法拉第效率
硫黄
阴极
纳米结构
电化学
化学工程
材料科学
多孔性
金属有机骨架
热解
锂硫电池
碳纤维
溶解
电池(电)
比表面积
纳米技术
电极
复合数
化学
催化作用
复合材料
有机化学
吸附
冶金
功率(物理)
物理化学
工程类
物理
量子力学
作者
Guiyin Xu,Bing Ding,Laifa Shen,Ping Nie,Jinpeng Han,Xiaogang Zhang
摘要
The wide-scale implementation of lithium–sulfur batteries is limited by their rapid capacity fading, which is induced by the pulverization of the sulfur cathode and dissolution of intermediate polysulfides. Herein, we reported the encapsulation of sulfur (S) into hierarchically porous carbon nanoplates (HPCN) derived from one-step pyrolysis of metal-organic frameworks (MOF-5). HPCN with an average thickness of ca. 50 nm exhibits a three-dimensional (3D) hierarchically porous nanostructure, high specific surface area (1645 m2 g−1) and large pore volume (1.18 cm3 g−1). When evaluated as a cathode for lithium–sulfur batteries, the HPCN–S composite demonstrates high specific capacity and excellent cycling performance. At a current rate of 0.1 C, the initial discharge capacity of HPCN–S is 1177 mA h g−1. Even at a current rate of 0.5 C, it still delivers a discharge capacity of 730 mA h g−1 after 50 cycles and the Coulombic efficiency is up to 97%. The enhanced electrochemical performance of HPCN–S is closely related to its well-defined 3D porous plate nanostructure which not only provides stable electronic and ionic transfer channels, but also plays a key role as a strong absorbent to retain polysulfides and accommodate volume variation during the charge–discharge process.
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