In situ formation of highly active Ni-Fe based oxygen-evolving electrocatalysts via simple reactive dip-coating

被引:106
作者
Dong, Guofa [1 ,2 ,3 ]
Fang, Ming [1 ,4 ]
Zhang, Jianshuo [3 ]
Wei, Renjie [1 ,4 ]
Shu, Lei [1 ,4 ]
Liang, Xiaoguang [1 ,4 ]
Yip, SenPo [1 ,4 ]
Wang, Fengyun [5 ]
Guan, Lunhui [3 ]
Zheng, Zijian [2 ]
Ho, Johnny C. [1 ,4 ,6 ]
机构
[1] City Univ Hong Kong, Dept Phys & Mat Sci, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Inst Text & Clothing, Nanotechnol Ctr, Kowloon, Hong Kong, Peoples R China
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350108, Peoples R China
[4] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen 518057, Peoples R China
[5] Qingdao Univ, Cultivat Base State Key Lab, Qingdao 266071, Peoples R China
[6] City Univ Hong Kong, State Key Lab Millimeter Waves, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
WATER-ELECTROLYSIS CATALYSTS; EVOLUTION ELECTROCATALYSTS; OXIDE-FILMS; OXIDATION CATALYSIS; XPS SPECTRA; IRON; NICKEL; COBALT; METAL; EFFICIENT;
D O I
10.1039/c7ta01134b
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
Since the oxygen evolution reaction (OER) is a key step in the process of water splitting, efficient catalysts are inevitably required to overcome energy barriers at the electrode-electrolyte interface in order to improve its reaction efficiency; as a result, developing highly active and low-cost catalysts is of the great importance. Herein, we report an extremely simple method to prepare OER catalysts, which exhibit excellent activity and superior OER stability in alkaline conditions. The OER catalysts are composed of mixed Ni-Fe oxides or hydroxides that can be easily obtained by in situ reactive dip-coating of nickel foams in a Fe3+-containing aqueous solution. In specific, the as-prepared composites can give an overpotential value of 210 mV under a current density of 10 mA cm(-2) in 1 M KOH aqueous solution and there is not any obvious degradation in OER activity even after 50 hour's chronopotentiometry measurement at a current density of 50 mA cm(-2). More importantly, the samples prepared by this method also illustrate the good uniformity, in which this particular synthesis scheme would hold the great potency for practical fabrication of high-performance and low-cost catalysts in the large-scale industrialization.
引用
收藏
页码:11009 / 11015
页数:7
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