Abstract
The successful implementation of direct seawater electrolysis for sustainable hydrogen production and seawater desalination hinges on the development of high-efficiency and durable catalysts. In this study, we report the fabrication of a self-supported bimetallic selenide heterostructure catalyst (NiSe2-RuSe2/NF), which achieves an ultralow overpotential of 26 mV at 10 mA cm−2 in natural seawater (unpurified, with 1 M KOH added), outperforming commercial Pt/C. Furthermore, it exhibits exceptional long-term stability, maintaining performance over 250 h at an industrial current density of 500 mA cm−2. Combined density functional theory (DFT) calculations and experimental analyses reveal that the heterostructure modulates the electronic structure, optimizing H* adsorption and enhancing HER catalytic activity. This work provides a straightforward yet effective strategy for designing highly active and efficient HER electrocatalysts for practical seawater electrolysis applications.
| Original language | English |
|---|---|
| Article number | 162567 |
| Journal | Chemical Engineering Journal |
| Volume | 512 |
| DOIs | |
| State | Published - 15 May 2025 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Bimetallic Selenides
- Electronic Interaction
- Heterostructure
- Hydrogen Evolution Reaction
- Seawater Electrolysis
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