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Covalent Organic Nanosheets with a Tunable Electronic Structure to Achieve Unprecedented Stability and High-Performance in Sodium-Ion Batteriesopen access

Authors
Lee, MinseopLee, NakyeongKwon, GuminOh, Jae-MinPark, Jin KuenPaek, Seung-Min
Issue Date
Sep-2025
Publisher
WILEY-V C H VERLAG GMBH
Keywords
bandgap engineering; covalent organic nanosheets; electron density control; push-pull electronic structure; sodium ion batteries
Citation
Small, v.21, no.36
Indexed
SCIE
SCOPUS
Journal Title
Small
Volume
21
Number
36
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/58284
DOI
10.1002/smll.202502368
ISSN
1613-6810
1613-6829
Abstract
This study develops a new type of fluorinated covalent organic nanosheets (CONs) as anode materials for sodium-ion batteries by incorporating an electron-withdrawing benzothiadiazole (BT) unit and F atom into the framework. These modifications lead to a reduced bandgap and electron density, generating strong permanent dipoles that increased Na+ accessible sites within the self-assembled solid-state structure. To elucidate the effect of these electronic changes, the Na+ storage performance of fluorinated D/A-CON-10-F is compared to that of nonfluorinated D/A-CON-10. The reduced electron density in D/A-CON-10-F weakens its interaction with Na+, yet enhances ion and charge carrier conductivities, leading to improved electrochemical performance. Notably, D/A-CON-10-F exhibits a reversible discharge capacity of approximate to 637 mA h g-1 at 100 mA g-1, maintaining structural stability over 5000 cycles with excellent rate capability. These results demonstrate that dipole engineering in CONs effectively enhances charge transport and long-term stability, offering a promising strategy for next-generation sodium-ion battery anodes.
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