Abstract
Nickel-molybdenum, nickel-zinc, nickel-cobalt, nickel-tungsten, nickel-iron and nickel chromium binary alloy codeposits, obtained through electrodeposition methods on mild steel strips, have been characterized with the objective of qualitatively comparing and assessing their electrocatalytic activities as hydrogen electrodes in alkaline solution. It has been concluded that their electrocatalytic effects for the hydrogen evolution reaction rank in the following order: Ni-Mo > Ni-Zn (after leaching Zn in KOH) > Ni-Co > Ni-W > Ni-Fe > Ni-Cr > Ni plated steel. Further investigations on the alloy electrocatalysts have revealed that the cathodic overpotential contribution to the electrolysis voltage can be brought down by 0.3 V when compared with conventional cathodes. The best and most stable hydrogen evolving cathode, based on nickel-molybdenum alloy, exhibited an overpotential of about 0.18 V for over 1500 h of continuous electrolysis in 6m KOH at 300 mA cm−2 and 353 K. The salient features of the coatings, such as physical characteristics, chemical composition, crystal structure of the alloy phases and the varying effects of the catalytic activation method were analysed with a view to correlating the micro-structural characteristics of the coatings with the hydrogen adsorption process. The stability under open-circuit conditions, the tolerance to electrochemical corrosion and the long term stability of nickel-molybdenum alloy cathodes were very encouraging. An attempt to identify the pathway for the hydrogen evolution reaction on these alloy coatings was made, in view of the very low apparent activation energy values obtained experimentally.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
I. Arul Raj and V. K. Venkatesan,Int. J. Hydrogen Energy 13 (1988) 215.
,Trans. SAEST 22 (1987) 189.
I. Arul Raj, K. Venkateswara Rao and V. V. Venkatesan,Bull. Electrochem. 2 (1986) 157.
D. E. Hall, J. M. Sarver and D. O. Gothard,Int. J. Hydrogen Energy 13 (1988) 547.
J. Divesk, P. Malinowski, J. Margel and H. Schmitz,13 (1988) 841.
M. R. Gennero de Chialvo and A. C. Chialvo,Electrochim. Acta 33 (1988) 825.
G. Fiori and C. M. Mari,Int. J. Hydrogen Energy 12 (1987) 159.
M. M. Jaksić,12 (1987) 727.
D. E. Brown, M. N. Mahmood, M. C. M. Man and A. K. Turner,Electrochim. Acta 29 (1984) 1551.
M. B. Janjua and R. L. Le Roy,Int. J. Hydrogen Energy 10 (1985) 11.
A. Brenner, in ‘Electrodeposition of Alloys, Principles and Practice’, Vol. 2, Academic, New York (1963) p. 430.
H. Wendt and V. Plzak,Electrochim. Acta 28 (1983) 27.
E. Beltowska-Lehman and K. Vu Quang,Surf. Coat. Technol. 27 (1986) 75.
C. Karwas and T. Hepel,J. Electrochem. Soc. 135 (1988) 839.
D. E. Hall,128 (1981) 740.
P. W. T. Lu and S. Srinivasan,125 (1978) 265.
B. Tereszko, A. Risenkampf and K. Vu Quang,Surf. Coat. Technol. 12 (1981) 301.
A. T. Wasko, ‘Electrochimia molibdena i wolframa’, Izd. Naukowa Dunka, Kiev (1977).
A. Nidola and R. Schira, in Proceedings of the Symposium Advances in Chlor Alkali and Chlorate Industry (edited by E. M. Spore and M. M. Silver), The Electrochemical Society, Pennington, New York (1984) p. 206.
E. R. Gonzales, L. A. Avaca, A. Carubelli, A. A. Tanaka and G. Tremiliosi-Filho,Int. J. Hydrogen Energy 9 (1984) 689.
D. E. Brown, M. N. Mahmood, A. K. Turner, S. M. Hall and P. O. Fogarty,7 (1982) 405.
B. E. Conway, H. Angerstein-Kozlowska, M. A. Sattar and B. V. Tilak,J. Electrochem. Soc.,130 (1983) 1825.
B. E. Conway and L. Bai,Int. J. Hydrogen Energy 11 (1986) 533.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Raj, I.A., Vasu, K.I. Transition metal-based hydrogen electrodes in alkaline solution — electrocatalysis on nickel based binary alloy coatings. J Appl Electrochem 20, 32–38 (1990). https://doi.org/10.1007/BF01012468
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF01012468