A Fractal-Tip Cu₃Ni/NiMoO₄Heterostructure for Efficient Hydrogen Evolution via an Accelerated Volmer–Tafel Mechanism

Achieving hydrogen evolution at industrial current densities requires optimized kinetics involving electron transfer, catalytic reactions, and mass transport. Here we report a Cu₃Ni alloy and amorphous NiMoO₄heterostructure featuring a Romanesco-like fractal-tip architecture grown on a copper mesh. This cathode exhibits outstanding catalytic activity, requiring low overpotentials of 144.0 and 122.5 mV to reach 1 A cm^–2in 1 M KOH and 100 mA cm^–2in 1 M PBS, respectively, along with a Tafel slope as low as 27.2 mV dec^–1in alkaline media. It also maintains long-term durability over 3000 h at 1 A cm^–2with negligible degradation. At the Cu₃Ni/NiMoO₄interface, the distinct chemical environments of Ni atoms result in hydrogen affinity in Cu₃Ni and oxygen affinity in NiMoO₄, promoting water dissociation (H*–*OH). Experimental results and theoretical calculations reveal that the interface lowers the energy barrier for water dissociation and increases H* coverage, shifting the reaction mechanism from the Volmer–Heyrovsky pathway to the more efficient Volmer–Tafel route. Furthermore, the fractal-tip structure boosts HER kinetics by amplifying local electric fields, concentrating protons, and accelerating bubble release. This work provides a rational design strategy for improving hydrogen evolution kinetics through combined structural and interfacial optimization.