阴极
硫黄
材料科学
两亲性
化学工程
表面改性
多硫化物
锂(药物)
碳纳米纤维
锂硫电池
碳纤维
聚合物
纳米技术
化学
电化学
电极
碳纳米管
共聚物
复合材料
物理化学
内分泌学
冶金
工程类
复合数
医学
电解质
作者
Guangyuan Zheng,Qianfan Zhang,J. Judy,Yuan Yang,Weiyang Li,Zhi Wei Seh,Yi Cui
出处
期刊:Nano Letters
[American Chemical Society]
日期:2013-02-08
卷期号:13 (3): 1265-1270
被引量:689
摘要
Tremendous effort has been put into developing viable lithium sulfur batteries, due to their high specific energy and relatively low cost. Despite recent progress in addressing the various problems of sulfur cathodes, lithium sulfur batteries still exhibit significant capacity decay over cycling. Herein, we identify a new capacity fading mechanism of the sulfur cathodes, relating to Li(x)S detachment from the carbon surface during the discharge process. This observation is confirmed by ex-situ transmission electron microscopy study and first-principles calculations. We demonstrate that this capacity fading mechanism can be overcome by introducing amphiphilic polymers to modify the carbon surface, rendering strong interactions between the nonpolar carbon and the polar Li(x)S clusters. The modified sulfur cathode show excellent cycling performance with specific capacity close to 1180 mAh/g at C/5 current rate. Capacity retention of 80% is achieved over 300 cycles at C/2.
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