多硫化物
锂硫电池
纳米结构
锂(药物)
纳米技术
硫黄
材料科学
电化学
化学
冶金
电极
电解质
医学
内分泌学
物理化学
作者
Wenchao Zhang,Kaixin Zhao,Qi Jin,Junpeng Xiao,Huiqing Lu,Xitian Zhang,Lili Wu
标识
DOI:10.1016/j.electacta.2022.141104
摘要
Lithium-sulfur (Li-S) batteries have received extensive attention in electrochemical energy storage systems due to their high theoretical energy density as well as natural abundance of sulfur and low cost. However, Li-S batteries exhibit rapid capacity decay and inferior rate performance due to polysulfides (LiPSs) shuttling and sluggish redox kinetics. Therefore, it is crucial that LiPSs are anchored and their conversion reactions are catalyzed in order to improve the performance of Li-S batteries. In this work, ZIF-67-derived carbon polyhedra decorated with ultrafine CoS 2 nanoparticles are interconnected by carbon nanotubes (CNTs). The uniformly distributed CoS 2 nanoparticles can immobilize LiPSs and catalyze their conversion of solid-to-liquid-to-solid reactions, which enhances the redox kinetics. Furthermore, the three-dimensional conductive network consisting of ZIF-67-derived carbon polyhedra and CNTs facilitates fast electron transport and thus leads to excellent rate and cycling performance. The cells were assembled using CoS 2 -NC@CNTs-pp and show a high initial discharge capacity of 1408.5 mAh g −1 at 0.1 C and 1186.7 mAh g −1 at 1 C, and they remain outstanding cycling stability for over 500 cycles. Even at a high C rate of 5 C, it still can deliver a high discharge capacity of 832.6 mAh g −1 . This work provides an efficient route to accelerate redox conversion and suppress the shuttle effect by designing a multifunctional separator.
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