Charge-Redistribution-Enhanced Nanocrystalline Ru@IrOx Electrocatalysts for Oxygen Evolution in Acidic Media

被引:479
作者
Shan, Jieqiong [1 ]
Guo, Chunxian [1 ]
Zhu, Yihan [2 ,3 ]
Chen, Shuangming [4 ]
Song, Li [4 ]
Jaroniec, Mietek [5 ]
Zheng, Yao [1 ]
Qiao, Shi-Zhang [1 ]
机构
[1] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
[2] Zhejiang Univ Technol, Dept Chem Engn, Hangzhou 310014, Zhejiang, Peoples R China
[3] Zhejiang Univ Technol, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310014, Zhejiang, Peoples R China
[4] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
[5] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
CATALYSTS; RUTHENIUM; NANOPARTICLES; STABILITY; DESIGN; ENERGY; OXIDES; OXIDATION; NANOSTRUCTURES; NANOCATALYSTS;
D O I
10.1016/j.chempr.2018.11.010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Achieving high activity and long-term stability is a major challenge in the design of catalysts. In particular, the oxygen evolution reaction (OER) in acidic media, which plays a key role in proton exchange membrane electrolyzers for fast hydrogen fuel generation, seriously suffers from rapid degradation of catalysts as a result of the harsh acidic and oxidative conditions. Here, we report a rational design strategy for the fabrication of a heterostructured OER electrocatalyst (Ru@IrOx) that has unique physicochemical properties and in which a strong charge redistribution exists between a highly strained ruthenium core and a partially oxidized iridium shell across the metal-metal oxide heterojunction. The increased valence of the iridium shell and the decreased valence of the ruthenium core activate a synergistic electronic and structural interaction, which results in the enhanced activity and stability of the catalyst compared with the majority of the state-of-the-art ruthenium- and iridium-based materials.
引用
收藏
页码:445 / 459
页数:15
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