Issue 3, 2025

An oxide-promoted, self-supported Ni4Mo catalyst for high current density anion exchange membrane water electrolysis

Abstract

Anionic exchange membrane (AEM) water electrolyzers are emerging as a cost-effective technology for green hydrogen production. However, state-of-the-art AEM electrolyzers rely on platinum group metal (PGM) catalysts for the hydrogen evolution reaction (HER). Currently, PGM-free HER catalysts exhibit inadequate activity and stability at high current densities in electrolyzer environments. Here, we report a simple electrodeposition method for a self-supported Ni4Mo–MoOx catalyst. This catalyst exhibits remarkable HER activity, as demonstrated both in three-electrode cells as well as in prototype AEM electrolyzers. In particular, the catalyst enables AEM electrolyzers to operate stably at current densities as high as 3 A cm−2, which had not been reported for a non-PGM HER catalyst. The performance (2 V@3 A cm−2) is comparable to the benchmark Pt/C, whereas the stability is even higher. Characterization and particularly operando X-ray diffraction and absorption spectroscopy reveal that the catalyst is an unconventional tetragonal Ni4Mo with a D1a superlattice whose surface contains in situ formed MoOx species. The cooperative action of MoOx and Ni4Mo enhances the volmer step of HER, attributing to the superior activity.

Graphical abstract: An oxide-promoted, self-supported Ni4Mo catalyst for high current density anion exchange membrane water electrolysis

Supplementary files

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Article information

Article type
Paper
Submitted
02 oct. 2024
Accepted
29 nov. 2024
First published
02 déc. 2024
This article is Open Access
Creative Commons BY license

Energy Environ. Sci., 2025,18, 1533-1543

An oxide-promoted, self-supported Ni4Mo catalyst for high current density anion exchange membrane water electrolysis

A. Serban, M. Liu, N. Chen, H. M. Chen and X. Hu, Energy Environ. Sci., 2025, 18, 1533 DOI: 10.1039/D4EE04528A

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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