Extended conjugation-induced π electron redistribution for stabilizing organic anodes in aqueous ammonium ion batteries

Organic molecules have attracted significant attention as potential anode materials for aqueous ammonium-ion batteries (AAIBs) due to their tunable structure, rich active sites, and abundant resources. However, their practical applications are hindered by structural instability and high solubility. Herein, we design an extended conjugated molecule, benzo[ a ]benzo[7,8]quinoxalino[2,3- i ]phenazine-8,17-dione (TABQ-NQ), by incorporating phenyl groups into the 5,7,12,14-tetraaza-6,13-pentacenequinone (TAPQ) structure. The strengthened intermolecular interactions arising from the extended conjugation contribute to the improved structural integrity of TABQ-NQ. Furthermore, the intramolecular charge redistribution facilitated by the extended conjugation enhances the binding affinity between TABQ-NQ and NH 4 + while reducing interactions of TABQ-NQ with H 2 O, thereby stabilizing discharge intermediates and preventing further dissolution. As a result, TABQ-NQ exhibits reduced solubility, improved stability, and superior electrochemical performance. The TABQ-NQ anode demonstrates a high initial specific capacity of 190 mAh g −1 , with a capacity of 146 mAh g −1 at 0.2 A g −1 after over 650 cycles, corresponding to the capacity retention of 76.8 %, and maintains an initial capacity of 127.5 mAh g −1 at 2 A g −1 . Ex-situ characterizations further reveal the low solubility and high redox reversibility of TABQ-NQ. This work provides new insights into the extension of conjugated structures in organic molecules and offers valuable guidance for the development of AAIBs research. • Extended conjugation optimizes NH 4 + storage performance of TABQ-NQ. • Intramolecular charge redistribution enhances NH 4 + binding and reduces dissolution of TABQ-NQ. • TABQ-NQ anode shows superior capacity, rate performance, and 10,000-cycle stability. • Theoretical calculations reveal unique trans-coordination mechanism for NH 4 + storage.

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Publication Details

Journal
Journal of Energy Storage
Published
2025-06-17
DOI
https://doi.org/10.1016/j.est.2025.117473
Citations
4
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
2.92

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article

Extended conjugation-induced π electron redistribution for stabilizing organic anodes in aqueous ammonium ion batteries

Xinlei Tang, Shan Hu, Haode Zhang, Wen Chen et al.
4 citations
Journal of Energy Storage
Advanced battery technologies research
2.92
article

Extended conjugation-induced π electron redistribution for stabilizing organic anodes in aqueous ammonium ion batteries

Xinlei Tang, Shan Hu, Haode Zhang, Wen Chen, Sensen Yu
article en
4 citations

Abstract

Organic molecules have attracted significant attention as potential anode materials for aqueous ammonium-ion batteries (AAIBs) due to their tunable structure, rich active sites, and abundant resources. However, their practical applications are hindered by structural instability and high solubility. Herein, we design an extended conjugated molecule, benzo[ a ]benzo[7,8]quinoxalino[2,3- i ]phenazine-8,17-dione (TABQ-NQ), by incorporating phenyl groups into the 5,7,12,14-tetraaza-6,13-pentacenequinone (TAPQ) structure. The strengthened intermolecular interactions arising from the extended conjugation contribute to the improved structural integrity of TABQ-NQ. Furthermore, the intramolecular charge redistribution facilitated by the extended conjugation enhances the binding affinity between TABQ-NQ and NH 4 + while reducing interactions of TABQ-NQ with H 2 O, thereby stabilizing discharge intermediates and preventing further dissolution. As a result, TABQ-NQ exhibits reduced solubility, improved stability, and superior electrochemical performance. The TABQ-NQ anode demonstrates a high initial specific capacity of 190 mAh g −1 , with a capacity of 146 mAh g −1 at 0.2 A g −1 after over 650 cycles, corresponding to the capacity retention of 76.8 %, and maintains an initial capacity of 127.5 mAh g −1 at 2 A g −1 . Ex-situ characterizations further reveal the low solubility and high redox reversibility of TABQ-NQ. This work provides new insights into the extension of conjugated structures in organic molecules and offers valuable guidance for the development of AAIBs research. • Extended conjugation optimizes NH 4 + storage performance of TABQ-NQ. • Intramolecular charge redistribution enhances NH 4 + binding and reduces dissolution of TABQ-NQ. • TABQ-NQ anode shows superior capacity, rate performance, and 10,000-cycle stability. • Theoretical calculations reveal unique trans-coordination mechanism for NH 4 + storage.

Journal of Energy StorageVol. 130
Wuhan University of Technology (CN)
Natural Science Foundation of Hubei Province
Openalex Percentile: Top 9%
Advanced battery technologies research
2.92
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