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具有可调电子结构的共价有机纳米片在钠离子电池中实现前所未有的稳定性和高性能。

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

作者信息

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

机构信息

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.

出版信息

Small. 2025 Sep;21(36):e2502368. doi: 10.1002/smll.202502368. Epub 2025 Apr 30.

DOI:10.1002/smll.202502368
PMID:40304161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12423913/
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 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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/acdcc806f9fa/SMLL-21-2502368-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/24570481e892/SMLL-21-2502368-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/d697e3a17627/SMLL-21-2502368-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/bd56196c39f6/SMLL-21-2502368-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/fdaea2c11e91/SMLL-21-2502368-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/be77003915ef/SMLL-21-2502368-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/8323ef70a038/SMLL-21-2502368-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/acdcc806f9fa/SMLL-21-2502368-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/24570481e892/SMLL-21-2502368-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/d697e3a17627/SMLL-21-2502368-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/bd56196c39f6/SMLL-21-2502368-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/fdaea2c11e91/SMLL-21-2502368-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/be77003915ef/SMLL-21-2502368-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/8323ef70a038/SMLL-21-2502368-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f1/12423913/acdcc806f9fa/SMLL-21-2502368-g007.jpg

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Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202417779. doi: 10.1002/anie.202417779. Epub 2024 Dec 2.
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High-Performance Polyimide Covalent Organic Frameworks for Lithium-Ion Batteries: Exceptional Stability and Capacity Retention at High Current Densities.用于锂离子电池的高性能聚酰亚胺共价有机骨架:在高电流密度下具有出色的稳定性和容量保持率。
Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202412452. doi: 10.1002/anie.202412452. Epub 2024 Nov 7.
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Integrating Multiple Redox-Active Units into Conductive Covalent Organic Frameworks for High-Performance Sodium-Ion Batteries.
将多个氧化还原活性单元集成到用于高性能钠离子电池的导电共价有机框架中。
Angew Chem Int Ed Engl. 2025 Jan 27;64(5):e202417493. doi: 10.1002/anie.202417493. Epub 2024 Oct 31.
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Biomass-Derived Materials for Advanced Rechargeable Batteries.用于先进可充电电池的生物质衍生材料。
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