In‐Built Compatible Electrode‐Electrolyte Interphases for Quasi‐Solid‐State Li‐SPAN Batteries

T Tao Zhang Z Zhengyuan Shen (Key Lab for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nano Science and Materials Engineering, Collaborative Innovation Center of Nano Functional Materials and Applications) X Xinhui Pan M Man Zhang (College of Chemistry) T Tong Lian (Shandong Key Laboratory of Advanced Chemical Energy Storage and Intelligent Safety Advanced Technology Research Institute Beijing Institute of Technology Jinan 250300 China) K Keqing Shi J Ji Qian (Beijing Key Laboratory of Environmental Science and Engineering School of Materials Science and Engineering Beijing Institute of Technology Beijing China) L Li Li F Feng Wu (Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering) R Renjie Chen (Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering)

Abstract

AbstractLithium‐sulfur batteries have been regarded as a promising candidate for next‐generation energy storage systems owing to their high energy density and low cost. Sulfurized polyacrylonitrile (SPAN) as a cathode material has received wide interest due to the solid‐solid conversion mechanism, while the Li‐SPAN cell performance has been limited by the notorious issue of lithium metal anode. Developing solid‐state electrolytes for lithium‐sulfur batteries with favorable electrode‐electrolyte compatibility is urgently desired. Herein, we demonstrate a dual‐interface optimization strategy through in‐situ polymerization interface construction, which synergistically enhances interfacial compatibility between the solid polymer electrolyte (SPE) and both the lithium metal anode and SPAN cathode. The initiator pre‐buried in the SPE triggers the in‐situ polymerization of 1,3‐dioxolane (DOL) at the interface, thereby greatly reducing the electrode/electrolyte interfacial impedance. Additionally, the released fluoroethylene carbonate (FEC) into the poly‐DOL interface could further reduce the impedance and enhance the interface stability during cycling, simultaneously preventing the dissolution of polysulfides, owing to the inorganic‐rich and dense cathode electrolyte interphase formed on SPAN. As a result, the Li‐SPAN cell could operate more than 200 cycles at 0.5C with a capacity retention of 90%. We believe that this strategy provides prospects for the development of high‐energy solid‐state lithium‐sulfur batteries.

Article Details

Volume / Issue Vol. 64, Issue 43
Published October 20, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

T

Tao Zhang

Z

Zhengyuan Shen

Key Lab for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nano Science and Materials Engineering, Collaborative Innovation Center of Nano Functional Materials and Applications

X

Xinhui Pan

M

Man Zhang

College of Chemistry

T

Tong Lian

Shandong Key Laboratory of Advanced Chemical Energy Storage and Intelligent Safety Advanced Technology Research Institute Beijing Institute of Technology Jinan 250300 China

K

Keqing Shi

J

Ji Qian

Beijing Key Laboratory of Environmental Science and Engineering School of Materials Science and Engineering Beijing Institute of Technology Beijing China

L

Li Li

F

Feng Wu

Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering

R

Renjie Chen

Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering