阴极
材料科学
电化学
共价有机骨架
氧化还原
储能
锂(药物)
电池(电)
碳纳米管
纳米技术
共价键
电化学储能
离子
多孔性
化学工程
聚合物
锂离子电池
扩散
电极
复合材料
化学
超级电容器
有机化学
医学
功率(物理)
物理
物理化学
量子力学
工程类
冶金
内分泌学
热力学
作者
Chao Jia,An Duan,Chao Liu,Wen‐Zhuang Wang,Shi‐Xian Gan,Qiao‐Yan Qi,Yongjun Li,Xiaoyu Huang,Xin Zhao
出处
期刊:Small
[Wiley]
日期:2023-03-14
卷期号:19 (24)
被引量:34
标识
DOI:10.1002/smll.202300518
摘要
Covalent organic frameworks (COFs) have emerged as a new class of cathode materials for energy storage in recent years. However, they are limited to two-dimensional (2D) or three-dimensional (3D) framework structures. Herein, this work reports designed synthesis of a redox-active one-dimensional (1D) COF and its composites with 1D carbon nanotubes (CNTs) via in situ growth. Used as cathode materials for Li-ion batteries, the 1D COF@CNT composites with unique dendritic core-shell structure can provide abundant and easily accessible redox-active sites, which contribute to improve diffusion rate of lithium ions and the corresponding specific capacity. This synergistic structural design enables excellent electrochemical performance of the cathodes, giving rise to 95% utilization of redox-active sites, high rate capability (81% capacity retention at 10 C), and long cycling stability (86% retention after 600 cycles at 5 C). As the first example to explore the application of 1D COFs in the field of energy storage, this study demonstrates the great potential of this novel type of linear crystalline porous polymers in battery technologies.
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