Micro-nano structure composite cathode material with high sulfur loading for advanced lithium-sulfur batteries

被引:39
|
作者
Zhang, Zhian [1 ]
Li, Qiang [1 ]
Zhang, Kai [1 ]
Lai, Yanqing [1 ]
Li, Jie [1 ]
机构
[1] Cent S Univ, Sch Met & Environm, Changsha 410083, Peoples R China
关键词
hybrid structure; hollow carbon nanofiber; polydopamine; high sulfur content; lithium-sulfur batteries; MESOPOROUS CARBON; HIGH-PERFORMANCE; GRAPHENE OXIDE; RATE CAPABILITY; NANOTUBES; NANOFIBER; NANOCOMPOSITE; ELECTROLYTE; EFFICIENCY; ROUTE;
D O I
10.1016/j.electacta.2014.11.099
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A micro-nano structure based on polydopamine-grafted hollow carbon nanofiber-sulfur composite (HCNF@PDA-S) is designed as a cathode material for effective trapping of sulfur and polysulfides for lithium-sulfur batteries. Hollow carbon nanofiber@polydopamine (HCNF@PDA) micro-nano structure hybrid is first prepared by an in-situ polymerization dopamine monomer decorating on the surface of HCNFs and then elemental sulfur is infiltrated into the HCNF@PDA hybrid nanostructure by thermal treatment. The obtained HCNF@PDA-S composite shows the micro-nano structure based on the micron-sized hollow carbon nanofiber in length and nano-sized polydopamine grafted on the outer surfaces of the HCNFs with homogeneously distribution of sulfur. Compared with the HCNF-S composite, HCNF@PDA-S composite with a high sulfur content of approximately 80 wt% exhibits better electrochemical performance, which delivers initial discharge capacity of 800 mAh g(-1) and maintains 530 mAh g(-1) after 200 cycles at 0.5 C rate. The enhancements of electrochemical performances may be attributed to the unique micro-nano hybrid structure based on HCNFs and PDA coating layer, in which the micro-sized HCNFs offer the electronic conductivity and provide a firm porous network of the cathode tolerating the volume expansion of sulfur cathode, and nano-sized PDA layers effectively prevent the dissolution of the polysulfides into the electrolyte. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:53 / 60
页数:8
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