Issue 42, 2025, Issue in Progress

Ruthenium-based electrocatalyst for efficient acidic water oxidation in PEM water electrolysis for H2 production

Abstract

Proton exchange membrane (PEM) water electrolysis is a promising and sustainable technology for hydrogen production. Currently, the anode catalysts used in PEM water electrolysis are predominantly iridium-based electrocatalysts, which are extremely precious and scarce. In this study, we report a mixed (Ru–W)Ox catalyst as a promising alternative to iridium-based catalysts. The (Ru–W)Ox catalyst was synthesized using a simple Pechini–Adams method, and its microstructure and electrochemical performance were optimized by controlling the Ru/W doping ratio and the synthesis temperature. Among the synthesized catalysts, the Ru6W4Ox catalyst prepared at 400 °C demonstrated the best oxygen evolution reaction (OER) activity and stability, achieving an overpotential of only 140.32 mV at 10 mA cm−2. Furthermore, after a 150 hours stability test, no significant loss in catalytic activity was observed. When applied to the anode of a PEM water electrolyzer, the Ru6W4Ox-400 °C catalyst exhibited an impressively low cell voltage of 1.784 V at 2 A cm−2. The energy consumption is as low as 4.34 kWh m−3 H2. These results provide new insights for developing efficient and stable non-iridium-based OER catalysts for PEM water electrolysis.

Graphical abstract: Ruthenium-based electrocatalyst for efficient acidic water oxidation in PEM water electrolysis for H2 production

Supplementary files

Article information

Article type
Paper
Submitted
17 Jul 2025
Accepted
17 Sep 2025
First published
23 Sep 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 34991-35002

Ruthenium-based electrocatalyst for efficient acidic water oxidation in PEM water electrolysis for H2 production

Y. Tao, R. Zhang, J. Chen, W. Weng, Y. He and Z. Wang, RSC Adv., 2025, 15, 34991 DOI: 10.1039/D5RA05145B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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