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DTSTART;TZID=Europe/London:20260625T153000
DTEND;TZID=Europe/London:20260625T170000
DTSTAMP:20260409T215725
CREATED:20251114T141624Z
LAST-MODIFIED:20260313T151924Z
UID:7164-1782401400-1782406800@thomasyoungcentre.org
SUMMARY:3rd TYC Early Career Award Symposium 2026
DESCRIPTION:3rd TYC Early Career Award 2026 Share on X\n\n\n\n\nThe TYC Early Career Prize\, will be awarded to an early career researcher in recognition of their original published research in the theory and/or simulation of materials or (bio)molecules. \n\n\n\nAre you an early career postdoctoral researcher eager to showcase your work and accelerate your professional growth? The TYC Early Career Prize\, established in 2022\, is a fantastic opportunity to gain recognition for your original published research in the theory and/or simulation of materials or (bio)molecules. Winning – or even being shortlisted – offers tremendous benefits: a prestigious accolade that strengthens your CV\, enhances your visibility in the scientific community\, and opens doors to future funding opportunities.  \n\n\n\nShortlisted candidates will be invited to present their research at a dedicated in-person Symposium at UCL on 25 June 2026\, providing invaluable networking and exposure to leading academics in the field. Plus\, the award comes with a £500 prize\, underscoring the value placed on your contributions. Don’t miss this chance to elevate your career and position yourself as a rising leader in computational and theoretical science! \n\n\n\nDetails of how to apply  in 2028 can be found here \n\n\n\n\n\n\n\nThe awardee will be selected by a panel of academics in the broad field of theory and simulation of materials and molecules.  \n\n\n\n\nRegister to attend here\n\n\n\n\n\n\n\n\nAttendance is free but we kindly ask you to register before Sunday 7th June 2026.
URL:https://thomasyoungcentre.org/event/3rd-tyc-early-career-award-2025/
LOCATION:Graduate Centre Foyer & Lecture Theatre\, Queen Mary University of London\, Mile End Road\, London\, E1 4NS\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260610T093000
DTEND;TZID=Europe/London:20260610T180000
DTSTAMP:20260409T215725
CREATED:20260223T170458Z
LAST-MODIFIED:20260227T120226Z
UID:7699-1781083800-1781114400@thomasyoungcentre.org
SUMMARY:TYC Postgraduate Student Day 2026
DESCRIPTION:Great Hall\, King’s College London\, Strand \n\n\n\n\n\n\n\n\n\n\nTYC Postgraduate Student Day 2026 Share on X\n\n\n\n\nThe TYC Student Day is a one‑day celebration showcasing PhD research in the theory and simulation of materials and molecules across the four London Colleges of the Thomas Young Centre (UCL\, Imperial\, King’s and QMUL)\, as well as Brunel University London and London South Bank University. \n\n\n\nThe programme features talks from selected final‑year students\, a poster session\, and invited guest speakers.  \n\n\n\nWe invite all TYC students to submit abstracts for poster presentations\, and final‑year students to submit abstracts for oral presentations. Around 12 talks will be selected (12‑minute presentation + 2‑minute Q&A). All posters from participating institutions will be displayed during the lunchtime poster session and again during the drinks reception at the end of the day. \n\n\n\nCash prizes will be awarded for the Best Talk and Best Poster. \n\n\n\n\n\n\n\n\nRegister and submit your abstract\n\n\n\n\n\n\n\n\nAbstract submission and registration deadline: Sunday 17 May 2026 \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nSchedule:\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nInvited speakers:
URL:https://thomasyoungcentre.org/event/tyc-postgraduate-student-day-2026/
LOCATION:The Great Hall\, King’s College London\, Strand\, London\, WC2R 2LS\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260601T133000
DTEND;TZID=Europe/London:20260603T183000
DTSTAMP:20260409T215725
CREATED:20260112T155046Z
LAST-MODIFIED:20260320T170737Z
UID:7520-1780320600-1780511400@thomasyoungcentre.org
SUMMARY:TYC 8th Energy Materials workshop: From Electron and Phonon Interactions to Net Zero
DESCRIPTION:Venue: The Great Hall\, King’s College London\, Strand \n\n\n\nMaterials for energy harvesting are pivotal to global decarbonisation efforts and the prevention of climate breakdown. This workshop will focus on photovoltaic and thermoelectric materials\, which generate electricity from solar energy and waste heat\, respectively. While both technologies are relatively mature and commercially available\, their adoption and the breadth of their applications could increase significantly if the efficiency of their energy conversion processes were substantially improved. \n\n\n\n\n\n\n\n\n\n\nTYC 8th Energy Materials workshop: From Electron and Phonon Interactions to Net Zero Share on X\n\n\n\n\nAchieving such improvements requires a deeper understanding of the fundamental interactions that govern material properties\, including electron-phonon and electron-electron interactions\, as well as interactions with defects and external perturbations such as light. Recent advances in modelling techniques have enabled unprecedented insight into these processes. The workshop will bring together leading experts in these areas to discuss recent breakthroughs and identify new directions for dramatically enhancing the performance of thermoelectric and photovoltaic materials. \n\n\n\nPhotovoltaic and thermoelectric technologies often rely on similar classes of materials\, including inorganic bulk compounds and their nanostructured forms\, and more recently\, two-dimensional\, organic\, and hybrid materials. In photovoltaics\, the operation is typically governed by electron-phonon\, electron-electron\, and electron-defect interactions\, alongside coupling with photons. In thermoelectrics\, phonon-phonon and electron-phonon interactions are considered central\, together with phonon-defect and electron-defect interactions. Therefore\, electron-phonon and electron-defect interactions are of significant interest to both communities. \n\n\n\nHowever\, emerging research has revealed a deeper set of commonalities between photovoltaics and thermoelectrics. For instance\, electron-electron interactions play a crucial role in accurately modelling electron-phonon interactions in narrow-bandgap and intermetallic thermoelectric materials. In halide perovskites\, strong phonon-phonon interactions can significantly influence photovoltaic performance. Similarly\, plasmons\, typically employed to enhance solar absorption in metallic nanostructures\, may also benefit thermoelectric materials with high doping levels. Finally\, polarons – quasiparticles formed by electrons interacting strongly with lattice vibrations are increasingly recognised as relevant to both fields\, particularly in oxides\, organic and two-dimensional materials. \n\n\n\nThis workshop will highlight recent advances in theoretical and computational methods used to characterise the interactions in realistic materials. Several invited talks will also explore the application of modern AI and machine learning techniques for the discovery of novel photovoltaic and thermoelectric materials. Approximately half of the invited presentations will focus on experimental research\, including the synthesis of new materials and the characterisation of key interaction mechanisms. Together\, these contributions aim to identify the most pressing challenges in designing next-generation materials with significantly improved energy conversion efficiencies. \n\n\n\n\n\n\n\n\n\n\n\n Registration\n\n\n\nRegister for the workshop here: \n\n\n\n\nRegistration\n\n\n\n\n\n\n\n\nThe registration deadline is 1 May 2026 \n\n\n\n\n\n\n\n\n\nIf you are attempting to register from a medical\, educational or governmental institution whether working onsite\, or remotely from home\, a firewall may prevent you from making the booking. You will therefore need to use another internet connection.  You should also use either a laptop or PC to make the booking\, and not iPhone or tablet\, and either Firefox or Microsoft Edge rather than Google Chrome. \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nInvited speakers\n\n\n\n\nDr. Keith Butler\, University College London\, UK \n\n\n\nProf. Emiliano Cortes\, Ludwig Maximilian University of Munich\, Germany \n\n\n\nDr. Jennifer Coulter\, Flatiron Institute\, USA \n\n\n\nProf. Janine George\, Friedrich Schiller University of Jena\, Germany \n\n\n\nDr. Samuele Giannini\, CNR Pisa\, Italy \n\n\n\nProf. Feliciano Giustino\, University of Texas Austin\, USA \n\n\n\nProf. Maria Ibanez\, Institute of Science and Technology\, Austria \n\n\n\nProf. Jenny Nelson\, Imperial College London\, UK \n\n\n\nProf. Neophytos Neophytou\, University of Warwick\, UK \n\n\n\nProf. Yu Pan\, Southwest University\, China \n\n\n\nProf. Andrej Pustogow\, Technical University of Vienna\, Austria \n\n\n\nProf. Sivan Refaeli-Abramson\, Weizman Institute of Science\, Israel \n\n\n\nProf. Henning Sirringhaus\, University of Cambridge\, UK \n\n\n\nProf. Kevin Sivula\, Ecole Polytechnique Federale de Lausanne\, Switzerland \n\n\n\nProf. G. Jeffrey Snyder\, Northwestern University\, USA \n\n\n\nDr. Terumasa Tadano\, National Institute for Materials Science\, Japan \n\n\n\nProf. Matthieu Verstraete\, University of Utrecht\, Netherlands \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nAbstract submission\n\n\n\nIn addition to invited talk\, we offer participants the opportunity to present their work through contributed talks (15 minutes + 5 minutes Q&A) and posters.  \n\n\n\n\n\n\n\n\nSubmit your abstract\n\n\n\n\n\n\n\n\nThe deadline for applications for contributed talks is 15 April 2026. \n\n\n\nThe deadline for poster abstracts is 1 May 2026. \n\n\n\nWe may be able to provide some financial assistance for delegates who experience financial strain byregistering for this workshop.  Please send an email to the organising committee at tyc-administrator@ucl.ac.uk justifying your reason for applying for support to attend the meeting. \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nSponsors\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nGenerously sponsored by Psi-K\, CCP9 and CECAM JC Maxwell \n\n\n\n\n\n\n\n\n\n\n\n\n\nContact\n\n\n\nIvana Savic – ivana.savic@kings.ac.uk \n\n\n\nOrganisers:Jochen Blumberger – University College LondonAlex Ganose – Imperial College LondonJohannes Lischner – Imperial College LondonAmel Mazari – Imperial College LondonIvana Savic – King’s College LondonAlex Shluger – University College LondonKaren Stoneham – University College LondonJan Tomczak – King’s College LondonMartijn Zwijnenburg – University College London \n\n\n\n\n\n\n\n\n\n\n\nBy registering for this conference\, you agree to our code of conduct for the event. \n\n\n\nCode of Conduct\n\n\n\nWe value the participation of every member of the materials and molecular modelling community and want to ensure that everyone has an enjoyable and fulfilling experience\, both professionally and personally. Accordingly\, all participants of the 7th Energy Materials Workshop are expected to always show respect and courtesy to others.  The TYC and its partners strive to maintain inclusivity in all of our activities.  All participants (staff and students) are entitled to a harassment-free experience\, regardless of gender identity and expression\, sexual orientation\, disability\, physical appearance\, body size\, race\, age\, and/or religion. Harassment in any form is not acceptable for any of us.  We respectfully ask all attendees of the 7th Energy Workshop to kindly conform to the following Code of Conduct: \n\n\n\n\nTreat all individuals with courtesy and respect.\n\n\n\nBe kind to others and do not insult or put down other members.\n\n\n\nBehave professionally. Remember that harassment and sexist\, racist\, or exclusionary jokes are not appropriate.\n\n\n\nHarassment includes\, but is not limited to\, offensive verbal comments related to gender\, sexual orientation\, disability\, physical appearance\, body size\, race\, religion\, sexual images in public spaces\, deliberate intimidation\, stalking\, following\, harassing photography or recording\, sustained disruption of discussions\, and unwelcome sexual attention.\n\n\n\nParticipants asked to stop any harassing behaviour are expected to comply immediately.\n\n\n\nContribute to communications with a constructive\, positive approach.\n\n\n\nBe mindful of talking over others during presentations and discussion and be willing to hear out the ideas of others.\n\n\n\nAll communication should be appropriate for a professional audience\, and be considerate of people from different cultural backgrounds. Sexual language and imagery are not appropriate at any time.\n\n\n\nChallenge behaviour\, action and words that do not support the promotion of equality and diversity.\n\n\n\nArrive at the conference events punctually where possible.\n\n\n\nShow consideration for the welfare of your friends and peers and\, if appropriate\, provide advice on seeking help.\n\n\n\nSeek help for yourself when you need it.\n\n\n\n\nYour data \n\n\n\nThank you for your interest in attending this workshop. Any information collected from you will be used to help us to organise the event\, and to contact you with details relevant to the event only. 
URL:https://thomasyoungcentre.org/event/tyc-8th-energy-materials-workshop/
LOCATION:King’s College London
CATEGORIES:Main event
ORGANIZER;CN="Scott Woodley":MAILTO:scott.woodley@ucl.ac.uk
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260513T130000
DTEND;TZID=Europe/London:20260513T150000
DTSTAMP:20260409T215725
CREATED:20260324T155229Z
LAST-MODIFIED:20260327T135724Z
UID:7796-1778677200-1778684400@thomasyoungcentre.org
SUMMARY:TYC Junior Research Fellowship talks
DESCRIPTION:TYC Junior Research Fellowship talks Share on X\n\n\n\n\nJRF Awardees present the outcomes of their visit to the TYC at a seminar at UCL. \n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nGianmarco Biagi\, University of Bologna – A computational study of polaron formation\, hopping mechanisms\, and dynamics in amorphous SiO₂\n\n\n\nI first generate realistic amorphous structures via melt–quench procedures\, then analyse polaronic states formed by additional electrons using density functional theory. \n\n\n\nThe aim of my work is to characterise polaron hopping between stable localisation sites and study the associated dynamics through ab initio molecular dynamics. \n\n\n\nEsmée Berger\, Chalmers University – Connecting ongoing work at Chalmers on machine-learned potentials and large-scale atomistic simulations with the TYC community.\n\n\n\nI am working on theoretical and computational modelling of molecular materials.  \n\n\n\nMy project demonstrates how machine-learned models can be combined with quantum simulation techniques to study complex interfacial systems relevant to chemistry\, materials science\, and nanotechnology. \n\n\n\n\n\n\n\nThe talks will be followed by snacks\, refreshments and networking in UCL Physics E7.
URL:https://thomasyoungcentre.org/event/tyc-junior-research-fellowship-talks/
LOCATION:UCL Physics A1/3\, Physics Building\, Gower Street\, London\, WC1E 6BT\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260430T140000
DTEND;TZID=Europe/London:20260430T170000
DTSTAMP:20260409T215725
CREATED:20260116T145316Z
LAST-MODIFIED:20260330T103905Z
UID:7546-1777557600-1777568400@thomasyoungcentre.org
SUMMARY:TYC Recently Appointed Academic Talks: Angela Casarella\, Imperial\, Francisco Martin-Martinez\, King’s\, Ricardo Grau-Crespo\, QMUL
DESCRIPTION:TYC Recently Appointed Academic Talks: Angela Casarella\, Imperial\, Francisco Martin-Martinez\, King’s\, Ricardo Grau-Crespo\, QMUL Share on X\n\n\n\n\nVenue: UCL Physics A1/3 (top floor)\, followed by networking in E7 (ground floor) \n\n\n\nTo Thomas Young Centre runs a continuous programme of Recently Appointed talks to welcome new PIs to the TYC\, and to introduce them and their research to the community.  \n\n\n\nThis session introduces Angela Casarella from Imperial\, Francisco Martin-Martinez from King’s\, and Ricardo Grau-Crespo from QMUL\, to the TYC. \n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nComputational modelling of nature-inspired bio-based materials – Francisco Martin-Martinez\, King’s College London\n\n\n\nValorising extensively available biomass wastes\, developing biobased materials\, and mimicking nature in its ability to design materials for circularity as well as performance are some of the avenues to achieve a more sustainable development. In our lab\, we seek material building blocks in biomass waste and non-critical material sources\, and we investigate structure-property relationships\, assembly\, and degradation mechanisms of biomolecules and biomass materials. We use computational chemistry\, atomistic modelling\, and machine learning to develop molecules and materials with applications in precision agriculture\, self-healing infrastructure\, or energy storage. \n\n\n\nTowards a Virtual Laboratory for Clay: from phenomenology to particle-scale modelling – Angela Casarella\, Imperial College London \n\n\n\nThe mechanical behaviour of clay is typically described using macroscopic constitutive models\, which are largely phenomenological and do not explicitly account for the underlying particle-scale mechanisms governing deformation and strength. Bridging this gap requires a mechanistic understanding of interactions between individual clay platelets\, where anisotropy\, electrochemical forces\, and pore fluid play a central role. \n\n\n\nIn this talk\, I present a multiscale framework combining coarse-grained molecular dynamics (CGMD) and finite element modelling (FEM). CGMD is used to simulate the collective behaviour of anisotropic clay platelets\, while FEM resolves electrochemical interactions and provides particle-to-particle constitutive laws that inform the simulations. \n\n\n\nThese modelling approaches are supported by synchrotron nano-holo-tomography\, enabling 3D imaging of clay particles in their natural saturated state and providing experimental validation of particle geometry\, arrangements and spacing.Together\, these developments contribute to a virtual laboratory for clay\, enabling a transition from phenomenological descriptions to predictive\, physics-based modelling.
URL:https://thomasyoungcentre.org/event/tyc-recently-appointed-academic-talks-angela-casarella-imperial-francisco-martin-martinez-kings-ricardo-grau-crespo-qmul-2/
LOCATION:UCL Physics A1/3\, Physics Building\, Gower Street\, London\, WC1E 6BT\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260417T170000
DTEND;TZID=Europe/London:20260417T210000
DTSTAMP:20260409T215725
CREATED:20260326T155920Z
LAST-MODIFIED:20260326T155921Z
UID:7805-1776445200-1776459600@thomasyoungcentre.org
SUMMARY:TYC  Early Career Researchers' 2026 Easter Bonanza
DESCRIPTION:TYC  Early Career Researchers' 2026 Easter Bonanza Share on X\n\n\n\n\n\n\n\n\nHappy Easter from the TYC ECR Committee! \n\n\n\nAs part of our mission\, we want to enhance socialising and networking outside of the academic environment with a series of events spread through the academic year. \n\n\n\nHence\, we are delighted to invite you to our Easter event\, which will take place the 17th of April at 5 pm in UCL —venue to be announced with a Teams calendar invite later on. \n\n\n\nWe have prepared exciting activities for everyone to take a part of. Join us and meet your fellow peers! \n\n\n\nPlease send a confirmation email to Britanny (britanny.klassen_gonzalez@kcl.ac.uk)\, so that we can keep track of anyone wanting to attend\, for organisation purposes. \n\n\n\nAll the best from us\,The TYC ECR Committee
URL:https://thomasyoungcentre.org/event/tyc-early-career-researchers-2026-easter-bonanza/
CATEGORIES:Main event
ORGANIZER;CN="Britanny Klassen Gonzalez":MAILTO:britanny.klassen_gonzalez@kcl.ac.uk
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260409T150000
DTEND;TZID=Europe/London:20260409T170000
DTSTAMP:20260409T215725
CREATED:20260119T120155Z
LAST-MODIFIED:20260326T113259Z
UID:7580-1775746800-1775754000@thomasyoungcentre.org
SUMMARY:TYC soiree: Non-adiabatic dynamics
DESCRIPTION:TYC soiree: Non-adiabatic dynamics Share on X\n\n\n\n\n\n\n\n\nJoin online: https://ucl.zoom.us/j/93561129864?pwd=hbMXSaN39kTe8a6LtUguqPDPuiqmqp.1 \n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nTheory and simulation of ultrafast processes in molecules – Federica Agostini\, Sorbonne University\, Paris\n\n\n\nThe interaction of light and matter is responsible for a variety of photophysical and photochemical phenomena occurring in nature\, like photosynthesis\, in the human body\, like vision\, and in technological devices\, like photovoltaics. Theoretical modeling of these phenomena requires to be able to describe the complex interplay of electronic and nuclear motion beyond the Born-Oppenheimer approximation [1]\, ie including nonadiabatic effects\, over ultrafast time scales ranging from femtoseconds to picoseconds. \n\n\n\nThe exact factorization of the electron-nuclear wavefunction is a formalism introduced in 2010 by Gross and coworkers to analyze and to simulate nonadiabatic processes [2]. Its original electron-nuclear formulation has been used to derive various flavors of trajectory-based algorithms [3\,4] to simulate ultrafast relaxation processes initiated by photoexcitation\, like photoisomerizations or photodissociations. However\, extensions of the original formalism to treat electron-only systems (exact electron factorization) and photon-electron-nuclear systems (exact photon-electron-nuclear factorization) have been proposed to develop density functional theory or to study photodynamics in the strong light-matter coupling regime [5].  \n\n\n\nIn this talk\, I will present an introduction to the theory of nonadiabatic ultrafast dynamics with the exact factorization and I will give an overview of its recent applications. \n\n\n\n[1] F. Agostini\, B. F. E. Curchod\, WIREs Comput. Mol. Sci. (2019).[2] L.-M. Ibele\, E. Sangiogo Gil\, E. Villaseco Arribas\, F. Agostini\, Phys. Chem. Chem. Phys. (2024).[3] C. Pieroni\, E. Sangiogo Gil\, L.-M. Ibele\, M. Persico\, G. Granucci\, F. Agostini\,  J. Chem. Theory Comput. (2024).[4] L.-M. Ibele\, E. Sangiogo Gil\, P. Schürger\, B. Le Dé\, R. Noc\, F. Agostini\,  J. Chem. Theory Comput. (2026).[5] S. Giarrusso\, P. Schürger\, F. Agostini\, arXiv:2602.23914 [physics.chem-ph] (2026). \n\n\n\nImproving the accuracy of nonadiabatic surface-hopping simulations – Jonthathan Mannouch\, MPSD\, Hamburg\, Germany\n\n\n\nFewest-switches surface hopping (FSSH) is one of the most popular approaches for simulating photochemical experiments [1]\, even though it suffers from problems of inconsistency and overcoherence that often significantly degrade its accuracy. \n\n\n\nFor example\, FSSH is unable to correctly describe the dynamics under strong electromagnetic pulses [2\,3]\, such that a fully satisfactory approach for simulating the photoexcitation step of many experiments is currently lacking. Additionally\, using FSSH in systems containing a dense manifold of electronic states is also challenging[4\,5]\, because trivial crossings must be correctly accounted for. \n\n\n\nIn this talk\, I will discuss some of my recent work in alleviating these problems in surface-hopping based simulations. First\, I will demonstrate how the advantageous features of a newly developed surface-hopping algorithm (the mapping approach to surface hopping [6]) can be utilized to provide an improved description of the photoexcitation step for a series of molecular systems. Finally\, I will present an improved expression for the FSSH hopping probability\, which in tandem with state tracking provides a robust strategy for computing charge mobilities in molecular materials. \n\n\n\n[1] J. E. Subotnik et. al.\, Annu. Rev. Phys. Chem. 2016\, 67\, 387–417.[2] B. Mignolet\, B. F. E. Curchod\, J. Phys. Chem. A 2019\, 123\, 3582–3591.[3] T. Fiedlschuster\, et al.\, Phys. Rev. A\, 95\, 063424 (2017)[4] T. Qiu\, C. Climent\, J. E. Subotnik\, J. Chem. Theory Comput. 19\, 2744-2757 (2023)[5] A. Carof\, S. Giannini\, J. Blumberger\, Phys. Chem. Chem. Phys. 21\, 26368 (2019)[6] J. R. Mannouch\, J. O. Richardson\, J. Chem. Phys. 2023\, 158\, 104111.
URL:https://thomasyoungcentre.org/event/tyc-soiree-non-adiabatic-dynamics/
LOCATION:UCL Physics A1/3\, Physics Building\, Gower Street\, London\, WC1E 6BT\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260326T160000
DTEND;TZID=Europe/London:20260326T180000
DTSTAMP:20260409T215725
CREATED:20260112T121547Z
LAST-MODIFIED:20260305T154433Z
UID:7513-1774540800-1774548000@thomasyoungcentre.org
SUMMARY:1st TYC Annual Lecture: Photon-Mediated Interactions and Quantum Material Control via QEDFT\, Prof. Angel Rubio
DESCRIPTION:1st TYC Annual Lecture: Photon-Mediated Interactions and Quantum Material Control via QEDFT\, Prof. Angel Rubio Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nJoin us for a special lecture in G20\, Royal School of Mines followed by a drinks reception in G01.  \n\n\n\nThis is also a hybrid event. For those who cannot attend in person you can join online via link.  \n\n\n\nDr Angel Rubio\, Max Planck Institute for the Structure and Dynamics of Matter & Initiative for Computational Catalysis (ICC) and Center for Computational Quantum Physics (CCQ) Flatiron Institute\n\n\n\nProf. Angel Rubio received his PhD in Physics with honors from the University of Valladolid in 1991 where he did fundamental work on the structural and optical properties of metallic clusters. Then moved to a postdoctoral position at UC Berkeley-Physics (92-95) where he predicted a new type of boron-nitride nanotubes (PRB1994) triggering their ensuing experimental synthesis. Between 1994 and 2001 as Professor at UVA he started the ab initio materials research open-source project octopus used now by over 1000 groups worldwide. Diverse Professorships at École Polytechnique Paris\, FU Berlin and Montpellier followed. In 2001 he moved as Chair of Condensed Matter Physics at UPV/EHU. There he engaged in highly successful work on modeling of excited-state properties of materials and nanostructures setting the foundations of modern theoretical spectroscopy (RMP2002). In August 2014 he accepted the position as Max Planck Director. There he has pioneered the development of quantum electrodynamical density functional theory (QEDFT)\, a novel theoretical framework for strong light-matter phenomena in chemistry and materials sciences (PNAS2015\, Nat.Rev.Chem.2018). His work has been recognized by several awards\, including the 2023 Spanish National Physics Prize “Blas Cabrera” 2018 Max Born medal and prize\, 2016 Medal of the Spanish Royal Physical Society and the 2014 Premio Rey Jaime I for basic research\, and more\, and elected member of different academies\, including the German Leopoldina Academy and Berlin-Brandenburgischen Akademie der Wissenschaften\, the European Academy of Sciences\, the Academia Europaea\, and a foreign associate member of the National Academy of Sciences (USA). \n\n\n\nTitle: Photon-Mediated Interactions and Quantum Material Control via QEDFT \n\n\n\nAbstract: The quantum vacuum is not empty: confined electromagnetic modes in cavities can mediate interactions that reshape material ground states. Embedding Cavity materials engineering is an emerging field at the intersection of quantum optics and condensed matter physics\, where the quantum vacuum fluctuations of confined electromagnetic fields can be harnessed to control and design material properties at equilibrium. Embedding quantum materials inside optical or microwave cavities enhances light–matter coupling to the point where even the vacuum field can induce macroscopic changes—such as shifts in superconductivity\, magnetism\, Dirac gaps\, Fermi velocity\, or interlayer spacing—without any external driving or photon excitation. This “dark” regime fundamentally differs from traditional light-driven approaches and opens a new route for modifying the ground state of matter. \n\n\n\nDescribing these effects requires theoretical frameworks that go beyond standard electronic structure methods. Quantum Electrodynamical Density Functional Theory (QEDFT) incorporates quantized photon fields directly into ab initio simulations\, providing a first-principles platform to predict cavity-induced modifications of electronic\, magnetic\, and structural properties. Complementary Hartree–Fock and many-body approaches reveal how photon-mediated interactions\, including anisotropic mode effects\, can control correlations and optical responses in two-dimensional and van der Waals materials. \n\n\n\nIn this talk\, I will present the principles of QEDFT\, highlight recent experimental and theoretical breakthroughs in cavity-engineered quantum materials\, and discuss emerging opportunities where vacuum fluctuations\, rather than classical light\, become a new tool for controlling correlated quantum phases.
URL:https://thomasyoungcentre.org/event/tyc-seminar-photon-mediated-interactions-and-quantum-material-control-via-qedft-dr-angel-rubio/
LOCATION:Imperial College London\, Room G20 - Royal School of Mines\, London\, SW7 2AZ
CATEGORIES:Main event
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260319T160000
DTEND;TZID=Europe/London:20260319T180000
DTSTAMP:20260409T215725
CREATED:20260219T114453Z
LAST-MODIFIED:20260313T125319Z
UID:7681-1773936000-1773943200@thomasyoungcentre.org
SUMMARY:TYC Soft & Bio Matter soiree: Gianni De Fabriitis & Daniel Cole\, Newcastle
DESCRIPTION:TYC Soft & Bio Matter soiree: Gianni De Fabriitis & Daniel Cole\, Newcastle Share on X\n\n\n\n\n\n\n\n\nData-driven Interatomic potentials for computer-aided drug design – Daniel Cole\n\n\n\nDrawing on computational methods that are based around training to extensive condensed phase physical property and quantum mechanical datasets\, I will describe some of our efforts to design accurate and transferable inter- and intra-molecular potentials\, with a view to applications in condensed phase atomistic modelling and computer-aided drug design. \n\n\n\nI will explain how recent collaborations with the Open Force Field Initiative \n\n\n\n(https://openforcefield.org) enable the automated development of fast\, accurate force field models. I will describe the development of a graph neural network based charge model targeting accurate electrostatic properties of organic molecules\, and the use of Open Force Field infrastructure to rapidly train valence parameters on the GPU. Finally\, I will describe MACE-OFF\, a transferable force field for organic molecules created using state-of-the-art machine learning technology and first principles reference data. \n\n\n\nBio: Dr Daniel Cole is a UKRI Future Leaders Fellow and Reader in Computational Chemistry at Newcastle University. He has worked previously as a Marie Curie Research Fellow in the group of Prof William Jorgensen at Yale University\, and as a Research Associate in the group of Prof Mike Payne at the University of Cambridge. He is a principal investigator at the Open Force Field Initiative and sits on the management group of the CCPBioSim collaborative computational project. \n\n\n\nSpeak to a Protein: AI Co-Scientists for Interactive Drug Discovery – Gianni De Fabriitis\n\n\n\nIn this talk\, we introduce Speak to a Protein\, an interactive multimodal AI co-scientist for drug discovery. The system brings together scientific literature\, structural biology\, ligand knowledge\, molecular visualization\, and code execution into a single conversational interface. It can answer questions grounded in a live 3D molecular scene\, highlight and manipulate structural features\, retrieve and synthesize evidence across sources\, and generate analyses on demand\, explaining results through words\, graphics\, and interactive views. \n\n\n\nRather than treating AI as a passive search or summarization tool\, Speak to a Protein points to a new model of scientific interaction: one in which researchers collaborate with systems that help them think\, interrogate evidence\, and generate hypotheses in real time. We show how this capability can accelerate tasks such as identifying binding pockets\, comparing conformational states\, exploring structure-activity relationships\, and moving rapidly from question to insight. \n\n\n\nMore broadly\, this work suggests a future in which AI co-scientists lower the barrier to complex molecular reasoning\, make advanced analysis more widely accessible\, and help reshape how discovery science is done. \n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nFor anyone attending online: \n\n\n\nJoin Zoom Meetinghttps://ucl.zoom.us/j/99936321012?pwd=aB2BHuszvdAJ9f2vVmONjgNiMqF2ZR.1 \n\n\n\nMeeting ID: 999 3632 1012Passcode: 140132
URL:https://thomasyoungcentre.org/event/tyc-soft-bio-matter-soiree-gianni-de-fabriitis-daniel-cole-newcastle/
LOCATION:Harrie Massey Lecture Theatre\, UCL\, 25 Gordon Street\, London\, WC1H 0AY
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260304T153000
DTEND;TZID=Europe/London:20260304T180000
DTSTAMP:20260409T215725
CREATED:20260206T154526Z
LAST-MODIFIED:20260302T110742Z
UID:7631-1772638200-1772647200@thomasyoungcentre.org
SUMMARY:TYC & WHPCLondon Early Career Researcher Talks
DESCRIPTION:TYC & WHPCLondon Early Career Researcher Talks Share on X\n\n\n\n\nInternational Women’s Day on 8th March\, will be marked by WHPC London on 4th of March with two talks from female Early Career researchers\, which aligns with the Materials Modelling Course session ‘Electronic excitations\, GW\, Bethe-Salpeter equation\, GF‘ which will be given by Johannes Lischner from Imperial from 1-3pm in UCL Physics E7 ground floor.  \n\n\n\nWe will follow the talks with networking\, snacks and refreshments. \n\n\n\nThis event is open to all TYC\, not just female members.  \n\n\n\nSelin Kilic\, UCL \n\n\n\nTitle: Modelling excited states of MOFs with cluster models and navigating early careers in academia; a first year PhD student’s perspective. \n\n\n\nAbstract: The growing interest in metal-organic frameworks (MOFs) for photoactive applications has increased the need for accurate modelling of their excited states.  However\, the large unit cells of MOFs make high-level excited state calculations computationally challenging. One approach is the use of embedded cluster techniques\, such as the ONIOM (QM:QM′) scheme\, where chemically relevant regions can be treated at a higher level of theory than the extended environment. Selin’s PhD focuses on developing workflows to apply these methods to large-scale MOF databases. Alongside introducing her research\, she will reflect on her first six months as a PhD student and her experiences navigating academia as a female early career researcher. \n\n\n\nWenxuan Cai\, Imperial College London \n\n\n\nTitle: Learning about gas sensing from calculations of core-electron binding energies \n\n\n\nAbstract: Metal-oxide gas sensors are widely used. However\, their microscopic operating mechanisms remain incompletely understood. This is primarily because the observable quantities measured in experiments are difficult to explain straightforwardly. X-ray photoemission spectroscopy (XPS) is a key technique for probing surface chemistry\, but the interpretation of XPS spectra is challenging when multiple terminations\, defects\, and adsorbates give rise to overlapping spectral features. A predictive theoretical framework that can directly link atomistic structure to measured spectra is therefore essential. In this talk\, I present a first-principles approach for modelling XPS spectra of metal oxides based on core-level calculations\, with based on the Z+1 approximation the ΔSCF method. After introducing the physical idea behind core-hole creation and relaxation\, I outline how these methods can be applied consistently across length scales\, starting from molecules\, bulk oxides\, and then extending to surface slab models. \n\n\n\nThe methodology is demonstrated in detail for rutile SnO₂ (110) surfaces\, which serve as a typical system for gas sensors. We consider the stoichiometric surface\, several reduced surfaces with distinct oxygen vacancy configurations (including the fully reduced surface)\, and the fully reduced surface decorated with OH and O₂ adsorbates. For each system\, O 1s core-electron binding energies are calculated for all oxygen sites and combined to generate simulated XPS spectra. The results explain the relationship between structure and spectroscopy. Bridging oxygen atoms on stoichiometric surfaces generate additional low-binding-energy features\, whilst hydroxyl and molecular oxygen adsorbates yield high-binding-energy components. Fully reduced surfaces exhibit highly symmetric O 1s peaks\, demonstrating high consistency with the initial material surface state in the experimental setup. Moreover\, the predicted spectral energies precisely reproduce measurements from reduced surfaces exposed to oxygen. \n\n\n\n \n\n\n\n \n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\n\n\n\n\nUpcoming WHPC events to mark International Women’s Day\n\n\n\nTYC & WHPC London Early Career Researcher Talks3:30pm-6pm GMT\, 4 March 2026\, 1.02\, Malet Place Engineering Building\, UCL \n\n\n\nWHPC Pittsburgh: Powered by AI: Best Practices for Staying Motivated and Working Smarter1-1:30pm PA (6pm UK time)\, 6 March 2026\, ONLINE \n\n\n\nGreat Plains WHPC Network: Panel Discussion: “A Day in the Life of HPC System Administrator”12pm CT (6pm UK time)\, 11 March 2026 \n\n\n\nCambridge and East Anglia WHPC: Queens’ Conversations – Impactful Women – International Women’s Day 20264pm-5:30pm GMT\, 10 March 2026
URL:https://thomasyoungcentre.org/event/whpc-early-career-researcher-talks/
LOCATION:1.02\, Malet Place Engineering Building\, 2 Malet Place\, London\, WC1E 7JE
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260226T093000
DTEND;TZID=Europe/London:20260226T113000
DTSTAMP:20260409T215725
CREATED:20260211T115524Z
LAST-MODIFIED:20260211T143542Z
UID:7640-1772098200-1772105400@thomasyoungcentre.org
SUMMARY:Strongly Correlated Materials — a Korean matinée
DESCRIPTION:Schedule \n\n\n\n09:30am – Ara Go \n\n\n\nData-Driven Bath Fitting for Hamiltonian-Diagonalization DMFT \n\n\n\n10:00am – Heung-Sik Kim \n\n\n\nCorrelation-induced flat bands in two- and three-dimensional transition metal compounds \n\n\n\n10:30am – Choong Hyun Kim \n\n\n\nFrom Jahn-Teller Distortions to Spin-Orbital Entanglement: Pathways to Mott Metal-Insulator \n\n\n\n11:00am – Bongjae Kim  \n\n\n\nStrain-Engineered Ruthenates: Controlling Correlated Quantum Phases \n\n\n\n \n\n\n\n\n\n\n\n \n\n\n\nAbstracts \n\n\n\nAra Go – Data-Driven Bath Fitting for Hamiltonian-Diagonalization DMFT \n\n\n\nDepartment of Physics\, Chonnam National University\, Gwangju\, Republic of Korea \n\n\n\nWe develop a machine-learning-based initialization strategy that alleviates a major practical bottleneck of Hamiltonian-diagonalization-based dynamical mean-field theory (HD-DMFT): nonlinear bath fitting. In HD-DMFT\, the continuous hybridization function is approximated by a finite set of bath-site energies and hybridization amplitudes obtained from a highly non-convex multivariable optimization. As the number of bath sites increases\, this optimization becomes increasingly sensitive to the initial guess and prone to trapping in suboptimal local minima\, slowing or destabilizing the DMFT self-consistency loop. \n\n\n\nWe recast bath fitting as a supervised regression problem and train a kernel ridge regression model to predict near-optimal discrete bath parameters directly from the target hybridization function on the Matsubara axis. A key methodological element is a physically grounded data-generation protocol: rather than random sampling\, we construct a diverse training set from tight-binding Hamiltonians of layered-perovskite-like ruthenate models across systematically deformed structures\, with high-quality labels obtained from fully converged conventional bath fitting. Time-reversal symmetry is explicitly incorporated in both feature and target representations\, reducing effective dimensionality and enforcing physical consistency. \n\n\n\nBenchmarks in the non-interacting limit show that the learned initialization systematically reduces the initial fitting error\, decreases the number of conjugate-gradient iterations\, and improves robustness against local minima over a wide range of bath sizes. We further demonstrate transferability to an interacting HD-DMFT calculation for Sr2RuO4 solved with an adaptive-truncation impurity solver\, where the ML initialization yields consistently faster convergence than a symmetry-preserving heuristic baseline while preserving the final fitted solution. \n\n\n\nHeung-Sik Kim – Correlation-induced flat bands in two- and three-dimensional transition metal compounds \n\n\n\nDepartment of Energy Engineering\, Korea Institute of Energy Technology\, Naju-si 58330\, Republic of Korea \n\n\n\nThe exploration of electronic flat bands has recently attracted considerable attention due to their potential to host emergent quantum phenomena\, including fractional Chern insulating phases\, charge density waves\, and superconductivity. Numerous theoretical proposals and candidate materials have been suggested; however\, realizing flat bands near the Fermi level remains challenging due to the intricate requirements of lattice structure\, chemical composition\, and symmetry considerations. In this study\, we propose an alternative pathway to achieve flat bands\, employing electron correlations in quasi-two- and three-dimensional transition-metal-based compounds. \n\n\n\nFirstly\, we examine α-RuI3\, demonstrating that the interplay between spin-orbit coupling and on-site Coulomb interactions stabilizes flat bands near the Fermi level\, thereby underpinning the compound’s peculiar bad-metallic behavior[1\,2]. Secondly\, we discuss Sc3Mn3Al7SI5\, illustrating that flat bands emerge due to the synergy between geometric frustration and Coulomb interactions; these correlation-driven flat bands are proposed as the source of intrinsic ferromagnetic fluctuations observed in this nominally nonmagnetic metal[3]. Lastly\, we show our preliminary results on a spinel compound CuV2S4\, employing our recent complex-time tensor-network impurity solver[4\,5]. This work highlights the crucial role of electron correlations combined with structural and geometric factors in engineering and identifying flat-band systems. \n\n\n\n[1] S. Samanta\, D. Hong\, and H.-S. Kim\, Nanomaterials 14\, 9 (2023). \n\n\n\n[2] D. A. S. Kaib et al.\, npj Quant. Mater. 7\, 75 (2022). \n\n\n\n[3] S. Samanta et al.\, Nat. Commun. 15\, 5376 (2024). \n\n\n\n[4] J. Huang et al.\, Nat. Phys. 20\, 603-609 (2024). \n\n\n\n[5] J. Cha\, H.-Y. Lee\, H.-S. Kim\, Sci. Rep. 15\, 37490 (2025).   \n\n\n\n \n\n\n\nChoong Hyun Kim  – From Jahn-Teller Distortions to Spin-Orbital Entanglement: Pathways to Mott Metal-Insulator \n\n\n\nDepartment of Physics\, Ajou University\, Suwon\, Republic of Korea \n\n\n\nMott metal-insulator transition (Mott MIT) is one of the most prominent emergent phenomena in strongly correlated systems. Unlike conventional band insulators\, Mott MIT arises from the interplay of Coulomb interaction\, spin-orbit coupling\, and lattice distortion\, leading to novel phase transitions and electronic states. In multi-orbital systems\, the lifting of orbital degeneracy plays a crucial role in determining the MIT. This can be driven by Jahn-Teller distortion\, spin-orbit coupling\, or a complex interplay of Hund’s coupling and Coulomb U\, which can either compete or cooperate in shaping the phase transition. \n\n\n\nIn this presentation\, we will discuss how key factors such as Coulomb U\, lattice distortion\, Hund’s coupling\, and spin-orbit coupling interact to produce intriguing phase diagrams in strongly correlated materials. Specifically\, we will focus on two systems: the CuAl₂O₄ spinel\, where strong spin-orbit coupling leads to a novel spin-orbital-entangled state\, and monolayer SrRuO₃ thin films\, where a new type of Jahn-Teller distortion drives the metal-insulator transition. These cases highlight the rich physics underlying Mott MIT and provide insights into the broader implications for correlated electron systems. \n\n\n\nBongjae Kim  – Strain-Engineered Ruthenates: Controlling Correlated Quantum Phases \n\n\n\nDepartment of Physics\, Kyungpook National University\, Dague\, Republic of Korea \n\n\n\nLayered ruthenates provide a clean platform in which small changes of lattice geometry reshuffle the hierarchy among superconducting\, magnetic\, and metallic ground states. In this talk\, we will discuss how uniaxial and epitaxial strain can be used as tuning parameters to manipulate correlated quantum phases in these systems. For Sr2RuO4\, we will discuss the microscopic origin of the counterintuitive emergence of static magnetism under uniaxial strain\, underlining the key role played by spin fluctuations. We will further show uniaxial strain can induce lattice softening driven by electronic instabilities and can stabilize distinct magnetic phases. We will then discuss the ruthenate heterostructures\, where dimensional confinement and epitaxial strain provide an effective route to engineer competing electronic and magnetic phases that go beyond what can be reached in bulk layered ruthenates. \n\n\n\n\nRegister Here
URL:https://thomasyoungcentre.org/event/strongly-correlated-materials-a-korean-matinee/
LOCATION:Kings College London\, Room S7.06 - The Strand Building\, London\, WC2R 2LS
CATEGORIES:Main event
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20260112T094500
DTEND;TZID=Europe/London:20260112T171500
DTSTAMP:20260409T215725
CREATED:20251120T134343Z
LAST-MODIFIED:20260109T135602Z
UID:7196-1768211100-1768238100@thomasyoungcentre.org
SUMMARY:M3-LEC (MMM-Learning\, Exchange & Collaboration) TYC-LJC
DESCRIPTION:Thomas Young Centre & Lennard Jones Centre collaborative conference \n\n\n\n\n\n\n\n\n\n\n\n\nM3-LEC (MMM-Learning\, Exchange & Collaboration) TYC-LJC Share on X\n\n\n\n\n\n\n\n\n\n\n\n\nJoin us for the 2026 joint Thomas Young Centre and Lennard-Jones Centre conference focusing on materials and molecular modelling. Designed primarily for early career researchers\, this event offers opportunities for learning\, collaboration\, and community building\, through talks\, poster sessions\, and breakout sessions. \n\n\n\nThis inaugural collaboration brings together TYC’s established network and extensive events programme with LJC’s Cambridge-based seminar programme\, covering molecular and material simulations\, electronic structures\, chemistry\, physics\, and engineering. By aligning our efforts\, we aim to foster deeper connections and shared learning across our communities.  \n\n\n\nA fantastic opportunity for early career researchers and established researchers alike to quickly build and enhance a broad network and disseminate research ideas. \n\n\n\n\n\n\nAI and Machine Learning \n\n\n\n\n\n\n\nMaterials Physics/ Biomolecules \n\n\n\n\n\n\n\nECR Skills \n\n\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\n09:45-10:00Introductions and Registration10:00-10:30Talk 1: Prof. Emilio Artacho\, University of Cambridge10:30-11:00Talk 2: Prof. Carla Molteni\, King’s College London11:00-11:30Coffee Break11:30-12:45Early Career Researcher Talks12:45-13:30Lunch: Informal Breakout Sessions and Posters13:30-14:00Breakout session 114:00-14:30Parallel Breakout sessions 2&314:30-15:00Breakout session 415:00-15:30Talk 3\, Prof. Sophia Yaliraki\, Imperial College London15:30-16:00Coffee Break16:00-16:30Talk 4: Prof. Ana Jorge Sobrido QMUL16:30-17:00Talk 5: Prof. Angelos Michaelides\, Yusuf Hamied Department of Chemistry\, University of Cambridge17:00-17:15Closing Remarks and Awards
URL:https://thomasyoungcentre.org/event/m3-lec-mmm-learning-exchange-collaboration-tyc-ljc/
LOCATION:Graduate Centre Foyer & Lecture Theatre\, Queen Mary University of London\, Mile End Road\, London\, E1 4NS\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251210T150000
DTEND;TZID=Europe/London:20251210T180000
DTSTAMP:20260409T215725
CREATED:20251128T190559Z
LAST-MODIFIED:20251128T190815Z
UID:7295-1765378800-1765389600@thomasyoungcentre.org
SUMMARY:TYC Christmas Party 2025
DESCRIPTION:UCL Physics E3/7 \n\n\n\n\n\n\n\n\n\n\nTYC Christmas Party 2025 Share on X\n\n\n\n\nThe Thomas Young Centre invites you all to our annual Festive Celebration event for snacks & drinks\, mulled wine (and non-alcoholic alternatives)\, music\, and Christmas inflatables! \n\n\n\n\nTell us you are joining
URL:https://thomasyoungcentre.org/event/tyc-christmas-party-2025/
LOCATION:UCL Physics E7\, Gower Place\, WC1E 6BN
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251201T160000
DTEND;TZID=Europe/London:20251201T170000
DTSTAMP:20260409T215725
CREATED:20251117T101759Z
LAST-MODIFIED:20251119T115939Z
UID:7175-1764604800-1764608400@thomasyoungcentre.org
SUMMARY:TYC Seminar: Ion-Specific Interactions in Nanoconfinement: Insights from Clay-like Materials
DESCRIPTION:TYC Highlight Seminar: Ion-Specific Interactions in Nanoconfinement: Insights from Clay-like Materials Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nDr Katerina Ioannidou\, CNRS & University of Montpellier\n\n\n\nKaterina Ioannidou is a CNRS Research Scientist at the Laboratory of Mechanics and Civil Engineering (LMGC)\, University of Montpellier. She holds a degree in Physics from the National and Kapodistrian University of Athens and a PhD in Science from ETH Zurich. Before joining CNRS\, she was a postdoctoral researcher in the Department of Civil and Environmental Engineering at MIT. \n\n\n\nHer research focuses on the physics of porous and disordered materials\, with an emphasis on reactive systems such as cement hydrates\, clays\, and geopolymers. She combines statistical-physics modelling\, granular and soft-matter simulations\, and 3D imaging and mechanical characterisation to understand how evolving microstructures control macroscopic mechanical and transport properties. Her work aims to establish predictive\, multi-scale frameworks for materials that are structurally complex and undergo continuous chemical or environmental transformations. \n\n\n\nIn 2024\, she was awarded the CNRS Bronze Medal for her contributions to the multi-scale physics of amorphous and reactive materials. \n\n\n\nTitle: Ion-Specific Interactions in Nanoconfinement: Insights from Clay-like Materials \n\n\n\nAbstract: Clays provide an archetypal example of matter under extreme confinement\, where charged surfaces\, hydration layers and ion-specific interactions create forces that cannot be captured by continuum theories. In this talk\, I will use clays and clay-like systems as a model to explore how molecular interactions shape mesoscale structure and macroscopic behavior in charged disordered materials. \n\n\n\nI will show how potentials of mean force extracted from atomistic simulations reveal the subtle role of hydration structure\, dielectric response and counter-ion identity in controlling swelling forces and aggregation. Using imogolite nanotubes and layered aluminosilicates as case studies\, I will demonstrate how nanoscale mechanisms translate into mesoscale cohesion\, network formation and mechanical response. Finally\, I will discuss how similar ideas underpin other reactive or confined materials such as cement hydrates\, nanoporous carbons and cohesive granular assemblies\, providing a unified physical framework for ion-mediated interactions in disordered solids. \n\n\n\nThe goal is to illustrate how multiscale modelling—from molecular simulations to coarse-grained descriptions—can reveal the physics of confined electrolytes and emergent cohesion in a broad class of soft and porous materials.
URL:https://thomasyoungcentre.org/event/tyc-highlight-seminar-ion-specific-interactions-in-nanoconfinement-insights-from-clay-like-materials/
LOCATION:Skempton Building Room 201\, Imperial College London\, South Kensington\, London\, SW7 2AZ\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251127T150000
DTEND;TZID=Europe/London:20251127T170000
DTSTAMP:20260409T215725
CREATED:20251008T131059Z
LAST-MODIFIED:20251125T130914Z
UID:7018-1764255600-1764262800@thomasyoungcentre.org
SUMMARY:TYC Soiree: Modelling and simulation of biomolecules: pathways\, kinetics and catalysis
DESCRIPTION:TYC Soiree: Modelling and simulation of biomolecules: pathways\, kinetics and catalysis Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nFor anyone attending online: \n\n\n\n\nhttps://ucl.zoom.us/j/99843406795\n\n\n\n\nMeeting ID: 998 4340 6795  \n\n\n\n\n\n\n\n15:00 – 15:40Gabriele Corso\, Massachusetts Institute of Technology15:40 – 16:20Marc Van der Kamp\, University of Bristol16:20 – 17:00Stefano Motta\, University of Milano Bicocca17:00 onwardsDrinks reception at UCL Physics E7\n\n\n\n \n\n\n\nBoltz: Towards Accurate Biomolecular Modeling and Design – Gabriele Corso\, Massachusetts Institute of Technology\n\n\n\nAccurately modeling biomolecular interactions remains a central challenge in modern biology. Breakthroughs such as AlphaFold3 and Boltz-1 have greatly advanced structure prediction of biomolecular complexes. Building on this progress\, we introduced Boltz-2\, the first AI model to approach the accuracy of free-energy perturbation (FEP) methods for estimating small molecule–protein binding affinities. Most recently\, with BoltzGen\, we demonstrated that fine-tuning large-scale structure prediction models for protein design enables a powerful end-to-end pipeline. We validated this pipeline experimentally with multiple wet-lab collaborators\, achieving successful designs across a wide range of novel targets. \n\n\n\nGabriele Corso recently received his PhD from MIT CSAIL where his research focused on developing novel ML frameworks to tackle challenging problems in drug discovery and he led the development of popular models in the space including DiffDock\, Boltz-1 and Boltz-2. \n\n\n\nMapping Biomolecular Conformational Pathways with Self-Organizing Maps – Stefano Motta\, University of Milano Bicocca\n\n\n\nUnderstanding complex biomolecular processes from molecular dynamics (MD) simulations requires interpreting large\, high-dimensional datasets. I will discuss how Self-Organizing Maps (SOMs)\, a type of unsupervised machine learning models\, can generate intuitive\, low-dimensional representations of the conformational space sampled during these simulations (1). I will then demonstrate how this approach\, implemented in our new R package SOMMD(2)\, can be used to reconstruct molecular pathways in processes such as protein unfolding and ligand binding\, and to build transition network models that characterize their key events(1\,3). \n\n\n\n1.      Motta\, S.\, Callea\, L.\, Bonati\, L.\, & Pandini\, A. (2022). PathDetect-SOM: A Neural Network Approach for the Identification of Pathways in Ligand Binding Simulations. Journal of Chemical Theory and Computation\, 18(3)\, 1957–1968. \n\n\n\n2.      Motta S.\, Callea L.\, Mulla S. I.\, Davoudkhani H.\, Bonati L.\, Pandini A. (2025). SOMMD: an R package for the analysis of molecular dynamics simulations using self-organizing map. Bioinformatics\, 41(6)\, btaf308. \n\n\n\n3.      Callea L.\, Caprai C.\, Bonati L.\, Giorgino T.\, Motta S. (2024). Self-organizing maps of unbiased ligand–target binding pathways and kinetics. The Journal of Chemical Physics\, 161\, 135102. \n\n\n\nStefano Motta obtained his PhD in Chemical Sciences from the University of Milano-Bicocca in 2018\, where he has been an Assistant Professor since 2022. His research focuses on the development and application of computational methods to investigate the structure and dynamics of biomolecular systems. His current research interests include the use of molecular dynamics to study protein-ligand recognition\, the mechanism of action of bHLH-PAS proteins\, the characterization of nanosystems for biomedical applications\, and the development of machine learning approaches for the analysis of complex simulations. \n\n\n\nMultiscale simulations for understanding and engineering enzymes: from QM/MM to ML/MM – Marc Van der Kamp\, University of Bristol\n\n\n\nEnzymes have excellent potential as selective and efficient biocatalysts for industry. Obtaining enzyme biocatalysts with both the desired selectivity and activity\, however\, remains a challenge. Atomistic simulations can provide valuable information for rational engineering. Ideally\, simulation protocols require limited computational resource (and thus energy) but maintain sufficient accuracy. Here\, the development of tools and methods for ‘in silico enzyme screening’ with reaction simulations are discussed\, highlighting applications to different enzymes. We have shown that short QM/MM reaction simulations with semi-empirical QM methods can be used to correctly indicate activity for certain enzymes\, such as serine beta-lactamases.1 When combined with automated protocols to set up simulations\, such as Enlighten2\,2 this can result in efficient evaluation of activity and selectivity. We demonstrate how this can be used to obtain key insights into natural beta-barrel Diels-Alderases\,3 which are promising stable and stereoselective biocatalysts.  \n\n\n\nFor highly efficient screening of enzyme activity\, such that calculations can be used during enzyme (re)design\, further increases in efficiency and accuracy are important. Replacing QM by machine-learning (ML) potentials can\, in principle\, offer QM accuracy at a fraction of the computational cost. However\, due to the absence of electrons in ML potentials\, properly describing the electrostatic interaction between ML and MM regions\, crucial for capturing enzyme catalysis\, is a challenge. We have developed the “electrostatic ML embedding” (EMLE) scheme that solves this issue\, allowing DFT/MM accuracy.4\,5 Here\, we show that this method can be applied for enzyme reaction simulations to capture key catalytic effects.  \n\n\n\nReferences:  \n\n\n\n\nV. H. A. Hirvonen\, K. Hammond\, E. I. Chudyk\, M. A. L. Limb\, J. Spencer\, A. J. Mulholland and M. W. van der Kamp. J. Chem. Inf. Model. 2019\, 59\, 3365-3369.\n\n\n\nK. Zinovjev and M. W. van der Kamp. Bioinformatics\, 2020\, 36\, 5104–5106.\n\n\n\nL. Maschio\, et al. Chem. Sci. 2024\, 15\, 11572-11583; Mbatha et al.\, Chem. Sci. 2024\, 15\, 14009-14015.\n\n\n\nK. Zinovjev\, L. Hedges\, R. M. Andreu\, C. Woods\, I. Tuñón and M. W. van der Kamp. J. Chem. Theory Comput. 2024\, 20\, 4514–4522.\n\n\n\nV. Gradisteanu\, E. W. Chan\, L. Hedges\, M. Malagarriga\, R. David\, M. de la Puente\, D. Laage\, I. Tuñón\, M. W. van der Kamp\, K. Zinovjev. ChemRxiv 2025\, DOI: 10.26434/chemrxiv-2025-nw9lt. \n\n\n\n\nMarc is Associate Prof. in Computational Biochemistry in the School of Biochemistry in Bristol\, and is an expert in biomolecular simulation of enzymes and their reactions. After obtaining a PhD in this field in Bristol (2008)\, he pursued postdoctoral research at the University of Washington (with Prof. Valerie Daggett) and in Bristol (with Prof. Adrian Mullholland). Then\, as a BBSRC David Phillips Fellow (2015-2021)\, he established a group with PDRAs and PhDs and advanced the use of detailed biomolecular simulation for understanding enzyme biocatalysts and predicting properties of their variants. The main research interests in the group include: enzymes involved in antibiotic resistance\, computational simulation methods to aid enzyme engineering and design of biologic drugs\, and further understanding the principles of enzyme catalysis and specificity.
URL:https://thomasyoungcentre.org/event/https-tyc-soiree-modelling-and-simulation-of-biomolecules-pathways-kinetics-and-catalysis/
LOCATION:Denys Holland Lecture Theatre\, Bentham House\, UCL\, 4–8 Endsleigh Gardens\, London\, WC1H 0EG\, United Kingdom
CATEGORIES:Main event
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251120T150000
DTEND;TZID=Europe/London:20251120T170000
DTSTAMP:20260409T215725
CREATED:20250529T124145Z
LAST-MODIFIED:20251113T161933Z
UID:6703-1763650800-1763658000@thomasyoungcentre.org
SUMMARY:TYC Highlight Seminar: Machine-Learned Force Fields for Molecular Simulations Beyond AlphaFold and Empirical Potentials
DESCRIPTION:TYC Highlight Seminar: Machine-Learned Force Fields for Molecular Simulations Beyond AlphaFold and Empirical Potentials Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nAlexander Tkatchenko\, University of Luxembourg\n\n\n\nThe convergence between accurate quantum-mechanical (QM) models (and codes) with efficient machine learning (ML) methods seem to promise a paradigm shift in all-atom simulations. Many challenging applications are now being tackled by increasingly powerful QM/ML methodologies (https://doi.org/10.1021/acs.chemrev.0c01111; https://doi.org/10.1021/acs.chemrev.1c00107). These include modeling covalent materials\, molecules\, molecular crystals\, surfaces\, and even whole proteins under physiological conditions (https://www.science.org/doi/abs/10.1126/sciadv.adn4397; https://doi.org/10.1021/jacs.5c09558).  \n\n\n\nIn this talk\, I will attempt to provide a reality check on these recent advances and on the developments required to enable fully predictive dynamics of complex functional (bio)molecular and material systems. Multiple challenges are highlighted\, in particular transferability in chemical space and interatomic interactions that should enable this field to grow for the foreseeable future.
URL:https://thomasyoungcentre.org/event/tyc-highlight-seminar-machine-learned-force-fields-for-molecular-simulations-beyond-alphafold-and-empirical-potentials/
LOCATION:Denys Holland Lecture Theatre\, Bentham House\, UCL\, 4–8 Endsleigh Gardens\, London\, WC1H 0EG\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251113T160000
DTEND;TZID=Europe/London:20251113T170000
DTSTAMP:20260409T215725
CREATED:20251014T104037Z
LAST-MODIFIED:20251014T104039Z
UID:7028-1763049600-1763053200@thomasyoungcentre.org
SUMMARY:TYC Seminar: Machine Learning for Periodic and Framework Materials
DESCRIPTION:TYC Seminar: Machine Learning for Periodic and Framework Materials Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nDr Ganna Gryn’ova\, University of Birmingham\n\n\n\nSignificant recent advances in chemical machine learning allow predictions of structures and physico-chemical properties of molecular systems with high accuracy and at a fraction of the computational cost of conventional quantum-chemical modelling. However\, the associated tools\, such as foundational models (e.g.\, MACE) or quantum-inspired representations (e.g.\, SPAHM and MAOC1) are not easily and directly transferrable to periodic materials due to the need to fine-tune the models on target materials\, sparsity of high-quality experimental training data\, and the higher costs of generating the presentations. In this talk\, we will discuss our recent efforts to address these limitations. Focusing on metal-organic and covalent organic frameworks\, we will present a new quantum-inspired representation for machine learning tasks and a new fragmentation algorithm2 enabling rational design of these systems. We will also demonstrate how persistent homology can be employed to coarse-grain the representation reducing the computational effort without sacrificing the accuracy of the predictions. \n\n\n\nReferences \n\n\n\nM. Ernst\, R. Fedorov\, A. Calzolari\, F. F. Grieser\, S. Ber\, G. Gryn’ova\, preprint DOI: 10.26434/chemrxiv-2025-zbc8x. \n\n\n\nS. Llenga\, G. Gryn’ova\, J. Chem. Phys. 2023\, 158\, 214116.
URL:https://thomasyoungcentre.org/event/tyc-seminar-machine-learning-for-periodic-and-framework-materials/
LOCATION:Royal School of Mines\, Room G05\, Royal School of Mines\, London\, South Kensington\, SW7 2AZ\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251105T153000
DTEND;TZID=Europe/London:20251105T170000
DTSTAMP:20260409T215725
CREATED:20250923T174410Z
LAST-MODIFIED:20251021T123952Z
UID:6988-1762356600-1762362000@thomasyoungcentre.org
SUMMARY:TYC Soiree: simulation of photo-excited and charge transport processes in organic semiconductors
DESCRIPTION:TYC Soiree: simulation of photo-excited and charge transport processes in organic semiconductors Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nAtomistic insights into the photodynamics of organic crystals and nanoclusters – Federico Hernandez\, QMUL\n\n\n\nExciton Delocalization and Dynamics: From Light Absorption to Charge Separation in Molecular Aggregates – Samuele Giannini\, University of Pisa\n\n\n\nLight absorption\, charge separation\, and electronic transport are vital for optimizing optoelectronic devices and designing new materials\, yet a fundamental understanding remains challenging because these processes span multiple time\, length\, and morphological scales. Quantum phenomena—arising from coupled electronic and vibrational (vibronic) interactions—govern both the optical response and electronic transport in supramolecular aggregates and molecular semiconductors.1\,2 \n\n\n\nI will show how first-principles-based Hamiltonians\, parametrized for realistic\, energetically disordered material morphologies and incorporating localized and charge transfer states\, can explain aggregation-induced changes in steady-state optical spectra.3\,4 By coupling these Hamiltonians with both full quantum dynamics and mixed quantum–classical dynamics\, we characterize the nature and evolution of electronic excitations across a broad range of timescales. Ultrafast dynamics in dense vibronic manifolds are resolved using efficient Multiconfigurational Time Dependent Hartree wavepacket propagation\, while a surface-hopping approach in the excitonic-state basis enables simulations at longer times. \n\n\n\nOur results clarify the role of exciton delocalization and coherence5 in enhancing the efficiency of important electronic processes such as charge separation in molecular aggregates6 and provide structure–property relationships that inform the design of more efficient optoelectronic devices. \n\n\n\nReferences: \n\n\n\n1. Giannini\, S. et al. Exciton transport in molecular organic semiconductors boosted by transient quantum delocalization. Nat. Commun. 13\, 2755 (2022).2. Giannini\, S. et al. Transiently delocalized states enhance hole mobility in organic molecular semiconductors. Nat. Mater. 22\, 1361–1369 (2023).3. Giannini\, S. et al. On the Role of Charge Transfer Excitations in Non-Fullerene Acceptors for Organic Photovoltaics. Mater. Today 80\, 308–326 (2024).4. Giannini\, S.\, Cerdá\, J.\, Prampolini\, G.\, Santoro\, F. & Beljonne\, D. Dissecting the nature and dynamics of electronic excitations in a solid-state aggregate of a representative non-fullerene acceptor. J. Mater. Chem. C 12\, 10009–10028 (2024).5. Giannini\, S.\, Segalina\, A.\, Padula\, D.\, Cantina\, M. & Pastore\, M. Disentangling Delocalization and Coherence in Photoexcited Noisy Supramolecular Aggregates. (submitted 2025)6. Ivanovic\, F.\, Peng\, W.-T.\, Giannini\, S.\, Blumberger\, J. Transiently Delocalised Hybrid Quantum States are the Gateways for Efficient Exciton Dissociation at Organic Donor-Acceptor Interfaces. (2025) https://doi.org/10.21203/rs.3.rs-7059572/v1.
URL:https://thomasyoungcentre.org/event/tyc-soiree-simulation-of-photo-excited-and-charge-transport-processes-in-organic-semiconductors/
LOCATION:Leolin Price Lecture Theatre in UCL GOSICH – Wellcome Trust Bldg\, 30 Guildford Street\, London\, WC1N 1DP\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251030T140000
DTEND;TZID=Europe/London:20251030T170000
DTSTAMP:20260409T215725
CREATED:20250529T124836Z
LAST-MODIFIED:20251120T113909Z
UID:6706-1761832800-1761843600@thomasyoungcentre.org
SUMMARY:TYC Symposium: Batteries
DESCRIPTION:TYC Symposium: Batteries Share on X\n\n\n\n\n\n\n\n\n\n\n\n\nProgramme\n\n\n\n\n14:00-14:05 welcome by Martijn Zwijnenburg\n\n\n\n14:05-14:45 Talk by Marie-Liesse Doublet\n\n\n\n14:45-14:55 questions\n\n\n\n14:55-15:35 Talk by Alex Squires\n\n\n\n15:35-15:45 question \n\n\n\n15:45-16:25 Talk by Benjamin Morgan\n\n\n\n15:25-16:35 questions\n\n\n\n\n\n\n\n\nThe Mirage of Anionic Redox for High-Energy Batteries – Marie-Liesse Doublet\, University of Montpelier\n\n\n\nOur growing reliance on lithium-ion batteries for energy storage demands continuous advancements in the performance of their positive electrodes. Traditionally\, these electrodes have relied exclusively on the cationic redox activity of transition-metal ions to drive electrochemical reactions. In recent years\, however\, the discovery of anionic redox has transformed strategies fordesigning advanced cathode materials. This phenomenon is most prominently observed in Li-rich transition-metal oxides (Li-rich TMOs)\, with Li₁.₂Ni₀.₁₃Co₀.₁₃Mn₀.₅₄O₂ (Li-rich NMC) serving as the archetypal example. [1–3]  \n\n\n\nUnlike conventional LiMO₂ oxides\, Li-rich TMOs can access an additional electron reservoir through anionic redox which enables theoretical capacities approaching 300 mAh/g\, [3] therefore offering the potential for improving energy density. Yet\, despite these advantages\, anionic redox introduces several critical challenges—including voltage fade\, O₂ release\, and voltage hysteresis—that severely compromise cycling stability and battery lifetime. [4] These limitations remain major obstacles to the commercialization of Li-rich cathodes. \n\n\n\nTo elucidate the origin and consequences of anionic redox\, we developed a theoretical framework based on chemical bonding concepts. [5] When integrated with electronic-structure DFT calculations and molecular dynamics simulations\, this framework revealed several key parameters governing both the onset and reversibility of the anionic reaction—most notably the material’selectronic ground state and the number of holes generated on the oxygen sublattice during charging. [5\,6] These parameters enable the reliable prediction of anionic redox behavior\, [7] providing critical insight for the rational design of Li-rich cathodes. Overall\, our results reveal that anionic redox is far from fulfilling its initial promise of enhancing battery energy density\, as its intrinsic limitations continue to undermine the practical viability of Li-rich materials. \n\n\n\n[1] Lu\, Z. et al. Layered cathode materials Li[NixLi(1/3−2x/3)Mn(2/3−x/3)]O2 for lithium-ion batteries. ElectrochemicalSolid-State Letters 4\, A191–A194 (2001).[2] Koga\, H. et al. Reversible oxygen participation to the redox processes revealed for Li1.20Mn0.54Co0.13Ni0.13O2Journal of the Electrochemical Society 160\, A786–A792 (2013).[3] Sathiya\, M. et al. Reversible anionic redox chemistry in high-capacity layered-oxide electrodes. NatureMaterials 12\, 827–835 (2013).[4] Assat\, G. et al. Fundamental understanding and practical challenges of anionic redox activity in Li-ionbatteries. Nature Energy 3\, 373–386 (2018).[5] Ben Yahia\, M. et al. Unified picture of anionic redox in Li/Na-ion batteries. Nature Materials 18\, 496–502(2019).[6] Xie\, Y. et al. Requirements for reversible extra-capacity in Li-rich layered oxides for Li-ion batteries. EnergyEnvironmental Science 10\, 266–274 (2017).[7] Gao et al. Clarifying the origin of molecular O2 in cathode oxides Nature Materials\, 24\, 743–752 (2025). \n\n\n\nMixed-anion NaTaOxCl6-2x oxychlorides: From crystalline to amorphous networks for high Na+ conductivity – Alexander Squires\, University of Birmingham\n\n\n\nAs the demand for efficient and sustainable energy storage solutions grows\, sodium-ion batteries have emerged as a promising alternative to lithium-ion batteries. With sodium’s abundance and wide geographical distribution\, they offer advantages in cost\, sustainability\, and economic viability. Solid-state sodium batteries\, in particular\, hold potential for enhanced safety\, higher energy density\, and longer lifetimes through the use of solid electrolytes. \n\n\n\nHalide-based electrolytes such as NaTaCl6 provide a useful starting point but exhibit limited ionic conductivities in their ordered form. Improvements have been achieved through disordering strategies\, while related chemistries such as NaTaOCl4 have recently shown much higher ionic conductivities and promising catholyte behaviour. Building on these advances\, the mixed-anion oxychloride series NaTaOxCl6–2x (x = 0.5\, 1) offers a platform to investigate how oxygen incorporation modifies structure and Na+ transport. \n\n\n\nHere\, we establish a computational workflow to probe this series\, combining density functional theory with ab initio random structure searching to identify low-energy configurations and the dominant local motifs. The calculations show that oxygen incorporation drives amorphization through the formation of corner-sharing TaCl5 dimers and ultimately trans-linked TaCl4O2 chains. These structural motifs generate percolating Na+ diffusion pathways\, rationalising the enhanced transport behaviour observed experimentally in compositions such as NaTaO0.5Cl5. \n\n\n\nThis work was carried out in close collaboration with experimental partners\, whose diffraction\, spectroscopy\, and electrochemical measurements provide critical validation of the structural and transport mechanisms identified in our simulations. By bridging computational predictions with experimental insights\, we establish a framework for understanding the atomistic origins of fast-ion conduction in amorphous oxyhalides. \n\n\n\nAbigail Parsons\, Alexander G. Squires*\, Justin Leifeld\, Alexandra Morscher\, Xabier Martinez de Irujo-Labalde\, Marvin A. Kraft\, Bibek Samantha\, Wiebke Zielasko\, Niina Jalarvo\, Michael Ryan Hansen\, David O. Scanlon\, Wolfgang G. Zeier* \n\n\n\nModelling Nanoscale Structural Changes in Layered Li-rich Mn Oxide Cathode Materials – Benjamin Morgan\, University of Bath\n\n\n\nLithium-rich manganese-based layered oxides are promising cathode materials for next-generation lithium-ion batteries\, offering exceptionally high energy densities through combined transition metal and oxygen redox. However\, this high energy density presents a critical limitation: these materials suffer progressive loss of energy density upon cycling\, due to progressive decrease in average voltage; a phenomenon termed ‘voltage fade’ [1–4]. Understanding and controlling the underlying mechanisms of voltage fade are essential to realise the full potential of these high-capacity cathode materials. \n\n\n\nVoltage fade has been linked to the formation and growth of nanoscale voids within the cathode bulk [1]\, but the atomic-scale mechanisms of this process are not well understood. The conventional approach for modelling battery cathode materials at the atomic scale is density functional theory (DFT). However\, DFT cannot be used to directly investigate nanoscale void formation and growth\, because the necessary system sizes are too large to be computed. \n\n\n\nTo investigate void formation over extended cycling\, we have developed a novel computational approach combining DFT calculations\, cluster expansion models\, and Monte Carlo simulations. By applying this methodology to Li-rich Mn-based cathodes across the Li2MnO3–LiMnO2 compositional space\, we find that nanoscale voids form through two concurrent processes: formation of O2 molecules within the bulk and extensive transition metal migration that forms transition-metal-deficient regions via phase segregation. Under extended cycling\, these voids coalesce\, driven by surface energy minimisation\, in a process analogous to Ostwald ripening. \n\n\n\nWe further find that void coalescence—and thus voltage fade—depends strongly on the initial Mn/Li configuration in the Mn-rich layer\, suggesting that targeting specific initial structures can inhibit deleterious structural evolution during cycling. By establishing the direct link between void growth and voltage loss\, we show that preventing coalescence offers a route to maintaining electrochemical performance. Through systematic mapping of voltage fade across the Li2MnO3–LiMnO2 compositional space\, we identify optimal structures and compositions that minimise degradation whilst retaining high energy density. These findings establish clear structural and compositional design principles for developing Li-rich cathodes with sustained performance over extended cycling. \n\n\n\n[1] McColl\, K.; Coles\, S. W.; Zarabadi-Poor\, P.; Morgan\, B. J.; Islam\, M. S. Phase Segregation and Nanoconfined Fluid O2 in a Lithium-Rich Oxide Cathode. Nat. Mater. 2024\, 23\, 826−833. \n\n\n\n[2] Csernica\, P. M.; McColl\, K.; Busse\, G. M.; Lim\, K.; Rivera\, D. F.; Shapiro\, D. A.; Islam\, M. S.; Chueh\, W. C. Substantial Oxygen Loss and Chemical Expansion in Lithium-Rich Layered Oxides at Moderate Delithiation. Nat. Mater. 2025\, 24\, 92−100. \n\n\n\n[3] House\, R. A.; Rees\, G. J.; McColl\, K.; Marie\, J. J.; Garcia-Fernandez\, M.; Nag\, A.; Zhou\, K.-J.; Cassidy\, S.; Morgan\, B. J.; Islam\, M. S.; Bruce\, P. G. Delocalized Electron Holes on Oxygen in a Battery Cathode. Nat. Energy 2023\, 8\, 351−360. \n\n\n\n[4] McColl\, K.; House\, R. A.; Rees\, G. J.; Squires\, A. G.; Coles\, S. W.; Bruce\, P. G.; Morgan\, B. J.; Islam\, M. S. Transition Metal Migration and O2 Formation Underpin Voltage Hysteresis in Oxygen-Redox Disordered Rocksalt Cathodes. Nat. Commun. 2022\, 13\, 5275.
URL:https://thomasyoungcentre.org/event/tyc-symposium-batteries/
LOCATION:Nyholm Room\, Christopher Ingold Building\, Gordon Street\, London
CATEGORIES:Main event
ORGANIZER;CN="Martijn Zwijnenburg":MAILTO:m.zwijnenburg@ucl.ac.uk
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DTSTART;TZID=Europe/London:20251029T150000
DTEND;TZID=Europe/London:20251029T170000
DTSTAMP:20260409T215725
CREATED:20250813T121618Z
LAST-MODIFIED:20251022T111301Z
UID:6843-1761750000-1761757200@thomasyoungcentre.org
SUMMARY:TYC Alumni Pathway Panel
DESCRIPTION:TYC Alumni Pathway Panel Share on X\n\n\n\n\nThe TYC is hosting the second in a series of alumni events\, led by recent former TYC member Vas Fotopoulos (now at MIT)\, at which former members come together to form a panel to present their career trajectory\, and to answer questions from current TYC students and PDRAs. \n\n\n\nThey will give a brief introduction to themselves\, share their journey so far and discuss their current work. The focus will be on career paths\, pursuing postdocs or industrial positions after completing a PhD\, and answering students’ questions. \n\n\n\nThe panel will be structured as an in-person event. \n\n\n\nVas has handpicked our panel\, who we believe will inspire you\, and provide a multitude of fascinating insights into life after PhD. \n\n\n\nThe event will be followed by a drinks social. \n\n\n\nRegistration is free but required \n\n\n\n\nRegister\n\n\n\n\nPanellists\n\n\n\nChair: Rashid E A M Al-Heidous – Lecturer at Qatar UniversityRashid achieved his Masters in nanotechnology at Imperial College London\, followed by a PhD. He took up a position as lecturer at Qatar in 2024. \n\n\n\nAbhishek Khedkar – Quantum Material Scientist at Phasecraft\, LondonAbhishek’s interest lies in studying complex molecular and material systems\, particularly those that feature strong electron correlation. He currently works as a Quantum Material Scientist at Phasecraft\, a company building the mathematical foundations for quantum computing applications that solve real-world problems. \n\n\n\nDaria Kieczka\, AnsysAfter Daria obtained her PhD she found opportunity at Ansys as an Academic Program Engineer\, working alongside the team on ways to support education and research. She is also working on a Horizon Europe-funded project called CE-RISE\, which explores ways in which information transparency can help products be more sustainable and circular (reducing waste). \n\n\n\nJoe Willis – Quantum Policy Adviser\, Office for Quantum\, Department for Science\, Innovation and TechnologyJoe is a policy adviser in the Office for Quantum\, part of the UK Government’s Department for Science\, Innovation and Technology. He leads work on regulation\, supply chains\, and quantum sensing for critical national infrastructure applications. Joe holds a Doctor of Engineering in Molecular Modelling and Materials Science from University College London\, where his research focused on simulation of defect chemistry in transparent conducting oxides\, power electronics materials\, thermoelectrics and photocatalysts.
URL:https://thomasyoungcentre.org/event/tyc-alumni-pathway-panel/
LOCATION:UCL Christopher Ingold Building\, Nyholm Room\, Gordon Street\, London\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251015T160000
DTEND;TZID=Europe/London:20251015T170000
DTSTAMP:20260409T215725
CREATED:20250903T140304Z
LAST-MODIFIED:20250905T121109Z
UID:6902-1760544000-1760547600@thomasyoungcentre.org
SUMMARY:TYC Seminar: The Crystal Isometry Principle infers chemistry from geometry - Vitaliy Kurlin\, University of Liverpool
DESCRIPTION:TYC Seminar: The Crystal Isometry Principle infers chemistry from geometry – Vitaliy Kurlin\, University of Liverpool Share on X\n\n\n\n\nRegistration is free but required: \n\n\n\n\n\n\n\nStructures of solid crystalline materials (periodic crystals) are determined in a rigid form and hence keep all their properties under rigid motion within the same ambient environment. However\, structures that have different rigid shapes can substantially differ in properties and hence should be reliably distinguished\, for example\, polymorphs with different solubility. Conventional representations based on reduced cells discontinuously change under almost any perturbation of atoms\, which led to the accumulation of near-duplicates in major databases of experimental structures [1]. \n\n\n\nThis ambiguity was resolved by generically complete and continuous invariants that distinguish all non-duplicate periodic crystals (about 1.5 million) in major databases within a few hours on a desktop [2]. Now\, any dataset of experimental or simulated crystals can be visualised on maps with analytically defined invariant coordinates [3]\, which are invertible to any generic periodic structure in 3 dimensions\, uniquely under any distance-preserving transformation [4]. Inspired by Richard Feynman’s hint in Fig.7 of his first lecture on physics\, the Crystal Isometry Principle says that any real periodic material is uniquely determined by a precise enough geometry of atomic centers without chemical elements\, under the same ambient conditions. \n\n\n\n[1] O.Anosova\, V.Kurlin\, M.Senechal. The importance of definitions in crystallography. IUCrJ 11 (4)\, 453-463 (2024). [2] D.Widdowson\, V.Kurlin. Resolving the data ambiguity for periodic crystals. NeurIPS 2022\, v.35\, p.24625-24638.[3] D.Widdowson\, V.Kurlin. Continuous invariant-based maps of the Cambridge Structural Database. Crystal Growth & Design\, 24(13)\, 5627–5636 (2024).[4] D.Widdowson\, V.Kurlin. Geographic-style maps with a local novelty distance help navigate in the materials space. Scientific Reports\, v.15\, 27588 (2025) \n\n\n\n\nRegister here
URL:https://thomasyoungcentre.org/event/tyc-seminar-vitaliy-kurlin-university-of-liverpool/
LOCATION:Room S7.06\, King’s College London\, Strand\, London\, United Kingdom
CATEGORIES:Main event
END:VEVENT
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DTSTART;TZID=Europe/London:20251008T151500
DTEND;TZID=Europe/London:20251008T171500
DTSTAMP:20260409T215725
CREATED:20250729T153140Z
LAST-MODIFIED:20251008T121710Z
UID:6806-1759936500-1759943700@thomasyoungcentre.org
SUMMARY:TYC Industry Focus Afternoon: “Quantum computing in materials and molecular sciences"
DESCRIPTION:TYC Industry Focus Afternoon: “Quantum computing in materials and molecular sciences Share on X\n\n\n\n\n\n\n\n\nComputational chemists in industry. An opportunity for Knowledge Exchange and networking between the TYC and industry\, and for us to find out about modelling opportunities outside of academia. The event will feature three short talks followed by a panel discussion. \n\n\n\nSchedule:\n\n\n\n15:15 Near-term quantum algorithms for many-body physics and material sciences: a path towards quantum utility – Ivano Tavernelli – IBM15:55 InQuanto: Quantum Chemistry on Quantum Computers – Gabriel Greene-Diniz\, Quantinuum16:35 Quantum Computing in Industry: Towards materials and chemistry simulation on near-term quantum devices – Abhishek Khedkar\, Phasecraft17:15 Refreshments in the cafe on the ground floor Roberts Building Foyer G02 \n\n\n\nNear-term quantum algorithms for many-body physics and material sciences: a path towards quantum utility – Ivano Tavernelli – IBMQuantum computing is emerging as a transformative paradigm\, offering solutions to problems that are intractable for classical computers. This potential is particularly pronounced in many-body physics\, quantum chemistry\, and materials science\, where the exponential complexity of classical methods can be efficiently addressed by quantum computing. Recent advancements in quantum technologies indicate that significant progress in these fields is achievable even with near-term noisy quantum computers. To realize this potential\, noise-resilient quantum algorithms and error mitigation strategies have been developed and integrated into hybrid quantum-classical workflows\, fostering a productive interplay between quantum and classical computational platforms. \n\n\n\nIn this talk\, I will present recent advancements in quantum algorithms for many-body physics and quantum chemistry\, emphasizing their relevance to near-term quantum computing. Key topics include error mitigation strategies critical for achieving accurate\, utility-scale results\, such as probabilistic error cancellation (PEC) and tensor network-based error mitigation (TEM). Additionally\, embedding techniques that integrate quantum electronic structure methods with density functional theory will be discussed and dynamical mean field theory\, enabling efficient problem partitioning while maintaining high accuracy. \n\n\n\nThese methods will be demonstrated through case studies on the computation of ground and excited-state properties in molecules and solids\, as well as simulations of quantum dynamics. Finally\, I will evaluate the performance of recent hardware calculations using IBM quantum computers and explore the future prospects of quantum computing in chemistry and materials science. \n\n\n\nInQuanto: Quantum Chemistry on Quantum Computers – Gabriel Greene-Diniz\, QuantinuumIn this talk\, I will present an overview of InQuanto\, Quantinuum’s state-of-the-art Python-based quantum computational chemistry platform. InQuanto is designed to facilitate quantum computational chemistry for researchers in industry and academia\, and to provide an ecosystem for quantum researchers to develop and implement novel algorithms for chemical problems. Following this overview\, I will report a recent application of InQuanto to an industrially interesting use-case: actinides chemistry. Actinides are important elements that are involved in many chemical applications\, such as nuclear energy\, power generation\, and single molecule magnets. However\, modelling the actinides chemistry is very challenging. I will present the use of InQuanto to quantum compute the energy of several molecules containing actinides which are involved in the plutonium oxidation. We devised chemical models\, performed classical CASSCF calculations and then carried out quantum calculations on both emulator and Quantinuum H2 hardware series. We have employed the stochastic Quantum Phase Estimation and the Quantum Computed Moments algorithms. The largest active space we have been able to run on hardware was 19 qubits. We have found promising results from the hardware output\, yielding energies at chemical accuracy or close to it. \n\n\n\nQuantum Computing in Industry: Towards materials and chemistry simulation on near-term quantum devices – Abhishek Khedkar\, PhasecraftAt Phasecraft we are developing and implementing methods that will lead to practical application on noisy near-term  and early fault-tolerant quantum devices. Performing molecule and material simulations on such devices requires deep understanding of the physics of the problem at hand in combination with efficient representation and encoding of the problem on a device\, to not only maximise use of limited resources\, but also to provide accurate results ultimately aiming to outperform classical computation on problems of interest.  \n\n\n\nStarting with a brief background of my career in industry I will discuss what has brought me to the field of quantum computing. Using examples from some recent consortia based programmes in materials and human health\, the talk will then introduce some of the considerations of representing and implementing your electronic structure problem on a quantum device. Following which  some of the key ideas in practical workflows and results from hybrid-classical algorithms will be presented. A brief discussion of open challenges and future directions will conclude the presentation. \n\n\n\n[1] L. Clinton et al.\, “Towards near-term quantum simulation of materials”\, Nature Communications 15\, 211 (2024)[2] E. Sheridan\, L. Mineh\, R.A. Santos\, and T. Cubitt\, “Enhancing density functional theory using the variational quantum eigensolver”\, arXiv: 2402.18534[3] Chaudhuri S\, et al. Challenges and Advances in the Simulation of Targeted Covalent Inhibitors Using Quantum Computing. J. Phys. Chem. Lett. 2025\, 16\, 33\, 8536-8545 \n\n\n\n \n\n\n\nRegistration is free: \n\n\n\n\nRegister here
URL:https://thomasyoungcentre.org/event/tyc-industry-focus-afternoon-quantum-computing-in-materials-and-molecular-sciences/
LOCATION:Roberts Building 106\, Roberts Building\, University College London\, Torrington Place\, London\, WC1E 7JE\, United Kingdom
CATEGORIES:Main event
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20251001T150000
DTEND;TZID=Europe/London:20251001T170000
DTSTAMP:20260409T215726
CREATED:20250813T150956Z
LAST-MODIFIED:20250926T153843Z
UID:6847-1759330800-1759338000@thomasyoungcentre.org
SUMMARY:TYC Welcome Day 2025
DESCRIPTION:TYC Welcome Day 2025 Share on X\n\n\n\n\nWe warmly invite you to attend our in-person TYC Welcome Event which is the perfect opportunity to hear about the fantastic benefits of being affiliated to this active and exciting institute and begin networking with your peers.  A panel of TYC students and postdocs will be on hand to answer your questions\, providing an overview of TYC activities and opportunities. \n\n\n\nTell us your PhD topic\, plus one (or more) burning question/s you have for the current TYC PhD students and postdocs\, to enable the panel to cover topics which are relevant to you. Ask them anything – from student life in London and at the TYC\, to what it’s like to undertake a PhD.  Questions will be answered anonymously. \n\n\n\nWe’ll need your confirmation by email to register you\, and send out details.  Don’t forget to include your question/s! Email Karen at tyc-administrator@ucl.ac.uk \n\n\n\n\n15:00 Gather in Nyholm Room\n\n\n\n15:15 Overview of TYC and Interest Groups – Jochen Blumberger\n\n\n\n15:25 Overview of TYC Early Career Researcher Committee – Ben Humphries (UCL) / Sophia Ber (QMUL)\n\n\n\n15:35 Panel\n\n\n\n16:20 Refreshments and social (snacks and refreshments will be provided)\n\n\n\n17:00 End
URL:https://thomasyoungcentre.org/event/tyc-welcome-day-2025/
LOCATION:Nyholm Room\, Christopher Ingold Building\, Gordon Street\, London
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20250915T130000
DTEND;TZID=Europe/London:20250918T140000
DTSTAMP:20260409T215726
CREATED:20250312T124352Z
LAST-MODIFIED:20250916T141030Z
UID:6415-1757941200-1758204000@thomasyoungcentre.org
SUMMARY:MMM Hub & UKCP Conference & User Meeting 2025
DESCRIPTION:MMM Hub & UKCP Conference & User Meeting 2025 Share on X\n\n\n\n\nIC7\, and Denise Coates building\, Keele University\, Staffordshire\, ST5 5AA\n\n\n\nThe Thomas Young Centre (University College London\, Imperial College London\, King’s College London\, and Queen Mary University of London) and its partners\, the University of Southampton\, Brunel University London\, and the University of Reading take great pleasure to announce the MMM Hub and UKCP Conference and User Meeting 2025\, to be held this year at Keele University\, between 15 – 18 September 2025.  \n\n\n\nWe are excited to announce that the Hub Conference will be preceded by a meeting of the United Kingdom Car-Parrinello Consortium (UKCP) community\, from Monday lunchtime to Tuesday lunchtime. Crossover talks will take place on Tuesday morning which will be of interest to everyone. \n\n\n\nA mix of leading expert invited and contributing speakers will deliver talks in state-of the art materials simulation techniques and software developments in High Performance Computing. Contributed talks from MMM Hub Users will inform the scientific innovations taking place at the MMM Hub\, addressing advanced materials\, biological and soft matter\, catalysis\, multi-scale modelling\, materials discovery and design and the impacts to society and industry seen through simulation of materials at the atomic scale. Attendees will be exposed to the latest technological advances in HPC\, which continues to play a fundamental role in driving forward the progress of computational science\, with a focus on software development and hardware advances.  \n\n\n\nThis 6th edition of the annual MMM Hub Conference will once again bring MMM Hub users and collaborators of this thriving community together\, alongside hardware manufacturers HPC and Intel\, and the first-class team who are key to the operational success of ‘Young’ at the Hub.  \n\n\n\n\n\nWe invite abstract submissions for contributed and 2-minute flash talks from across the community. We also invite participants\, particularly graduate student users of the Hub\, to contribute A1-size\, portrait orientation posters of their research. The posters will be on display to participants throughout\, and at a drinks reception and Poster Presentation. \n\n\n\n\n\n\n\nConference programme\n\n\n\nMMM Hub Conference & User Meeting Programme 2025Download\n\n\n\nMonday 15th September 2025 – UKCP meeting – IC7\, (51 on the map at the bottom of the page) \n\n\n\n\n\n\n\nTuesday 16th September 2025 IC7 am\, Denise Coates Building pm \n\n\n\n\n\n\n\nWednesday 17th September 2025 – Denise Coates Building & dinner in The Salvin Room\, Keele Hall \n\n\n\n\n\n\n\nThursday 18th September 2025 – Denise Coates Building \n\n\n\n\n\n\n\n\n\n\n\nRegistration for the conference is separate to submitting your abstract.   \n\n\n\nPlease submit your abstract and dietary requirements\, and register using the following two links:  \n\n\n\n\n\n\n\n \n\n\n\n\nSubmit your abstract and dietary requirements here\n\n\n\n\n\n\n\n\n\n\n\n\n \n\n\n\n\nRegister for the conference\n\n\n\n\n\n\n\n\n \n\n\n\nWe may be able to provide some financial assistance towards early career delegates’ participation.  Please send an email to the organising committee at tyc-administrator@ucl.ac.uk\, justifying your reason for applying for support to attend the meeting.  \n\n\n\n\n\n\n\n\n\n\n\nInvited speakers\n\n\n\nFirst Principles Calculations of Temperature Dependent Exciton Binding Energies and Dissociation Rates in Semiconductors and Insulators – Marina Filip\, University of OxfordIn this talk\, Marina will present a recent first principle framework that have been developed to understand the impact of ionic vibrations on the binding energy\, fine structure and dissociation of excitons in semiconductors and insulators[1\,2]. Our new framework builds upon standard state-of-the art Bethe-Salpeter Equation [3]\, and includes the effect of ionic vibrations at the level of the electron-hole interaction kernel. \n\n\n\nMarina will first introduce the theoretical background of this approach\, from the point of view of scattering theory [4]. Furthermore\, Marina will describe the implementation\, and discuss its applications to several examples of semiconductor and insulators studied recently [4-5]. These applications will be discussed\, starting from model theoretical approaches within the Wannier-Mott and Frohlich models\, followed by direct and fully converged first principles calculations of exciton binding energies and dissociation rates for binary and ternary semiconductors andinsulators [1\,2\,4\,5]. The talk will show how the recently developed framework allows for compute temperature dependent exciton binding energies and exciton dissociation rates with good accuracy\, and trends in agreement with experimental measurements. \n\n\n\nReferences: \n\n\n\n[1] Filip\, Haber & Neaton\, Phys. Rev. Lett.\, 127\, 067401 (2021).[2] Alvertis\, Haber\, Li\, Coveney\, Louie\, Filip & Neaton\, Proc. Natl. Acad. Sci\, 121\, 30\,e2403434121 (2024).[3] Rohlfing & Louie\, Phys. Rev. Lett. 81\, 2312 (1998).[4] Coveney\, Haber\, Alvertis\, Neaton & Filip\, Phys. Rev. B\, 110\, 5\, 054307 (2024).[5] Gant\, Alvertis\, Coveney\, Haber\, Filip & Neaton\, arXiv:2504.00110 (2025).Work supported by the EPSRC\, with computational resources from TACC at UT Austin. \n\n\n\nAn exploration of molecular structures and reaction pathways using adaptive learning and neural networks – Vanda Glezakou\, Oak Ridge National LaboratoryComputer simulations\, modern algorithms and data science have elevated our ability to better understand chemical structure\, reactivity and reactive pathways. Determining transition states in large molecular models still constitutes a computational challenge due to the increasing number of comparable configurational isomers and intermediates. In my presentation\, I will summarize our recent work in developing a computational protocol that explores minima and intermediates on a potential energy surface through an adaptive learning global optimization process. For a given reactive scheme\, once a set of low-lying reactants and products is identified\, generative adversarial networks (GANs) are used to connect a given set of initial and final states. For example\, an ensemble of N reactant and M product states can potentially lead to up to NxM reactive processes and associated transition states. GANs are able to identify energy barriers connecting reactants and products at a fraction of the computational cost\, facilitating the discovery of reaction pathways\, the construction of kinetic models and extraction of descriptors of reactivity. Examples from the literature and our current research will be also presented and discussed. \n\n\n\nVassiliki-Alexandra Glezakou\,* Difan Zhang\, Roger Rousseau1 Chemical Sciences Division\, Oak Ridge National Laboratory\, Oak Ridge\, TN\, 37830 \n\n\n\nWalking the Edge: Developments in Integrated Materials Design for Alternative Energy Technologies – Denis Kramer\, Helmut Schmidt University \n\n\n\nStrong electron correlations in Novel Battery materials – Andrew J. Morris\, University of BirminghamThe lithium nickel manganese cobalt oxides\, LiNixMnyCozO2 (x+y+z=1) (NMC) are a promising family of materials for the cathodes of lithium-ion batteries (LIB). The Ni-rich NMCs especially\, exhibit excellent performance as high-voltage cathode materials\, enabling batteries with high energy densities and high capacities of around 200- 275mAh/g. However Ni-rich NMCs are prone to structural instabilities and oxygen loss leading to electrode degradation\, a hurdle that must be overcome before widespread commercialisation. \n\n\n\nDensity-functional theory (DFT) is now the standard modelling technique for atomistic physics\, chemistry and materials science. It allows us to solve a single-particle Schrödinger-like equation for the energies of electrons in molecules and solids\, thereby allowing us to deduce the material’s crystal structure and properties. I introduce DFT and show how it can clarify the complex behaviour of a class of LIB cathodes\, the tungsten niobates. Indeed\, this behaviour may then be rationalised within the much simpler crystal-field theory. \n\n\n\nHowever\, for describing the crystal and electronic structure of NMCs\, DFT falls short due to a lack of ability to account for strong electron correlations. I introduce the more advanced dynamical-mean-field theory (DMFT) and show that it correctly describes the electronic properties of the NMC family. This\, in turn allows us to uncover the mechanism of oxygen loss on delithiation of NMC. \n\n\n\nMolecular materials: From accurate numbers to detailed chemical insight – Felix Plasser\, Loughborough UniversityMolecular materials provide a highly promising new design space for the development of solar cells\, light sources\, and batteries. Tremendous effort is invested in developing optimized molecules for these applications. Computational methods have become in many cases powerful enough to provide accurate numbers and\, thus\, accurately predict the properties of interest. However\, new challenges come into play when interpreting the results of the computations in order to obtain general chemical insight and\, ultimately\, develop new design guidelines. It is the purpose of this talk to present our computational tools (1\,2) allowing to gain detailed insight even from challenging computations on complex systems and to illustrate the further path of developing general design rules. \n\n\n\nTo date only a small number of design rules exist\, mostly based on the energies and shapes of the frontier molecular orbitals (FMO)\, meaning that extensive screening is often necessary. It is the purpose of this work to highlight two alternative strategies\, going beyond the standard FMO picture\, to explain photophysical behavior and ultimately design new molecules: (i) modulation of singlet-triplet gaps via the transition density\, and (ii) tuning of excitation energies via excited-state aromaticity. \n\n\n\nThis talk will first address the development of new design rules for materials with large singlet-triplet gaps\, as are needed for singlet fission solar cells. Previously\, we have shown that the transition density provides an intuitive way for explaining\, both\, optical brightness and singlet-triplet gaps (3). Applied to the case of singlet fission\, this framework was used to devise three now rules for maximizing S1/T1 gaps: (i) reducing the number of p-electrons\, (ii) localizing the excited electrons within the p-system\, and (iii) optimizing specific through-space interactions (4\, 5). We highlight the applicability of this model bridging from simple hydrocarbon backbones to realistic dyes. \n\n\n\nAs a second example\, we will investigate the optical properties of bridged p-conjugated diradicals. Firstly\, we will discuss the different types of diradical\, zwitterionic and charge-transfer states that are accessible in these systems (6). Using this framework we will explain the unexpected absorption and luminescence properties of a cyclopenta-dithiophene bridged tris(2\,4\,6­trichlorophenyl)methyl (TTM) diradical (7). \n\n\n\nReferences \n\n\n\n1. F. Plasser. JCP\, 2020\, 152\, 084108.2. F. Plasser\, A. Krylov\, A. Dreuw. WIREs CMS\, 2022\, 12\, e1595.3. P. Kimber\, F. Plasser. PCCP\, 2020\, 22\, 60584. A. V. Girija\, W. Zeng\, W. K. Myers\, R. C. Kilbride\, D. T. W. Toolan\, C. Zhong\, F. Plasser\, A. Rao\, H. Bronstein. JACS\, 2024\, 146\, 182535. W. Zeng\, C. Zhong\, H. Bronstein\, F. Plasser. ANIE\, 2025\, DOI: 10.1002/anie.202502485.6. L. Matasović\, H. Bronstein\, R. H. Friend\, F. Plasser. Faraday Disc. 2024\, 254\, 107.7. C. Yu et al. Sci. Adv. 2024\, 10\, DOI: 10.1126/sciadv.ado3476.Multiscale Modelling : An Industrial Perspective – Misbah Sarwar\, Johnson Matthey \n\n\n\nComputational techniques to model material properties and catalytic behaviour have now become mainstream tools in an industrial setting. This is due to two main factors: improved algorithms that accurately model material behaviour and increased computational power enabling faster simulations. As such\, multi-scale simulations\, ranging from electronic structure to continuum-based approaches have become embedded in product development cycles\, innovating the way in which new products are developed. \n\n\n\nThe talk will give an overview of how multi-scale modelling combined with advanced characterization techniques are being used in industry to understand the structure and activity of catalytic materials that are used to accelerate the transition to net zero. Multi-scale modelling aims to tackle the “grand challenge” of simulating catalytic processes by bridging atomic\, molecular\, pore\, and reactor scales. However\, it brings substantial challenges due to the complexity and diversity of phenomena involved\, combined by the difficulties in aligning differences in temporal and spatial scales and handling the computational demands across each model layer. Using methane oxidation as a test case a multiscale workflow developed as part of the EU funded ReaxPro project will be presented. The developed models were validated against experimental data collected through different reactive characterisation techniques. Model predictions demonstrated reasonable agreement with experimental results without any experimental fitting of parameters\, highlighting the workflow’s potential for tackling the complexities inherent to industrial catalytic processes. The talk will also discuss how newly developed approaches such as MLIPs might fit into such a workflow and be used to accelerate the catalyst discovery process. \n\n\n\n\n\n\n\n\n\n\n\nThis year’s MMM Hub Conference is supported by Keele University School of Chemical and Physical Sciences\, Hewlett Packard Enterprise\, AWE\, CCP5\, CCP-NC\, The American Society for Mechanical Engineers (ASME)\, RSC Advances\, RSC Physical Chemistry Chemical Physics (PCCP)\, RSC Digital Discovery and RSC Molecular Systems Design & Engineering (MSDE) \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n \n\n\n\n\n\n\n\nGetting to Keele University\n\n\n\n\nHow to find us – Keele University\n\n\n\n\nkeele-campus-map-june25Download\n\n\n\nACCESS\n\n\n\nSuggested hotels: \n\n\n\n\nCourtyard Keele Staffordshire – https://www.marriott.com/en-gb/hotels/manck-courtyard-keele-staffordshire/overview/ (on campus hotel – 0.2 miles from venue)\n\n\n\nTravelodge Newcastle Under Lyme – https://www.travelodge.co.uk/hotels/424/Newcastle-Under-Lyme-Central-hotel (2.2 miles from venue – 7 min by car – 15-20 min by bus) \n\n\n\nThe Crewe Arms Hotel – https://thecrewearmshotelmadeley.co.uk/ (2.5 miles – 5 min by car – 11 min by bus)\n\n\n\nBorough Arms Hotel – https://direct-book.com/borough-arms/properties/directborougharms?locale=en&items[0][adults]=2&items[0][children]=0&items[0][infants]=0&currency=GBP&checkInDate=2024-11-27&checkOutDate=2024-11-28&trackPage=yes – (2.4 miles from venue – 7 min by car – 20-30 min by bus)\n\n\n\nDoubleTree by Hilton Stoke on Trent – https://www.hilton.com/en/hotels/mandidi-doubletree-stoke-on-trent/  (4.8 miles – 13 min by car – 35-55 min by bus)\n\n\n\nPremier Inn Stoke-On-Trent (Hanley) hotel – https://www.premierinn.com/gb/en/hotels/england/staffordshire/stoke-on-trent/stoke-on-trent-hanley.html (4.3 miles from venue – 13 min by car – 45min-1h by bus)\n\n\n\nPremier Inn Stoke/Trentham Gardens hotel – https://www.premierinn.com/gb/en/hotels/england/staffordshire/stoke-on-trent/stoke-on-trent-hanley.html (5.0 miles from venue – 15 min by car – 45min-1h by bus)\n\n\n\nPremier Inn Newcastle Under Lyme hotel – https://www.premierinn.com/gb/en/hotels/england/staffordshire/newcastle-under-lyme/newcastle-under-lyme.html (6.4 miles – 15 min by car – 30-50 min by bus)\n\n\n\nHoliday Inn Stoke on Trent M6\, JCT.15\, an IHG Hotel – https://www.ihg.com/holidayinn/hotels/gb/en/newcastle-under-lyme/xwhsf/hoteldetail (3.5 miles – 10 min by car – not easy access via public transport)\n\n\n\nHoliday Inn Express Stoke on Trent by IHG – https://www.ihg.com/holidayinnexpress/hotels/gb/en/stoke-on-trent/xwhuk/hoteldetail (6.4 miles from venue – 17 min by car – 1h by bus)\n\n\n\n\nIn this link https://www.keele.ac.uk/about/howtofindus/ you can find information on how to travel to Keele University. \n\n\n\n\n\n\n\nMMM-Hub-conference-2025-privacy-notice \n\n\n\n\n\n\n\nCode of conduct: \n\n\n\nWe value the participation of every member of the materials and molecular modelling community and want to ensure that everyone has an enjoyable and fulfilling experience\, both professionally and personally. Accordingly\, all participants of the MMM Hub Conference and User meeting are expected to always show respect and courtesy to others.  The MMM Hub and its partners strive to maintain inclusivity in all of our activities.  All participants (staff and students) are entitled to a harassment-free experience\, regardless of gender identity and expression\, sexual orientation\, disability\, physical appearance\, body size\, race\, age\, and/or religion. Harassment in any form is not acceptable for any of us.  We respectfully ask all attendees of the MMM Hub Conference and User meeting to kindly conform to the following Code of Conduct: \n\n\n\n\nTreat all individuals with courtesy and respect.\n\n\n\nBe kind to others and do not insult or put down other members.\n\n\n\nBehave professionally. Remember that harassment and sexist\, racist\, or exclusionary jokes are not appropriate.\n\n\n\nHarassment includes\, but is not limited to\, offensive verbal comments related to gender\, sexual orientation\, disability\, physical appearance\, body size\, race\, religion\, sexual images in public spaces\, deliberate intimidation\, stalking\, following\, harassing photography or recording\, sustained disruption of discussions\, and unwelcome sexual attention.\n\n\n\nParticipants asked to stop any harassing behaviour are expected to comply immediately.\n\n\n\nContribute to communications with a constructive\, positive approach.\n\n\n\nBe mindful of talking over others during presentations and discussion and be willing to hear out the ideas of others.\n\n\n\nAll communication should be appropriate for a professional audience\, and be considerate of people from different cultural backgrounds. Sexual language and imagery are not appropriate at any time.\n\n\n\nChallenge behaviour\, action and words that do not support the promotion of equality and diversity.\n\n\n\nArrive at the conference events punctually where possible.\n\n\n\nShow consideration for the welfare of your friends and peers and\, if appropriate\, provide advice on seeking help.\n\n\n\nSeek help for yourself when you need it.\n\n\n\n\nMMM Hub Conference 2025 Organising Committee George Booth\, King’s College LondonAlejandro Santana Bonilla\, King’s College LondonPhil Hasnip\, University of YorkJuliana Morbec\, Keele UniversityChris Skylaris\, University of SouthamptonEd Smith\, Brunel University of LondonKaren Stoneham\, University College LondonMatt Watkins\, University of LincolnScott Woodley\, University College LondonJun Xia\, Brunel University of London
URL:https://thomasyoungcentre.org/event/mmm-hub-conference-user-meeting-2025/
LOCATION:Denise Coates building\, Keele University\, Staffordshire\, ST5 5AA\, United Kingdom
CATEGORIES:Main event
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20250910T150000
DTEND;TZID=Europe/London:20250910T160000
DTSTAMP:20260409T215726
CREATED:20250828T111112Z
LAST-MODIFIED:20250909T190423Z
UID:6879-1757516400-1757520000@thomasyoungcentre.org
SUMMARY:TYC - CCP9 Visiting Professor Seminar: Mark van Schilfgaarde\, NREL
DESCRIPTION:TYC – CCP9 Visiting Professor Seminar: Mark van Schilfgaarde\, NREL Share on X\n\n\n\n\n\n\n\n\n\nRegister here\n\n\n\n\nResponse functions of correlated systems within Green’s function theory \n\n\n\nWe present a detailed examination of one- and two-particle spectral functions in a vari- ety of correlated systems within diagrammatic many-body perturbation theory (MBPT). Diagrammatic Green’s function methods provide a natural path for an ab initio description of many-body phenomena. Diagrams generate both response functions and the effective time-dependent potential\, which is generated from response functions. This makes it a natural vehicle to model probes such as inelastic neutron neutron scattering\, ARPES\, EELS\, and RIXS. However\, much depends on the fidelity of the theory used to generate the Green’s functions. Finding adequate prescriptions for constructing Green’s functions is particularly daunting when systems are strongly correlated. \n\n\n\nIn traditional ab initio formulations\, the potential is calculated at the lowest order (GW) as a perturbative correction to density functional theory. However\, uncontrolled approximations in the reference propagate to MBPT\, which obscures and also limits the range of validity. We present an approach developed within the Questaal community code\, which starts at its lowest level the quasiparticle self-consistent GW (QSGW ) approxima- tion. Self-consistency can sometimes be essential\, as we show for TiSe2 and the 1D cuprate SrCuO2. Through self-consistency discrepancies with experiment become highly system- atic\, allowing us to identify which missing diagrams are the most important. This enables the theory to be refined in a systematic manner. We will show how addition of electron- hole diagrams dramatically improves its fidelity. The need for other diagrams become apparent when spin fluctuations become important. These we include by augmenting QSGW with dynamical mean field theory. \n\n\n\nQSGW is particularly effecting at characterizing spectral functions in magnetic van der Waals insulators. We present a detailed analysis of one- and two-body spectral functions in CrSBr\, a new 2D magnetic system that shows much promise for superseding the well- known transition metal dichalcogenides\, as a medium for integrated circuitry in quantum photonics\, optoelectronics\, and spintronics. Experimental observations of one-body and excitonic spectra\, their dependence on temperature\, magnetic field\, and layer thickness can be explained in detail. These excitons are intermediate between the Frenkel and Wannier limits. We show the connection between MBPT and ligand field theory traditionally used to describe them\, and the range of validity and limits to each.
URL:https://thomasyoungcentre.org/event/tyc-ccp9-visiting-professor-seminar-mark-van-schilfgaarde-nrel/
LOCATION:S3.30 Strand Building\, King’s College London\, Strand\, London\, WC2R 2LS\, United Kingdom
CATEGORIES:Main event
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/London:20250904T140000
DTEND;TZID=Europe/London:20250904T160000
DTSTAMP:20260409T215726
CREATED:20250724T132705Z
LAST-MODIFIED:20250904T123118Z
UID:6798-1756994400-1757001600@thomasyoungcentre.org
SUMMARY:Navigating Technology in Industry and Academia - Afternoon Tea with WHPC & the TYC
DESCRIPTION:Navigating Technology in Industry and Academia – Afternoon Tea with WHPC & the TYC Share on X\n\n\n\n\n\n\n\n\nWe’re excited to welcome Industry experts from Lenovo\, and Teresa Schofield who is a Freelance Chartered Electronic Engineer with a passion for semiconductor and software technologies\, RISC-V\, High Performance Computing (HPC)\, and Open Source. Our speakers will share insights into their career journeys\, current roles\, and how they found their way into the world of HPC. \n\n\n\nFollowing the talks\, we’ll host a panel discussion where you’ll have the opportunity to ask questions and engage with our speakers. The event will conclude with a networking session over some afternoon tea. \n\n\n\n14.00–14.15 Arrival\, registration\, refreshments•    Sign-up for newsletter and mailing list•    Informal welcome and mingling \n\n\n\n14.15-14.45 Lightning Talks •    3 short talks from invited speakers•    Focused insights to spark discussion \n\n\n\n14.45–15.15 Panel Discussion + Audience Q&A•    Moderated discussion with all speakers•    Open floor for questions and reflections \n\n\n\n15.15–16.00 Networking & Refreshments•    Opportunity to connect with speakers and attendees•    Explore collaboration and follow-up ideas \n\n\n\nAttendance is free\, however we do require people to register via the link below.  \n\n\n\n\nRegister here
URL:https://thomasyoungcentre.org/event/navigating-ai-in-industry-and-academia-afternoon-tea-with-whpc-the-tyc/
LOCATION:G06\, Royal School of Mines\, South Kensington\, London\, SW7 2AZ\, United Kingdom
CATEGORIES:Main event
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DTSTART;TZID=Europe/London:20250724T150000
DTEND;TZID=Europe/London:20250724T163000
DTSTAMP:20260409T215726
CREATED:20250626T150750Z
LAST-MODIFIED:20250723T145348Z
UID:6769-1753369200-1753374600@thomasyoungcentre.org
SUMMARY:TYC Junior Research Fellowship visitor talk: Extending Machine Learning Models Beyond Energy and Forces
DESCRIPTION:TYC Junior Research Fellowship talk: Extending Machine Learning Models Beyond Energy and Forces Share on X\n\n\n\n\nNils Gönnheimer\, University of Bayreuth \n\n\n\n\n\n\n\nAbstract: The development of machine‑learning interatomic potentials (MLIPs) has revolutionized computational chemistry by combining the accuracy of first‑principles methods with the computational speed of empirical force fields. Many important properties\, such as heat capacities\, vibrational spectra\, dielectric responses and optical activities\, require either higher‑order derivatives (e.g. Hessians) or direct learning of non‑scalar quantities beyond energies and forces. In the first part of the talk\, Hessian matrix evaluation is addressed: most MLIPs lack analytical second derivatives and must resort to costly\, error‑prone finite differences\, whereas implementing automatic‑differentiation (AD) Hessians within the equivariant MACE framework delivers both efficiency and numerical stability. In the second part\, MACE‑μ‑α\, a polarizability‑and‑dipole model built on the same equivariant architecture\, is trained directly on molecular dipole moments and polarizability tensors\, enabling accurate prediction of both infrared absorption and Raman scattering intensities. Together\, these advances form a unified\, beyond‑scalar MLIP platform for comprehensive spectroscopic characterization and rapid multi‑property prediction of complex materials.
URL:https://thomasyoungcentre.org/event/tyc-junior-research-fellowship-visitor-talk-extending-machine-learning-models-beyond-energy-and-forces/
LOCATION:LG17\, Bentham House\, UCL\, 4-8 ENDSLEIGH GARDENS\, LONDON\, WC1H 0EG
CATEGORIES:Main event
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DTSTART;TZID=Europe/London:20250723T120000
DTEND;TZID=Europe/London:20250723T133000
DTSTAMP:20260409T215726
CREATED:20250320T115839Z
LAST-MODIFIED:20250721T144532Z
UID:6482-1753272000-1753277400@thomasyoungcentre.org
SUMMARY:MMM Hub Software Spotlight: ML force fields
DESCRIPTION:Venue: ONLINE \n\n\n\n\n\n\n\n\n\n\nMMM Hub Software Spotlight: ML force fields Share on X\n\n\n\n\nVenkat Kapil from UCL and Ilyes Batatiya from the University of Cambridge will give an overview of ML force fields – their generation\, use and software which can enable this (inc. its use on HPC/Young). \n\n\n\nFuture talks aim to include commonly codes used on Young\, such as Quantum ESPRESSO and Casino and include some emerging technologies such as machine learning with Keras\, Tensorflow and Torch \n\n\n\nJoin Zoom Meeting: \n\n\n\nMeeting ID: 991 6854 2304Passcode: TYCSWS
URL:https://thomasyoungcentre.org/event/mmm-hub-software-spotlight-ml-force-fields/
CATEGORIES:Main event
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BEGIN:VEVENT
DTSTART;TZID=Europe/London:20250611T093000
DTEND;TZID=Europe/London:20250611T180000
DTSTAMP:20260409T215726
CREATED:20250204T161945Z
LAST-MODIFIED:20250605T114131Z
UID:6330-1749634200-1749664800@thomasyoungcentre.org
SUMMARY:TYC Postgraduate Student Day 2025
DESCRIPTION:Arts Two LT and foyer space\, Queen Mary University of London \n\n\n\n\n\n\n\n\n\n\nTYC Postgraduate Student Day 2025 Share on X\n\n\n\n\nThe TYC Student Day is a one-day celebration of the research in theory and simulation of materials and molecules that is done by PhD students in the four London Colleges that make up the TYC (UCL\, Imperial\, King’s and QMUL)\, and Brunel University London and London South Bank University. There is a programme of talks given by a selection of final year students\, together with a poster session\, and invited guest speakers. \n\n\n\nCash prizes will be awarded for the ‘Best Talk’ and ‘Best Poster’. \n\n\n\nWe invite all TYC students to submit abstracts to present a poster of their research\, and for final year students to submit abstracts for talks.  ~12 talks will be selected (12 minute presentations and 2 minute Q&A)\, and all of the posters from across the four London TYC colleges\, plus LSBU and Brunel\, will be on display at the poster presentation during lunch and at a drinks reception at the end of the day. \n\n\n\n\n\n\n\n\n\n\n\nSchedule:\n\n\n\nTYC Student Day 11 June 2025 ScheduleDownload\n\n\n\nInvited speakers:\n\n\n\nAn Industrial Perspective on the Challenges and Opportunities in Multiscale Materials Modelling – Dr Davide Di Stefano – Ansys\, Inc https://www.ansys.com/company-information/the-ansys-storyMaterials are at the core of engineering simulations\, directly influencing the accuracy and reliability of performance predictions. However\, materials data is often treated as static input derived from costly and time-consuming experimental testing. Increasing material complexity and performance demands require more precise\, adaptable\, and predictive data. Multiscale materials modelling offers a powerful solution to the problem\, providing mechanistic insights that can contribute to the reduction of experimental efforts\, and enhancing accuracy and efficiency. Despite its promise\, multiscale modelling is not yet widely adopted in industry. \n\n\n\nIn this talk\, we will provide an industrial perspective on the open challenges in fulfilling the “multiscale promise” and share examples of effort within Ansys to address these challenges. Examples will include physics-based workflows for multiscale modelling\,  use of machine learning for scale-bridging\, and advanced multiscale characterization techniques for calibration and validation. \n\n\n\nDr. Davide Di Stefano1\, Dr. David Mercier2\, Dr. Pascal Salzbrenner1\, Bhanuj Jain1 \n\n\n\nDavide is lead R&D Project Manager at Ansys in the office of the CTO. Davide’s expertise lies in multiscale modelling\, microstructure modelling\, atomic diffusion\, materials design\, and materials intelligence. \n\n\n\nBind – Making Disordered Proteins Druggable – Thomas Löhr\, Head of Compute – Bind Research https://bindresearch.org/We are a UK-based not-for-profit Focused Research Organisation (FRO) committed to improving patient outcomes by turning disordered proteins into viable drug targets. \n\n\n\nMany incurable diseases (e.g.\, cancer\, neurodegeneration) involve biomolecules called ‘disordered proteins’. Considered ‘undruggable’ by the mainstream pharmaceutical industry\, disordered proteins continuously change their three-dimensional shapes and lack long-lived sites with which drug-molecules can interact. \n\n\n\nOur mission is to make disordered proteins druggable. We are screening millions of disordered protein/drug-molecule pairs to learn the rules of drugging disordered proteins. \n\n\n\nBuilding on our expertise and working with academic and industrial partners\, we are leveraging cutting-edge biology\, engineering\, and AI to deliver new drugs and tools. We are building comprehensive datasets of disordered protein-drug interactions to create public assets to fuel AI models and accelerate the discovery process. To accomplish this in a manner for maximum societal benefit\, we have established a Focused Research Organisation (FRO)\, a fully-independent not-for-profit entity dedicated to this goal. \n\n\n\nThomas is a Computational biophysicist who is passionate about the intersection of simulation and machine learning to study challenging systems. \n\n\n\n\n\n\n\nThe TYC Postgraduate Student Day 2025 has been generously sponsored by Ansys
URL:https://thomasyoungcentre.org/event/tyc-postgraduate-student-day-2025/
LOCATION:Queen Mary University of London\, 327 Mile End Road\, London\, E1 4NS\, United Kingdom
CATEGORIES:Main event
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DTSTART;TZID=Europe/London:20250605T150000
DTEND;TZID=Europe/London:20250605T170000
DTSTAMP:20260409T215726
CREATED:20250110T102200Z
LAST-MODIFIED:20250327T110801Z
UID:6197-1749135600-1749142800@thomasyoungcentre.org
SUMMARY:TYC Highlight Seminar: Modelling the structure of the carbon/electrolyte interface
DESCRIPTION:TYC Highlight Seminar: Modelling the structure of the carbon/electrolyte interface Share on X\n\n\n\n\n\n\n\n\n\nRegister\n\n\n\n\n\n\n\n\nPaola Carbone\, University of Manchester\n\n\n\nThe physical-chemistry of the graphene/aqueous–electrolyte interface underpins the operational conditions of a wide range of devices. Despite its importance\, this interface is poorly understood due to the challenges faced in its experimental characterization and the difficulty of developing models that encompass its full physics. In this talk I’ll present the simulation methods we have developed to model such interface also under confinement and how modelling can aid the full characterization of this interface.
URL:https://thomasyoungcentre.org/event/tyc-highlight-seminar-prof-paola-carbonne-university-of-manchester/
LOCATION:1.02\, Malet Place Engineering Building\, 2 Malet Place\, London\, WC1E 7JE
CATEGORIES:Main event
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