Budding willow branches shaped Na3V2(PO4)3/C nanofibers synthesized via an electrospinning technique and used as cathode material for sodium ion batteries

被引:145
作者
Li, Hui [1 ]
Bai, Ying [1 ,2 ]
Wu, Feng [1 ,2 ]
Li, Yu [1 ]
Wu, Chuan [1 ,2 ]
机构
[1] Beijing Inst Technol, Sch Chem Engn & Environm, Beijing Key Lab Environm Sci & Engn, Beijing 100081, Peoples R China
[2] Natl Dev Ctr High Technol Green Mat, Beijing 100081, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Sodium ion batteries; Electrospin; Cathode; Nanofibers; Na3V2(PO4)(3)/C; Carbon; CARBON-COATED NA3V2(PO4)(3); ELECTROCHEMICAL PROPERTIES; ELECTRODE MATERIAL; INSERTION CATHODE; ANODE MATERIAL; PERFORMANCE; STORAGE; COMPOSITE; MORPHOLOGY; NANOWIRES;
D O I
10.1016/j.jpowsour.2014.09.153
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
Budding willow branches shaped Na3V2(PO4)(3)/C nanofibers were successfully synthesized by a simple electrospinning technique with Poly(vinyl pyrrilidone) (PVP). The Na3V2(PO4)(3)/C nanoparticles that anchored on the nanofibers surface seemed like the willow buds; the inner core of the nanofibers, which composed Na3V2(PO4)(3), looked like willow twig and the uniform carbon layer was same with willow bark. Such special morphology played a vital role in improving cycle stability and rate capability of the electrode due to the conductive network built up by nanofibers. The Na3V2(PO4)(3)/C nanofibers cathode exhibited an initial specific capacity of 106.8 mAh g(-1) at a current density of 0.2C, still stabling at 107.2 mAh g(-1) after 125 cycles with excellent cycle stability. Moreover, a capacity retention of 95.7% was obtained when Na3V2(PO4)(3)/C nanofibers cycled stepwise from 0.2 to 2C. Good electrochemical performance should be ascribed to both the special morphology and preferential growth of the (113) plane. The simple synthesis technique and good electrochemical performance suggests that this material with the special shape of budding willow branches is a promising cathode for sodium ion batteries. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:784 / 792
页数:9
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