In Situ Polymerized Polyfluorinated Crosslinked Polyether Electrolytes for High‐Voltage Lithium Metal Batteries

S Shimei Li (Department of Mechanical Engineering) H Hu Hong (Department of Mechanical Engineering) X Xinru Yang (Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China) D Dedi Li (Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China) Q Qi Xiong (Department of Materials Science and Engineering) D Dechao Zhang (Department of Mechanical Engineering) S Shixun Wang (Department of Mechanical Engineering) Z Zhaodong Huang (Department of Chemical and Biological Engineering, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China) H Haiming Lv (Department of Materials Science and Engineering City University of Hong Kong 83 Tat Chee Avenue Hong Kong SAR 999077 P. R. China) C Chunyi Zhi (Department of Mechanical Engineering)

Abstract

AbstractIn situ polymerized polyether electrolytes are promising for solid‐state Li metal batteries due to their high ionic conductivity and excellent interfacial contact. However, their practical application is hindered by Li dendrite formation, interfacial degradation, and limited oxidative stability. Herein, we propose an in situ polymerized polyfluorinated crosslinked polyether electrolyte (PDOL‐OFHDBO), synthesized by copolymerizing 1,3‐dioxolane (DOL) with 2,2′‐(2,2,3,3,4,4,5,5‐octafluorohexane‐1,6‐diyl)bis(oxirane) (OFHDBO) as a polyfluorinated crosslinker. The electron‐withdrawing polyfluorinated groups endow PDOL‐OFHDBO with enhanced oxidative stability and interfacial compatibility, while reducing the solvation power of the polymer matrix to promote an anion‐derived inorganic‐rich solid electrolyte interphase for uniform Li deposition. Consequently, PDOL‐OFHDBO exhibits a wide electrochemical stability window (>5.6 V) and enables long‐term stable Li plating/stripping for over 1100 h. Furthermore, Li||LiNi0.8Co0.1Mn0.1O2 (NCM811) full cells utilizing PDOL‐OFHDBO demonstrate outstanding cycling stability with high‐loading cathodes (≈3.8 mAh cm−2) and thin Li anodes (50 µm), achieving capacity retention of 95.5% and 89.1% over 100 cycles at cut‐off voltages of 4.3 and 4.5 V, respectively. Remarkably, Ah‐level Li||NCM811 pouch cells deliver an impressive specific energy of 401.8 Wh kg−1, highlighting their potential for practical solid‐state Li metal batteries.

Article Details

Volume / Issue Vol. 37, Issue 29
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

S

Shimei Li

Department of Mechanical Engineering

H

Hu Hong

Department of Mechanical Engineering

X

Xinru Yang

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China

D

Dedi Li

Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China

Q

Qi Xiong

Department of Materials Science and Engineering

D

Dechao Zhang

Department of Mechanical Engineering

S

Shixun Wang

Department of Mechanical Engineering

Z

Zhaodong Huang

Department of Chemical and Biological Engineering, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong 999077, China

H

Haiming Lv

Department of Materials Science and Engineering City University of Hong Kong 83 Tat Chee Avenue Hong Kong SAR 999077 P. R. China

C

Chunyi Zhi

Department of Mechanical Engineering