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

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/cm2, which had not been reported for a non-PGM HER catalyst. The performance (2 V@3 A/cm2) 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

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-12-04
DOI
https://doi.org/10.5281/zenodo.14276766
Primary Topic
Hybrid Renewable Energy Systems
Type
article
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article

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

Zenodo (CERN European Organization for Nuclear Research)
Hybrid Renewable Energy Systems
article

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

article en

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/cm2, which had not been reported for a non-PGM HER catalyst. The performance (2 V@3 A/cm2) 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

Zenodo (CERN European Organization for Nuclear Research)
École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 54%
Hybrid Renewable Energy Systems
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