Dual‐Redox Conjugated Bipolar Covalent Organic Framework Enables High‐Voltage Symmetric Proton Batteries
Symmetric all-organic proton batteries (SAOPBs) attract increasing attention for large-scale energy storage due to their safe and superior rate performance, which is severely limited by the lack of suitable bipolar electrode materials that integrate reversible dual-redox activity and high operating voltage within a single structure. Herein, we report a bipolar covalent organic framework (TAPT-HAT-COF) as both cathode and anode in symmetric proton battery. In this COF, the electron-deficient pyrazine/carbonyl units and electron-rich phenylimine groups establish two independent and reversible redox couples, achieving a high operating voltage of up to 0.83 V. Combined with in situ FTIR spectroscopy and theoretical calculations, TAPT-HAT-COF shows bipolar charge storage mechanism with the C═N and C═O groups served as reversible redox centers. Benefiting from the fully conjugated structure and abundant active sites, the assembled SAOPB exhibits high specific capacity of 108.5 mAh g<sup>-1</sup> under 5 A g<sup>-1</sup> with stable cycling over 3000 cycles. Moreover, when applied in a practical pouch cell, which delivers a specific capacity of 145.8 mAh g<sup>-1</sup> at 0.5 A g<sup>-1</sup>, confirming the material's potential for practical applications. The work can provide viable design strategy and model of bipolar COF materials for symmetric energy storage systems.
Authors
- Yangyang Feng (ORCID: https://orcid.org/0009-0005-0926-8809)
- Zhendong Wang
- Yaobing Wang
- Yang Xu
Institutions
- Fujian Normal University (CN)
- Chongqing University (CN)
- Fujian Institute of Research on the Structure of Matter (CN)
- Tan Kah Kee Innovation Laboratory (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-03-08
- DOI
- https://doi.org/10.1002/anie.9770638
- Primary Topic
- Advanced battery technologies research
- Type
- article
- Field-Weighted Citation Impact
- 0.00