Abstract
AbstractIn aqueous zinc (Zn) batteries, the Zn anode suffers from severe corrosion reactions and consequent dendrite growth troubles that cause fast performance decay. Herein, we uncover the corrosion mechanism and confirm that the dissolved oxygen (DO) other than the reputed proton is a principal origin of Zn corrosion and by‐product precipitates, especially during the initial battery resting period. In a break from common physical deoxygenation methods, we propose a chemical self‐deoxygenation strategy to tackle the DO‐induced hazards. As a proof of concept, sodium anthraquinone‐2‐sulfonate (AQS) is introduced to aqueous electrolytes as a self‐deoxidizing additive. As a result, the Zn anode sustains a long‐term cycling of 2500 h at 0.5 mA cm−2 and over 1100 h at 5 mA cm−2 together with a high Coulombic efficiency up to 99.6 %. The full cells also show a high capacity retention of 92 % after 500 cycles. Our findings provide a renewed understanding of Zn corrosion in aqueous electrolytes and also a practical solution towards industrializing aqueous Zn batteries.
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Metrics
114
Citations
30
References
Details
Published
Jun 06, 2023
Vol/Issue
62(28)
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Authors
Funding
National Natural Science Foundation of China Award: 22109116
Fundamental Research Funds for the Central Universities
China Postdoctoral Science Foundation Award: 2022T150468
National Key Research and Development Program of China Award: 2022YFB2404500
Cite This Article
Rui Sun, Daliang Han, Changjun Cui, et al. (2023). A Self‐Deoxidizing Electrolyte Additive Enables Highly Stable Aqueous Zinc Batteries. Angewandte Chemie International Edition, 62(28). https://doi.org/10.1002/anie.202303557
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