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

  • Minseop Lee
  • , Nakyeong Lee
  • , Gumin Kwon
  • , Jae Min Oh
  • , Jin Kuen Park
  • , Seung Min Paek

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

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 ≈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.

Original languageEnglish
Article number2502368
JournalSmall
Volume21
Issue number36
DOIs
StatePublished - 11 Sep 2025

Keywords

  • bandgap engineering
  • covalent organic nanosheets
  • electron density control
  • push–pull electronic structure
  • sodium ion batteries

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