Metal-Free Electron Donor-Acceptor Pair Enabled Long-Term Stability of Li-CO 2 Battery

The challenges of Lithium-carbon dioxide (Li-CO ) batteries for ensuring long-term cycling stability arise from the thermodynamically stable and electrically insulating discharge products (e.g., Li CO ), which primarily rely on their interaction with the active materials. To achieve the optimized in...

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Bibliographic Details
Published in:Small (Weinheim an der Bergstrasse, Germany) Vol. 20; no. 34; p. e2400619
Main Authors: Liu, Zhihao, Zhai, Xingwu, Wei, Tianchen, Liu, Yuchun, Sun, Zhixin, Zhang, Jing, Ding, Honghe, Xia, Yujian, Zhou, Min
Format: Journal Article
Language:English
Published: Germany 01-08-2024
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Summary:The challenges of Lithium-carbon dioxide (Li-CO ) batteries for ensuring long-term cycling stability arise from the thermodynamically stable and electrically insulating discharge products (e.g., Li CO ), which primarily rely on their interaction with the active materials. To achieve the optimized intermediates, the bifunctional electron donor-acceptor (D-A) pairs are proposed in cathode design to adjust such interactions in the case of B-O pairs. The inclusion of BC O sites allows for the optimized redistribution of electrons via p-π conjugation. The as-obtained D -A pairs endow the enhanced interactions with Li , CO , and various intermediates, accompanied by the adjustable growth mode of Li CO . The shift from solvation-mediated mode into surface absorption mode in turn manipulates the morphology and decomposition kinetics of Li CO . Therefore, the corresponding Li-CO battery got twofold improved in both the capacity and reversibility. The cycling prolongs exceed 1300 h and well operates at a wide temperature range (20-50 °C) and different folding angles (0-180°). Such a strategy of introducing electron donor-acceptor pairs provides a distinct direction to optimize the lifetime of Li-CO battery from local structure regulation at the atomic scale, further inspiring in-depth understandings for developing electrochemical energy storage and carbon capture technologies.
ISSN:1613-6810
1613-6829
DOI:10.1002/smll.202400619