Nitrile‐Assisted Hybrid‐Solvation Electrolyte Enables Wide‐Temperature, High‐Voltage, and Ultrafast‐Charging Lithium‐Metal Batteries

Y Yuhao Liang (Institute for Sustainable Transformation School of Chemical Engineering and Light Industry Guangdong University of Technology Guangzhou China) T Ting He (Division of Thyroid Surgery, Department of General Surgery and Laboratory of Thyroid and Parathyroid Disease, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University) Z Zimo Huang (Department of Neuroscience, Physiology and Pharmacology, University College London) W Wei Chen J Juncheng Wang H Hao Long X Xueming Chen (Institute for Sustainable Transformation School of Chemical Engineering and Light Industry Guangdong University of Technology Guangzhou China) M Meng Li Q Qifeng Zheng (School of Chemistry) H Hao Chen S Shanqing Zhang (Institute for Sustainable Transformation, School of Chemical Engineering and Light Industry)

Abstract

ABSTRACT The stable operation of lithium metal batteries (LMBs) requires simultaneous stabilization of anode and cathode interfaces, a challenge that intensifies under extreme operating conditions due to divergent formation mechanisms. Here, we present a hybrid‐solvation electrolyte design employing isobutyronitrile (IBN) as the primary solvent to regulate both Li + solvation and interfacial protection. Functioning as a bifunctional modulator, IBN drives dual‐source interfacial chemistry at the anode where anion‐enriched solvation and coordinated‐solvent decomposition co‐generate an inorganic‐ and nitrogen‐rich solid–electrolyte interphase (SEI) while lowering Li + desolvation barriers. At the cathode surface, excess IBN molecules form an adsorption‐derived protective layer that effectively suppresses solvent oxidation and stabilizes the cathode–electrolyte interface (CEI) under high‐voltage and high‐temperature conditions. Enabled by this design, Li||LiNi 0.8 Co 0.1 Mn 0.1 O 2 coin cells exhibit robust operation across wide temperatures (−40°C∼60°C) and high voltages (4.6 V), alongside ultrafast charging capabilities (20 C). Upscaling to practical pouch cells under lean‐electrolyte conditions (1.2 g Ah −1 ) yields a high energy density of 403 Wh kg −1 with a 12‐min fast‐charging/discharging capability. The hybrid solvation design framework integrates solvent‐ and anion‐driven chemistries in a unified electrolyte, enabling high‐energy LMB operation under demanding conditions.

Article Details

Volume / Issue Vol. 65, Issue 29
Published July 13, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

Y

Yuhao Liang

Institute for Sustainable Transformation School of Chemical Engineering and Light Industry Guangdong University of Technology Guangzhou China

T

Ting He

Division of Thyroid Surgery, Department of General Surgery and Laboratory of Thyroid and Parathyroid Disease, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University

Z

Zimo Huang

Department of Neuroscience, Physiology and Pharmacology, University College London

W

Wei Chen

J

Juncheng Wang

H

Hao Long

X

Xueming Chen

Institute for Sustainable Transformation School of Chemical Engineering and Light Industry Guangdong University of Technology Guangzhou China

M

Meng Li

Q

Qifeng Zheng

School of Chemistry

H

Hao Chen

S

Shanqing Zhang

Institute for Sustainable Transformation, School of Chemical Engineering and Light Industry