Assessment of the roughness factor effect and the intrinsic catalytic activity for hydrogen evolution reaction on Ni-based electrodeposits

被引:168
作者
Herraiz-Cardona, I. [1 ]
Ortega, E. [1 ]
Garcia Anton, J. [1 ]
Perez-Herranz, V. [1 ]
机构
[1] Univ Politecn Valencia, Dept Ingn Quim & Nucl, IEC Grp, Valencia 46022, Spain
关键词
Porous Ni electrodeposits; NiCo alloys; Surface roughness factor; Electrochemical impedance spectroscopy; COMPOSITE-COATED ELECTRODE; ELECTROCHEMICAL IMPEDANCE; CATHODE MATERIAL; AC-IMPEDANCE; NICKEL; KINETICS; COATINGS; ELECTROCATALYSIS; MORPHOLOGIES; MECHANISM;
D O I
10.1016/j.ijhydene.2011.05.047
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
The hydrogen evolution reaction (HER) was studied in 30 wt.% KOH solution at temperatures ranging between 30 and 80 degrees C on three type of electrodes: (i) rough pure Ni electrodeposits, obtained by applying a large current density; (ii) smooth NiCo electrodeposits; smooth commercial Ni electrodes. By using steady-state polarization curves and electrochemical impedance spectroscopy (EIS) the surface roughness factor and the intrinsic activities of the catalytic layers were determined. These techniques also permitted us to determine the mechanism and kinetics of the HER on the investigated catalysts. Different AC models were tested and the appropriate one was selected. The overall experimental data indicated that the rough/porous Ni electrode yields the highest electrocatalytic activity in the HER. Nevertheless, when the effect of the surface roughness was taken into consideration, it was demonstrated that alloying Ni with Co results in an increased electrocatalytic activity in the HER when comparing to pure Ni. This is due to an improved intrinsic activity of the material, which was explained on the basis of the synergism among the catalytic properties of Ni (low hydrogen overpotential) and of Co (high hydrogen adsorption). Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:9428 / 9438
页数:11
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