Sulfur embedded in metal organic framework-derived hierarchically porous carbon nanoplates for high performance lithium-sulfur battery

被引:266
作者
Xu, Guiyin [1 ]
Ding, Bing
Shen, Laifa
Nie, Ping
Han, Jinpeng
Zhang, Xiaogang
机构
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Engn, Nanjing 210016, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
DIRECT CARBONIZATION; ACTIVATED CARBON; CATHODE; CAPACITY; POROSITY;
D O I
10.1039/c3ta00004d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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 m(2) g(-1)) and large pore volume (1.18 cm(3) 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.
引用
收藏
页码:4490 / 4496
页数:7
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