TY - JOUR
T1 - Mortise-Tenon Joint Inspired Weakly Solvated Gel Electrolyte Based on Halogen Bonds for High-Voltage Lithium Metal Batteries
AU - Liu, Shuohan
AU - Tian, Wensheng
AU - Pan, Hui
AU - Chen, Shunwei
AU - Han, Xiujun
AU - Quan, Hengdao
AU - Zhu, Shenmin
N1 - Publisher Copyright:
© 2025 The Author(s). Advanced Science published by Wiley-VCH GmbH.
PY - 2025
Y1 - 2025
N2 - 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.
AB - 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.
KW - functional polymer frameworks
KW - gel electrolytes
KW - lithium metal batteries
KW - weak solvation structures
UR - https://www.scopus.com/pages/publications/105021839383
U2 - 10.1002/advs.202518448
DO - 10.1002/advs.202518448
M3 - Article
AN - SCOPUS:105021839383
SN - 2198-3844
JO - Advanced Science
JF - Advanced Science
ER -