Abstract

Active layers for hydrogen evolution were prepared electrolytically from nickel-plating baths containing various amounts of thiourea. The sulphur content of the deposited layers, which is dependent on the thiourea content of the electroplating bath, ranged between 10 and 20 wt%. X-ray photoelectron spectroscopic (XPS) analysis revealed that sulphur was present in the layers not only in the form of sulphide, but also in the forms of thiourea and sulphate entrained from the nickel-plating bath. X-ray diffraction analysis showed that the coatings were poorly crystalline. Nickel sulphide, which produces an X-ray diffraction pattern, was present only in coatings deposited from baths with higher amounts of thiourea. The surface layers of such coatings contained a maximum of 10 at % nickel in the form of Ni3S2. When the Ni−Sx electrodes were under load in 1m KOH over a long period, the hydrogen overpotential was found to vary with time. On the basis of XPS measurements, the initial decrease in hydrogen overpotential was ascribed to the washing-out of adsorbed residues of thiourea. The subsequent increase in the overpotential was due to the deposition of iron on to the surface of the layers from the electrolyte used.

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