Self-supported Ni3S2 nanostructures on nickel foam as bifunctional electrodes for efficient urea oxidation and hydrogen evolution reactions
摘要
Developing low-cost, efficient bifunctional electrocatalysts for urea-assisted water splitting is of paramount importance for sustainable hydrogen production and wastewater remediation. Herein, we report the in-situ growth of nickel trisulfide (Ni3S2) nanostructures on nickel foam (NF) (denoted as Ni3S2@NF) via a simple hydrothermal method. The three-dimensional (3D) conductive architecture of NF provides robust mechanical support and efficient electron transport, while the Ni3S2 nanoparticles exhibit abundant active sites for electrocatalysis. Electrochemical measurements demonstrate that Ni3S2@NF delivers superior urea oxidation reaction (UOR) performance with a potential of 1.38 V versus RHE at 10 mA cm−2 and a Tafel slope of 48.38 mV dec−1 in 1 M KOH with 0.33 M urea, along with excellent hydrogen evolution reaction (HER) activity featuring a low overpotential of 192 mV and a Tafel slope of 83.02 mV dec−1 in the same electrolyte. When assembled into a two-electrode urea electrolyzer, Ni3S2@NF requires only 1.53 V to achieve 10 mA cm−2, significantly lower than the 1.76 V needed for conventional water splitting. This work provides a viable strategy for designing cost-effective bifunctional electrodes for energy-efficient hydrogen production coupled with urea oxidation reaction.
Graphical Abstract