聚吡咯
多硫化物
硫黄
复合数
材料科学
炭黑
电解质
锂(药物)
阴极
溶解
化学工程
复合材料
化学
电极
冶金
聚合物
物理化学
聚合
工程类
天然橡胶
内分泌学
医学
作者
Yang Wu,Wang Yang,Jiani Feng,Xiujuan Qin
标识
DOI:10.1016/j.jechem.2017.05.007
摘要
Lithium–sulfur batteries are promising next-generation energy storage devices beyond conventional lithium ion batteries. However, it suffers from rapid capacity fading and poor cyclic stability. Here we report a facile in situ sulfur deposition and chemical oxidative polymerization method for preparing acetylene black/[email protected] (AB/[email protected]) composite as a cathode material for lithium–sulfur batteries. It is demonstrated that PPy is covered uniformly onto the surface of the AB/S composite forming a core–shell structure. In the structure, AB in the matrix and PPy on the surface acts as a combined conductive framework to provide ions and electrons transport pathways, and to inhibit the dissolution or diffusion of polysulfide into the electrolyte. The as-designed AB/[email protected] composite exhibits excellent rate capability and cyclic stability. The initial discharge specific capacity is as high as 1179.4 mAh/g, and remains at 769.3 mAh/g after 80 cycles at 0.2 C. Even at a high rate (0.5 C), a maximum discharge capacity of 811.1 mAh/g is still achieved for the AB/[email protected] composite after activation, and the capacity retention is over 62.5% after 200 cycles.
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