A polypyrrole-coated acetylene black/sulfur composite cathode material for lithium-sulfur batteries

被引:46
|
作者
Yang, Wu [1 ,2 ]
Yang, Wang [1 ]
Feng, Jiani [1 ]
Qin, Xiujuan [1 ,2 ]
机构
[1] Yanshan Univ, Coll Environm & Chem Engn, Hebei Key Lab Appl Chem, Qinhuangdao 066004, Hebei, Peoples R China
[2] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-sulfur batteries; Acetylene black; Polypyrrole; Core-shell; LI-S BATTERIES; GEL POLYMER ELECTROLYTE; ELECTROCHEMICAL PERFORMANCE; BLACK COMPOSITES; SHELL; POLYSULFIDES; SEPARATOR; ANODE; SUPERCAPACITORS; NANOSHEETS;
D O I
10.1016/j.jechem.2017.05.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
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/sulfur@polypyrrole (AB/S@PPy) 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 coreshell 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/S@PPy 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/S@PPy composite after activation, and the capacity retention is over 62.5% after 200 cycles. (C) 2017 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B. V. and Science Press. All rights reserved.
引用
收藏
页码:813 / 819
页数:7
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