Free-standing, curled and partially reduced graphene oxide network as sulfur host for high-performance lithium–sulfur batteries

被引:0
作者
陈辉亮 [1 ,2 ,3 ]
肖卓建 [1 ,2 ,3 ]
张楠 [1 ,2 ,3 ]
肖仕奇 [1 ,2 ,3 ]
夏晓刚 [1 ,2 ,3 ]
席薇 [1 ,2 ,3 ]
王艳春 [1 ,2 ]
周维亚 [1 ,2 ,3 ]
解思深 [1 ,2 ,3 ]
机构
[1] Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences
[2] Beijing Key Laboratory for Advanced Functional Materials and Structure Research
[3] School of Physical Sciences, University of Chinese Academy of Sciences
基金
中国国家自然科学基金;
关键词
lithium–sulfur batteries; sulfur cathode; curled reduced graphene oxide;
D O I
暂无
中图分类号
TM912 [蓄电池];
学科分类号
0808 ;
摘要
Lithium–sulfur(Li–S) batteries have received more and more attention because of higher specific capacity and energy density of sulfur than current lithium–ion batteries. However, the low electrical conductivity of sulfur and its discharge product, and also the high dissolution of polysulfides restrict the Li–S battery practical applications. To improve their performances, in this work, we fabricate a novel free-standing, curled and partially reduced graphene oxide(CPrGO for short) network and combine it with sulfur to form a CPrGO–S composite as a cathode for Li–S battery. With sulfur content of 60 wt%, the free-standing CPrGO–S composite network delievers an initial capacity of 988.9 m Ah·g-1. After 200 cycles,it shows a stable capacity of 841.4 m Ah·g-1at 0.2 C, retaining about 85% of the initial value. The high electrochemical performance demonstrates that the CPrGO–S network has great potential applications in energy storage system. Such improved properties can be ascribed to the unique free-standing and continous CPrGO–S network which has high specific surface area and good electrical conductivity. In addition, oxygen-containing groups on the partially reduced graphene oxide are beneficial to preventing the polysulfides from dissolving into electrolyte and can mitigate the "shuttle effect".
引用
收藏
页码:463 / 469
页数:7
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  • [1] Wang Z Y,Dong Y F,Li H J,Zhao Z B,Wu H B,Hao C,Liu S H,Qiu J S,Lou X W. Nat.Commun . 2014