High‐Performance Lithium‐Sulfur Batteries: Medium‐Entropy Alloys Embedded in CeO <sub>2</sub> for Polysulfide/Sulfide Bidirectional Catalysis

C Chuanhuang Wu (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) Y Yong‐Peng Wang (Key Laboratory of Wind and Solar Energy Utilization Technology of Ministry of Education Inner Mongolia Key Laboratory of New Energy and Energy Storage Technology Inner Mongolia University Renewable Energy Engineering Research Center, School of Energy and Power Engineering Inner Mongolia University of Technology Hohhot 010051 China) Y Yuchuan Zhu (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) H Haili Luo (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) L Longyang Zhou (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) D Daying Guo (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) G Guoyong Fang (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) H Huile Jin (Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering) X Xi'an Chen (College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China) S Shun Wang (Department of Mathematics)

Abstract

Abstract The slow kinetics of the sulfur reduction reaction (SRR) and Li 2 S oxidation reaction (SOR) in lithium‐sulfur batteries (LSBs) seriously affect their practical applications. Herein, we prepared a functional interlayer for LSBs consisting of hydroxylated carbon nanotubes dispersed with NiCoMoIr medium‐entropy alloys embedded in CeO 2 surface materials. Experimental results revealed a bidirectional catalytic mechanism involving different elements, verifying that Ir and Ni promote the SRR of Li 2 S 6 to Li 2 S. Meanwhile, Co and Mo were found to primarily promote the conversion process of Li 2 S to Li 2 S 6 . CeO 2 exhibits a bidirectional synergistic effect on enhancing the kinetics of the SRR and SOR. The battery exhibits a specific capacity of 1535.7 mAh g −1 at 0.2 C, and the decay rate is only 0.051% for per‐cycle of 1000 cycles at 1 C. More importantly, a 2 Ah‐level pouch cell with an energy density of 436.4 Wh kg −1 and the capacity decay rate was 0.039% per‐cycle after 800 cycles.

Article Details

Volume / Issue Vol. 64, Issue 52
Published December 22, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

C

Chuanhuang Wu

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

Y

Yong‐Peng Wang

Key Laboratory of Wind and Solar Energy Utilization Technology of Ministry of Education Inner Mongolia Key Laboratory of New Energy and Energy Storage Technology Inner Mongolia University Renewable Energy Engineering Research Center, School of Energy and Power Engineering Inner Mongolia University of Technology Hohhot 010051 China

Y

Yuchuan Zhu

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

H

Haili Luo

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

L

Longyang Zhou

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

D

Daying Guo

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

G

Guoyong Fang

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

H

Huile Jin

Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering

X

Xi'an Chen

College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 China

S

Shun Wang

Department of Mathematics