Solid Catholyte with Regulated Interphase Redox for All‐Solid‐State Lithium‐Sulfur Batteries

K Kaier Shen W Weize Shi H Huimin Song C Chenxi Zheng (International Center for Quantum Materials, School of Physics) Y Yingjing Yan X Xufeng Hong X Xu Liu Y Yun An (Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China) Y Yuanrui Li (Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China) F Fei Ye M Mengxue He G Guo Ye (State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China) C Chenyan Ma (Institute of High Energy Physics Chinese Academy of Sciences Beijing 100049 China) L Lei Zheng P Peng Gao Q Quanquan Pang

Abstract

Abstract All‐solid‐state lithium‐sulfur battery (ASSLSB) is considered one of the ultimate next‐generation energy storage technologies due to the expected low cost, high safety, and high specific energy. The high‐conductivity and low‐modulus sulfide electrolytes hold promise as electrolytes in the cathode (i.e., solid catholytes) for ASSLSBs, but their parasitic decomposition and reactions over cycling lead to degradation of the active material−catholyte interphases and hence limited cycling life. Herein a strategy is described to stabilize the ASSLSBs by regulating the interphase redox reversibility of the sulfide catholyte, which is validated on a new sulfide electrolyte formulated as Li 6+x P 1−x W x S 5 I (LPWSI). The experiments show that the presence of mixed ionic‐electronic conducting WS 2 boosts the Li 4 P 2 S 7 −to−Li 3 PS 4 reaction in the interphase, which prevents irreversible accumulation of impeding P 2 S 7 4− and thereby improves the catholyte's interphase stability. With the LPWSI catholyte, the ambient‐temperature ASSLSB exhibits stable cycling sustaining 92.2% capacity over 400 cycles at C/5 with an initial areal capacity of 1.95 mA h cm −2 . Furthermore, the cells demonstrate excellent high‐rate stability over 1000 cycles at rates of 1C and 2C. The reported strategy contributes to reshaping the understanding of how solid catholyte can function in composite cathodes and provides new guidelines for designing catholyte for high‐capacity conversion‐based electrodes that involve complex evolution of interphases.

Article Details

Volume / Issue Vol. 37, Issue 11
Published March 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (16)

K

Kaier Shen

W

Weize Shi

H

Huimin Song

C

Chenxi Zheng

International Center for Quantum Materials, School of Physics

Y

Yingjing Yan

X

Xufeng Hong

X

Xu Liu

Y

Yun An

Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China

Y

Yuanrui Li

Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 China

F

Fei Ye

M

Mengxue He

G

Guo Ye

State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xueyuan Road, Beijing 100191, China

C

Chenyan Ma

Institute of High Energy Physics Chinese Academy of Sciences Beijing 100049 China

L

Lei Zheng

P

Peng Gao

Q

Quanquan Pang