Zwitterionic Engineering of Vinylene‐Linked Covalent Organic Frameworks for Superior Protonic Electrolytes

H Hao‐Yu Li (State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China) G Guo‐Qin Zhang (State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China) H Hong‐Bin Luo (State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China) J Jin Zhang D Dong‐Sheng Shao (State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China) Q Qiao Qiao (Department of Chemistry) F Fengdong Wang (College of Chemistry, Frontiers Science Center for New Organic Matter) Y Yangyang Liu (State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology) Z Zhenjie Zhang (College of Chemistry, Frontiers Science Center for New Organic Matter) X Xiao‐Ming Ren (State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China)

Abstract

ABSTRACT Solid protonic electrolytes are a promising avenue for advanced solid‐state proton batteries, offering enhanced safety, long‐term cycling stability, and high energy density. However, achieving high proton conductivity under ambient conditions remains a formidable challenge. In this study, we demonstrate a highly robust zwitterionic vinylene‐linked covalent organic framework (COF) engineered with sulfobetaine functionalities that promote efficient proton dissociation and migration, enabling superior proton conduction under ambient conditions and setting a new benchmark in the COF field. The solid protonic electrolyte comprising phosphoric acid‐modified zwitterionic COFs achieved the highest proton conductivity (5.34 × 10 −2 S cm −1 ) under ambient conditions among all reported COF‐based protonic electrolytes, along with incredible long‐term stability. Furthermore, solid‐state proton batteries assembled using the solid electrolyte delivered a record‐high specific capacity (108.5 mAh g −1 at 1.0 A g −1 ), good cycling durability (90% capacity retention after 2000 charge‐discharge cycles at 1.0 A g −1 ), and excellent rate capability. This study presents a viable and effective strategy for constructing high‐performance COF‐based protonic electrolytes tailored for advanced solid‐state proton battery technologies.

Article Details

Volume / Issue Vol. 65, Issue 16
Published April 13, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

H

Hao‐Yu Li

State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China

G

Guo‐Qin Zhang

State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China

H

Hong‐Bin Luo

State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China

J

Jin Zhang

D

Dong‐Sheng Shao

State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China

Q

Qiao Qiao

Department of Chemistry

F

Fengdong Wang

College of Chemistry, Frontiers Science Center for New Organic Matter

Y

Yangyang Liu

State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology

Z

Zhenjie Zhang

College of Chemistry, Frontiers Science Center for New Organic Matter

X

Xiao‐Ming Ren

State Key Laboratory of Materials‐Oriented Chemical Engineering and School of Chemistry and Molecular Engineering Nanjing Tech University Nanjing China