Electrospun Carbon-Tin Oxide Composite Nanofibers for Use as Lithium Ion Battery Anodes

被引:150
作者
Bonino, Christopher A. [1 ]
Ji, Liwen [2 ]
Lin, Zhan [2 ]
Toprakci, Ozan [2 ]
Zhang, Xiangwu [2 ]
Khan, Saad A. [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Text Engn Chem & Sci, Raleigh, NC 27695 USA
基金
美国国家科学基金会;
关键词
composite nanofibers; electrospinning; lithium-ion battery; tin oxide; anode;
D O I
10.1021/am2004015
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Composite carbon tin oxide (C-SnO2) nanofibers are prepared by two methods and evaluated as anodes in lithium. ion battery half cells. Such an approach complements the long cycle life of carbon with the high lithium storage capacity of tin oxide. In addition, the high surface-to-volume ratio of the nanofibers improves the accessibility for lithium intercalation as compared to graphite-based anodes, while eliminating the need for binders or conductive additives. The composite nanofibrous anodes have first discharge capacities of 788 mAh g(-1) at 50 mA g(-1) current density, which are greater than pure carbon nanofiber anodes, as well as the theoretical capacity of graphite (372 mAh g(-1)) the traditional anode material. In the first protocol to fabricate the C-SnO2 composites, tin sulfate is directly incorporated within polyacrylonitrile (PAN) nanofibers by electrospinning. During a thermal treatment the tin salt is converted to tin oxide and the polymer is carbonized, yielding carbon-SnO2 nanofibers. In the second approach, we soak the nanofiber mats in tin sulfate solutions prior to the final thermal treatment, thereby loading the outer surfaces with SnO2 nanoparticles and raising the tin content from 1.9 to 8.6 wt %. Energy-dispersive spectro;copy and X-ray diffraction analyses confirm the formation of conversion of tin sulfate to tin oxide. Furthermore, analysis with Raman spectroscopy reveals that the additional salt soak treatment from the second fabrication approach increases in the disorder of the carboxystructure, as compared to the first approach. We also discuss the performance of our C-SnO2 compared with its theoretical capacity and other nanofiber electrode composites previously reported in
引用
收藏
页码:2534 / 2542
页数:9
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