Tuning Ion Transport at the Anode‐Electrolyte Interface via a Sulfonate‐Rich Ion‐Exchange Layer for Durable Zinc‐Iodine Batteries

  • Leiqian Zhang
    School of Chemical Engineering Zhengzhou University Zhengzhou 450001 P. R. China
  • Jiajia Huang
    School of Chemical Engineering Zhengzhou University Zhengzhou 450001 P. R. China
  • Hele Guo
    Department of Chemistry KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium
  • Lingfeng Ge
    School of Chemistry University of Bristol Cantock's Close Bristol BS8 1TS UK
  • Zhihong Tian
    Engineering Research Center for Nanomaterials Henan University Kaifeng 475004 P. R. China
  • Mingjie Zhang
    School of Chemical Engineering Zhengzhou University Zhengzhou 450001 P. R. China
  • Guanjie He
    Electrochemical Innovation Lab Department of Chemical Engineering University College London London WC1E 7JE UK
  • Tianxi Liu
    Key Laboratory of Synthetic and Biological Colloids Ministry of Education School of Chemical and Material Engineering Jiangnan University Wuxi 214122 P. R. China
  • Johan Hofkens
    Department of Chemistry KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium
  • Dan J.L. Brett
    Electrochemical Innovation Lab Department of Chemical Engineering University College London London WC1E 7JE UK
  • Jingtao Wang
    School of Chemical Engineering Zhengzhou University Zhengzhou 450001 P. R. China
  • Feili Lai
    Department of Chemistry KU Leuven Celestijnenlaan 200F 3001 Leuven Belgium

書誌事項

公開日
2023-02-05
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/aenm.202203790
公開者
Wiley

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説明

<jats:title>Abstract</jats:title><jats:p>Rechargeable aqueous zinc‐iodine batteries (ZIBs) are considered a promising newly‐developing energy‐storage system, but the corrosion and dendritic growth occurring on the anode seriously hinder their future application. Here, the corrosion mechanism of polyiodide is revealed in detail, showing that it can spontaneously react with zinc and cause rapid battery failure. To address this issue, a sulfonate‐rich ion‐exchange layer (SC‐PSS) is purposely constructed to modulate the transport and reaction chemistry of polyiodide and Zn<jats:sup>2+</jats:sup> at the zinc/electrolyte interface. The resulting ZIBs can work properly over 6000 cycles with high‐capacity retention (90.2%) and reversibility (99.89%). Theoretical calculations and experimental characterization reveal that the SC‐PPS layer blocks polyiodide permeation through electrostatic repulsion, while facilitating desolvation of Zn(H<jats:sub>2</jats:sub>O)<jats:sub>6</jats:sub><jats:sup>2+</jats:sup> and restricting undesirable 2D diffusion of Zn<jats:sup>2+</jats:sup> by chemisorption.</jats:p>

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