Electrospun Carbon-Tin Oxide Composite Nanofibers for Use as Lithium Ion Battery Anodes
Citations Over TimeTop 1% of 2011 papers
Abstract
Composite carbon-tin oxide (C-SnO(2)) 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-SnO(2) 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-SnO(2) 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 SnO(2) nanoparticles and raising the tin content from 1.9 to 8.6 wt %. Energy-dispersive spectroscopy 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 carbon structure, as compared to the first approach. We also discuss the performance of our C-SnO(2) compared with its theoretical capacity and other nanofiber electrode composites previously reported in the literature.
Related Papers
- → The degradation and stabilization of polyacrylonitrile. I. Evidence for β‐ketonitrile defect structures as initiators of degradation(1982)11 cited
- → Use of X-Ray Structure Analysis to Study the Fine Structure of Carbon and Polyacrylonitrile Fibers(2016)2 cited
- Preparation of Carrier of Enzyme-immobilization-magnetic Polyacrylonitrile Microsphere by Spray Method(2002)
- Structure Characteristic of Polyacrylonitrile Copolymer by IR Spectrometry(2012)
- Study on polyacrylonitrile-based activated carbon hollow fiber(2003)