A Strongly Coupled Cluster Heterostructure with Pt–N-Mo Bonding for Durable and Efficient H2 Evolution in Anion-Exchange Membrane Water Electrolyzers

Creating strongly coupled heterostructures with favorable catalytic activities is crucial for promoting the performance of catalytic reactions, especially those involve multiple intermediates. Herein, we fabricated a strongly coupled platinum/molybdenum nitrides nanocluster heterostructure on nitrogen-doped reduced graphene oxide (Pt/Mo₂N-NrGO) for alkaline hydrogen evolution reaction. The well-defined Pt-containing Anderson-type polyoxometalates promote strong interfacial Pt-N-Mo bonding in Pt/Mo<sub>2</sub>N-NrGO, which exhibits a remarkably low overpotential, high mass activity, and exceptional long-term durability (> 500 h at 1500 mA cm⁻<sup>2</sup>) in an anion-exchange membrane water electrolyzer (AEMWE). Operando Raman spectroscopy and density functional theory reveal that pronounced electronic coupling at the Pt/Mo₂N cluster interface facilitates the catalytic decomposition of H<sub>2</sub>O through synergistic stabilization of intermediates (Pt-H* and Mo-OH*), thereby enhancing the kinetics of the rate-determining Volmer step. Techno-economic analysis indicates a levelized hydrogen production cost of $2.02 kg⁻<sup>1</sup>, meeting the US DOE targets. Our strategy presents a viable pathway to designing next-generation catalysts for industrial AEMWE for green hydrogen production.

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Publication Details

Journal
Nano-Micro Letters
Published
2025-06-13
DOI
https://doi.org/10.1007/s40820-025-01798-x
Citations
12
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
4.36

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article

A Strongly Coupled Cluster Heterostructure with Pt–N-Mo Bonding for Durable and Efficient H2 Evolution in Anion-Exchange Membrane Water Electrolyzers

Jing Hua Gu, Wenpei Gao, Hanqing Cai, Zhuangjun Fan et al.
12 citations
Nano-Micro Letters
Electrocatalysts for Energy Conversion
4.36
article

A Strongly Coupled Cluster Heterostructure with Pt–N-Mo Bonding for Durable and Efficient H2 Evolution in Anion-Exchange Membrane Water Electrolyzers

Jing Hua Gu, Wenpei Gao, Hanqing Cai, Zhuangjun Fan, Zhiqing Tang, Lianming Zhao, Meihong Liao, Lulu Chen, Kai Chen, Haitao Li, Tao Wang, Chao Zhang, Yichao Huang, Wenbo Zhou, Zhenhai Wen
article en
12 citations

Abstract

Creating strongly coupled heterostructures with favorable catalytic activities is crucial for promoting the performance of catalytic reactions, especially those involve multiple intermediates. Herein, we fabricated a strongly coupled platinum/molybdenum nitrides nanocluster heterostructure on nitrogen-doped reduced graphene oxide (Pt/Mo₂N-NrGO) for alkaline hydrogen evolution reaction. The well-defined Pt-containing Anderson-type polyoxometalates promote strong interfacial Pt-N-Mo bonding in Pt/Mo<sub>2</sub>N-NrGO, which exhibits a remarkably low overpotential, high mass activity, and exceptional long-term durability (> 500 h at 1500 mA cm⁻<sup>2</sup>) in an anion-exchange membrane water electrolyzer (AEMWE). Operando Raman spectroscopy and density functional theory reveal that pronounced electronic coupling at the Pt/Mo₂N cluster interface facilitates the catalytic decomposition of H<sub>2</sub>O through synergistic stabilization of intermediates (Pt-H* and Mo-OH*), thereby enhancing the kinetics of the rate-determining Volmer step. Techno-economic analysis indicates a levelized hydrogen production cost of $2.02 kg⁻<sup>1</sup>, meeting the US DOE targets. Our strategy presents a viable pathway to designing next-generation catalysts for industrial AEMWE for green hydrogen production.

Nano-Micro LettersVol. 17(1)
San Diego State University (US)
National Natural Science Foundation of China, Chinese Academy of Sciences, Shanghai Jiao Tong University, Natural Science Foundation of Shandong Province, Institute of High Energy Physics, Fundamental Research Funds for the Central Universities, Beijing Synchrotron Radiation Facility, High Energy Physics
Openalex Percentile: Top 5%
Electrocatalysts for Energy Conversion
4.36
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