材料科学
共价有机骨架
共价键
动力学
电极
化学工程
苯
扩散
锂(药物)
共轭体系
离子
纳米技术
有机化学
复合材料
化学
聚合物
物理化学
工程类
内分泌学
物理
热力学
医学
量子力学
多孔性
作者
Xiudong Chen,Yusen Li,Liang Wang,Yi Xu,Anmin Nie,Qianqian Li,Fan Wu,Weiwei Sun,Xiang Zhang,Róbert Vajtai,Pulickel M. Ajayan,Long Chen,Yong Wang
标识
DOI:10.1002/adma.201901640
摘要
Covalent organic frameworks (COFs) with reversible redox behaviors are potential electrode materials for lithium-ion batteries (LIBs). However, the sluggish lithium diffusion kinetics, poor electronic conductivity, low reversible capacities, and poor rate performance for most reported COF materials limit their further application. Herein, a new 2D COF (TFPB-COF) with six unsaturated benzene rings per repeating unit and ordered mesoporous pores (≈2.1 nm) is designed. A chemical stripping strategy is developed to obtain exfoliated few-layered COF nanosheets (E-TFPB-COF), whose restacking is prevented by the in situ formed MnO2 nanoparticles. Compared with the bulk TFPB-COF, the exfoliated TFPB-COF exhibits new active Li-storage sites associated with conjugated aromatic π electrons by facilitating faster ion/electron kinetics. The E-TFPB-COF/MnO2 and E-TFPB-COF electrodes exhibit large reversible capacities of 1359 and 968 mAh g-1 after 300 cycles with good high-rate capability.
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