Study of the hydrogen evolution reaction on nickel-based composite coatings containing molybdenum powder

被引:210
作者
Kubisztal, J.
Budniok, A.
Lasia, A.
机构
[1] Univ Silesia, Inst Mat Sci, PL-40007 Katowice, Poland
[2] Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, Canada
关键词
nickel; molybdenum; electrolytic composite coatings; galvanostatic deposition; hydrogen evolution reaction; kinetics; real surface area; electrochemical impedance spectroscopy;
D O I
10.1016/j.ijhydene.2006.11.020
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
Ni + Mo composite coatings were prepared by electrodeposition of nickel from a nickel bath containing Mo particles suspended by stirring. All the coatings have been deposited under galvanostatic conditions. It was found, that molybdenum content depends on the deposition current density and changes between 28 and 46 wt%. The thickness of the Ni + Mo composite coatings was between 100 and 130 mu m depending on the deposition current density. Ni + Mo coatings were characterized by larger surface area than the Ni electrodeposits. Structural investigation carried out by X-ray diffraction (XRD) method show that the obtained coatings consist of crystalline Mo phase incorporated into Ni matrix. The apparent and intrinsic coating activity and the mechanism of the hydrogen evolution reaction (HER) were studied by electrochemical impedance spectroscopy (EIS) and steady-state polarization methods. The results demonstrate greater apparent activity of Ni + Mo composite coatings towards hydrogen evolution in comparison with pure Ni matrix. For the Ni + Mo composite electrodes, increase of the amount of molybdenum particles embedded into Ni matrix causes simultaneously important increase in the apparent activity, increase in the electrochemically accessible surface area, and a small decrease in the intrinsic activity. (c) 2006 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1211 / 1218
页数:8
相关论文
共 20 条
[1]   Electrochemical investigation of the Ni-Cu-Mo electrodeposition system [J].
BeltowskaLehman, E ;
Chassaing, E .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1997, 27 (05) :568-572
[2]   THE STRUCTURAL IDENTIFIABILITY OF THE VOLMER-HEYROVSKY REACTION [J].
BERTHIER, F ;
DIARD, JP ;
MONTELLA, C ;
PRONZATO, L ;
WALTER, E .
JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1993, 90 (11-12) :2069-2081
[3]   Identifiability and distinguishability concepts in electrochemistry [J].
Berthier, F ;
Diard, JP ;
Pronzato, L ;
Walter, E .
AUTOMATICA, 1996, 32 (07) :973-984
[4]   Studies of the hydrogen evolution reaction on Raney nickel-molybdenum electrodes [J].
Birry, L ;
Lasia, A .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2004, 34 (07) :735-749
[5]   Hydrogen evolution on RuxTi1-xO2 in 0.5 M H2SO4 [J].
Borresen, B ;
Hagen, G ;
Tunold, R .
ELECTROCHIMICA ACTA, 2002, 47 (11) :1819-1827
[6]   A NONLINEAR LEAST-SQUARES FIT PROCEDURE FOR ANALYSIS OF IMMITTANCE DATA OF ELECTROCHEMICAL SYSTEMS [J].
BOUKAMP, BA .
SOLID STATE IONICS, 1986, 20 (01) :31-44
[7]   THE ANALYSIS OF ELECTRODE IMPEDANCES COMPLICATED BY THE PRESENCE OF A CONSTANT PHASE ELEMENT [J].
BRUG, GJ ;
VANDENEEDEN, ALG ;
SLUYTERSREHBACH, M ;
SLUYTERS, JH .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 176 (1-2) :275-295
[8]   STUDY OF THE KINETICS OF HYDROGEN EVOLUTION REACTION ON NICKEL-ZINC POWDER ELECTRODES [J].
CHEN, LL ;
LASIA, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1992, 139 (11) :3214-3219
[9]   ELECTRODEPOSITION AS A MEANS OF PRODUCING LARGE-SURFACE ELECTRODES REQUIRED IN WATER ELECTROLYSIS [J].
FAN, CL ;
PIRON, DL .
SURFACE & COATINGS TECHNOLOGY, 1995, 73 (1-2) :91-97
[10]   Kinetic analysis of hydrogen evolution at Ni-Mo alloy electrodes [J].
Jaksic, JM ;
Vojnovic, MV ;
Krstajic, NV .
ELECTROCHIMICA ACTA, 2000, 45 (25-26) :4151-4158