Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Key Laboratory of Cluster Science, Ministry of Education, School of Chemistry and Chemical Engineering, Beijing Institute of Technology , Beijing 100081, P. R. China.
J Am Chem Soc. 2017 Mar 29;139(12):4258-4261. doi: 10.1021/jacs.7b02648. Epub 2017 Mar 21.
Covalent organic frameworks (COFs) have attracted growing interest by virtue of their structural diversity and tunability. Herein, we present a novel approach for the development of organic rechargeable battery cathodes in which three distinct redox-active COFs were successfully prepared and delaminated into 2D few-layer nanosheets. Compared with the pristine COFs, the exfoliated COFs with shorter Li diffusion pathways allow a significant higher utilization efficiency of redox sites and faster kinetics for lithium storage. Unlike diffusion-controlled manners in the bulk COFs, the redox reactions in ECOFs are mainly dominated by charge transfer process. The capacity and potential are further engineered by reticular design of COFs without altering the underlying topology. Specifically, DAAQ-ECOF exhibits excellent rechargeability (98% capacity retention after 1800 cycles) and fast charge-discharge ability (74% retention at 500 mA g as compared to at 20 mA g). DABQ-ECOF shows a specific capacity of 210 mA h g and a voltage plateau of 2.8 V.
共价有机框架(COFs)因其结构多样性和可调谐性而引起了越来越多的关注。本文提出了一种开发有机可充电电池正极的新方法,其中成功制备了三种不同的氧化还原活性 COF,并将其剥离成 2D 少层纳米片。与原始 COF 相比,具有较短 Li 扩散途径的剥离 COF 允许更高的氧化还原位点利用率和更快的储锂动力学。与体相 COF 中的扩散控制方式不同,ECOF 中的氧化还原反应主要由电荷转移过程控制。通过不改变基本拓扑结构的 COF 的网状设计进一步设计容量和电位。具体来说,DAAQ-ECOF 表现出优异的可充电性(1800 次循环后容量保持率为 98%)和快速充放电能力(与 20 mA g 相比,在 500 mA g 时保留 74%)。DABQ-ECOF 的比容量为 210 mA h g,电压平台为 2.8 V。