Interfacial Photoelectrochemistry in Organic Synthesis
Abstract
Abstract Photoelectrodes have traditionally enjoyed widespread attention as heterogeneous catalysts for the activation of water and CO 2 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.
Article Details
Authors (5)
Gabriel Chan
Colloid Chemistry Department Max Planck Institute of Colloids and Interfaces Am Mühlenberg 1 14476 Potsdam Germany
Daria Corsi
Institute of Organic Chemistry University of Regensburg Universitätsstr. 31 93053 Regensburg Germany
Oleksandr Savateev
Paolo Giusto
Joshua P. Barham
Department of Pure & Applied Chemistry University of Strathclyde Glasgow UK