IrCuNi Deeply Concave Nanocubes as Highly Active Oxygen Evolution Reaction Electrocatalyst in Acid Electrolyte

被引:72
作者
Liu, Di [1 ]
Lv, Qingqing [1 ]
Lu, Siqi [1 ]
Fang, Jinjie [2 ]
Zhang, Yufeng [1 ]
Wang, Xingdong [1 ]
Xue, Yanrong [1 ]
Zhu, Wei [1 ]
Zhuang, Zhongbin [1 ,2 ,3 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
[3] Beijing Univ Chem Technol, Beijing Key Lab Energy Environm Catalysis, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
iridium; concave nanostructure; oxygen evolution reaction; water electrolyzer; HIGH-INDEX FACETS; IRIDIUM; CATALYSTS; EFFICIENT; OXIDE; IR; NANOPARTICLES; NANOCRYSTALS; OXIDATION; CU;
D O I
10.1021/acs.nanolett.0c04878
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Proton exchange membrane water electrolyzer can sustainably and environmentally friendly produce hydrogen. However, it is hindered by the lack of high-performance anode catalysts for oxygen evolution reaction (OER) in acid electrolyte. Herein, IrCuNi deeply concave nanocubes (IrCuNi DCNCs) are successfully synthesized from the selective etching of the facet of cubic nanoparticles, and they significantly boost the OER. The obtained IrCuNi DCNCs show high activity toward OER in the acidic electrolyte, which only requires an overpotential of 273 mV to achieve the OER current density of 10 mA cm(-2) at a low Ir loading of 6.0 mu g(Ir) cm(-2). The precious metal based mass activity is 6.6 A mg(Ir)(-1) at 1.53 V, which is 19 times as high as that of pristine Ir. It demonstrates that the outstanding catalytic performance is beneficial from the well-defined multimetal concave nanostructures, which may shed light on the fabrication of efficient water electrolyzers.
引用
收藏
页码:2809 / 2816
页数:8
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