Construction of Fe regulated NiMoN nanorods as an efficient electrocatalyst for overall water splitting and urea electrolysis

Abstract

Rational design of low-cost, highly-efficient electrocatalysts for hydrogen and oxygen evolution reactions (HER/OER) is critical to enable sustainable hydrogen production via water electrolysis. Herein, a novel nanorod arrays catalyst, Fe-NiMoN, has been rationally designed and directly grown on nickel foam (NF) via a facile hydrothermal method followed by a nitridation treatment. The novel 3D porous nanorod architecture is favorable for providing abundant active sites, accelerating mass diffusion/electron transfer, and facilitating gas release. In addition, density functional theory (DFT) simulations reveal that Fe doping shifts the d-band center of NiMoN away from the Fermi level compared to the undoped NiMoN, thereby reducing the hydrogen adsorption free energy (ΔGH*) toward 0, and which in turn enhances the HER activity. Consequently, the Fe-NiMoN catalyst delivers exceptional bifunctional electrocatalytic activity in alkaline media, requiring low overpotentials of 17 mV (HER) and 238 mV (OER) to achieve 10 mA cm–2. Notably, the Fe-NiMoN catalyst assembled into a two-electrode alkaline electrolyzer, requires only a voltage of 1.504 to achieve a current density value of 10 mA cm−2, with no performance declining after 100 h of steady operation. Moreover, for urea-assisted electrolysis, it can deliver 10 mA cm−2 at only 1.367 V. Overall, this work provides a strategy for synthesizing desirable electrocatalysts for green hydrogen production coupled with wastewater treatment.

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Article information

Article type
Paper
Submitted
22 Aug 2025
Accepted
06 Nov 2025
First published
11 Dec 2025

Nanoscale, 2025, Accepted Manuscript

Construction of Fe regulated NiMoN nanorods as an efficient electrocatalyst for overall water splitting and urea electrolysis

L. Liu, L. Chen, H. Zhang, M. Humayun, Y. Liu, J. Duan, Y. Fu, M. Bououdina, X. Xue and C. Wang, Nanoscale, 2025, Accepted Manuscript , DOI: 10.1039/D5NR03552J

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