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X-ORIGINAL-URL:https://remade-project.eu
X-WR-CALDESC:Events for a hub for materials research
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TZID:Europe/Paris
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20260222
DTEND;VALUE=DATE:20260330
DTSTAMP:20260405T214620
CREATED:20250922T143200Z
LAST-MODIFIED:20250922T143200Z
UID:10000071-1771718400-1774828799@remade-project.eu
SUMMARY:HERCULES European School 2026: Neutrons and synchrotron radiation for science
DESCRIPTION:HERCULES EUROPEAN SCHOOL is a five weeks course coordinated by the Université Grenoble Alpes (UGA). The school provides training for students\, postdoctoral and senior scientists from European and non-European universities and laboratories\, in the field of Neutrons\, X-ray Synchrotron Radiation\, and Free Electron Laser for condensed matter studies (Biology\, Chemistry\, Physics\, Materials Science\, Geosciences\, Industrial applications). Neutron and X-ray science is integrated with complementary techniques like (but not only) optical and electron microscopy\, NMR\, optical spectroscopy. \nThe school includes lectures\, practicals\, tutorials\, and visits of large-scale facilities.\nA poster session is organised\, where each participant puts up a poster presenting her/his thesis or research topic for a half-day. \nThe partner Large Scale Facilities for HERCULES 2026 will be: ALBA (Spain)\, KIT (Germany)\, MAX IV / ESS / LINXS (Sweden)\, and SOLEIL (France). \nThe language of the course is English. \nSee the general programme for more information. \n⭐️Join the 2026 HERCULES European School! Advance Your Knowledge in Neutron and Synchrotron Radiation for Science!\n📆 Dates: 22nd February 2026 to 29th March 2026\n📍 Location: in and outside of Grenoble\, France\n⏳Applications to the 2026 HERCULES school are welcomed until October 1st\, 2025!
URL:https://remade-project.eu/index.php/event/hercules-european-school-2026-neutrons-and-synchrotron-radiation-for-science/
LOCATION:in Grenoble (France) and other cities in Europe
CATEGORIES:School
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2025/09/flyer-HERCULES-2026.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260313T100000
DTEND;TZID=Europe/Paris:20260313T110000
DTSTAMP:20260405T214620
CREATED:20260302T184856Z
LAST-MODIFIED:20260313T175130Z
UID:10000072-1773396000-1773399600@remade-project.eu
SUMMARY:Operando adsorption of heavy metals and their recycling into electrodes for energy storage
DESCRIPTION:Zoom webinar | Replay on Youtube\nMarcelo AMARO DE ANDRADE\,  \nInstitut des Matériaux Jean Rouxel de Nantes\, France \nTreating wastewater contaminated with heavy metals often relies on passive adsorption using high-surface area materials\, but once these adsorbents are saturated\, they become hazardous waste themselves. In this work\, Hg2+ cations uptake by reduced graphene oxide (rGO) was tracked under continuous-flow conditions\, using operando techniques to get a realistic picture of the adsorption process. A microfluidic platform was combined with Hg L3-edge synchrotron X-ray absorption spectroscopy (XAS) to monitor\, in real time\, how mercury coordinates and loads onto rGO during adsorption. At the same time\, an electrochemical quartz-crystal microbalance (EQCM) was used to independently follow changes in mass and viscoelastic properties of the rGO layer under model wastewater flow. This approach allowed to distinguish between strongly bound (chemisorbed) and more weakly coordinated (physisorbed) mercury species\, and to observe how these forms changed dynamically as adsorption progressed. 1 \nOn top of that\, the metals captured in these materials can also be used as redox-active components for further applications. Our group previously showed how rGO foams used to capture Hg2+ cations from model wastewater (rGO/Hgads) can be directly recycled into self-standing electrodes without extra chemical or thermal steps. In H2SO4\, these electrodes combine double-layer capacitance with redox-based faradaic reactions\, resulting in about 33% higher gravimetric capacity compared to pristine rGO (Figure 1 – left). 2 \nTo understand the charge-storage mechanism\, operando synchrotron Hg L3-edge XAS was used\, in addition to operando EQCM. Time-resolved XANES revealed two main mercury states: oxidized Hg(II) and a reduced state most consistent with Hg(I). Their concentration profiles show reversible cycling between Hg(II) and Hg(I)\, which corresponds to the electrochemical features observed in cyclic voltammetry. Hg(II) is consumed at the reduction peak around 0.60 V\, and regenerated at the oxidation peak near 0.64 V\, starting as early as 0.45 V (Figure 1 – right). This suggests that redox changes are not limited by simple thermodynamics\, and the capacity gain comes indeed from the adsorbed cations. L₃-edge jump analysis shows that the total mercury content changes with potential\, showing considerable mercury movement in and around the electrode during cycling\, which was correlated to EQCM-D measures. Overall\, this ReMade project allowed to understand both the heavy-metal capture mechanism\, and their later contribution to the electrochemistry by redox changes\, helping to advance new ways of combining environmental remediation with energy storage materials. \nReferences: \n\nAndrade\, M. A.\, Bugaev\, A. L.\, Skorynina\, A. & Douard\, C. Tracking Hg2+ adsorption by reduced graphene oxide in continuous flow by in situ techniques. J. Environ. Chem. Eng. 13\, 118680 (2025).\n\n2. Andrade\, M.\, Crosnier\, O.\, Johansson\, P. & Brousse\, T. Energy from Garbage: Recycling Heavy Metal‐Containing Wastewater Adsorbents for Energy Storage. Adv. Energy Sustain. Res. 6\, (2024).
URL:https://remade-project.eu/index.php/event/operando-adsorption-of-heavy-metals-and-their-recycling-into-electrodes-for-energy-storage/
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2026/03/260313_ReMade@ARI-seminar_AMARO-DE-ANDRADE.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260327T100000
DTEND;TZID=Europe/Paris:20260327T110000
DTSTAMP:20260405T214620
CREATED:20260313T081247Z
LAST-MODIFIED:20260330T115331Z
UID:10000073-1774605600-1774609200@remade-project.eu
SUMMARY:Mechanisms of Pd nanoparticle formation and strong metal-support interaction in Pd/TiO2 revealed by operando XAS
DESCRIPTION:Zoom webinar | Replay on Youtube\nElizaveta KOZYR\,  \nE. Kozyr1\, P. Paciok2\, R. Pellegrini3\, M. Chiesa1\, Elena Groppo1\, L. Mino1\, A. Bugaev4 \n1University of Turin\, Italy; 2Forschungszentrum Jülich GmbH\, Germany; 3ALBAChimet S.p.A\, Italy;\n4Paul Scherrer Institute\, Switzerland; elizaveta.kozyr@unito.it \nUnderstanding the formation of active phases and metal-support interactions is essential for the rational design of efficient photocatalysts. In this work\, Pd/TiO2 catalysts prepared by photodeposition and deposition-precipitation were investigated using a combination of operando synchrotron-based X-ray absorption spectroscopy (XAS) and complementary microscopic and spectroscopic techniques. A custom operando photocatalytic cell enabled in situ monitoring of the Pd photodeposition process\, revealing the formation of single-atom Pd(0) sites as an initial step followed by the growth of ~1 nm Pd nanoparticles with narrow size distribution. Photodeposited catalysts exhibit strong metal-support interaction (SMSI)\, associated with the presence of Ti³⁺ sites at the Pd/TiO2 interface and direct Pd-Ti interactions observed by XAS\, EPR\, and EELS. These features lead to enhanced stabilization of metallic Pd even under oxidizing conditions\, in contrast to catalysts prepared by deposition-precipitation. The results highlight how synthesis pathways govern nanoparticle formation mechanisms and metal-support interactions in Pd/TiO2 photocatalysts. \nAcknowledgements \nWe thank ReMade@ARIE funded by the European Union as part of the Horizon Europe call HORIZON-INFRA-2021-SERV-01 under grant agreement number 101058414 and co-funded by the Swiss State Secretariat for Education\, Research and Innovation (SERI) under contract number 22.00187 for the access to the HR-STEM measurements (ERC\, Julich\, Germany) and XAS measurements at SuperXAS beamline of Swiss Light Source.
URL:https://remade-project.eu/index.php/event/mechanisms-of-pd-nanoparticle-formation-and-strong-metal-support-interaction-in-pd-tio2-revealed-by-operando-xas/
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2026/03/260327_ReMade@ARI-seminar_KOZYR.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260424T100000
DTEND;TZID=Europe/Paris:20260424T110000
DTSTAMP:20260405T214620
CREATED:20260313T081801Z
LAST-MODIFIED:20260313T082013Z
UID:10000074-1777024800-1777028400@remade-project.eu
SUMMARY:Designing better Metal-Organic Framework catalysts for CO2 conversion:  what characterization teaches us
DESCRIPTION:Zoom webinar | Replay on Youtube (soon)\nAnna LIUTKOVA \nPSI (Switzerland) \nMetal-organic frameworks are increasingly explored as materials that can both interact with CO2 and host catalytic sites for its conversion into useful chemicals. This talk discusses how advanced characterization techniques help reveal how these materials behave under reaction conditions. Using Cu and Zn modified UiO-66 catalysts for CO2-to-methanol conversion as an example\, it illustrates how in situ X-ray methods and microscopy guide the design of better catalytic materials.
URL:https://remade-project.eu/index.php/event/designing-better-metal-organic-framework-catalysts-for-co2-conversion-what-characterization-teaches-us/
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2026/03/260424_ReMade@ARI-seminar_LIUTKOVA.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20260515T100000
DTEND;TZID=Europe/Paris:20260515T110000
DTSTAMP:20260405T214620
CREATED:20250514T092613Z
LAST-MODIFIED:20260313T082639Z
UID:10000067-1778839200-1778842800@remade-project.eu
SUMMARY:Synergies between Molecular Spectroscopy and Computational Chemistry and their role in the Characterization and Design of Sustainable Materials
DESCRIPTION:Zoom webinar | Replay on Youtube (soon)\nLicinia L. G. Justino\,  \nUniversity of Coimbra\, Portugal \nAbstract TBC.
URL:https://remade-project.eu/index.php/event/synergies-between-molecular-spectroscopy-and-computational-chemistry-and-their-role-in-the-characterization-and-design-of-sustainable-materials/
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2025/05/260515_ReMade@ARI-seminar_JUSTINO.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261023T100000
DTEND;TZID=Europe/Paris:20261023T110000
DTSTAMP:20260405T214620
CREATED:20260313T082957Z
LAST-MODIFIED:20260313T084320Z
UID:10000075-1792749600-1792753200@remade-project.eu
SUMMARY:Scalable and longer-lasting bulk metals for public health and infrastructure
DESCRIPTION:Zoom webinar | Replay on Youtube (soon)\nLiliana ROMERO RESENDIZ \nBournemounth University\, UK \nImagine a structural metal that is simultaneously stronger and more ductile (flexible) than conventional options – and can even kill bacteria on contact. This is now possible through heterostructured materials\, which combine soft and hard regions within the same metal to create internal mechanical interactions that enhance overall performance. \nThis talk introduces the design principles of these architectures and explains why they outperform traditional alloys across multiple metrics. Using results from the ReMade@ARI initiative\, I will show how cryogenic deformation triggers a cascade of crystal defect mechanisms that progressively sustain work hardening. \nBeyond mechanical superiority\, heterostructuring can embed antimicrobial functionality into bulk metals without sacrificing durability. These findings open pathways toward scalable\, multifunctional materials for demanding applications: from safer medical devices and water infrastructure to resilient energy systems and cryogenic transport.
URL:https://remade-project.eu/index.php/event/scalable-and-longer-lasting-bulk-metals-for-public-health-and-infrastructure/
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2026/03/261023_ReMade@ARI-seminar_Romero-Resendiz.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20261127T100000
DTEND;TZID=Europe/Paris:20261127T110000
DTSTAMP:20260405T214620
CREATED:20260313T084204Z
LAST-MODIFIED:20260313T084353Z
UID:10000076-1795773600-1795777200@remade-project.eu
SUMMARY:In situ characterization of food and plastic waste carbonized under pressure
DESCRIPTION:Zoom webinar | Replay on Youtube (soon)\nFrancesco D’ACIERNO \nKU Leuven\, Belgium \n  \nIn situ investigations of soft-matter carbonization are essential to connect processing conditions with final carbon structure and function. Here we report time-resolved structural and chemical monitoring of autogenic pressure carbonization of non-recyclable commodity plastics performed directly inside sealed quartz capillaries. We also treated food waste-derived sugars through alkaline and neutral hydrothermal carbonization in water and ionic liquids. By combining synchrotron-grade WAXS and SAXS with in-situ Raman spectroscopy\, and supporting ex-situ XPS surface analysis\, we follow the transformation from disordered organic networks to carbonaceous solids under self-generated pressure in real time.\n\nSAXS reveals the emergence and coarsening of nanoscale porosity and density inhomogeneities early in the heating profile\, while WAXS captures the progressive development of short-range aromatic stacking (broadening and gradual appearance of 002-type scattering). Raman spectra recorded concurrently track the evolution of sp2 domains and defect populations via the D and G bands\, allowing kinetic comparison between plastic and sugar routes. Ex-situ XPS indicates contrasting heteroatom retention: hydrothermal-derived chars retain higher oxygen functionality\, whereas plastic-derived carbons show lower O/C ratios and more pronounced graphitization signatures at equivalent processing stages.\n\nTogether the multimodal dataset supports a unifying mechanism in which precursor chemistry controls the balance between intramolecular rearrangement and intermolecular crosslinking\, setting the pathway for pore formation and aromatic ordering under pressure.
URL:https://remade-project.eu/index.php/event/in-situ-characterization-of-food-and-plastic-waste-carbonized-under-pressure/
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://remade-project.eu/wp-content/uploads/2026/03/261127_ReMade@ARI-seminar_DACIERNO.jpg
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