économique et culturel. Les solutions fondées sur la nature mobilisent ces capacités par la conservation\, la gestion durable et la restauration de la biodiversité. Dans cette présentation vous verrez comment elles peuvent être mises en œuvre dans nos territoires\, en concertation avec leurs acteurs. \nÀ propos de l’intervenant : \nSandra Lavorel est directrice de recherche au CNRS. Elle est une figure majeure de l’écologie scientifique. Elle travaille au Laboratoire d’Écologie Alpine à Grenoble. Pionnière de l’écologie fonctionnelle des plantes\, ses recherches portent sur les effets du changement climatique et des usages des sols sur la biodiversité\, et le fonctionnement des écosystèmes. Elle applique ces approches à la quantification des services écosystémiques et à l’adaptation au changement climatique. Avec ses travaux interdisciplinaires et transdisciplinaires\, elle figure parmi les leaders mondiaux de l’analyse des trajectoires d’adaptation fondée sur la nature. Très impliquée dans le dialogue science-politique\, elle a contribué aux évaluations internationales (IPBES\, GIEC) et nationales (Evaluation Française des Ecosystème et des Services Ecosystémiques). \n_ \nContact : contact@giant-grenoble.org \n 
URL:https://sfp-alpes.fr/event/sandra-lavorel-laboratoire-decologie-alpine-grenoble/
LOCATION:Amphi Minatec\, 3 parvis Louis Néel\, Grenoble\, 38054\, France
CATEGORIES:Séminaire
ORGANIZER;CN="GIANT":MAILTO:giant.campus@cea.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260914T110000
DTEND;TZID=Europe/Paris:20260914T120000
DTSTAMP:20260910T140135Z
CREATED:20260910T140135Z
LAST-MODIFIED:20260910T140135Z
UID:10000241-1789383600-1789387200@sfp-alpes.fr
SUMMARY:Daniel DUFFY (Cambridge\, UK)
DESCRIPTION:Mechanics and geometry of nematic shape-morphing sheets\n\nRésumé : \nThin ‘shape-programmed’ sheets morph into curved shapes when stimulated by heat\, light\, or chemical fuel. Biology is full of intricate examples (leaves\, petals\, etc)\, and soft synthetic materials such as liquid-crystal elastomers have begun to approach similar levels of richness\, opening doors to bio-inspired soft machines. Such machines can lift\, pump\, push\, pull\, . . . etc\, promising myriad applications including microfluidic components\, deployable structures\, switchable surfaces\, and robotic actuators. I’ll present work on nematic shape morphers\, in which the direction of anisotropic deformation is patterned\, while deformation magnitudes are spatially uniform. The focus will be on encoding Gauss curvature\, which imparts mechanical strength to the resultant structures\, as Gauss understood centuries ago. The patterned deformation direction must typically be chosen at the time of manufacture\, leading to a design limitation: the morphing sheet can only realise a single target shape. I will then show how to overcome this limitation\, by varying the deformation magnitude (e.g. via patterned illumination) in both space and time. This new paradigm allows a single physical sample to be morphed into arbitrarily many different shapes at will. Thus a designer can specify entire time-dependent motions of the sheet. This capability could greatly increase the versatility of soft robots\, e.g. when operating in confined environments or performing complex tasks. Furthermore\, it facilitates swimming\, which typically requires non-reciprocal motion. More generally\, it unlocks the full potential of shape-morphing sheets\, allowing them to progress from being merely functional to being truly multi-functional. \n_ \nContact : emmanuel.siefert@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/daniel-duffy-cambridge-uk/
LOCATION:LiPhy – Salle de conférence\, LiPhy 140 avenue de la Physique\, St Martin d'Hères\, 38402\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260914T140000
DTEND;TZID=Europe/Paris:20260914T150000
DTSTAMP:20260903T152520Z
CREATED:20260903T152520Z
LAST-MODIFIED:20260903T152520Z
UID:10000237-1789394400-1789398000@sfp-alpes.fr
SUMMARY:Gabriel GARCIA JIMENEZ  (Institut Laue-Langevin)
DESCRIPTION:Proton-induced reactions on 238U in inverse kinematics : probing fission through nucleon knockout\nRésumé : \nIn this seminar\, I will present a study of proton-induced reactions on 238U in inverse kinematics\, performed at 540 AMeV with the R3B/SOFIA setup at GSI. The experiment provides access to the different reaction channels and\, in particular\, to the fission of the protactinium residue following nucleon knockout. \nI will discuss how the excitation energy of the residual nucleus was reconstructed from the kinematics of the emitted nucleons and how it can be correlated with the charge distribution of the fission fragments. This provides a way to investigate the evolution of shell effects with excitation energy and to test different theoretical descriptions of this process. The experimental results will be compared with calculations based on the INCL and ABLA07 models. \nFinally\, I will show the measured cross sections for the main spallation-evaporation and spallation-fission channels and compare them with previous experimental data and theoretical predictions. Overall\, the results provide insight into the interplay between nucleon knockout\, nuclear excitation\, and fission in relativistic proton-induced reactions on heavy nuclei. \nHenry Fischer (College 3 Secretary) \nExternal visitors may ask for a site access to : dubouloz@ill.fr \nZoom link : https://ill.zoom.us/j/7804743065?pwd=vYbib10VNk56W5mHOHB2QhzTBEyT0J.1&omn=95143035964 – Password : SeminarC3 \n 
URL:https://sfp-alpes.fr/event/gabriel-garcia-jimenez-institut-laue-langevin/
LOCATION:ILL – Salle de Séminaire (110-111)\, ILL 50 71 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260914T140000
DTEND;TZID=Europe/Paris:20260914T150000
DTSTAMP:20260910T141150Z
CREATED:20260910T141150Z
LAST-MODIFIED:20260910T141150Z
UID:10000242-1789394400-1789398000@sfp-alpes.fr
SUMMARY:Alberto CARTA ( Laboratory for Material simulations\, Paul Scherrer Institut\, Villigen)
DESCRIPTION:Of bandits and Bohr magnetons : balancing exploration and exploitation in magnetic landscapes\nRésumé : \nThe energy landscape of strongly interacting magnetic materials is a high-dimensional\, rugged terrain populated by a multitude of metastable states with distinct magnetizations\, oxidation states\, and orbital orders. Identifying the true ground state within this complexity remains a significant hurdle for the computational design of materials with tunable magnetic properties.\nBuilding on the work of Ponet et al. [1\,2]\, we systematically characterize this terrain to reveal the fundamental drivers of its complexity. We trace its origins to a core competition between the DFT functional’s preference for delocalization and the Hubbard +U correction’s drive for localization. This primary conflict is further modulated by a hierarchy of magnetic interactions\, including Hund’s coupling\, superexchange\, and Kugel-Khomskii physics\, which collectively define the energetic valleys and barriers across both high and low energy scales.\nTo overcome these barriers\, we propose a novel approach inspired by a completely different field: advertisement/recommendation engines (contextual Bandits) currently powering social media feeds and large parts of the Internet. By leveraging bandit strategies that balance the exploration of unknown configurations with the exploitation of known areas\, we demonstrate an efficient method for navigating this landscape. Our results show that these strategies successfully identify the lowest energy states where traditional methods often fail\, providing a robust framework for predicting and engineering the properties of strongly correlated magnetic materials. \n[1] Ponet\, L.\, Di Lucente\, E.\, & Marzari\, N. (2024). The energy landscape of magnetic materials. npj Computational Materials\, 10(1)\, 151.\n[2] Haddadi\, F.\, Campi\, D.\, dos Santos\, F.\, Mounet\, N.\, Ponet\, L.\, Marzari\, N.\, & Gibertini\, M. (2025). Exploring the magnetic landscape of easily-exfoliable two-dimensional materials (arXiv:2509.09531v2). \n_ \nContact : matteo.dastuto@neel.cnrs.fr
URL:https://sfp-alpes.fr/event/alberto-carta-laboratory-for-material-simulations-paul-scherrer-institut-villigen/
LOCATION:CNRS – Salle Louis Weil (E424)\, CNRS - Institut Néel 25 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260915T110000
DTEND;TZID=Europe/Paris:20260915T120000
DTSTAMP:20260910T142118Z
CREATED:20260910T142118Z
LAST-MODIFIED:20260910T142118Z
UID:10000243-1789470000-1789473600@sfp-alpes.fr
SUMMARY:Thomas KISBY (Centre for Nanotechnology in Medicine\, Manchester (UK)
DESCRIPTION:Nanoscale approaches to brain tumour therapy : harnessing biology for targeted therapeutics\nRésumé : \nGlioblastoma remains one of the most challenging cancers to treat\, in part because conventional approaches struggle to selectively access and target the cells responsible for recurrence. This talk will explore how nanoscale technologies can exploit the biology of brain tumours and the brain to create new therapeutic opportunities. Using graphene oxide\, a nanomaterial with preferential interaction with tumour-associated immune cells\, I will describe how we can use this as a locally administered platform for both more localised chemotherapy and targeted tumour immunomodulation. \nI will then discuss a new approach that exploits the biological response to tumour resection itself : a transient postoperative window in which the blood–brain barrier becomes selectively\npermeable to clinically used liposomal nanomedicines. By linking the timing and biology of surgery with nanoscale drug delivery\, we have developed an approach to specifically target residual disease at the site of recurrence. Together\, these studies illustrate how understanding and exploiting biological processes can guide the design and application of nanotherapeutics for brain cancer. \n_ \nContact : anne-laure.bulin@univ-grenoble-aleps.fr
URL:https://sfp-alpes.fr/event/thomas-kisby-centre-for-nanotechnology-in-medicine-manchester-uk/
LOCATION:IAB – Salle de séminaire\, IAB Site Santé - Allée des Alpes\, La Tronche\, 38700\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IAB":MAILTO:appaixfl@univ-grenoble-alpes.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260918T100000
DTEND;TZID=Europe/Paris:20260918T110000
DTSTAMP:20260828T133335Z
CREATED:20260828T133107Z
LAST-MODIFIED:20260828T133335Z
UID:10000233-1789725600-1789729200@sfp-alpes.fr
SUMMARY:Sandrine GERBER (Deputy Director of the Institute of Chemical Sciences and Engineering (ISIC) at EPFL) -  Franck LEBRIN (PhD​ Director of an international Inserm JointLab at Leiden University Medical Center​ (LUMC\, Department of Internal Medicine))
DESCRIPTION:1) Multifunctional harmonic nanoparticles for targeted bioimaging and drug delivery.\n\n\n​​​​​​​2) Targeting pericytes for microvascular stabilization.\nRésumé : \n\nSandrine GERBER\nIs e​xpert in organic synthesis\, engineering of polymer and lipid-based nanoparticles for gene delivery\, surface functionalization of nanomaterials for theranostic applications as well as DNA biosensors for viral screening.\nThe research program of her group is devoted to the development of new chemical entities for bio-applications. Her team is mainly interested in the design\, synthesis and evaluation of functionalized nanomaterials and biomaterials for therapeutic applications as imaging probes\, drug nanocarriers and biosensors. In particular\, harmonic nanoparticles are bioconjugated to cancer targeting ligands\, caged therapeutic cargos and complementary contrast agents to develop new theranostic tools. Chitosan-based copolymers are engineered for the delivery of plasmid DNA and siRNA in the context of liver metabolic diseases and oncology. The functionalization of glass slides and gold interdigitated electrodes with peptide- and polymer-based spacers is used for the development of DNA biosensors for viral screening.​\n​\nFranck LEBRIN\n​Is a vascular biologist​ and a member of Inserm Abroad. His research focuses on microvascular disorders\, particularly Hereditary Hemorrhagic Telangiectasia (HHT)\, with an emphasis on endothelial–pericyte interactions. He develops advanced human hiPSC- and mouse-based models\, combined with ultrasound imaging\, to investigate disease mechanisms and support translational research. His work has contributed to the development of AKT inhibitors currently in Phase I and III clinical trials\, as well as small molecules promoting vessel stability and integrity for HHT and pericyte-related diseases affecting the brain\, eye\, and kidney. He is Vice-Chair of Cure HHT International and founder of RougeTX\, a spin-off developing pericyte-focused therapies.​\n\n\n_\n\n\n\n\n\nATTENTION ! L’accès à Clinatec est réservé aux porteurs de laissez-passer CEA
URL:https://sfp-alpes.fr/event/sandrine-gerber-deputy-director-of-the-institute-of-chemical-sciences-and-engineering-isic-at-epfl-franck-lebrin-phd-director-of-an-international-inserm-jointlab-at-leiden-university/
LOCATION:Clinatec\, amphithéâtre\, 17\, avenue des Martyrs\, Grenoble\, 38000\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IRIG - CEA":MAILTO:irig.communication@cea.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260918T110000
DTEND;TZID=Europe/Paris:20260918T120000
DTSTAMP:20260910T150555Z
CREATED:20260910T150555Z
LAST-MODIFIED:20260910T150555Z
UID:10000244-1789729200-1789732800@sfp-alpes.fr
SUMMARY:Yuzhu WANG (LPMMC)
DESCRIPTION:Geometric excitations in topological flat bands\nLe séminaire théorie est financé par la fédération de recherche Quantalps. \nRésumé : \nGeometric excitations provide a new way of probing the internal structure of fractional quantum Hall (FQH) states beyond their more familiar topological properties. In this talk\, we will focus on a particular class of such excitations\, known as graviton modes\, and ask how their physics changes when we move from Landau levels to fractional Chern insulators (FCIs). \nWe will start with a brief introduction to the basic concepts and formalisms used to describe FQH states\, with an emphasis on the guiding center degree of freedom and its connection to quantum geometry. This will provide the background for understanding the microscopic origin of graviton modes and how they can be identified in strongly correlated topological bands. We then turn to FCIs\, where an intriguing contrast can be found. Despite the absence of continuous rotational symmetry in the underlying lattice\, both the FCI ground state and the graviton mode exhibit an emergent guiding center rotational symmetry. The excitation continuum\, however\, does not share this symmetry. This mismatch allows the graviton mode to couple much more strongly to the continuum\, giving it a much shorter lifetime than in Landau levels. We will introduce a simple microscopic model that helps explain why this happens. \nFinally\, we will discuss how the graviton mode may be enhanced and detected experimentally in moiré materials\, and what kinds of tuning strategies could make it more visible. We will also briefly discuss how this picture can be generalized beyond spin-two graviton modes to geometric excitations with higher spins and what exciting physics can be expected there. \n_ \nContact : cecile.repellin@lpmmc.cnrs.fr 
URL:https://sfp-alpes.fr/event/yuzhu-wang-lpmmc/
LOCATION:LPMMC – salle Roger Maynard (G421)\, CNRS - LPMMC 25 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260918T110000
DTEND;TZID=Europe/Paris:20260918T120000
DTSTAMP:20260910T151054Z
CREATED:20260910T151054Z
LAST-MODIFIED:20260910T151054Z
UID:10000245-1789729200-1789732800@sfp-alpes.fr
SUMMARY:Wilson POON (University of Edinburgh\, UK)
DESCRIPTION:Cooking crystalline candies and the ductile to brittle transition in concentrated suspensions\nRésumé : \nThe existence and origin of the ductile to brittle transition in non-Brownian suspensions and pastes is under-explored despite the ubiquity of such materials in practical applications. We demonstrate the phenomenon in candies of sugar crystals in a water-protein-fat matrix prepared by boiling a sugar-cream-butter mixture (known as `fudge’ in some countries). As cooking time or final cooking temperature increases\, we observe a transition from a fluid to a ductile solid\, then to a brittle solid that abruptly fractures in compression. We propose that this is driven by rising solid sugar crystal volume fraction\, and indeed find the same sequence of behaviour in a suspension of non-Brownian calcite particles as the solid fraction moves from frictional jamming to random close packing. Particle-based simulations reveal the sensitivity of the observed phenomenon to boundary conditions. \n_ \nContact : samantha.micciulla@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/wilson-poon-university-of-edinburgh-uk/
LOCATION:LiPhy – Salle de conférence\, LiPhy 140 avenue de la Physique\, St Martin d'Hères\, 38402\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260922T103000
DTEND;TZID=Europe/Paris:20260922T113000
DTSTAMP:20260917T141914Z
CREATED:20260917T141914Z
LAST-MODIFIED:20260917T141914Z
UID:10000256-1790073000-1790076600@sfp-alpes.fr
SUMMARY:1) João BORGES (University of Aveiro\, Portugal)  - 2) Dominique VAUTIER (Université de Strasbourg – Centre de Recherche en Biomédecine de Strasbourg)
DESCRIPTION:1) Supramolecular design of cell-instructive materials for regenerative medicine strategies.\n2) Les forces intracellulaires dans le remodelage de la chromatine : mécanotransduction directe et inversée​.\nRésumé : \nThese two presentations will provide complementary perspectives on how cells interact with and respond to their physical and material environment\, from the design of cell-instructive biomaterials to the role of intracellular forces in chromatin remodeling.\n\nThey will be followed in the afternoon by Nathan Thibieroz’s Phd defence at 14:00\, on his work at GreEn-ER – Amphithéâtre 2A003\n\n_\n\n\n\n​ATTENTION ! L’accès au CEA​ est réservé aux porteurs de laissez-passer. Merci de contacter au préalable Elisa Migliorini​
URL:https://sfp-alpes.fr/event/1-joao-borges-university-of-aveiro-portugal-2-dominique-vautier-universite-de-strasbourg-centre-de-recherche-en-biomedecine-de-strasbourg/
LOCATION:CEA – Salle de séminaire IRIG (104 – bâtiment C3)\, 17\, avenue des Martyrs\, Grenoble\, 38000\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IRIG - CEA":MAILTO:irig.communication@cea.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260922T140000
DTEND;TZID=Europe/Paris:20260922T150000
DTSTAMP:20260910T151656Z
CREATED:20260910T151623Z
LAST-MODIFIED:20260910T151656Z
UID:10000246-1790085600-1790089200@sfp-alpes.fr
SUMMARY:Joseph KIOSEOGLOU (Department of Physics\, Aristotle University of Thessaloniki\, Greece)
DESCRIPTION:Atomistic & AI Discovery of Functional Nanomaterials & Thin Films\nRésumé : \nFunctional nanomaterials and thin films play a central role in emerging technologies for microelectronics\, optoelectronics\, energy conversion\, sensing\, and health-related applications. Their properties are often governed by atomic-scale mechanisms\, including defects\, dopant incorporation\, surface and interface stability\, strain fields\, morphology evolution\, growth pathways\, and phase transformations. In this seminar\, predictive atomistic modelling strategies will be presented as a way to connect these mechanisms with experimentally measurable properties and data-driven materials design. Selected examples will include semiconductors\, oxide materials\, nanowires\, nanoparticles\, low-dimensional systems\, and bio-related/pharmaceutical materials\, with emphasis on first-principles calculations\, molecular dynamics\, interatomic potentials\, machine-learning interatomic potentials\, and microscopy-informed simulations. Recent opportunities opened by artificial intelligence and generative modelling\, including sustainable-by-design materials discovery\, will also be discussed. These approaches enable the exploration of large chemical and structural spaces\, the simultaneous optimization of multiple properties\, and the proposal of experimentally relevant candidate materials. The broader perspective is to show how computation can move beyond interpretation and become part of a predictive\, collaborative workflow integrating modelling\, synthesis\, characterization\, and materials optimization for next-generation functional materials. \nShort Bio/CV\nPr. Joseph Kioseoglou research focuses on atomistic modelling\, first-principles calculations\, molecular dynamics\, machine-learning interatomic potentials\, and AI-assisted materials design\, with applications to semiconductors\, oxide materials\, nanostructures\, thin films\, surfaces\, interfaces\, defects\, nanoparticles\, and bio-related/pharmaceutical materials. He has coordinated and participated in numerous European and national research projects and has extensive experience in doctoral supervision\, international scientific collaborations and conference organization. He has held visiting professor/research positions in France\, Germany\, Japan\, including Grenoble INP/LMGP. \n_ \nContact : deborah.verger@grenoble-inp.fr
URL:https://sfp-alpes.fr/event/joseph-kioseiglou-department-of-physics-aristotle-university-of-thessaloniki-greece/
LOCATION:LMGP – salle des séminaires\, Grenoble INP -Phelma 3 parvis Louis Néel\, Grenoble\, 38054\, France
CATEGORIES:Séminaire
ORGANIZER;CN="LMGP":MAILTO:deborah.verger@grenoble-inp.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260922T140000
DTEND;TZID=Europe/Paris:20260922T150000
DTSTAMP:20260917T152447Z
CREATED:20260917T152447Z
LAST-MODIFIED:20260917T152447Z
UID:10000260-1790085600-1790089200@sfp-alpes.fr
SUMMARY:Klaus ENSSLIN (ETH Zürich)
DESCRIPTION:Bilayer graphene : rich in physics and good for devices\nRésumé : \nElectrons have a charge and a spin degree of freedom. The primitive unit cell in graphene honeycomb lattice has 2 atoms. As a consequence\, there is an additional valley degree of freedom in graphene that can be tuned by gate voltages. For electrostatically-defined quantum dots in bilayer graphene this leads to a particular filling sequence\, with the first 4 electrons in the s-shell and the next 8 electrons in the p-shell. The details of the level spectrum reveals many surprises\, such as a singly-degenerate spin-triplet/valley-singlet states for the two carrier state. When building a qubit\, one can utilize all available degrees of freedom: charge\, spin and valley. For the so-called Kramers qubits\, where spin and valley need to be flipped for relaxation from the excited to the ground state\, lifetimes as long as 100 s have been experimentally observed. For graphene layer twisted at the magic angle one can fabricate superconducting devices such as Josephson junctions\, SQUIDs and Cooper pairs boxes. In this talk I will present the prospects that graphene offers to investigate physics questions related to topology\, superconductivity\, spin-orbit interactions and spin-valley coupling as well as device concepts with unprecedented tuning opportunities. \n_ \n\n\n\nATTENTION : Pour accéder au site du CNRS (sans badge)\, envoyez-nous un e-mail plus de 24 heures avant le séminaire.\nATTENTION : To enter the CNRS site (without a badge)\, send us an email more than 24 hours before the seminar.\n\n\n\nContact : equipe-seminaires-nano@listes.grenoble.cnrs.fr
URL:https://sfp-alpes.fr/event/klaus-ensslin-eth-zurich/
LOCATION:CNRS – Salle Rémy Lemaire (K223)\, CNRS - Institut Néel 25 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260924T100000
DTEND;TZID=Europe/Paris:20260924T110000
DTSTAMP:20260917T151916Z
CREATED:20260917T151850Z
LAST-MODIFIED:20260917T151916Z
UID:10000259-1790244000-1790247600@sfp-alpes.fr
SUMMARY:Laura B. STEREN (Instituto de Nanociencia y Nanotecnologia CNEA/CONICET\, Buenos Aires\, Argentina)
DESCRIPTION:Emergent phenomena at Oxides surface and Interfaces\nRésumé : \nComplex oxides exhibit a rich variety of optical\, electronic\, and magnetic behaviours. When these materials are confined to the nanoscale\, they can display interfacial and size-dependent effects that are not present in bulk materials. The ability to design and fabricate artificial oxide heterostructures with tailored functionalities has therefore made them an important platform within the broader field of quantum materials. In this talk\, I will present our most recent results in oxide spintronics\, describe the main research directions pursued by our team\, and discuss the experimental challenges of controlling these materials at the nanometre scale\, where structure\, interfaces\, and functionality must be precisely managed to advance future oxide-based spintronic technologies. \n_ \nCollege 5B Secretary \nEdmond CHAN \nExternal visitors may ask for a site access to Brigitte Dubouloz (dubouloz@ill.fr)
URL:https://sfp-alpes.fr/event/laura-b-steren-instituto-de-nanociencia-y-nanotecnologia-cnea-conicet-buenos-aires-argentina/
LOCATION:ILL 50 building – room 101\, EPN Campus - 71 avenue des Martyrs\, Grenoble\, 38000\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260924T113000
DTEND;TZID=Europe/Paris:20260924T123000
DTSTAMP:20260917T150745Z
CREATED:20260917T150745Z
LAST-MODIFIED:20260917T150745Z
UID:10000258-1790249400-1790253000@sfp-alpes.fr
SUMMARY:Jérémie POSCHMANN (Université de Nantes)
DESCRIPTION:Functional genomics of brain disease : linking regulatory mechanisms\, circulating immune states and clinical trajectories\nRésumé : \nMy research uses func-onal genomics to characterize disease associated molecular states and to understand how they relate to biological mechanisms\, clinical heterogeneity and patient trajectories. I first used functional genomics directly in human brain tissue to identify regulatory alterations associated with disease. In autism spectrum disorder\, genome wide profiling revealed that clinically and genetically heterogeneous patients nevertheless shared convergent changes in regulatory activity. Subsequent studies in other brain disorders showed that this convergence at the molecular level was a recurrent feature and established functional genomics as a powerful approach to resolve disease-associated regulatory states. I subsequently extended this approach to circulating cells\, with the objective of accessing disease associated molecular states in living patients. In severe brain injury and psychiatric disorders\, our studies identified\nimmune and regulatory signatures associated with clinical trajectories and disease severity. These results support the use of circulating immune states to characterize biological heterogeneity beyond conventional diagnostic categories and provide a basis for patient stratification. A complementary programme in genetically defined neurodevelopmental disorders allows us to investigate these molecular alterations in a causal framework. By profiling patient blood cells carrying pathogenic variants in chromatin and proteostasis regulators\, we can connect a defined genetic alteration to its molecular consequences and to disease-relevant cellular pathways. \nTogether\, these studies establish a func-onal genomics framework that links regulatory mechanisms to accessible biomarkers and clinical trajectories in neurological and psychiatric disease. \n_ \nContact : yury.lages@univ-grenoble-alpes.fr ou sebastien.carnicella@univ-grenoble-alpes.fr \n 
URL:https://sfp-alpes.fr/event/jeremie-poschmann-universite-de-nantes/
LOCATION:GIN – Amphi Serge Kampf\, Grenoble Institut des Neurosciences (GIN) Bât. Edmond J. Safra\, Chemin Fortune Ferrini CHU\, La Tronche\, 38700\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260924T140000
DTEND;TZID=Europe/Paris:20260924T150000
DTSTAMP:20260827T153130Z
CREATED:20260827T153130Z
LAST-MODIFIED:20260827T153130Z
UID:10000225-1790258400-1790262000@sfp-alpes.fr
SUMMARY:Alexandre BERNARD (Walter Schottky Institute\, TU Munich)
DESCRIPTION:Remanent anomalous Hall effect from dual spin-orbit and exchange proximity in graphene heterostructure\nRésumé : \nThe coexistence of induced spin-orbit coupling (SOC) and magnetic exchange fields is predicted to drive graphene into topological phases\, such as the quantum anomalous Hall state. In this talk\, I will discuss the prospect of using monolayer graphene proximitized by WSe2 (SOC) and Cr2Ge2Te6 (magnetic exchange) to reach such “ex-so-tic” states. Low-temperature magnetotransport measurements of the heterostructures reveal a large and gate-tunable remanent anomalous Hall effect (AHE) persisting at zero magnetic field. Combining data analysis over various magnetic field ranges and a simple model\, we explain our findings by an intrinsic AHE regime\, where Berry curvature hot-spots from the interplay of SOC and magnetism dominate the Hall response\, but disorder broadening prevents quantization and a full topological phase transition. These results demonstrate the potential of double proximity effects in graphene-based van der Waals heterostructures as a route toward gate-tunable topological graphene phases and devices based on chiral edge states. \n_ \nContact : florence.levy-bertrand@neel.cnrs.fr \n 
URL:https://sfp-alpes.fr/event/alexandre-bernard-walter-schottky-institute-tu-munich/
LOCATION:CNRS – Salle Rémy Lemaire (K223)\, CNRS - Institut Néel 25 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260925T110000
DTEND;TZID=Europe/Paris:20260925T120000
DTSTAMP:20260827T154550Z
CREATED:20260827T154550Z
LAST-MODIFIED:20260827T154550Z
UID:10000227-1790334000-1790337600@sfp-alpes.fr
SUMMARY:Toyoyuki OSE (Hokkaido University\, Japon​)
DESCRIPTION:Viral strategies for immune evasion targeting the JAK-STAT pathway\nRésumé : \n\nThe capacity of viruses to target and inhibit immune signaling by the principal antiviral cytokines\, interferons (IFNs)\, is critical to the outcomes of infection and disease\, and is mediated by viral IFN-antagonist proteins. We have been working on viral IFN-antagonists from the order Mononegavirales such as genus Lyssavirus (e.g.\, rabies virus) and Morbillivirus (e.g.\, measles virus) that counteract the JAK-STAT system. STAT family members mediate signaling in the JAK–STAT pathway and are activated by phosphorylation at a conserved tyrosine residue\, resulting in dimerization through reciprocal interactions between the phosphotyrosine and a SH2 domain.\nTyrosine-phosphorylated STAT (pY-STAT) then translocates to the nucleus to induce the expression of genes encoding antiviral proteins. Although the active and functional forms of STATs are conventionally considered to be dimers\, STATs can undergo higher-order oligomerization\, which is implicated in regulating transcriptional activity. \nWe presented the cryo-EM structures of the tetrameric form of intact pY-STAT1 in complex with DNA or the P protein of rabies viruses [1\,2]. We explained the molecular architecture of the interactions by which P protein selectively antagonizes phosphorylated\, activated STAT1. This novel binding mode explains previously undefined mechanisms by which P protein inhibits importin binding\, DNA binding\, and the conformational transition of activated STAT1 into its DNA-binding form\, thus efficiently shutting down antiviral signaling. We also clarified that the C-terminal domain of the V protein from measles virus selectively binds to the core-region of STAT2 but not STAT13. We were able to monitor that binding of V and IRF9 to STAT2-core is competitive ; V disrupts a preformed STAT2–IRF9 interaction\, suggesting a new mechanism by which V can prevent type I IFN signaling by preventing STAT1–STAT2–IRF9 (the ISGF3 complex) formation [3\,4]. Taken together\, our findings substantially advance molecular understanding of viral evasion of antiviral immunity\, with high resolution molecular insights having the potential to inform novel intervention strategies for a lethal viral disease. \n1. Rabies virus antagonizes interferon signaling by targeting phosphorylated STAT1 tetramers. bioRxiv 2026.07.29.741124 (2026) doi:10.64898/2026.07.29.741124.\n2. Structural analysis reveals how tetrameric tyrosine-phosphorylated STAT1 is targeted by the rabies virus P-protein. Sci. Signal. 18\, eads2210 (2025).\n3. The Measles Virus V Protein Binding Site to STAT2 Overlaps That of IRF9. J. Virol. 94\, e01169-20 (2020).\n4. Solution structure of the C-terminal domain of the measles virus V protein in its free form and mechanistic analysis of STAT2 targeting. J. Virol. 99\, e00739-25 (2025).​ \n_\n\n\n\n\nLes séminaires et soutenances sont ouverts à tous\, notez toutefois que l’accès au campus EPN nécessite un avis de rendez-vous. Merci de remplir ce formulaire  et de l’adresser\, plus de 48h à l’avance\, à ce contact.\nPensez à vous munir d’une pièce d’identité le jour de votre visite.
URL:https://sfp-alpes.fr/event/toyoyuki-ose-hokkaido-university-japon/
LOCATION:IBS – Salle des séminaires\, IBS 71 avenue des Martyrs\, Grenoble\, 38042\, France
CATEGORIES:Séminaire
ORGANIZER;CN="IBS":MAILTO:ibs.seminaires@ibs.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260929T140000
DTEND;TZID=Europe/Paris:20260929T150000
DTSTAMP:20260910T152942Z
CREATED:20260910T152942Z
LAST-MODIFIED:20260910T152942Z
UID:10000248-1790690400-1790694000@sfp-alpes.fr
SUMMARY:Natali PLANK (School of Chemical and Physical Sciences and the MacDiarmid Institute for Advanced Materials and Nanotechnology\, Victoria University of Wellington\, New Zealand)
DESCRIPTION:Nanowire and carbon nanotube device structures for Biosensors and Artificial Neural Networks\nRésumé : \nCarbon nanotube (CNT) networks offer a particularly attractive platform due to their simple fabrication\, tunable electronic properties\, and ability to be interrogated through multiple electrical contacts on a single chip [1]. Functionalised carbon nanotube and graphene field effect transistors (CNTFETs and GFETs) have been used as the active channel in biosensors\, with the future promise of lab-on-a-chip diagnostics strongly motivating the research [2]. The ability to effectively sense analytes depends on multiple factors\, the conductivity of the platform [3]\, the robustness of the functionalisation and the selectivity and function of the receptor [4]. \nCarbon nanotubes also offer an interesting base platform for neuromorphic computing via physical reservoirs. Physical reservoir computing exploits the intrinsic dynamics of complex materials to perform temporal information processing with low power consumption and minimal training requirements. Disordered networks of memristive nanowires have emerged as promising neuromorphic architectures\, as they can host large numbers of nonlinear junctions that collectively generate rich spatiotemporal dynamics [5-7]. \nHere I will present our recent work on the development of the CNTFET and GFET platforms with aptamers and insect odorant receptors and the different challenges and device constraints we have encountered. I will also present our work on the development of the CNT platform for physical reservoir computing applications. \n[1]      Topinka\, M. A\, et al. Nano Lett. 2009 9\, 1866–1871 \n[2]      T An et al\, Lab Chip\, 2010\,10\,2052-2056 \n[3]      M Thanihaichelvan M\, et al\, Biosensors and Bioelectronics\, 2019\, 130\, 408-413 \n[4]      Nguyen et al.\, Nanomaterials\, 2021 11 (9)\, 2280 \n[5]      Milano\, G\, et al. Nat. Mater. 2022\, 21 (2)\, 195–202. \n[6]      Kotooka\, T.\, et al. Thermally Stable Ag 2 Se Nanowire Network as an Effective In-Materio Physical Reservoir Computing Device. 2024\, 2400443\, 1–10.  \n[7]      Zhu\, R.\, et al Online Dynamical Learning and Sequence Memory with Neuromorphic Nanowire Networks. Nat. Commun. 2023\, 14 (1)\, 6697.  \n\nShort Bio/CV\nDr Natalie Plank is Deputy Director for Commercialisation and Industry Engagement and an Associate Professor in Physics in the School of Chemical and Physical Sciences at Victoria University of Wellington. Natalie completed a BSc (Hons) in Astrophysics at The University of Edinburgh before doing an MSc in Microelectronics. She then completed her PhD on the functionalisation of carbon nanotubes for molecular electronics with Rebecca Cheung also at The University of Edinburgh. \nNatalie’s research interests are in the area of nanomaterial device fabrication and the characterisation of novel materials. Her current work focuses on nanomaterial device platforms for sensing technology and artificial neural networks. She is interested in carbon nanotubes and ZnO nanowires for nanowire transistor applications and in particular the ability to functionalise the nanomaterial channels with specific biomarkers or memristive molecules. Natalie’s core interests are in low cost fabrication techniques which allow for high throughput of devices whilst maintaining the particular material properties of the unique nanowire system. \n_ \nContact : deborah.verger@grenoble-inp.fr
URL:https://sfp-alpes.fr/event/natali-plank-school-of-chemical-and-physical-sciences-and-the-macdiarmid-institute-for-advanced-materials-and-nanotechnology-victoria-university-of-wellington-new-zealand/
LOCATION:LMGP – salle des séminaires\, Grenoble INP -Phelma 3 parvis Louis Néel\, Grenoble\, 38054\, France
CATEGORIES:Séminaire
ORGANIZER;CN="LMGP":MAILTO:deborah.verger@grenoble-inp.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261001T130000
DTEND;TZID=Europe/Paris:20261001T140000
DTSTAMP:20260917T134744Z
CREATED:20260917T134744Z
LAST-MODIFIED:20260917T134744Z
UID:10000255-1790859600-1790863200@sfp-alpes.fr
SUMMARY:Alice CLEYNEN (LJK\, Grenoble)
DESCRIPTION:Les différentes facettes de l’ARN : les opportunités ouvertes par le séquençage direct par nanopore\nRésumé : \nLe séquençage direct de l’ARN (Direct RNA Sequencing\, DRS) par nanopore (Oxford Nanopore Technologies) est une technologie qui lit les molécules d’ARN telles qu’elles existent dans la cellule\, sans jamais les copier. Cette absence d’amplification change la donne à plusieurs titres : elle évite les biais d’estimation de l’abondance des ARN inhérents à toute étape de PCR\, et surtout elle préserve les modifications chimiques qui décorent nativement les molécules — des marques aujourd’hui reconnues comme un véritable langage réactionnel. Autre atout\, les lectures produites (des « long-reads ») couvrent la molécule dans son intégralité\, ce qui permet d’assigner directement chaque lecture à un isoforme\, plutôt que de devoir les reconstruire a posteriori à partir de données au niveau du gène. Cerise sur le gâteau\, le DRS donne aussi accès à la longueur de la queue poly(A)\, dont un nombre croissant d’études souligne le rôle déterminant dans la stabilité et la traduction des ARN. \n_ \nContact : lucie.lamothe@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/alice-cleynen-ljk-grenoble/
LOCATION:IMAG – Salle de Réunion\, 150 place du Torrent\, St Martin d’Hères\, 38400\, France
CATEGORIES:Séminaire
ORGANIZER;CN="TIMC - IMAG":MAILTO:lucie.lamothe@univ-grenoble-alpes.fr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261001T140000
DTEND;TZID=Europe/Paris:20261001T150000
DTSTAMP:20260911T092949Z
CREATED:20260911T092949Z
LAST-MODIFIED:20260911T092949Z
UID:10000250-1790863200-1790866800@sfp-alpes.fr
SUMMARY:Zacharias AMARA (Conservatoire National des Arts et Métiers\, Paris)
DESCRIPTION:From Interface Engineering to Wavelength Control: Selective Photocatalytic Oxidations\nRésumé : \nIn this research seminar\, we present our group’s recent advances in the development of heterogenized photocatalytic systems for selective oxidation reactions. Central to our approach is the creation of well-defined catalytic interfaces through simple and scalable heterogenization strategies\, enabling the use of green solvents while simultaneously enhancing catalyst reactivity\, robustness\, and long-term stability. These engineered interfaces provide a versatile platform for efficient photo-oxidation under mild and sustainable reaction conditions. \nBeyond catalyst design\, control over interfacial phenomena is extended to the reactor level through the implementation of continuous-flow processing. Flow photoreactors offer precise control over mass and heat transfer\, as well as improved photon management\, allowing these heterogenized systems to operate at significantly higher space–time yields. As a result\, photo-\noxidation reactions can be performed with unprecedented productivity\, reproducibility\, and scalability. \nFinally\, an additional level of control is achieved by tuning the excitation wavelength across the visible spectrum and toward lower-energy photons in the near-infrared (NIR) region. Access to wavelength-selective photoactivation enables new photo-oxygenation pathways and unlocks levels of chemoselectivity that are inaccessible under conventional higher-energy irradiation. Together\, the combined control of catalytic interfaces\, reactor architecture\, and light energy establishes a unified strategy for highly selective and efficient photocatalytic oxidation processes. \nFor key references from our group\, see: a) Amara\, Zimberlin\, Atakpa\, Al Ayi\, Lancel\, ACS Inorg. Org. Chem. Au\, 2026\, 6\, 8–22 ; b) Al Ayi\, Atakpa\, Arab\, Lancel\, Amara\, Eur. J. Org. Chem.\, 2024 e202400634 ; c) Lancel\, Lindgren\, Monnereau\, Amara\, Photochem. Photobiol. Sci. 2023\, 23\, 79-92 ; d) Lancel\, Golisano\, Monnereau\, Gomez\, Port\, Amara\, ACS Sustain. Chem. Eng. 2023\, 11\, 15674–15684 ; e) Lancel\, Zimberlin\, Gomez\, Port\, Khrouz\, Monnereau\, Amara J. Org. Chem. 2023\, 88\, 10\, 6498–6508; f) Terra\, Desgranges\, Amara\, Moores\, Catalysis Today\, 2023\, 407\, 52-58 ; g) Lancel\, Gomez\, Port\, Amara\, Front. Chem. Eng.\, 2021\, 3\, 752364. ; h) Gellé\, Price\, Voisard\, Brodusch\, Gauvin\, Amara\, Moores\, ACS Appl. Mater. Interfaces\, 2021\, 13\, 35606-35616 ; i) Blanchard\, Asbai\, Cottet\, Boissonnat\, Port\, Amara\, Org. Process Res. Dev.\, 2020\, 24\, 822-826 ; j) Tambosco\, Segura\, Seyrig\, Cabrera\, Port\, Ferroud\, Amara\, ACS Catal. 2018\, 8\, 4383-4389 \n_ \nContact : adrien.quintard@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/zacharias-amara-conservatoire-national-des-arts-et-metiers-paris/
LOCATION:DCM – Salle C209\, DCM - Bât Chimie Recherche 301 rue de la Chimie\, St Martin d'Hères\, 38400\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261008T160000
DTEND;TZID=Europe/Paris:20261008T170000
DTSTAMP:20260409T110853Z
CREATED:20260409T110848Z
LAST-MODIFIED:20260409T110853Z
UID:10000124-1791475200-1791478800@sfp-alpes.fr
SUMMARY:Cecile ENGRAND
DESCRIPTION:Les micrométéorites : les messagères de notre origine\n_ \nToutes les informations sont disponibles sur : https://indico.ijclab.in2p3.fr/event/13491/ \nContact : louis.fayard@IJCLAB.INP3.FR \n  \n 
URL:https://sfp-alpes.fr/event/cecile-engrand/
LOCATION:Laboratoire IJCLab – Auditorium Pierre Lehmann\, Rue Ampère\, Orsay cedex\, 91898\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261013T140000
DTEND;TZID=Europe/Paris:20261013T150000
DTSTAMP:20260918T144108Z
CREATED:20260918T143923Z
LAST-MODIFIED:20260918T144108Z
UID:10000265-1791900000-1791903600@sfp-alpes.fr
SUMMARY:Chung-Hou CHUNG (1 Department of Electrophysics\, National Yang Ming Chiao Tung University\, Hsinchu\, Taiwan -  2 Physics Division\, National center for Theoretical Sciences\, Taipei\,Taiwan)
DESCRIPTION:A theory for quantum-critical Planckian strange metal phase in high-Tc cuprate superconductors\nRésumé : \nThe strange metallic state showing incoherent charge transport with universal linear-in-temperature scattering rate: 1/τ = αP kB T / ħ with αP ~ 1 and logarithmic-in-temperature singular specific heat coefficient\, so-called “Planckian metal”\, has been observed in various high-Tc cuprate superconductors over a finite range in doping near optimal doping [1]. Understanding this state is believed to be the key to revealing the mechanism for high-Tc superconductivity. Here\, we propose a generic microscopic mechanism for this state based on quantum-critical local bosonic charge Kondo fluctuations coupled to both spinon and a heavy conduction-electron Fermi surfaces within the heavy-fermion formulated slave-boson t-J model [2]. Our theory is motivated by the striking similarity in strange metal phenomenology between cuprates and heavy-fermion Kondo lattice systems [3]. By a controlled perturbative renormalization group analysis of our effective heavy-fermion model\, we examine the competition between the pseudogap phase\, characterized by Anderson’s Resonating-Valence-Bond spin-liquid made of fermionic spin-singlet spinons\, and the Fermi-liquid state modeled by coherent electron hopping (charge Kondo hybridization). We find an extended quantum-critical metallic phase with a universal Planckian ħω/kBT scaling in scattering rate near a localized-delocalized (pseudogap-to-Fermi liquid) charge-Kondo breakdown transition of the model. The d-wave superconducting ground state emerges near the transition. Unprecedented qualitative and quantitative agreements are reached between our theoretical predictions and various experiments\, including ħω/kBT scaling in optical conductivity [4]\, universal doping-insensitive field-to-temperature (B/T-) scaling in magnetoresistance [5]\, singular specific heat coefficient [6]\, marginal Fermi-liquid spectral function observed in ARPES [7]\, and Fermi surface reconstruction observed in Hall coefficients in various overdoped cuprates [5\,8]. We further applied this framework to obtain a universal quantum-critical B/T-scaling in magneto-transport and unify the B-linear and T-linear Planckian scattering rate observed in LSCO over an extended doping range\, pointing toward a unified quantum–critical origin of Planckian transport in cuprates [9]. This universal Planckian metal phase can be realized within a solvable large-N multi-channel Kondo lattice model generalized from this heavy-fermion formulated tJ model [10]. Our mechanism offers a microscopic understanding of the quantum-critical Planckian metal phase observed in cuprates and its link to the pseudogap\, d-wave superconducting\, and Fermi liquid phases. It offers a promising route for understanding how d-wave superconductivity emerges from such a strange metal phase in cuprates–one of the long-standing open problems in condensed matter physics since 1990s. \nReferences  \n\nLegros et al.\, Nat. Phys. 15\, 142 (2019).\nA mechanism for quantum-critical Planckian metal phase in high-temperature cuprate superconductors\, YY Chang\, K Van Nguyen\, K Remund\, C.H. Chung*\, Reports on Progress in Physics\, 88\, 048001 (2025).\nThe scaled-invariant Planckian metal and quantum criticality in Ce1-xNdxCoIn5\, Yung-Yeh Chang\, Hechang Lei\, Cedomir Petrovic*\, Chung-Hou Chung*\, Nature Communications 14 (581) (2023); A mechanism for the strange metal phase in rare-earth intermetallic compounds”\, Jiangfan Wang\, Yung-Yeh Chang and Chung-Hou Chung*\, Proceedings of the National Academy of Sciences (PNAS)\, Volume 119(10) e2116980119 March 1\, 2022; Strange superconductivity near an antiferromagnetic heavy fermion quantum critical point\, Y. Y. Chang\, F. Hsu\, S. Kirchner\, C. Y. Mou\, T. K. Lee\, C. H. Chung*\, Phys. Rev. B 99\, 094513 (2019); Mechanism of a strange metal state near a heavy-fermion quantum critical point\, Yung-Yeh Chang\, Silke Paschen\, Chung-Hou Chung*\, Phys. Rev. B 97\, 035156 (2018).\nB. Michon et al.\, Nature Communications 14\, 3033 (2023).\nJ. Ayres et al.\, Nature 595\, 661 (2021).\nB. Michon et al.\, Nature 567\, 218 (2019).\nS.D. Chen et al.\, Science\, 366\, 1099 (2019).\nC. Proust et al.\, Annual Review of Condensed Matter Physics 10\, 409 (2019).\nUniversality of T –linear and B–linear Planckian scattering rate in high–Tc cuprate superconductors\, K. Remund\, K. V. Nguyen\, P.-H. Chou\, P. Giraldo-Gallo\, J. A. Galvis\, G. S. Boebinger\, and C.-H. Chung*\, arXiv:2602.10627.\nTheory of universal Planckian metal phase in t-J model: application for high-temperature cuprate superconductors\, YY Chang\, K Van Nguyen\, K Remund\, CH Chung*\, arXiv:2506.15552\n\n_ \nContact : david.leboeuf@lncmi.cnrs.fr
URL:https://sfp-alpes.fr/event/chung-hou-chung-1-department-of-electrophysics-national-yang-ming-chiao-tung-university-hsinchu-taiwan-2-physics-division-national-center-for-theoretical-sciences-taipeitaiwan/
LOCATION:CNRS – Salle René Pauthenet (J229)\, CNRS – LNCMI\, 25 avenue des Martyrs\, Grenoble\, 38000\, France
CATEGORIES:Séminaire
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BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261015T140000
DTEND;TZID=Europe/Paris:20261015T150000
DTSTAMP:20260911T130347Z
CREATED:20260911T130150Z
LAST-MODIFIED:20260911T130347Z
UID:10000251-1792072800-1792076400@sfp-alpes.fr
SUMMARY:Elise DUMONT (Institut de Chimie de Nice\, Université Côte d’Azur)
DESCRIPTION:Modeling the dynamics of DNA (photo)lesions: from reactivity to repair\nRésumé : \nFormation and repair of DNA lesions embrace a rich and combinatorial chemistry\, where atomic-scale simulations are increasingly helpful to complement and extent experimental evidences. \nThe modeling of DNA structure\, dynamics\, and (photo)chemistry has benefited from a series of recent methodological developments that now allow\, for instance capturing DNA-photosensitizers interactions\, probing new excited-state mechanisms for DNA lesions induction or photostability [1]\, and rationalize the photochemistry or photocatalytic properties of drugs within DNA owing to hybrid QM/MM-MD schemes. \nI will present a series of examples where computational approaches can palliate\, at least partly\, the absence of NMR\, FRET or X-ray data for damaged DNA oligonucleotides\, DNA-drug\nbinding modes or even DNA-proteins interactions at the nucleosomal scale [2\,3]. I will also situate DNA-ligand interactions\, which can be helpful for the design of next-generation G-\nquadruplex-specific photosensitizers [4] or new DNA-inspired photocatalysts [5]. \n[1] A. Frances-Monerris\, H. Gattuso\, D. Roca-Sanjuan\, I. Tunon\, M. Marazzi\, E. Dumont\, A. Monari\, Chem. Sci.\, 2018\, 9:7902-7911\n[2] E. Matouskova\, E. Bignon\, V. E. P. Claerbout\, T. Drsata\, N. Gillet\, A. Monari. E. Dumont\, F. Lankas\, J. Chem. Theory. Comput.\, 2020\, 16(9):5972-5981\n[3] T. Wen\, M. Kermarrec\, E. Dumont\, N. Gillet\, M. M. Greenberg\, J. Am. Chem. Soc.\, 2023\, 145(43):23702-23714\n[4] M. Deiana et al.\, Nucl. Acids. Res.\, 2023\, 51(12):6264-6285\n[5] Z. Pastorel\, J. Zani\, M. Noël\, A. Bartocci\, S. Arseniyadis\, E. Dumont\, Y. Canac\, O. Baslé\, M. Smietana\, Nat. Comm.\, 2026\, 17:7527 \n_ \nContact : anne.milet@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/elise-dumont-institut-de-chimie-de-nice-universite-cote-dazur/
LOCATION:DCM – Salle C209\, DCM - Bât Chimie Recherche 301 rue de la Chimie\, St Martin d'Hères\, 38400\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261015T160000
DTEND;TZID=Europe/Paris:20261015T170000
DTSTAMP:20260409T111459Z
CREATED:20260409T111456Z
LAST-MODIFIED:20260409T111459Z
UID:10000125-1792080000-1792083600@sfp-alpes.fr
SUMMARY:Christophe SALOMON
DESCRIPTION:Atomes froids et mesure précise du temps\n_ \nToutes les informations sont disponibles sur : https://indico.ijclab.in2p3.fr/event/13426/ \nContact : louis.fayard@IJCLAB.INP3.FR
URL:https://sfp-alpes.fr/event/christophe-salomon/
LOCATION:Laboratoire IJCLab – Auditorium Pierre Lehmann\, Rue Ampère\, Orsay cedex\, 91898\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261016T103000
DTEND;TZID=Europe/Paris:20261016T113000
DTSTAMP:20260918T091036Z
CREATED:20260918T091036Z
LAST-MODIFIED:20260918T091036Z
UID:10000261-1792146600-1792150200@sfp-alpes.fr
SUMMARY:Xavier RIBAS SALAMAÑA (Universitat de Girona)
DESCRIPTION:Supramolecular Nanocages as Masks for Fullerene Regiofunctionalization and Beyond\nRésumé : \nThe design of a confined cavity dictates the type of guest to be encapsulated\, and supramolecular cages are tunable scaffolds that allow the rational design of their cavities. Nowadays\, easily accessible C60 and C70 fullerene mono-adducts are mainly used in any application (1) due to the hampered accessibility to pure alternative fullerene poly-adduct derivatives. In general\, multi-adduct mixtures with uncontrolled regioselectivity (multi-isomers) are obtained\, and chromatographic purification is too costly and time-consuming. Herein\, porphyrin-based supramolecular nanocapsules (2\,3) are used as supramolecular shadow masks to tame the over-reactivity of Bingel-type cyclopropanation reactions and to have full control over the equatorial regioselectivity\nand the number of additions. Furthermore\, the regioselectivity control is finely tuned using a three-shell Matryoshka-like assembly towards synthesizing a single trans-3 bis-Bingel-C60 for the first time (4). Also\, the mask strategy is extended to C60 and C70 for Bingel and Diels-Alder (5\,6). We envision that the described protocol will produce a plethora of derivatives for applications such as solar cells. We will also discuss our recent selective purification of fullertube mixtures and beyond (7\,8). \nReferences :\n1. E. Castro\, L. Echegoyen et al. J. Mater. Chem. C\, 2018\, 6\, 2635.\n2. C. García-Simón\, X. Ribas\, et al. Nat. Commun. 2014\, 5:5557.\n3. C. Fuertes-Espinosa\, X. Ribas\, et al\, Chem 2020\, 6\, 169–186.\n4. E. Ubasart\, X. Ribas\, et al\, Nat. Chem. 2021\, 13\, 420-427.\n5. V. Iannace\, X. Ribas et al\, J. Am. Chem. Soc. 2024\, 146\, 5186−5194.\n6. T. Pèlachs\, X. Ribas et al\, CCS Chem. 2025\, 7\, 703–715\n7. V. Iannace\, X. Ribas et al\, J. Am. Chem. Soc. 2025\, 147\, 36079−36084\n8. V. Iannace\, X. Ribas\, Acc. Chem. Res. 2026\, 59\, 1414−1425 \n_ \nContact : noemie.lalaoui@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/xavier-ribas-salamana-universitat-de-girona/
LOCATION:DCM – Salle C209\, DCM - Bât Chimie Recherche 301 rue de la Chimie\, St Martin d'Hères\, 38400\, France
CATEGORIES:Séminaire
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261016T111500
DTEND;TZID=Europe/Paris:20261016T121500
DTSTAMP:20260918T092550Z
CREATED:20260918T092501Z
LAST-MODIFIED:20260918T092550Z
UID:10000262-1792149300-1792152900@sfp-alpes.fr
SUMMARY:Gyorgy SZALOKI (Université Paul Sabatier – Toulouse)
DESCRIPTION:Towards confined gold catalysis\nRésumé : \nGold complexes have been the subject of an intense research over the past decade.[1] The main driving force to this interest is to impart new reactivity to these complexes\, that can be leveraged in catalysis. In addition to the widely used ligand engineering strategy\,[2] the concept of confining gold complexes within supramolecular cages has also shown a great\npotential.[3] Toste et coll. have demonstrated\, that small cationic gold complexes (LAu+\, L = Me3P)\, generated within anionic cages show a markedly different reactivity compared to their non-confined analogues. However\, the small cavity size of the cage (251 Å3) has not allowed to extend this concept to larger complexes (L = tBuP\, NHC) and substrates. Indeed\, one obstacle\nto overcome is the synthesis of large anionic cages\, that is far from being straightforward.\nIn order to design and synthesize large anionic cages\, we have implemented a rational approach combining modellizations and cavity size calculations.[4] As a result\, we have prepared an anionic\, cyclotricatechylene based supramolecular cage 1 with a large cavity (558 Å3).[5] Recently\, we have been studying the host-guest chemistry of this cage\, in order to prepare the confined gold-catalyst (Au+@1\, Figure 1). The catalytic activity of Au+@1 is being studied\, with special attention to the synthetically challenging gold catalyzed macrocyclizations. \nFigure 1. Concept: Using the confinement effect to alter the reactivity of gold complexes. \nAcknowledgements\nThe CNRS\, the ANR and the French Ministry of Higher Education and Research is gratefully acknowledged for funding. \nReferences\n[1] L. Rochigiani\, M. Bochmann Chem. Rev. 2021\, 121\, 8364.\n[2] J. Rodriguez\, G. Szalóki\, E. D. Sosa Carizzo\, N. Saffon-Merceron\, K. Miqueu\, D. Bourissou Angew. Chem. Int. Ed.\, 2020\, 59\, 1511;\n(b) G. Szalóki\, J. Babinot\, V. Martin-Diaconescu\, S. Mallet-Ladeira\, Y. Garcia-Rodeja\, K. Miqueu\, D. Bourissou Chem. Sci. 2022\, 13\, 10499.\n[3] M. Morimoto\, S. M. Bierschenk\, K. T. Xia\, R. G. Bergman\, K. N. Raymond\, D. F. Toste Nat. Catal. 2020\, 3\, 969.\n[4] J. V. S. Guerra\, L. F. G. Alves\, D. Bourissou\, P. S. Lopes-de-Oliveira\, G. Szalóki J. Chem. Inf. Model. 2023\, 63\, 3772.\n[5] Y. Diack\, S. Mallet-Ladeira\, D. Lesage\, J. V. S. Guerra\, D. Bourissou\, G. Szalóki Chem. Commun. 2025\, 61\, 8003 \n_ \nContact : noemie.lalaoui@univ-grenoble-alpes.fr
URL:https://sfp-alpes.fr/event/gyorgy-szaloki-universite-paul-sabatier-toulouse/
LOCATION:DCM – Salle C209\, DCM - Bât Chimie Recherche 301 rue de la Chimie\, St Martin d'Hères\, 38400\, France
CATEGORIES:Séminaire
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