Solid Polymer Electrolyte with Compatible Cathode‐Electrolyte Interfacial Design Enabling Lithium Metal Batteries Operation at 4.8 V with Long Cycle Life

J Jiajia Li H Haiman Hu (Energy Engineering Division of Energy Science Luleå University of Technology Luleå 97187 Sweden) J Jiufu Zhu (CAS Key Laboratory of Green Process and Engineering Beijing Key Laboratory of Ionic Liquids Clean Process Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 P. R. China) X Xinyu Ma (Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Suzhou Key Laboratory of Soft Material and New Energy, College of Chemistry, Chemical Engineering and Materials Science) Y Yin Hu (Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Suzhou Key Laboratory of Soft Material and New Energy, College of Chemistry, Chemical Engineering and Materials Science) H Haitao Zhang F Fengming Liu S Suojiang Zhang X Xiaoyan Ji (Energy Engineering Division of Energy Science Luleå University of Technology Luleå 97187 Sweden)

Abstract

Abstract Lithium metal batteries (LMBs) with solid polymer electrolytes (SPEs) offer higher energy density and enhance safety compared to the Li‐ion batteries that use a graphite anode and organic electrolytes. However, achieving long cycle life for LMBs while enabling the use of high‐voltage cathodes required the compatibility between cathode‐SPE, rather than focusing solely on the individual components. This study presente a dual‐functional poly(ionic liquid) (PolyIL)‐based material that simultaneously serves as an SPE matrix and a cathode binder, constructing a cathode‐SPE interface with exceptional (electro)chemical compatibility owing to the high ionic conductivity and wide electrochemical stability window. Additionally, a modified cellulose acetate (CA)‐based PolyIL substrate, enriched with C═O and ─OH groups, is designed rationally and incorporated to assist the Li + migration, leveraging their highly negative charge, and enhancing the mechanical strength of the SPE. Furthermore, an in situ polymerization approach is employed to assemble the cells, improving the physical compatibility at the cathode‐SPE interface. As a result, the Li||LFP cell demonstrate stable cycling beyond 1100 cycles, and the Li||NCM811 cell reliably operates at a high cut‐off voltage of up to 4.8 V.

Article Details

Volume / Issue Vol. 37, Issue 19
Published May 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (9)

J

Jiajia Li

H

Haiman Hu

Energy Engineering Division of Energy Science Luleå University of Technology Luleå 97187 Sweden

J

Jiufu Zhu

CAS Key Laboratory of Green Process and Engineering Beijing Key Laboratory of Ionic Liquids Clean Process Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 P. R. China

X

Xinyu Ma

Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Suzhou Key Laboratory of Soft Material and New Energy, College of Chemistry, Chemical Engineering and Materials Science

Y

Yin Hu

Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Suzhou Key Laboratory of Soft Material and New Energy, College of Chemistry, Chemical Engineering and Materials Science

H

Haitao Zhang

F

Fengming Liu

S

Suojiang Zhang

X

Xiaoyan Ji

Energy Engineering Division of Energy Science Luleå University of Technology Luleå 97187 Sweden