Recent progress and perspective for oxygen evolution reaction under acidic environments

被引:3
|
作者
Chen, Lianhua [1 ]
Liu, Yuting [1 ]
Cong, Hang [1 ]
Ge, Qingmei [1 ]
Zhao, Wenfeng [1 ]
Jiang, Nan [1 ,2 ]
Zhang, Qian [3 ]
机构
[1] Guizhou Univ, Sch Chem & Chem Engn, Guiyang 550025, Guizhou, Peoples R China
[2] Guizhou Univ, Collaborat Innovat Ctr Guizhou Prov Efficient Util, Minist Educ, Guiyang 550025, Guizhou, Peoples R China
[3] Nanjing Forestry Univ, Coll Sci, Nanjing 210037, Jiangsu, Peoples R China
关键词
WATER OXIDATION; BIFUNCTIONAL ELECTROCATALYST; STABLE ELECTROCATALYST; RUTHENATE PYROCHLORE; ENHANCED ACTIVITY; DOPED CARBON; CATALYSTS; EFFICIENT; IRIDIUM; OXIDE;
D O I
10.1039/d3qm00801k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Proton exchange membrane (PEM) electrolyzers play a vital role in sustainable energy conversion and storage. However, the oxygen evolution reaction (OER) is considered to be their major bottleneck, limiting their overall efficiency due to its sluggish kinetics and vulnerability under acidic and oxidative conditions. Furthermore, it is still a challenge to design and develop competent and robust electrocatalysts for OER in acidic media. In this case, achieving the rational design of high-performance OER catalysts relies on a comprehensive understanding of the reaction mechanism and structure-activity relationships. In this review, we address the recent progress on the OER mechanisms, including the deactivation mechanisms, scaling relations, and electronic descriptors of OER catalysts with the help of theoretical computations and advanced operando characterization. Then, the strategies for enhancing the OER performance and stability of catalysts are introduced. Finally, the representative catalysts ranging from noble metal-based catalysts and transition metal-based catalysts to metal-free catalysts reported in the last five years for acidic OER are described, followed by a future perspective for developing OER catalysts. Proton exchange membrane (PEM) electrolyzers play a vital role in sustainable energy conversion and storage.
引用
收藏
页码:986 / 1014
页数:29
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