A CuMo dual-doped Ni3S2 porous ultrathin nanosheet as an efficient bifunctional electrocatalyst for urea–water electrolysis

Abstract

The development of efficient and energy-saving electrocatalysts for urea-assisted hydrogen production has attracted considerable attention in sustainable energy technologies. In this work, a three-dimensional porous CuMo dual-doped Ni3S2 ultrathin nanosheet (CuMo–Ni3S2) catalyst was successfully synthesized via a one-step hydrothermal method on Ni foam. The synergistic doping of Cu and Mo elements induced a remarkable morphology transformation of Ni3S2 from nanofold structures to porous ultrathin nanosheets, significantly enhancing the electrochemical active surface area and exposing abundant active sites. The resulting catalyst exhibited excellent activity and durability for both the urea oxidation reaction (UOR) and the hydrogen evolution reaction (HER). Specifically, the catalyst required only 1.40 V (vs. RHE) to achieve a current density of 10 mA cm−2 for the UOR, and a low overpotential of 115 mV for the HER at the same current density. Notably, the catalyst maintained stable performance after 50 h of continuous operation with no significant activity decay. Furthermore, the overall urea electrolyzer constructed with CuMo–Ni3S2 as both UOR and HER catalysts only required a cell voltage of 1.55 V to deliver a current density of 10 mA cm−2. This study provides an effective approach for developing low-cost, high-performance electrocatalysts for sustainable hydrogen production through urea electrolysis.

Graphical abstract: A CuMo dual-doped Ni3S2 porous ultrathin nanosheet as an efficient bifunctional electrocatalyst for urea–water electrolysis

Supplementary files

Article information

Article type
Paper
Submitted
04 Jul 2025
Accepted
20 Aug 2025
First published
27 Aug 2025

New J. Chem., 2025, Advance Article

A CuMo dual-doped Ni3S2 porous ultrathin nanosheet as an efficient bifunctional electrocatalyst for urea–water electrolysis

J. Li, M. Song, X. Meng and X. Qi, New J. Chem., 2025, Advance Article , DOI: 10.1039/D5NJ02719E

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