阴极
共价键
锂(药物)
共价有机骨架
硫黄
扩散
吸附
储能
多硫化物
材料科学
纳米技术
化学
化学工程
电极
有机化学
电解质
工程类
冶金
物理化学
功率(物理)
内分泌学
物理
热力学
医学
量子力学
作者
Shaobo Cai,Runlin Ma,Ke Wang,Hao Zhang,Yiyang Liu,Menggai Jiao,Y. Tian,Yongzheng Fang,Manman Wu,Zhen Zhou
标识
DOI:10.1016/j.cej.2024.151979
摘要
Lithium-sulfur (Li-S) batteries have emerged as a promising alternative energy storage system due to their high energy density and cost-effectiveness. However, practical applications of Li-S batteries are hindered by challenges such as the shuttle effect and sluggish redox kinetics. In this study, a three-dimensional (3D) flower-like diaminoanthraquinone (DAAQ)-covalent organic framework (COF) was developed, featuring nanorod-like petals and enriched with abundant N and O adsorption sites, serving as a host material for the sulfur cathode of Li-S batteries. Through a process of sulfur melting-diffusion, the resulting DAAQ-COF@S cathode material demonstrated a stable 3D cross-linked morphology with a hierarchical pore structure, maximizing the exposure of N/O adsorptive sites and facilitating rapid ion diffusion. This effectively inhibited the shuttling effect of lithium polysulfides (LiPSs) and enhanced rate performance. Consequently, DAAQ-COF@S cathodes exhibited a high initial discharge capacity of 1182.0 mAh g−1 at 0.1 C, with a capacity retention rate of 79.6% after 500 cycles at 2 C. Even at a high current density of 4 C, they maintained a high capacity of 616.8 mAh g−1, surpassing the majority of previously reported COF-based host materials for Li-S batteries. This work underscores the significance of COF micromorphology and advances the development of high-performance cathodes for Li-S batteries.
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