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- Language
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- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
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Received April 19, 2025
Revised May 24, 2025
Accepted June 7, 2025
Available online December 25, 2025
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This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits
unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Development of Co(OH)2/FeOOH Heterostructured Electrode via Sacrificial Template Strategy for Anion Exchange Membrane Water Electrolyzer
https://doi.org/10.1007/s11814-025-00498-x
Abstract
Improving the efficiency of water electrolysis is essential for reducing electrical energy consumption and enabling costeffective
hydrogen production. Among the key challenges, the oxygen evolution reaction (OER) remains a major bottleneck
due to its inherently sluggish kinetics. Although platinum group metal (PGM)-based electrocatalysts offer high OER activity,
their high-cost limits large-scale commercialization. In this study, we developed a non-PGM-based heterostructured
electrocatalyst composed of Co(OH)2 and FeOOH (Co(OH)2–FeOOH/NF) on commercial nickel foam (NF), synthesized
via a sacrificial template method using zeolitic imidazolate framework-67 (ZIF-67). The Co(OH)2–FeOOH/NF electrode
demonstrated outstanding OER performance, primarily due to the synergistic interaction between Co(OH)2 and FeOOH.
When applied to an anion exchange membrane water electrolyzer (AEM electrolyzer), the system achieved a hydrogen
production efficiency of 46.7 kWh kg−
1
H2, highlighting the strong potential of Co(OH)2–FeOOH/NF as a cost-effective and
efficient alternative to conventional PGM-based OER electrode.

