The mechanism of water oxidation using transition metal-based heterogeneous electrocatalysts

被引:40
作者
Yang, Shujiao [1 ]
Liu, Xiaohan [1 ]
Li, Sisi [1 ]
Yuan, Wenjie [1 ]
Yang, Luna [1 ]
Wang, Ting [1 ]
Zheng, Haoquan [1 ]
Cao, Rui [1 ]
Zhang, Wei [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Appl Surface & Colloid Chem, Minist Educ, Xian 710119, Peoples R China
基金
中国国家自然科学基金;
关键词
O BOND-FORMATION; OXYGEN-EVOLUTION REACTION; X-RAY-ABSORPTION; OXIDE THIN-FILM; FE-57 SYNCHROTRON MOSSBAUER; SINGLE-ATOM CATALYSTS; AMBIENT-PRESSURE XPS; IN-SITU FORMATION; PHOTOSYSTEM-II; EVOLVING COMPLEX;
D O I
10.1039/d3cs01031g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The water oxidation reaction, a crucial process for solar energy conversion, has garnered significant research attention. Achieving efficient energy conversion requires the development of cost-effective and durable water oxidation catalysts. To design effective catalysts, it is essential to have a fundamental understanding of the reaction mechanisms. This review presents a comprehensive overview of recent advancements in the understanding of the mechanisms of water oxidation using transition metal-based heterogeneous electrocatalysts, including Mn, Fe, Co, Ni, and Cu-based catalysts. It highlights the catalytic mechanisms of different transition metals and emphasizes the importance of monitoring of key intermediates to explore the reaction pathway. In addition, advanced techniques for physical characterization of water oxidation intermediates are also introduced, for the purpose of providing information for establishing reliable methodologies in water oxidation research. The study of transition metal-based water oxidation electrocatalysts is instrumental in providing novel insights into understanding both natural and artificial energy conversion processes. The oxygen evolution reaction (OER) mechanisms using transition metal-based electrocatalysts are instrumental in providing novel insights into both natural and artificial energy conversion processes.
引用
收藏
页码:5593 / 5625
页数:33
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