Amorphous Nitride‐chloride Solid‐State Electrolytes for High Performance All‐Solid‐State Lithium Batteries

T Ting‐Ting Wu (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P.R. China) S Si‐Jie Guo (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P.R. China) H Hong‐Shen Zhang (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P.R. China) Y Yue Jiang J Jun Wang J Jiacheng Zhu X Xusheng Zhang P Pengfei Wei (State Key Laboratory of Catalysis Dalian Institute of Chemical Physics) Z Ziyang Hu (Department of Chemistry, The University of Hong Kong 1 , Pokfulam Road, Hong Kong,) R Rongzhi Gao G Guanhua Chen (Department of Chemistry, The University of Hong Kong, Pok Fu Lam Road, Kowloon 999077, Hong Kong, P. R. China) R Rui Wen X Xuefeng Wang (Beijing National Laboratory for Condensed Matter Physics) A An‐Min Cao (CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing China)

Abstract

Abstract High‐performance solid‐state electrolytes (SSEs) are crucial for advancing all‐solid‐state batteries (ASSBs). Amorphous SSEs, in particular, offer promising advantages due to their grain‐boundary‐free nature, which facilitates intimate solid‐to‐solid contact and uniform lithium‐ion flux, thereby improving composite electrode performance. Here, we report a class of SSEs based on a nitrogen–chlorine dual‐anion framework, formulated as Li 3 x +0.1 ZrN x Cl 4.1 , for high‐voltage ASSBs. Unlike widely studied crystalline Li 2 ZrCl 6 with a triclinic structure, increased N 3− substitution drives a structural transition to an amorphous phase (Li 1.3 ZrN 0.4 Cl 4.1 ), which achieves a significant enhancement in Li + conductivity from 0.46 to 3.01 mS cm −1 , alongside improved oxidative stability up to 4.8 V. This dual‐anion SSEs exhibits excellent compatibility with high‐energy LiNi 0.83 Co 0.06 Mn 0.11 O 2 (NCM83) cathodes. The corresponding full cells deliver a high reversible capacity of 200.1 mAh g −1 at 4.5 V with outstanding capacity retention of 95.1% after 150 cycles at 0.2 C, along with remarkable long‐term cycling stability exceeding 3000 cycles at 3 C. Furthermore, the electrochemical stability of Li 1.3 ZrN 0.4 Cl 4.1 in conjunction with NCM83 is still preserved under elevated temperatures (50  °C) and higher cut‐off voltages (up to 4.8 V). These results highlight the promise of dual‐anion amorphous electrolytes, paving the way for the design of next‐generation SSEs beyond traditional single‐anion systems.

Article Details

Volume / Issue Vol. 64, Issue 36
Published September 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

T

Ting‐Ting Wu

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P.R. China

S

Si‐Jie Guo

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P.R. China

H

Hong‐Shen Zhang

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry Chinese Academy of Sciences (CAS) Beijing 100190 P.R. China

Y

Yue Jiang

J

Jun Wang

J

Jiacheng Zhu

X

Xusheng Zhang

P

Pengfei Wei

State Key Laboratory of Catalysis Dalian Institute of Chemical Physics

Z

Ziyang Hu

Department of Chemistry, The University of Hong Kong 1 , Pokfulam Road, Hong Kong,

R

Rongzhi Gao

G

Guanhua Chen

Department of Chemistry, The University of Hong Kong, Pok Fu Lam Road, Kowloon 999077, Hong Kong, P. R. China

R

Rui Wen

X

Xuefeng Wang

Beijing National Laboratory for Condensed Matter Physics

A

An‐Min Cao

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology Beijing National Laboratory For Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing China