Electrocatalytic properties of porous Ni-Co-WC composite electrode toward hydrogen evolution reaction in acid medium

被引:24
作者
Yang, Yufang [1 ]
Zhu, Xun [1 ]
Zhang, Bodong [1 ]
Yang, Huan [1 ]
Liang, Changjin [1 ]
机构
[1] Hanshan Normal Univ, Sch Mat Sci & Engn, Chaozhou 521041, Peoples R China
关键词
Electrodeposition; Porous Ni-Co-WC; Composite materials; Foam Ni; Electrocatalysis; Hydrogen evolution reaction; ELECTROCHEMICAL PREPARATION; CATALYTIC-ACTIVITY; EFFICIENT ELECTROCATALYST; MACROPOROUS NI; ALLOY; COATINGS; CATHODES; MO; CARBON; NANOFIBERS;
D O I
10.1016/j.ijhydene.2019.05.088
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
Porous Ni-Co-(WC)(x) ternary composite electrodes were fabricated by means of electrode position on a foam Ni substrate. The surface morphology and microstructure of the electrodes were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The electrocatalytic properties of porous Ni-Co-(WC)(x) electrodes for hydrogen evolution reaction (HER) in 0.5 M H2SO4 solution at temperatures from 25 to 50 degrees C were conducted by means of cathodic polarization, electrochemical impedance spectroscopy (EIS), cyclic voltammetry and chronoamperometry (CA). These Ni-Co-WC electrodes are efficient electrocatalysts for HER. Compared with the porous Ni-Co electrode, the porous Ni-Co-(WC)(x) electrode exhibited a lower HER overpotential, a lower electrochemical impedance, a lower apparent activation energy and a higher exchange current density. The apparent exchange current density of porous Ni-Co-(WC)(x) (x = 10, 20, 30 and 40 g/l) is 2.01, 3.01, 7.8 and 19.91 times of porous Ni-Co electrode, respectively. With the increase of WC concentration and temperature, the apparent exchange current density of HER was enhanced. With the increase of WC concentration and potential, the HER resistance and the activation energy decreased. The Ni-Co-(WC)(x) electrode exhibited superior corrosion resistance and stability for HER. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19771 / 19781
页数:11
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