Engineering Robust Hydrophilic–Hydrophobic Interface via π‐electron Delocalization for Ultralong‐Lived Zinc–Ion Batteries

Y Yudong Sang (Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) J Jing Wang (Hunan Cancer Hospital Changsha China) M Mi Xu (Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) B Beinuo Zhang (Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) Q Qiongying Huang (Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) D Dongdong Wang C Chuangwei Liu (School of Materials Science and Engineering) Y Yatao Zhang (State Key Laboratory of Critical Metals Beneficiation, Metallurgy and Purification, School of Chemical Engineering) H Haozhen Dou (Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) Z Zhongwei Chen (Power Battery & Systems Research Center, State Key Laboratory of Catalysis)

Abstract

Abstract Aqueous zinc ion batteries (AZIBs) are hindered by the severe interfacial issues of Zn anode such as side reactions and dendrite growth. The in‐situ construction of robust interface to tackle above issues remains a grand challenge and lacks rational design principles, especially under high current density. Herein, a π‐electron delocalization strategy is proposed to in‐situ construct the self‐assembled hydrophilic–hydrophobic interface layer (HHIL) for ultralong‐lived AZIBs, where interface design principles are built based on the electronic structure and spatial configuration of additives. Encouragingly, HHIL derived by π‐π interactions and ion–dipole interactions is robust during long‐term cycling and facilitates the generation of an inorganic‐rich interface chemistry. The flexible HHIL and rigid inorganic‐rich interface afford the rapid interface kinetics, and effectively suppresses side reactions and dendrite growth. Notably, Zn//Zn cells deliver the cycling life over 900 h at 20 mA cm −2 and 10 mAh cm −2 , and Zn//NVO full cells stably perform over 25 000 cycles at 10 A g −1 . Furthermore, the practical pouch cell is also demonstrated.

Article Details

Volume / Issue Vol. 64, Issue 31
Published July 28, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

Y

Yudong Sang

Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

J

Jing Wang

Hunan Cancer Hospital Changsha China

M

Mi Xu

Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

B

Beinuo Zhang

Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

Q

Qiongying Huang

Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

D

Dongdong Wang

C

Chuangwei Liu

School of Materials Science and Engineering

Y

Yatao Zhang

State Key Laboratory of Critical Metals Beneficiation, Metallurgy and Purification, School of Chemical Engineering

H

Haozhen Dou

Power Battery and Systems Research Center State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

Z

Zhongwei Chen

Power Battery & Systems Research Center, State Key Laboratory of Catalysis