Directional Catalysis of Sulfur at Highly Ordered Triple‐Phase Interfaces in All‐Solid‐State Lithium‐Sulfur Batteries

X Xinxin Zhu (Xi’an Key Laboratory of Functional Supramolecular Structure and Materials, Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of Education, College of Chemistry and Materials Science) W Wenbo Wang W Wendi Dou (College of Chemical and Biological Engineering Zhejiang University Hangzhou China) X Xucheng Lv J Junxiu Wu (School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study) M Mengting Zheng N Ning Qin (Institute of Gene Science and Industrialization for Bamboo and Rattan Resources, International Centre for Bamboo and Rattan) Z Ziqing Wang J Jun Zhong (Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices) X Xingzhong Guo (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) J Jun Lu

Abstract

ABSTRACT Sluggish sulfur reaction kinetics present a critical barrier to the practical application of sulfide‐electrolyte (SE) based all‐solid‐state lithium‐sulfur batteries (ASSLSBs). Achieving high performance requires both lowering the intrinsic energy barrier for sulfur conversion and engineering efficient transport pathways. Herein, we address these challenges by designing atomically dispersed cobalt sites on carbon nanotubes to directionally catalyze sulfur conversion at the triple phase interface. Strong orbital hybridization between Co 3d and S 3p states strengthens chemical bonding, effectively accelerating both sulfur reduction and lithium sulfide oxidation. The interfaces tailored for directional catalysis maximize highly ordered C/S/SE triple‐phase interfaces and minimize SE/C interfaces, establishing hierarchical ionic/electronic transport networks while mitigating side reactions. Consequently, the engineered cathode delivers a high reversible capacity of 1108 mAh g − 1 at 0.5 C, retaining 97 % capacity over 500 cycles. The resulting batteries also demonstrate remarkable robustness under demanding conditions. This work offers a powerful catalysis‐driven strategy for high‐performance ASSLSBs.

Article Details

Volume / Issue Vol. 38, Issue 14
Published March 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

X

Xinxin Zhu

Xi’an Key Laboratory of Functional Supramolecular Structure and Materials, Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of Education, College of Chemistry and Materials Science

W

Wenbo Wang

W

Wendi Dou

College of Chemical and Biological Engineering Zhejiang University Hangzhou China

X

Xucheng Lv

J

Junxiu Wu

School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study

M

Mengting Zheng

N

Ning Qin

Institute of Gene Science and Industrialization for Bamboo and Rattan Resources, International Centre for Bamboo and Rattan

Z

Ziqing Wang

J

Jun Zhong

Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices

X

Xingzhong Guo

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

J

Jun Lu