A Corrosion‐Resistant Amorphous/Crystalline Heterostructured Catalyst for Industrial‐Level Seawater Electrolysis in Membrane Electrode Assembly Electrolyzer

Abstract The oxygen evolution reaction (OER) is integral to the production of green hydrogen via seawater electrolysis. However, it faces significant challenges, including suboptimal catalytic activity, pronounced corrosion induced by Cl − ions, and restricted operational lifetimes. In this study, a heterostructured hybrid catalyst composed of an amorphous NiFe‐layered double hydroxide (LDH) and a crystalline NiMoO₄ is presented. Leveraging the synergistic coupling interactions, the NiFe‐LDH/NiMoO₄ demonstrates a remarkable OER performance in seawater electrolysis, requiring a minimal overpotential of merely 339 mV to attain an industrial‐level current density of 500 mA cm − 2 . Experimental findings reveal that the constructed NiFe‐LDH/NiMoO₄ architecture significantly enhances electron transfer between the Ni and Fe sites, resulting in the formation of high‐valent Ni species that are beneficial for OER catalysis. A mechanistic analysis elucidates the phenomenon whereby the integration of NiFe‐LDH and NiMoO₄ mitigates Cl − ions corrosion and optimizes the adsorption of vital oxygen‐containing intermediates, accelerating the kinetics of alkaline seawater OER and improving catalytic performance during the seawater electrolysis process.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-05-15
DOI
https://doi.org/10.1002/adfm.202417603
Citations
23
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
8.36

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article

A Corrosion‐Resistant Amorphous/Crystalline Heterostructured Catalyst for Industrial‐Level Seawater Electrolysis in Membrane Electrode Assembly Electrolyzer

Yingnan Liu, Cheng Lian, Qizhou Dai, Zhengfei Chen et al.
23 citations
Advanced Functional Materials
Electrocatalysts for Energy Conversion
8.36
article

A Corrosion‐Resistant Amorphous/Crystalline Heterostructured Catalyst for Industrial‐Level Seawater Electrolysis in Membrane Electrode Assembly Electrolyzer

Yingnan Liu, Cheng Lian, Qizhou Dai, Zhengfei Chen, Zhongjian Li, Kai Huang, Lecheng Lei, Yang Hou, Xiaohe Zheng, Jiadong Wu, Bin Yang, Lin Wang
article en
23 citations

Abstract

Abstract The oxygen evolution reaction (OER) is integral to the production of green hydrogen via seawater electrolysis. However, it faces significant challenges, including suboptimal catalytic activity, pronounced corrosion induced by Cl − ions, and restricted operational lifetimes. In this study, a heterostructured hybrid catalyst composed of an amorphous NiFe‐layered double hydroxide (LDH) and a crystalline NiMoO₄ is presented. Leveraging the synergistic coupling interactions, the NiFe‐LDH/NiMoO₄ demonstrates a remarkable OER performance in seawater electrolysis, requiring a minimal overpotential of merely 339 mV to attain an industrial‐level current density of 500 mA cm − 2 . Experimental findings reveal that the constructed NiFe‐LDH/NiMoO₄ architecture significantly enhances electron transfer between the Ni and Fe sites, resulting in the formation of high‐valent Ni species that are beneficial for OER catalysis. A mechanistic analysis elucidates the phenomenon whereby the integration of NiFe‐LDH and NiMoO₄ mitigates Cl − ions corrosion and optimizes the adsorption of vital oxygen‐containing intermediates, accelerating the kinetics of alkaline seawater OER and improving catalytic performance during the seawater electrolysis process.

Advanced Functional MaterialsVol. 35(42)
East China University of Science and Technology (CN), Ningbo University of Technology (CN), Zhejiang Energy Research Institute (CN), State Key Laboratory of Chemical Engineering (CN), Zhejiang University of Technology (CN), Zhejiang University (CN), Taizhou University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 2%
Electrocatalysts for Energy Conversion
8.36
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