Mortise-Tenon Joint Inspired Weakly Solvated Gel Electrolyte Based on Halogen Bonds for High-Voltage Lithium Metal Batteries

  • Shuohan Liu
  • , Wensheng Tian
  • , Hui Pan*
  • , Shunwei Chen
  • , Xiujun Han*
  • , Hengdao Quan*
  • , Shenmin Zhu*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

In situ gel polymer electrolytes (GPEs) offer a promising approach to improve safety and cycling stability in lithium metal batteries (LMBs), yet often suffer from poor electrode compatibility, especially at high temperatures. This work reports a “mortise-tenon joint” inspired non-covalent interaction — “π-hole” based halogen bond, that enables solvation structure regulation beyond traditional van der Waals force or hydrogen bond. The electrophilic π-hole on the polymer skeleton engages in halogen bonding with solvents, thereby weakening their coordination with Li+ to form a weakly solvated structure. Moreover, the fluorine-rich skeleton participates in the formation of the electrode-electrolyte interphases, achieving good anode compatibility and high-voltage stability simultaneously. The resulting electrolyte exhibits high ionic conductivity (0.30 mS cm−1) and a Li+ transference number of 0.84. Li symmetric cells stably cycle over 1000 h. The Li/LiNi0.8Co0.1Mn0.1O2 (NCM811) cell delivers discharge specific capacities of 161.0 mAh g−1 after 500 cycles at 1C. Especially, the cell can work stably for 100 cycles at 80 °C (1C, 156.0 mAh g−1). Furthermore, the pouch cell achieves an energy density of 462.2 Wh kg−1. This study demonstrates that the concept of a weakly solvated gel electrolyte based on halogen bonds provides a new approach to achieving high-energy-density LMBs.

Original languageEnglish
JournalAdvanced Science
DOIs
Publication statusAccepted/In press - 2025
Externally publishedYes

Keywords

  • functional polymer frameworks
  • gel electrolytes
  • lithium metal batteries
  • weak solvation structures

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