Improved cyclability of lithium-sulfur battery cathode using encapsulated sulfur in hollow carbon nanofiber@nitrogen-doped porous carbon core-shell composite

被引:109
|
作者
Li, Qiang [1 ]
Zhang, Zhian [1 ,2 ]
Guo, Zaiping [2 ]
Lai, Yanqing [1 ]
Zhang, Kai [1 ]
Li, Jie [1 ]
机构
[1] Cent S Univ, Sch Met & Environm, Changsha 410083, Hunan, Peoples R China
[2] Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2522, Australia
关键词
MESOPOROUS CARBON; GRAPHENE OXIDE; PERFORMANCE; EFFICIENCY; CHALLENGES; CAPACITY; SOLVENT; FACILE;
D O I
10.1016/j.carbon.2014.05.047
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
Hollow carbon nanofiber@nitrogen-doped porous carbon (HCNF@NPC) core-shell composite, which was carbonized from HCNF@polyaniline, was prepared as an improved high conductive carbon matrix for encapsulating sulfur as a cathode composite material for lithium-sulfur batteries. The prepared HCNF@NPC-S composite with high sulfur content of 77.5 wt.% showed an obvious core-shell structure with an NPC layer coating on the surface of the HCNFs and sulfur homogeneously distributed in the coating layer. This material exhibited much better electrochemical performance than the HCNF-S composite, delivered initial discharge capacity of 1170 mAh g(-1), and maintains 590 mAh g(-1) after 200 cycles at the current density of 837.5 mA g(-1) (0.5 C). The significantly improved electrochemical performance of the HCNF@NPC-S composite was attributed to the synergetic effect between HCNF cores, which provided electronic conduction pathways and worked as mechanical support, and the NPC shells with relatively high surface area and pore volume, which could trap sulfur/polysulfides and provide Li+ conductive pathways. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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