Ce-Doped IrO2 Electrocatalysts with Enhanced Performance for Water Oxidation in Acidic Media

被引:64
|
作者
Wang, Yahui [1 ]
Hao, Shaoyun [1 ]
Liu, Xiangnan [1 ]
Wang, Qiqi [1 ]
Su, Zhiwei [1 ]
Lei, Lecheng [1 ,2 ]
Zhang, Xingwang [1 ,2 ]
机构
[1] Zhejiang Univ, Key Lab Biomass Chem Engn, Minist Educ, Coll Chem & Biol Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Inst Zhejiang Univ Quzhou, Quzhou 324000, Zhejiang, Peoples R China
关键词
acidic media; density functional theory; doping; OER; water splitting; OXYGEN EVOLUTION; IRIDIUM OXIDE; STABILITY; EFFICIENT; CATALYST; NANOPARTICLES; VACANCIES;
D O I
10.1021/acsami.0c00389
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Electrocatalytic water splitting in acidic media based on a proton-exchange membrane (PEM) is a promising technique for the large-scale production of hydrogen. However, developing electrocatalysts with high activity and excellent stability for an oxygen evolution reaction (OER) in acidic media is still a big challenge. Herein, a Ce-x-IrO2 catalyst supported on N-doped porous carbon (NPC) was developed via doping Ce into IrO2 nanoparticles. The Ce-x-IrO2 nanoparticles were uniformly distributed on NPC due to the high surface area. The optimized Ce-0.2-IrO2 @NPC delivers a low overpotential of 224 mV and excellent stability of 100 h in 0.5 M H2SO4 at 10 mA cm(-2). Density functional theory (DFT) calculations indicated that the introduction of Ce could modify the electronic structure of IOr(2), decreasing the energy barrier of the rate-determining step for OER and enhancing the electrochemical OER performance. Our work opens up a new way of developing anodic electrocatalysts, which can be stably applied in acidic media.
引用
收藏
页码:37006 / 37012
页数:7
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