Cathodic hydrogen evolution in acidic solutions using electrodeposited nano-crystalline Ni-Co cathodes

被引:59
作者
Badawy, W. A. [1 ]
Nady, H. [2 ]
Negem, M. [2 ]
机构
[1] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt
[2] Fayoum Univ, Fac Sci, Dept Chem, Al Fayyum, Egypt
关键词
Nano-crystalline electrodes; Ni-Co deposit; Hydrogen evolution; EIS; Polarization; ELECTROCHEMICAL IMPEDANCE; ELECTROCATALYTIC BEHAVIOR; WATER ELECTROLYSIS; WORK FUNCTION; ALLOY; KINETICS; ELECTRONEGATIVITY; SYNERGISM; METALS; CU;
D O I
10.1016/j.ijhydene.2014.05.049
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
Nano-crystalline Ni and Ni-Co electrodes were prepared by electrodeposition on copper substrates. The obtained materials were characterized morphologically and chemically by XRD and scanning electron microscopy, SEM, coupled with EDX analysis. The incorporation of Co into the Ni matrix causes surface modification, which catalyzes the hydrogen evolution reaction, HER. The electro-catalytic performance of the prepared electrode layers was studied by means of polarization techniques and electrochemical impedance spectroscopy, EIS, in acidic solutions. The Results reveal a decrease in the hydrogen overpotential by increasing the Co content up to approximate to 50 at% in the deposited cathode layer. The Nyquist impedance plots of the different investigated materials at different potentials in the hydrogen evolution region showed a single semicircle, which means that a single time constant is controlling the HER. Ni Co deposits with approximate to 50 at% Co contents show the highest rate of hydrogen evolution as a consequence of the synergetic combination of Ni and Co. The increase of the Co content more than approximate to 50 at% was accompanied by a decrease in the rate of HER. The low hydrogen over-potential and high hydrogen adsorption on the Ni-50 at% Co is attributed to the synergetic effects of Co and Ni together. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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页码:10824 / 10832
页数:9
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