Abstract
The hydrogen evolution reaction (HER) on polished pure cobalt cathodes in 30 w/o KOH at 70°C in the presence of dissolved metallic impurities has been investigated in constant current and potential modes combined with the potential-sweep method. Potentiostatic tests show that the cell current decreases with time during the first 1000 s, which is tentatively attributed to the penetration of atomic hydrogen into the metal lattice. The deposition of copper, iron and zinc, observed after several hours' incubation significantly influences the Tafel parameters for HER.
Marked improvement in the electrocatalytic activity of the cathode in the presence of dissolved sodium molybdate is ascribed mainly to the deposition of molybdenum on the electrode surface, which lowers the Tafel slope and considerably increases the exchange-current density. The current increase is observed after an incubation period which is closely related to the concentration of dissolved sodium molybdate, whereas the rate of current increase with time is largely influenced by the applied potential.
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Huot, J.Y., Brossard, L. In situ activation of cobalt cathodes in alkaline water electrolysis. J Appl Electrochem 18, 815–822 (1988). https://doi.org/10.1007/BF01016036
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DOI: https://doi.org/10.1007/BF01016036