Urea-assisted water electrolysis integrated by a urea
oxidation
reaction (UOR) and a hydrogen evolution reaction (HER) is an efficient
strategy for energy-saving hydrogen production. However, its practical
application requires catalysts with sufficient durability and high-strength
reactant/product diffusion capability under large current densities.
Herein, the Co0.5NiS2–Ni3S2 coral-like nanorods (Co0.5NiS2–Ni3S2/NF) of electronic structure and morphology regulation
are rationally constructed. The heterostructure and sulfur vacancies
induce interfacial charge redistribution, thus promoting the adsorption
of urea and *OH intermediates, accompanied by accelerating the dissociation
of H2O. Moreover, the hierarchical nanorod structure ensures
mass transfer and gas product rapid escape. As a result, Co0.5NiS2–Ni3S2/NF only takes
1.45 V and −345 mV to reach large current densities of ±1500
mA cm–2 for the UOR and HER, respectively. Notably,
the overall urea electrolysis system needs only 2.00 V to obtain 1500
mA cm–2, and it can operate stably for 120 h at
500 mA cm–2. This work illustrates the importance
of regulating the adsorption energy of intermediates to design advanced
catalysts for energy-efficient H2 production from urea
electrolysis.