Compact Ion‐Pair Aggregates Dominated Electrolytes Enable High‐Performance Low‐Temperature Lithium‐Ion Batteries

F Feng Su (State Key Laboratory of Radio Frequency Heterogeneous Integration, College of Chemistry and Environmental Engineering) Y Yiting Lin X Xin Dou (Key Laboratory for Ultrafine Materials of Ministry of Education, School of Chemical Engineering East China University of Science and Technology Shanghai 200237 China) H Haipeng You (Department of Chemical Engineering, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 China) S Shang Gao Z Zheng Bai (Key Laboratory for Ultrafine Materials of Ministry of Education, School of Chemical Engineering East China University of Science and Technology Shanghai 200237 China) J Jiajun Jiang (Department of Physics, Shanghai University of Electric Power 1 , Shanghai 200090,) L Long Chen (Department of Chemistry, Frontiers Science Center for New Organic Matter and State Key Laboratory of Advanced Chemical Power Sources, College of Chemistry) C Chunzhong Li (Key Laboratory for Ultrafine Materials of Ministry of Education, School of Chemical Engineering)

Abstract

Abstract Lithium‐ion batteries (LIBs) are widely used due to their high energy density, long cycle life, and environmental friendliness. However, at sub‐zero temperatures, the operation of LIBs is constrained by degraded electrolyte ion transport performance and severe charge transfer polarization. In this work, we proposed a strategy for the construction of solvation structures dominated by compact ion‐pair aggregates (CIPAs) through weak lithium‐solvent interactions design, which significantly improved the lithium‐ion transference number and reduced the de‐solvation energy barrier. Excitingly, this strategy can induce the formation of a robust anion‐derived solid electrolyte interface, thereby enabling the rapid transport of lithium ions across the interface even at extremely low temperatures. This electrolyte provides excellent electrochemical performance of practical natural graphite and LiNi 0.8 Co 0.1 Mn 0.1 (NCM811) electrodes. The NCM811||graphite full cell exhibits capacity retention of 84.7% of its room temperature capacity at a high rate of 0.5C at −20 °C, and can be cycled stably for over 200 cycles at −40 °C without obvious capacity degradation. This work presents an innovative avenue for high performance LIBs at low temperature.

Article Details

Volume / Issue Vol. 64, Issue 38
Published September 15, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

F

Feng Su

State Key Laboratory of Radio Frequency Heterogeneous Integration, College of Chemistry and Environmental Engineering

Y

Yiting Lin

X

Xin Dou

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Chemical Engineering East China University of Science and Technology Shanghai 200237 China

H

Haipeng You

Department of Chemical Engineering, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 China

S

Shang Gao

Z

Zheng Bai

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Chemical Engineering East China University of Science and Technology Shanghai 200237 China

J

Jiajun Jiang

Department of Physics, Shanghai University of Electric Power 1 , Shanghai 200090,

L

Long Chen

Department of Chemistry, Frontiers Science Center for New Organic Matter and State Key Laboratory of Advanced Chemical Power Sources, College of Chemistry

C

Chunzhong Li

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Chemical Engineering