Low-iridium electrocatalysts for acidic oxygen evolution

被引:18
|
作者
Fan, Meihong [1 ,2 ]
Liang, Xiao [1 ]
Chen, Hui [1 ]
Zou, Xiaoxin [1 ]
机构
[1] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Coll Chem, Changchun 130012, Peoples R China
[2] Jilin Univ, Coll Phys, State Key Lab Superhard Mat, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
WATER OXIDATION; REACTION-MECHANISM; DISSOLUTION; STABILITY; CATALYST;
D O I
10.1039/d0dt02676j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The widespread use of proton-exchange membrane water electrolysis is limited by the dynamically sluggish oxygen evolution reaction (OER), which is mediated by noble iridium-based materials as active and stable electrocatalysts. Significant efforts have been made to decrease the amount of iridium in OER catalysts without sacrificing their catalytic performances. In this frontier paper, we present the main common issues relevant to the iridium-catalyzed OER, including catalytically active species, catalytic mechanisms and activity-stability relation. We also take iridium-based perovskites as an example, and summarize the recent theoretical and experimental advances in available strategies that can lead to highly efficient, low-iridium oxygen evolution electrocatalysts under acidic conditions. Finally, we propose the remaining challenges and future directions for exploring acidic OER catalysts.
引用
收藏
页码:15568 / 15573
页数:6
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