Various platinum-free electrocatalysts have been explored for hydrogen evolution reaction in acidic solutions. However, in economical water-alkali electrolysers, sluggish water dissociation kinetics (Volmer step) on platinum-free electrocatalysts results in poor hydrogen-production activities. Here we report a MoNi₄ electrocatalyst supported by MoO₂ cuboids on nickel foam (MoNi₄/MoO₂@Ni), which is constructed by controlling the outward diffusion of nickel atoms on annealing precursor NiMoO₄ cuboids on nickel foam. Experimental and theoretical results confirm that a rapid Tafel-step-decided hydrogen evolution proceeds on MoNi₄ electrocatalyst. As a result, the MoNi₄ electrocatalyst exhibits zero onset overpotential, an overpotential of 15 mV at 10 mA cm⁻² and a low Tafel slope of 30 mV per decade in 1 M potassium hydroxide electrolyte, which are comparable to the results for platinum and superior to those for state-of-the-art platinum-free electrocatalysts. Benefiting from its scalable preparation and stability, the MoNi₄ electrocatalyst is promising for practical water-alkali electrolysers.

Engineering the water dissociation sites of MoS ₂ nanosheets can efficiently enhance the electrocatalytic hydrogen evolution under alkaline conditions.

Nanoporous bimetallic (Co_1−xFe_x)₂P phosphides with tuneable Co/Fe ratios exhibit versatile catalytic activities for highly efficient electrochemical water splitting.