三嗪
共价键
阴极
共价有机骨架
锂(药物)
阳极
多硫化物
材料科学
化学工程
微型多孔材料
化学
电极
纳米技术
高分子化学
有机化学
复合材料
物理化学
电解质
内分泌学
工程类
医学
作者
Mingkai Li,Yingming Wang,Shuzheng Sun,Yanqin Yang,GU Guo-xian,Zisheng Zhang
标识
DOI:10.1016/j.cej.2021.132254
摘要
To overcome the loss of soluble lithium polysulfides (LiPSs) generated during the discharge process of lithium-sulfur (Li-S) batteries, a lot of efforts have been devoted to the design of novel micro- or nano-structured host materials, aiming to trap soluble polysulfide within the network. Covalent organic framework (COF) as porous materials have been receiving a great deal of attention. Herein, an allyl-rich triazine covalent organic framework (ART-COF) synthesized by 5-(allyloxy) isophthalaldehyde and 4,4′,4″-(1,3,5-triazine-2,4,6-triyl) trianiline (TAPT) is used as cathode host material for Li-S batteries. Owning to the synergistic effect of physical force (through microporous channel) and chemical force (through C-S covalent bond and dipole–dipole interaction between nitrogen and lithium), the shuttle action of LiPSs to anode electrode can be effectively limited. ART-COF shows a high initial specific capacity of 1270 mAh g−1 which retains 1220 mAh g−1 after 100 charge–discharge cycles at 0.2C, and even at 1C it also demonstrates an initial specific capacity of 993 mAh g−1 which retains 818 mAh g−1 after 500 cycles with a low fading rate of 0.035% per cycle. This work represents a sustainable approach for developing highly stable and long-lived Li-S batteries.
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