Robust and Antioxidative Quasi‐Solid‐State Polymer Electrolytes for Long‐Cycling 4.6 V Lithium Metal Batteries

C Congping Li (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China) Y Yue Zhong (Mount Sinai Center for Therapeutics Discovery, Departments of Pharmacological Sciences, Oncological Sciences and Neuroscience, Tisch Cancer Institute) R Rongfeng Liao (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China) T Tan Yi (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) M Minghong Zhou (Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P. R. China) R Ruliang Liu (School of Chemistry and Materials Science Guangdong University of Education Guangzhou P. R. China) S Shaohong Liu (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou P. R. China) D Dingcai Wu

Abstract

Abstract Quasi‐solid‐state polymer electrolytes (QSPEs) have been considered as one of the most promising electrolytes for high‐safety high‐energy‐density lithium metal batteries (LMBs). However, their inadequate mechanical properties and instability under high voltages pose significant challenges for practical applications. Herein, robust and antioxidative QSPEs are developed based on a polymer‐brush‐based rigid supporting film (BC‐ g ‐PLiMTFSI‐ b ‐PPFEMA, BC: bacterial cellulose, PLiMTFSI: poly(lithium (3‐methacryloyloxypropylsulfonyl) (trifluoromethylsulfonyl)imide), PPFEMA: poly(2‐(perfluorohexyl)ethyl methacrylate)). The robust BC nanofibril backbone can produce a highly porous supporting structure with outstanding mechanical strength. More importantly, the PLiMTFSI‐ b ‐PPFEMA side‐chains can not only obviously increase the conversion ratio of easily oxidized monomers in QSPEs, but also possess strong interaction with unstable electrolyte components. With such QSPEs as solid‐state electrolytes, the Li/LiNi 0.8 Mn 0.1 Co 0.1 O 2 full cell with a high cathode loading (20.3 mg cm −2 ) exhibits a specific discharge capacity of 200.7 mAh g −1 at 0.5 C and demonstrates a long lifespan of 137 cycles with a highly retained capacity of 170.7 mAh g −1 under a cut‐off voltage of 4.5 V. More importantly, under a high cut‐off voltage of 4.6 V, a high specific capacity of 147.0 mAh g −1 after 187 cycles can be retained for solid‐state Li/LiCoO 2 cells. This work provides a feasible development strategy of QSPEs for practical long‐cycling high‐voltage LMBs.

Article Details

Volume / Issue Vol. 37, Issue 21
Published May 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (8)

C

Congping Li

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China

Y

Yue Zhong

Mount Sinai Center for Therapeutics Discovery, Departments of Pharmacological Sciences, Oncological Sciences and Neuroscience, Tisch Cancer Institute

R

Rongfeng Liao

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China

T

Tan Yi

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

M

Minghong Zhou

Medical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences) Southern Medical University Guangzhou P. R. China

R

Ruliang Liu

School of Chemistry and Materials Science Guangdong University of Education Guangzhou P. R. China

S

Shaohong Liu

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou P. R. China

D

Dingcai Wu