Halide perovskites and organic bulk heterojunctions in photoelectrodes for solar chemical devices
Salvador Eslava a
a Department of Chemical Engineering and Centre for Processable Electronics, Imperial College London, SW7 2AZ, London, United Kingdom
Proceedings of MATSUS Fall 2025 Conference (MATSUSFall25)
E.21 Photo-assisted chemical reactions: materials, characterization and mechanisms - #PhotoChem
València, Spain, 2025 October 20th - 24th
Organizers: Josep Albero Sancho and Menny Shalom
Invited Speaker, Salvador Eslava, presentation 231
Publication date: 17th July 2025

Direct solar conversion of abundant reactants in photoelectrochemical devices offers a promising pathway for producing clean fuels and chemicals. Achieving high efficiency and long-term stability in these systems demands innovative strategies that build on advances in mature fields such as photovoltaics and electrocatalysis. This presentation highlights recent progress in integrating halide perovskite- and organic bulk heterojunction-based photovoltaic devices with electrocatalytic sheets to develop high-performance photoelectrodes for solar fuel and chemical production. For example, we demonstrate CsPbBr3-based photoanodes delivering stable photocurrents >6 mA cm² at 1.23 V vs. RHE, and organic bulk heterojunction photoanodes (e.g., PM6/PTQ10 blends) achieving photocurrents of 25 mA cm-2 or over 5% unassisted solar-to-hydrogen efficiency in tandem configurations. Electrocatalytic sheets composed of carbon allotropes (graphite, glassy carbon, boron-doped diamond) and Ni- or NiFeOOH-based catalysts enable efficient oxygen evolution, while confined Pt catalysts support hydrogen evolution at photocathodes. Minimizing voltage losses and optimizing charge injection into electrolytes are critical to drive solar fuel and chemical production. Our characterization studies underscore key strengths of these devices, including strong solar absorption and substantial photovoltage generation, pointing to new opportunities for unassisted solar chemical synthesis.

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