Hydrogen Evolution Reaction in Alkaline Media: Alpha- or Beta-Nickel Hydroxide on the Surface of Platinum?

被引:268
|
作者
Yu, Xiaowen [1 ]
Zhao, Jun [2 ]
Zheng, Li-Rong [3 ]
Tong, Yue [1 ]
Zhang, Miao [1 ]
Xu, Guochuang [1 ]
Li, Chun [1 ]
Ma, Jing [2 ]
Shi, Gaoquan [1 ]
机构
[1] Tsinghua Univ, Dept Chem, MOE Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210093, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
来源
ACS ENERGY LETTERS | 2018年 / 3卷 / 01期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
WATER OXIDATION; ELECTROCHEMICAL EVOLUTION; RAMAN-SPECTROSCOPY; OXIDE CATALYSTS; OXYGEN; ELECTROCATALYST; ELECTROLYTES; ELECTRODES; NANOSHEETS; NITRIDES;
D O I
10.1021/acsenergylett.7b01103
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reducing the energy consumption of a hydrogen evolution reaction (HER) at a platinum (Pt) electrode is important for the hydrogen economy. Herein, we report the loading of alpha- or beta-nickel hydroxide (alpha- or beta-Ni(OH)(2)) nanostructures on the surface of a Pt electrode to improve its catalytic activity and stability for HER in alkaline electrolytes. Both experimental and theoretical studies reveal that beta-Ni(OH)(2) is a better co-catalyst of Pt than alpha-Ni(OH)(2) for promoting the HER, attributed to the higher water dissociation ability of beta-Ni(OH)(2), as well as the stronger interactions between beta-Ni(OH)(2) and the Pt electrode. Particularly, the over potential of the HER in 0.1 M KOH at 10 mA cm(-2) is decreased from 278 mV at the Pt electrode to 92 mV at the beta-Ni(OH)(2)/Pt electrode, and the Tafel slope decreased from 62 to 42 mV dec(-1), correspondingly. The performance of the beta-Ni(OH)(2)/Pt catalytic electrode surpasses that of most of the previously reported electrodes for the same purpose.
引用
收藏
页码:237 / 244
页数:8
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