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Research Article | Open Access

Acetone CoSolvent Reconstructs the Zn2+ Solvation Sheath for Ultra-Stable Zinc-Ion Battery

Jinyu ZhangYu LiuXiaosheng ZhangLingyang XueLinlin Zhang ( )Xuying Liu( )
School of Materials Science and Engineering, Zhengzhou Key Laboratory of Flexible Electronic Materials and Thin-Film Technologies, Zhengzhou University, Zhengzhou 450001, China
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Abstract

The uncontrollable growth of zinc metal dendrites and the water-induced parasitic reaction in pure aqueous electrolyte cause the poor cycling stability of zinc ion battery. Herein, a stable electrode/electrolyte interface with a dendrite-free zinc anode is developed by adding acetone into the aqueous electrolyte. The as-formed water/acetone hybrid solvent effectively optimizes the Zn2+ solvation structure (coordinated water changes from 6 to 4) and induces the uniform zinc ion deposition through the high adsorption energy with the Zn (002) surface. It also stabilizes the zinc metal by reducing the corrosion reaction (hydrogen evolution) with water and the formation of a basic zinc salt by-product. As a result, the symmetrical cell with the acetone/water electrolyte exhibits a superior stability of 3700 h (154 days) at 1 mA cm−2. The battery with the Na2V6O16·3H2O cathode delivers an 84.1% capacity retention after 1000 cycles at 1.0 A g−1. The organic/aqueous electrolyte provides a new insight into understanding the relationship between solvation structure, electrode/electrolyte interface, and the performance of the zinc ion battery.

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Cite this article:
Zhang J, Liu Y, Zhang X, et al. Acetone CoSolvent Reconstructs the Zn2+ Solvation Sheath for Ultra-Stable Zinc-Ion Battery. Energy & Environmental Materials, 2026, 9(1). https://doi.org/10.1002/eem2.70098

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Received: 12 April 2025
Revised: 26 June 2025
Published: 05 July 2025
© 2025 The Author(s).

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.