Abstract

The electrocatalytic behavior of electrodeposited Ni and Ni–Mo alloy coatings in the hydrogen evolution reaction in a 1 M NaOH aqueous solution was investigated by means of the electrochemical impedance spectroscopy method. The electrochemical deposition of electrocatalytic coatings was carried out using electrolytes based on deep eutectic solvents (eutectic mixtures of choline chloride with ethylene glycol or urea). To simulate the recorded Nyquist plots reflecting the electrocatalytic performance of deposited coatings, a modified Armstrong-Henderson equivalent circuit was employed, which accounts for the involvement of adsorbed intermediates in the reaction. The equivalent circuit included three polarization resistances and three constant phase elements, allowing for the consideration of the localization of the electrochemical process on different surface microdomains. It was found that the electrocatalytic activity of nickel coatings deposited from deep eutectic solvents exceeded the activity of nickel fabricated in an aqueous electrolyte. The increase in molybdenum content in the coating was shown to enhance electrocatalytic activity. It was established that the main reasons for improving the electrocatalytic properties of the Ni–Mo alloy coatings are structural-morphological factors (increase in the degree of microheterogeneity of the surface and the development of the surface area available for electrochemical reaction) and the formation of a favorable electronic structure of the metal, leading to the acceleration of the rate-determining Volmer step.

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