Six-electron-conversion selenium cathodes stabilized by dead-selenium revitalizer for aqueous zinc batteries
Abstract Aqueous zinc batteries are attractive for large-scale energy storage due to their inherent safety and sustainability. However, their widespread application has been constrained by limited energy density, underscoring a high demand of advanced cathodes with large capacity and high redox pote...
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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-04-01
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| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-58859-3 |
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| Summary: | Abstract Aqueous zinc batteries are attractive for large-scale energy storage due to their inherent safety and sustainability. However, their widespread application has been constrained by limited energy density, underscoring a high demand of advanced cathodes with large capacity and high redox potential. Here, we report a reversible high-capacity six-electron-conversion Se cathode undergoing a ZnSe↔Se↔SeCl4 reaction, with Br−/Brn − redox couple effectively stabilizes the Zn | |Se cell. This Se conversion, initiated in a ZnCl2-based hydrogel electrolyte, presents rapid capacity decay (from 1937.3 to 394.1 mAh gSe −1 after only 50 cycles at 0.5 A gSe −1) primarily due to the dissolution of SeCl4 and its subsequent migration to the Zn anode, resulting in dead Se passivation. To address this, we incorporate the Br−/Brn − redox couple into the Zn | |Se cell by introducing bromide salt as an electrolyte additive. The generated Brn − species acts as a dead-Se revitalizer by reacting with Se passivation on the Zn anode and regenerating active Se for the cathode reaction. Consequently, the cycling stability of the Zn | |Se cell is improved, maintaining 1246.8 mAh gSe −1 after 50 cycles. Moreover, the Zn | |Se cell exhibits a specific capacity of 2077.6 mAh gSe −1 and specific energy of 404.2 Wh kg−1 based on the overall cell reaction. |
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| ISSN: | 2041-1723 |