Hydrogen‐Bond‐Networked Robust Binder Enabling Long‐Cycling Sulfide‐Based All‐Solid‐State Lithium Batteries

W Wenjun Zhang P Pengzhou Mu (Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao China) C Chenghao Sun J Junjie Li (Physics Department, University of California, San Diego, La Jolla, CA, USA.) J Jiedong Li (Department of Chemistry and Biochemistry) X Xi Wu (Institute of Materials Research, Tsinghua Shenzhen International Graduate School) Y Yifan Gong J Jiangwei Ju D Decai Guo (Dalian Research Institute of Petroleum and Petrochemicals Dalian China) H Huanrui Zhang C Cizhen Luo (Yibin Fengyuan New Material Co., Ltd Yibin China) J Ju Xiao (Qinghai Salt Lake Industry Co., Ltd Geermu China) X Xinhong Zhou (College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao China) G Guanglei Cui (Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology)

Abstract

ABSTRACT Wet processing is promising for scalable manufacture of sulfide‐based all‐solid‐state lithium batteries (ASSBs), but it demands binders compatible with low‐polarity solvents and sulfides while enabling thin sulfide solid electrolyte (SSE) films (≤ 30 µm) and high‐loading composite cathodes (≥ 30 mg cm −2 ). To address these, we present a dynamic hydrogen bonding‐empowered robust polymer (denoted as PNO) binder via soft‐hard segment synergism design. In the PNO binder, the polybutadiene‐based soft segments retain easy processability of SSE films and composite cathodes, while carbamate motif‐containing hard segments improve the mechanical strength of them mainly via forming dynamic hydrogen bonding interactions not only among adjacent PNO chains but also between PNO chains and the surface of sulfide or cathode particles. The breaking and reforming of hydrogen bonds enable effective stress dissipation, thereby maintaining the structural stability of both SSE films and composite cathodes during processing and battery cycling. Benefiting from these, ASSBs assembled with PNO binder‐based LiNi 0.8 Co 0.1 Mn 0.1 O 2  cathodes and Li 6 PS 5 Cl films exhibit outstanding cycling stability, which compares favorably with recently reported sulfide‐based ASSBs. This work highlights a soft‐hard segment synergism binder design strategy that overcomes the bottleneck in wet processing of practical ASSBs, conducive to accelerating the scale‐up production of advanced sulfide‐based ASSBs.

Article Details

Volume / Issue Vol. 65, Issue 28
Published July 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

W

Wenjun Zhang

P

Pengzhou Mu

Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao China

C

Chenghao Sun

J

Junjie Li

Physics Department, University of California, San Diego, La Jolla, CA, USA.

J

Jiedong Li

Department of Chemistry and Biochemistry

X

Xi Wu

Institute of Materials Research, Tsinghua Shenzhen International Graduate School

Y

Yifan Gong

J

Jiangwei Ju

D

Decai Guo

Dalian Research Institute of Petroleum and Petrochemicals Dalian China

H

Huanrui Zhang

C

Cizhen Luo

Yibin Fengyuan New Material Co., Ltd Yibin China

J

Ju Xiao

Qinghai Salt Lake Industry Co., Ltd Geermu China

X

Xinhong Zhou

College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao China

G

Guanglei Cui

Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology