Lee Minseop, Lee Nakyeong, Kwon Gumin, Oh Jae-Min, Park Jin Kuen, Paek Seung-Min
Department of Chemistry, Kyungpook National University, Daegu, 41566, Republic of Korea.
Department of Chemistry, Hankuk University of Foreign Studies, Gyenggi-do, Yongin, 17035, Republic of Korea.
Small. 2025 Sep;21(36):e2502368. doi: 10.1002/smll.202502368. Epub 2025 Apr 30.
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 at 100 mA g, 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.
本研究通过将吸电子的苯并噻二唑(BT)单元和氟原子引入框架中,开发出一种新型的氟化共价有机纳米片(CONs)作为钠离子电池的负极材料。这些修饰导致带隙和电子密度降低,产生强永久偶极,增加了自组装固态结构内可接触钠的位点。为了阐明这些电子变化的影响,将氟化的D/A-CON-10-F的钠存储性能与非氟化的D/A-CON-10进行了比较。D/A-CON-10-F中降低的电子密度削弱了其与钠的相互作用,但提高了离子和电荷载流子的电导率,从而改善了电化学性能。值得注意的是,D/A-CON-10-F在100 mA g下表现出约637 mA h g的可逆放电容量,在5000次循环中保持结构稳定性,具有出色的倍率性能。这些结果表明,CONs中的偶极工程有效地增强了电荷传输和长期稳定性,为下一代钠离子电池负极提供了一种有前景的策略。