Weakly‐Solvated and Co‐Intercalation‐Free Ether‐Based Electrolytes Enhance the Low‐ Temperature and Fast‐Charging Performance of LiFePO <sub>4</sub> ||Graphite Batteries

Z Ziwei Wang X Xuewei Gu (Institute of Functional Nano and Soft Materials Soochow University Suzhou 215123 China) J Jiacheng Zhu C Cong Zhong (Beijing National Laboratory for Condensed Matter Physics) S Shiwei Xu S Suting Weng B Bowen Liu (College of Chemistry and Chemical Engineering) Z Zhaoxiang Wang (Department of Pathophysiology, School of Basic Medicine, Key Laboratory for Epigenetics of Dongguan City, Guangdong Provincial Key Laboratory of Medical Immunology and Molecular Diagnostics, Guangdong Medical University) Y Yejing Li (State Key Laboratory of Advanced Metallurgy School of Metallurgical and Ecological Engineering University of Science and Technology Beijing Beijing 100083 China) T Tao Cheng (Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies) X Xuefeng Wang (Beijing National Laboratory for Condensed Matter Physics)

Abstract

Abstract Lithium‐ion batteries (LIBs) employing lithium iron phosphate (LiFePO 4 , LFP) cathodes and graphite (Gr) anodes are extensively utilized for energy storage applications because of their exceptional cycle life and inherent safety characteristics. However, sluggish desolvation kinetics and interfacial Li⁺ transport hinder their fast‐charging capability and low‐temperature performance, limiting broader applications. In this work, we propose a weakly solvating ether (WSE) electrolyte based on 2‐methyl‐tetrahydrofuran (2MT) as the main solvent. This electrolyte results in considerable steric hindrance, effectively preventing co‐intercalation with Gr, while also providing a weak solvation capability for Li⁺ ions and facilitating rapid interfacial Li⁺ transport. WSE, formulated with 2MT and fluoroethylene carbonate (FEC) as a co‐solvent, combines fast desolvation kinetics with an extremely low freezing point of −117.67 °C. This electrolyte induces the formation of a LiF‐, Li 3 N‐, Li 2 CO 3 ‐, and Li 2 O‐rich solid electrolyte interphase (SEI) on the Gr anode, thereby enhancing low‐temperature interfacial transport. Consequently, the Gr||Li half‐cell and the LFP||Gr full cell with this WSE demonstrates excellent rate performance, stable cycling stability, and a high specific capacity at −30 °C while also delivering reliable power even at −60 °C. These results underscore the electrolyte's efficient desolvation process, stable SEI layer, and excellent compatibility with graphite, rendering it ideal for extreme‐temperature applications.

Article Details

Volume / Issue Vol. 65, Issue 1
Published January 02, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

Z

Ziwei Wang

X

Xuewei Gu

Institute of Functional Nano and Soft Materials Soochow University Suzhou 215123 China

J

Jiacheng Zhu

C

Cong Zhong

Beijing National Laboratory for Condensed Matter Physics

S

Shiwei Xu

S

Suting Weng

B

Bowen Liu

College of Chemistry and Chemical Engineering

Z

Zhaoxiang Wang

Department of Pathophysiology, School of Basic Medicine, Key Laboratory for Epigenetics of Dongguan City, Guangdong Provincial Key Laboratory of Medical Immunology and Molecular Diagnostics, Guangdong Medical University

Y

Yejing Li

State Key Laboratory of Advanced Metallurgy School of Metallurgical and Ecological Engineering University of Science and Technology Beijing Beijing 100083 China

T

Tao Cheng

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Jiangsu Key Laboratory of Advanced Negative Carbon Technologies

X

Xuefeng Wang

Beijing National Laboratory for Condensed Matter Physics