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Updated: May 11, 2025

Zinc-Sponge Battery Electrodes that Suppress Dendrites
Published on: September 29, 2020
Six-electron-conversion selenium cathodes stabilized by dead-selenium revitalizer for aqueous zinc batteries
Jingwei Du1, Jiaxu Zhang1, Xingyuan Chu1
1Faculty of Chemistry and Food Chemistry & Center for Advancing Electronics Dresden (cfaed), Technische Universität Dresden, Dresden, 01062, Germany.
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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