All‐Solid‐State Lithium Metal Batteries with Microdomain‐Regulated Polycationic Solid Electrolytes

G Guo Ye (State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China) X Xufeng Hong M Mengxue He J Junjie Song L Lujun Zhu (Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering) C Chengxi Zheng (International Centre for Quantum Materials Collaborative Innovation Centre of Quantum Matter Peking University Beijing 100871 China) Y Yue Ma Y Yun An (Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China) K Kaier Shen W Weize Shi Y Yongfeng Jia (Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering) M Muhammad Burhan Shafqat (Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China) P Peng Gao D Dingguo Xia (Beijing Key Laboratory of Theory and Technology for Advanced Batteries Materials, School of Materials Science and Engineering) F Fangfang Chen Q Quanquan Pang

Abstract

AbstractSolid polymer electrolytes (SPEs) are promising for high‐energy and high‐safety solid‐state lithium metal batteries (LMBs). Here, a polycationic solid electrolyte (PCSE) is described that leverages the inherent high thermal/chemical stability of the polycationic domain and the anion trapping (FMAT) effect of another fluorinated microdomain for stable and fast‐charging high‐voltage LMBs. Specifically, while the polycationic imidazolium backbone ensures high segmental flexibility facilitating the Li+ mobility, the fluorinated microdomain effectively traps the bis(trifluoromethanesulfonyl)imide anions by strong dipole interactions, imparting localized solvation and restricted mobility of the anions, as well as improved oxidation stability. As a result, the PCSE exhibits a high ionic conductivity of 1.4 mS cm−1, a high Li+ transference number of 0.50, and a wide electrochemical window of ∼5.5 V at 25 °C. By way of in situ thermal polymerization of the electrolyte within assembled cells, the PCSE enables ultra‐stable cycling of Li|LiNi0.8Co0.1Mn0.1O2 cells with a capacity retention of 98.1% after 500 cycles at 0.2 C at ambient temperatures. The work on the molecular design of PCSEs represents a fundamentally unique perspective for the rational design of SPEs with balanced properties that are historically challenging for high‐energy, long‐life, ambient‐temperature solid‐state LMBs.

Article Details

Volume / Issue Vol. 37, Issue 12
Published March 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (16)

G

Guo Ye

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China

X

Xufeng Hong

M

Mengxue He

J

Junjie Song

L

Lujun Zhu

Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering

C

Chengxi Zheng

International Centre for Quantum Materials Collaborative Innovation Centre of Quantum Matter Peking University Beijing 100871 China

Y

Yue Ma

Y

Yun An

Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China

K

Kaier Shen

W

Weize Shi

Y

Yongfeng Jia

Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering

M

Muhammad Burhan Shafqat

Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China

P

Peng Gao

D

Dingguo Xia

Beijing Key Laboratory of Theory and Technology for Advanced Batteries Materials, School of Materials Science and Engineering

F

Fangfang Chen

Q

Quanquan Pang