Engineering cobalt molybdate nanosheet arrays with phosphorus-modified nickel as heterogeneous electrodes for...

Electrochemical urea electrolysis has been regarded as a promising strategy to replace traditional water-splitting technology to achieve hydrogen fuel due to its cost savings and high energy efficiency. Designing efficient bifunctional electrocatalysts easily is important but still faces significant challenges. Herein, an interface engineering strategy is used to construct a hybrid material by coupling cobalt molybdate (CoMoO₄) nanosheet arrays with phosphorus-modified nickel (P-Ni) particles on copper foam (P-Ni@CoMoO₄/CF) through the hydrothermal and in-situ electrodeposition process. Benefiting from the abundant catalytic active sites, low charge transfer resistance, and synergistic coupling effect, the optimal P-Ni@CoMoO₄/CF electrocatalyst presents a superior bifunctional activity for urea oxidation reaction (UOR) and hydrogen evolution reaction (HER). In detail, a small overpotential of 125 mV and a low potential of 1.36 V is required to attain the current density of 100 mA cm^-2 for HER and UOR, respectively. In the process of urea electrolysis, the P-Ni@CoMoO₄/CF-based electrolyzer provides a current density of 100 mA cm^-2 with an overall voltage of 1.50 V, about 170 mV less than that in a traditional water electrolyzer. The high performance of P-Ni@CoMoO₄/CF outperforms many recently reported electrodes, suggesting its promising application in energy-saving hydrogen production. Our work proposes a novel idea for the rational design and exploitation of low-cost and robust bifunctional electrodes for electrocatalysis.