Three‐Motif Molecular Junction Covalent Organic Frameworks for Symmetric All‐Organic Lithium‐Ion Battery

W Wenhai Feng (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou 510006 P.R. China) Z Zhi Yang C Can Guo H Huifen Zhuang (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou 510006 P.R. China) R Rui Xu (College & Hospital of Stomatology) H Haifu Zhang (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry South China Normal University Guangzhou 510006 P.R. China) M Mingjin Shi (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry South China Normal University Guangzhou 510006 P.R. China) Z Zhengyang Chen (Guizhou Province Key Laboratory of Metallurgical Engineering and Process Energy Saving, College of Materials and Metallurgy Guizhou University Guiyang Guizhou 550025 China) Y Yifa Chen Y Ya‐Qian Lan (Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China)

Abstract

Abstract The symmetric all‐organic batteries (SAOBs) based on the same organic electrode materials for both cathode and anode are promising in achieving an efficient battery system with excellent electrode compatibility, compensable volume change, full discharge ability, low preparation cost, and simple operation procedure, etc. Herein, for the first time, we have designed a kind of anhydride‐based three‐motif molecular junction COFs (i.e., TAT‐AZO‐COF) through a melt polymerization method that can serve as dual‐electrode active materials for SAOBs. The prepared TAT‐AZO‐COF with three‐motif molecular junction units, resulting from the integration of a cathode‐active carbonyl group, an anode‐active azo group, and a changeably bipolar‐active triazin group, could provide a tunable voltage inductive effect to simultaneously meet the requirements of SAOBs. Thus‐assembled SAOBs display excellent rate performance, high energy density (125 Wh kg −1 ) at 1 A g −1 and superior long‐cycle property (90 mAh g −1 over 10 000 cycles) at 10 A g −1 , which is represented to be the best high‐current density performance among all the organic electrode materials in dual‐electrode available SAOBs. The Li + storage mechanisms of three‐motif molecular junction COFs are thoroughly scrutinized by experimental and theoretical identification, and the feasibility in practical application has been validated by a successfully assembled pouch cell.

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)

W

Wenhai Feng

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou 510006 P.R. China

Z

Zhi Yang

C

Can Guo

H

Huifen Zhuang

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou 510006 P.R. China

R

Rui Xu

College & Hospital of Stomatology

H

Haifu Zhang

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry South China Normal University Guangzhou 510006 P.R. China

M

Mingjin Shi

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry South China Normal University Guangzhou 510006 P.R. China

Z

Zhengyang Chen

Guizhou Province Key Laboratory of Metallurgical Engineering and Process Energy Saving, College of Materials and Metallurgy Guizhou University Guiyang Guizhou 550025 China

Y

Yifa Chen

Y

Ya‐Qian Lan

Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization School of Chemistry South China Normal University Guangzhou P. R. China