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使用可逆氧粘合剂在颗粒光催化全水分解中解耦氢和氧的释放

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

作者信息

Liu Dan, Xu Huihui, Shen Jinni, Wang Xun, Qiu Chengwei, Lin Huaxiang, Long Jinlin, Wang Ying, Dai Wenxin, Fang Yuanxing, Yang Yanhui, Wang Xuxu, Fu Xianzhi, Zhang Zizhong

机构信息

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

College of Materials and Chemical Engineering, Minjiang University, Fuzhou, 350108, China.

出版信息

Angew Chem Int Ed Engl. 2025 Feb 24;64(9):e202420913. doi: 10.1002/anie.202420913. Epub 2025 Jan 3.

Abstract

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.

摘要

在传统的颗粒光催化全水分解(PPOWS)过程中,氢气和氧气的析出同时发生,导致显著的逆反应并形成爆炸性的氢/氧气体混合物。这是PPOWS工业化之前必须解决的一个问题。在此,引入了一种便捷、经济高效且可扩展的概念,用于使PPOWS中的氢气和氧气生成解耦。基于这一想法,构建了一种三元光催化剂Co(5 %)-HPCN/(rGO/Pt),它由光响应芯片(HPCN)、析氢助催化剂(rGO/Pt)和能够可逆结合氧的钴配合物(Co)组成,以实现在交替紫外光和可见光照射下PPOWS的解耦。异步析氧和析氢策略在适用于PPOWS的光催化剂结构和光源方面具有相当大的灵活性。

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