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Rechargeable aqueous Zn–I2 batteries face challenges from zinc anode degradation (dendrites, corrosion) and polyiodide (I3−/I5−) shuttling at the cathode, limiting cycle life. To address these issues simultaneously, a novel ion-selective, solvation-regulating, and flexible sulfonic acid-based water reducer gel electrolyte (polyacrylamide (PAM)-polynaphthalene sulphonate (FDN)-carboxylated chitosan (CCS)/zinc sulfate (ZSO)) is designed in this work. This electrolyte features a three-dimensional (3D) porous structure and abundant polar groups enabling efficient Zn2+ transport and solvation structure regulation, promoting uniform zinc deposition and suppressing water-related side reactions (e.g., hydrogen evolution) at the anode. Crucially, the strongly negatively charged sulfonic acid groups impart exceptional ion selectivity: They electrostatically repel polyiodide anion, effectively blocking their shuttle to the anode and minimizing active iodine loss, while permitting unimpeded Zn2+ diffusion. Consequently, Zn–I2 full cells employing this multifunctional gel electrolyte achieve outstanding cycling stability, retaining 118.5 mAh·g−1 after 9000 cycles at 5 A·g−1. This work achieves the synergistic optimization of interface issues in Zn–I2 batteries by constructing an ion-selective multifunctional gel electrolyte, significantly enhancing their overall electrochemical performance.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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