Bimetallic iron cobalt oxide self-supported on Ni-Foam: An efficient bifunctional electrocatalyst for oxygen and hydrogen evolution reaction

被引:122
|
作者
Bandal, Harshad A. [1 ]
Jadhav, Amol R. [1 ]
Tamboli, Asif H. [1 ]
Kim, Hern [1 ]
机构
[1] Myongji Univ, Dept Energy Sci & Technol, Smart Living Innovat Technol Ctr, Yongin 17058, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Bifunctional electrocatalyst; Water electrolysis; Hydrogen evolution; Oxygen evolution; WATER OXIDATION ACTIVITY; MESOPOROUS CO3O4; FILM ELECTRODES; RAMAN-SPECTRA; THIN-FILM; CO; CATALYST; NANOPARTICLES; GENERATION; ARRAY;
D O I
10.1016/j.electacta.2017.07.178
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Water electrolysis offers an efficient way to store energy derived from renewable sources in the form of hydrogen. However, the practical implication of this technology is hindered by the lack of efficient earth abundant catalyst capable of accelerating both half reaction of water electrolysis. In this regards, herein; we have prepared a highly active composite electrode by depositing hierarchical spinel iron cobalt oxide on the surface of nickel foam. The layered morphology of iron cobalt oxide is ideal for effective transfer of electrolyte and facile dissipation of gaseous product. Moreover, intimate contact between the catalyst and the current collector caused a significant reduction in charge transfer resistance. Consequently, composite electrode displayed enhanced catalytic activity for HER and OER, achieving the benchmark current density of 10 mA cm(-2) at a low overpotential of 205 mV and 244 mV respectively. In addition, a two-electrode alkaline water electrolyzer constructed by employing the composite electrode as anode and cathode yielded a current density of 10 mA cm(-2) at an applied potential of only 1.62 V. The long-lasting stability of iron cobalt oxide-Ni foam electrode along with its exceptional catalytic activity makes it a promising alternative to substitute the precious metal catalyst used in commercial water electrolyzer. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:253 / 262
页数:10
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