Non-critical Raw Material Based Oxides as Efficient and Stable Catalyst for Acidic Water Oxidation
Ranit Ram a, Lu Xia a, Hind Benzidi b, Anku Guha a, Nuria Lopez b, F. Pelayo García de Arquer a
a ICFO Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, Castelldefels (Barcelona) 08860, Spain
b ICIQ – Institute of Chemical Research of Catalonia, The Barcelona Institute of Science and Technology, Tarragona 43007, Spain
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Spring 2024 Conference (MATSUS24)
#MatInter - Materials and Interfaces for emerging electrocatalytic reactions
Barcelona, Spain, 2024 March 4th - 8th
Organizers: Marta Costa Figueiredo and María Escudero-Escribano
Oral, Ranit Ram, presentation 137
DOI: https://doi.org/10.29363/nanoge.matsus.2024.137
Publication date: 18th December 2023

The oxygen evolution reaction (OER) is the predominant overall reaction bottleneck in water electrolysis towards achieving the large-scale production of sustainable H2. A proton exchange membrane-based water electrolyzer (PEMWE) shows advantages in operating at higher current densities, low H2 cross-over, and improved energy efficiency; over diaphragm and anion transport-based water electrolysers [1]. However, today´s OER catalysts in acid rely on rare and expensive critical raw materials such as Ir, Pt, or Ru. This limits the broad-scale implementation of PEMWE technology. Hence, the development of new platinum-group metal (PGM)-free electrocatalysts for the OER that combine efficiency and robustness in acidic conditions is paramount for clean H2 production from water [2–3]. We present new Co-based anode catalysts that achieve high activity and stable operation. Our synthetic strategy triggers a structural reconstruction of Co-based oxides that enables a different OER pathway by controlling the local oxide structure. The catalyst achieves 1.8 A‧cm−2 of current density at 2.0 V in PEMWE system at 80˚C using milli-Q water as electrolyte. It exhibited 278 h and 250 h of durability at 0.2 and 1.0 A‧cm−2 of current density, respectively, in industrial relevant conditions. Our study outperforms the durability of benchmark non-PGM catalysts over eight-times in the PEMWE system [2–3].

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