Accepted Articles e202424300
Review
Open Access

Interfacial Photoelectrochemistry in Organic Synthesis

Gabriel Chan

Gabriel Chan

Max Planck Institute of Colloids and Interfaces: Max-Planck-Institut fur Kolloid und Grenzflachenforschung, Department of Colloid Chemistry, GERMANY

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Daria Corsi

Daria Corsi

University of Regensburg: Universitat Regensburg, Fakultat fur Chemie und Pharmazie, GERMANY

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Oleksandr Savateev

Oleksandr Savateev

The Chinese University of Hong Kong, Department of Chemistry, HONG KONG

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Paolo Giusto

Paolo Giusto

Max Planck Institute of Colloids and Interfaces: Max-Planck-Institut fur Kolloid und Grenzflachenforschung, Department of Colloid Chemistry, GERMANY

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Joshua Philip Barham

Corresponding Author

Joshua Philip Barham

Universitat Regensburg, Fakultat fur Chemie und Pharmazie, Universität Regensburg, Fakultät für Chemie und Pharmazie, 93040 Regensburg, GERMANY

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First published: 19 May 2025

Abstract

Photoelectrodes have traditionally enjoyed widespread attention as heterogeneous catalysts for the activation of water and CO2 in energy research, while photoelectrochemistry with homogeneous molecular catalysts dominates the activations of more complex molecules in organic synthesis. Nonetheless, interfacial photoelectrochemistry (iPEC) offers great benefits to organic synthesis, including catalyst cost-efficiency, reusability and stability. This review aims i) for a comprehensive collection of historical and recent examples of iPEC and ii) to present the field in manner and language accessible to synthetic chemists. Conceptual comparisons from photoelectrodes to homogeneous (electro-activated) photocatalysts to dye-sensitized photoelectrodes will be drawn, with advantages and limitations of each catalyst archetype discussed. Surface techniques for fabrication of photoelectrodes will be introduced. Future semiconductor photoelectrode materials, substrate targets and conceptual challenges in the field will be highlighted.

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