A Self‐Phase‐Separated Deep Eutectic Solvent‐Based Biphasic Electrolyte for Durable Four‐Electron Zn‐I <sub>2</sub> Batteries Across Wide‐Temperature Range

W Wenhui Wang (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, Frontiers Center for Materiobiology and Dynamic Chemistry) Y Yangyang Liu (State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology) S Shilong Li H Hongwei Kang (Anhui Provincial Key Laboratory of Green Carbon Chemistry Fuyang Normal University Fuyang Anhui P. R. China) J Jian Shi R Rui Wang L Longhai Zhang Y Yun Gao (Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry) S Shilin Zhang (School of Chemical Engineering, Faculty of Sciences, Engineering and Technology) C Chaofeng Zhang (Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Leibniz International Joint Research Centre of Materials Sciences of Anhui Province)

Abstract

ABSTRACT Aqueous four‐electron zinc‐iodine batteries (4eZIBs) hold great promise for long‐term energy storage, but their practical application is severely hindered by the multiple drawbacks, including Zn dendrite growth, polyiodide shuttle, and I + hydrolysis. Such limitations can be effectively mitigated by employing biphasic electrolytes featuring a liquid‐liquid interface, which enables efficient immobilization of the dissolved reaction intermediates. However, such systems frequently employ toxic organic solvents, which not only pose flammability risks but also struggle to adapt to extreme temperature conditions. Herein, we design a novel self‐stratified biphasic electrolyte via liquid‐liquid phase separation of choline chloride (ChCl)‐trifluoroacetamide (TFA) deep eutectic solvent (DES) and ZnSO 4 /H 2 O/ ethylene glycol solution. The upper DES phase effectively confines polyiodide anions, suppresses shuttle effect and stabilizes I + species, while the bottom aqueous phase regulates Zn 2+ solvation structure and inhibits dendrite formation and side reactions. Benefiting from the synergistic functional separation, the Zn‐I 2 battery realizes highly reversible four‐electron conversion, effectively suppresses battery self‐discharge, and delivers superior cycling stability over 21000 cycles as well as wide temperature tolerance ranging from −30°C to 50°C. This work offers novel insights into the design of safe and eco‐friendly biphasic electrolytes and provides an effective strategy for the construction of high‐performance 4eZIBs.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 12, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

W

Wenhui Wang

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, Frontiers Center for Materiobiology and Dynamic Chemistry

Y

Yangyang Liu

State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology

S

Shilong Li

H

Hongwei Kang

Anhui Provincial Key Laboratory of Green Carbon Chemistry Fuyang Normal University Fuyang Anhui P. R. China

J

Jian Shi

R

Rui Wang

L

Longhai Zhang

Y

Yun Gao

Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry

S

Shilin Zhang

School of Chemical Engineering, Faculty of Sciences, Engineering and Technology

C

Chaofeng Zhang

Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Leibniz International Joint Research Centre of Materials Sciences of Anhui Province