Biswas Sandip, Pramanik Atin, Dey Anupam, Chattopadhyay Shreyasi, Pieshkov Tymofii S, Bhattacharyya Sohini, Ajayan Pulickel M, Maji Tapas Kumar
Molecular Materials Laboratory, Chemistry and Physics of Materials Unit, School of Advanced Materials (SAMat), International Centre for Materials Science, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore, 560064, India.
Department of Material Science and NanoEngineering, Rice University, Houston, TX, 77005, USA.
Small. 2024 Nov;20(48):e2406173. doi: 10.1002/smll.202406173. Epub 2024 Sep 3.
Covalent organic frameworks (COFs), featuring structural diversity, permanent porosity, and functional versatility, have emerged as promising electrode materials for rechargeable batteries. To date, amorphous polymer, COF, or their composites are mostly explored in lithium-ion batteries (LIBs), while their research in other alkali metal ion batteries is still in infancy. This can be due to the challenges that arise from large volume changes, slow diffusion kinetics, and inefficient active site utilization by the large Na or K ion. Herein, microwave-assisted imide-based 2D COF, TAPB-NDA covalently connected with amine-functionalized carbon nanotubes (TAPB-NDA@CNT) targeting the application in both Li-/Na-ion batteries, is synthesized. As-synthesized, TAPB-NDA@CNT50 displays the good performance as LIB cathode with a specific capacity of ≈138 mAh g at 25 mA g, long cycling stability (81.2% retention after 2000 cycles at 300 mA g), with excellent reversible capacity retention of ≈79.6%. Similarly, TAPB-NDA@CNT50, when employed in sodium-ion battery (SIB), exhibited 136.7 mAh g specific capacity at 25 mA g, retained ≈80% of the reversible capacity after 1000 cycles at 300 mA g and showing excellent rate performance. The structural advantage of TAPB-NDA@CNT will encourage researchers to design COF-based cathodes for the alkali ion batteries.
共价有机框架(COFs)具有结构多样性、永久孔隙率和功能多样性,已成为有前景的可充电电池电极材料。迄今为止,非晶态聚合物、COF或它们的复合材料大多在锂离子电池(LIBs)中得到探索,而它们在其他碱金属离子电池中的研究仍处于起步阶段。这可能是由于大体积变化、缓慢的扩散动力学以及大的Na或K离子对活性位点利用效率低下所带来的挑战。在此,合成了基于微波辅助酰亚胺的二维COF,即与胺官能化碳纳米管共价连接的TAPB-NDA(TAPB-NDA@CNT),其目标应用于锂/钠离子电池。合成后的TAPB-NDA@CNT50作为LIB阴极表现出良好的性能,在25 mA g时比容量约为138 mAh g,具有长循环稳定性(在300 mA g下2000次循环后保留率为81.2%),具有约79.6%的优异可逆容量保持率。同样,TAPB-NDA@CNT50在钠离子电池(SIB)中使用时,在25 mA g时表现出136.7 mAh g的比容量,在300 mA g下1000次循环后保留了约80%的可逆容量,并显示出优异的倍率性能。TAPB-NDA@CNT的结构优势将鼓励研究人员设计用于碱离子电池的基于COF的阴极。