阳极
材料科学
锂(药物)
离子
共价键
电极
化学工程
氧化还原
共价有机骨架
纳米技术
复合材料
化学
有机化学
物理化学
多孔性
工程类
内分泌学
医学
冶金
作者
Manman Wu,Zhao Yang,Hongtao Zhang,Jie Zhu,Yanfeng Ma,Chenxi Li,Yamin Zhang,Yongsheng Chen
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2021-11-22
卷期号:15 (11): 9779-9784
被引量:43
标识
DOI:10.1007/s12274-021-3950-6
摘要
Covalent organic frameworks (COFs) have been broadly investigated for energy storage systems. However, many COF-based anode materials suffer from low utilization of redox-active sites and sluggish ions/electrons transport caused by their densely stacked layers. Thus, it is still a great challenge to obtain COF-based anode materials with fast ions/electrons transport and thus superior rate performance. Herein, a redox-active piperazine-terephthalaldehyde (PA-TA) COF with ultra-large interlayer distance is designed and synthesized for high-rate anode material, which contains piperazine units adopting a chair-shaped conformation with the nonplanar linkages of a tetrahedral configuration. This unique structure renders PA-TA COF an ultra-large interlayer distance of 6.2 Å, and further enables it to achieve outstanding rate and cycling performance. With a high specific capacity of 543 mAh·g−1 even after 400 cycles at 1.0 A·g−1, it still could afford a specific capacity of 207 mAh·g−1 even at a high current density of 5.0 A·g−1. Our study indicates that expanding the interlayer distance of COFs by rational molecular design would be of great importance to develop high-rate electrode materials for lithium-ion batteries.
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