High-conductivity NiFe@Ni@Cu composite electrodes for durable and efficient industrial oxygen evolution

Abstract

The oxygen evolution reaction (OER) is a key bottleneck in water electrolysis due to its sluggish kinetics. Although nickel–iron layered double hydroxides (NiFe LDHs) are promising OER catalysts in alkaline media, their low electrical conductivity hinders industrial-scale applications. Copper mesh substrates offer excellent conductivity and low cost but suffer from poor corrosion resistance, limiting their use as electrode supports. Herein, we report a self-supported NiFe@Ni@Cu composite electrode, fabricated by sequential electrodeposition of a nickel interlayer and Ni3Fe alloy–NiFe LDH hybrid nanosheets onto a copper mesh. This hierarchical structure synergistically combines the high conductivity of copper and the corrosion resistance of the nickel interlayer, leading to a substantial enhancement in OER activity and stability. The electrode shows a low overpotential of 283 mV at 100 mA cm−2 and a Tafel slope of 33.4 mV dec−1 in 1 M KOH. As a full water-splitting electrocatalyst, it operates stably at 500 mA cm−2, with a 23.3% reduction in cell voltage compared to NiFe@Ni, and demonstrates outstanding durability under industrial conditions (30 wt% KOH, 80 °C) for over 80 hours. Moreover, coupled with a NiFe@Ni@Cu cathode, the integrated electrolyzer delivers 100 mA cm−2 at 1.53 V. This substrate engineering strategy offers a scalable and cost-effective approach to efficient and durable alkaline water electrolysis.

Graphical abstract: High-conductivity NiFe@Ni@Cu composite electrodes for durable and efficient industrial oxygen evolution

Supplementary files

Article information

Article type
Paper
Submitted
16 Aug 2025
Accepted
29 Oct 2025
First published
03 Nov 2025

New J. Chem., 2026, Advance Article

High-conductivity NiFe@Ni@Cu composite electrodes for durable and efficient industrial oxygen evolution

Y. Zhu, X. Zheng, S. Ming, H. Li, X. Han, Y. Wang, H. Li and Z. Wang, New J. Chem., 2026, Advance Article , DOI: 10.1039/D5NJ03318G

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