Tracking and Controlling Reaction Intermediates in Transition Metal Oxides with Ultrafast Spectroscopy
Hanna Strojecka a, Felipe A. Garcés-Pineda b, José Ramón Galán-Mascarós b, Simon Gwénaël Mizrahi a, Nicolas Godin a, Guy Pecheul a, Maciej Lorenc a, Ernest Pastor a
a Univ Rennes, CNRS, IPR (Institut de Physique de Rennes) - UMR 6251, Rennes France
b Institute of Chemical Research of Catalonia (ICIQ-CERCA), The Barcelona Institute of Science and Technology (BIST), Av. Paisos Catalans 16, Tarragona, Spain
Proceedings of MATSUS Spring 2026 Conference (MATSUSSpring26)
E3 Photocatalysis for solar fuel and chemical synthesis
Barcelona, Spain, 2026 March 23rd - 27th
Organizers: Demetra Achilleos, Virgil Andrei and Sixto Gimenez Julia
Poster, Hanna Strojecka, 972
Publication date: 15th December 2025

Earth-abundant transition metal oxides (TMOs) based on Ni, Fe and Co are being widely explored as potential electrocatalysts. [1,2] Their low production costs and high availability make them promising candidates for applications in energy and chemical product generation. [3] However, achieving the high catalytic efficiencies and stabilities required for industrial implementation remains challenging. [4] Electrochemical reactions, driven by an external electric field, occur as a series of proton - coupled electron transfer steps in which reaction intermediates are generated. [5] However, the exact mechanism behind the generation and stabilisation of those intermediates in TMOs is not well understood. [6] In this poster, I will discuss how ultrafast spectroscopy can be used as a tool to monitor and control the formation of reaction intermediates at the electrochemical interface. Specifically, I will report data on Ni-based oxides used for the oxygen evolution reaction (OER), tracking the spectroscopic fingerprints of different intermediates and demonstrating how they can be manipulated using light. Finally, I will examine the opportunities and constraints associated with light-driven control of pre-catalytic species and the reaction mechanism.

This work was supported by the European Research Council (ERC) and the Agence Nationale de la Recherche (ANR).

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