Author
Listed:
- Yuan, Yubin
- Sun, Shengwei
- Chen, Feng
- Zhao, Zikang
- Wang, Tianshuo
- Ma, Xiangyuan
- Xie, Tianxiao
- Luo, Yide
- Zhou, Zongtai
- Zhou, Junshuang
- Gao, Faming
Abstract
Seawater electrolysis powered by renewable energy sources, such as solar and wind, presents a promising approach for green hydrogen production, but still faces some challenges. In this study, we developed a highly efficient seawater electrolysis catalyst, SNiFeMo@NF, featuring a unique nanowire-flower structure. SNiFeMo@NF exhibits outstanding bifunctional catalytic activity for seawater electrolysis. The introduction of sulfur to adjust the electronic structure of the catalyst, along with the incorporation of molybdate (MoO42−) to boost OH− adsorption, dramatically improved both catalytic activity and resistance to chloride-induced corrosion. In natural seawater with 6 M KOH, SNiFeMo@NF demonstrates remarkable stability, operating continuously for 300 h. At a current density of 100 mA cm−2, it achieves low overpotentials of 95 mV for the hydrogen evolution reaction (HER) and 236 mV for the oxygen evolution reaction (OER). In industrial settings (6 M KOH, 80 °C), an electrolyzer utilizing SNiFeMo@NF as the catalyst attained a current density of 100 mA cm−2 with a cell voltage of just 1.46 V. The low energy consumption of the electrolyzer, combined with its integration with solar cells, underscores the economic viability and feasibility of renewable energy-driven seawater electrolysis for hydrogen production. This study offers fresh insights into hydrogen generation via seawater electrolysis.
Suggested Citation
Yuan, Yubin & Sun, Shengwei & Chen, Feng & Zhao, Zikang & Wang, Tianshuo & Ma, Xiangyuan & Xie, Tianxiao & Luo, Yide & Zhou, Zongtai & Zhou, Junshuang & Gao, Faming, 2026.
"Nanowire-flower structured catalysts regulated by MoO42−/SO42− dual anion layers for efficient seawater electrolysis,"
Renewable Energy, Elsevier, vol. 256(PC).
Handle:
RePEc:eee:renene:v:256:y:2026:i:pc:s096014812501777x
DOI: 10.1016/j.renene.2025.124113
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