The oxygen evolution reaction enabled by transition metal phosphide and chalcogenide pre-catalysts with dynamic changes

被引:282
作者
Li, Wei [1 ,2 ]
Xiong, Dehua [1 ,3 ]
Gao, Xuefei [2 ]
Liu, Lifeng [1 ]
机构
[1] Int Iberian Nanotechnol Lab INL, Ave Mestre Jose Veiga S-N, P-4715330 Braga, Portugal
[2] West Virginia Univ, Dept Mech & Aerosp Engn, Morgantown, WV 26506 USA
[3] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Hubei, Peoples R China
基金
欧盟地平线“2020”;
关键词
EFFICIENT BIFUNCTIONAL CATALYSTS; ONE-STEP SYNTHESIS; HYDROGEN EVOLUTION; HIGHLY EFFICIENT; WATER OXIDATION; NICKEL PHOSPHIDE; ELECTROCHEMICAL OXIDATION; HIGH-PERFORMANCE; COBALT OXIDE; ELECTROCATALYST;
D O I
10.1039/c9cc02845e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxygen evolution reaction represents an important electrochemical reaction in several energy storage and conversion devices such as water electrolyzers and metal-air batteries. Developing efficient, inexpensive and durable electrocatalysts for the oxygen evolution reaction (OER) has been one of the major focuses of applied electrochemistry and has attracted considerable research attention in the past decades. Non-oxide based transition metal compounds, typically transition metal phosphides (TMPs) and chalcogenides (TMCs), have recently emerged as new categories of OER pre-catalysts, demonstrated outstanding electrocatalytic performance as compared to the conventional oxide- or hydroxide-based OER catalysts for alkaline water electrolysis, and even shown promise to replace noble metals for proton-exchange membrane (PEM) water electrolysis. In this feature article, we will summarize the latest advances in the development of TMP- and TMC-based OER electrocatalysts. In particular, we will discuss the electrochemical stability of TMPs and TMCs predicted using Pourbaix diagrams and their morphological, structural and compositional evolution under OER conditions. We will also point out some challenges to be addressed in this specific area of research and propose further investigations yet to be done.
引用
收藏
页码:8744 / 8763
页数:20
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