Decoupling H and O Release in Particulate Photocatalytic Overall Water Splitting Using a Reversible O Binder.

Angew Chem Int Ed Engl

Research Institute of Photocatalysis, State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, 350116, China.

Published: December 2024

H and O evolutions occur simultaneously for conventional particulate photocatalytic overall water splitting (PPOWS), leading to a significant backward reaction and the formation of an explosive H/O gas mixture. This is an issue that must be addressed prior to industrialization of PPOWS. Here, a convenient, cost-effective, and scalable concept is introduced to uncouple hydrogen and oxygen production for PPOWS. Based on this idea, a three-component photocatalyst, Co(5 %)-HPCN/(rGO/Pt), is constructed, consisting of a photoresponsive chip (HPCN), a H evolution cocatalyst (rGO/Pt), and a cobalt complex capable of reversibly binding O (Co), to achieve the decoupling of PPOWS under alternating UV and visible light irradiations. The asynchronous O and H evolution strategy have considerable flexibility regarding the photocatalyst structure and light sources suitable for PPOWS.

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http://dx.doi.org/10.1002/anie.202420913DOI Listing

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