4.6 Article

Solvent-assisted molten salt process: A new route to synthesise α-Fe2O3/C nanocomposite and its electrochemical performance in lithium-ion batteries

期刊

ELECTROCHIMICA ACTA
卷 55, 期 17, 页码 5006-5013

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2010.04.006

关键词

Molten salt; Iron oxide; Nanocomposite; Carbon coating; Lithium-ion batteries

资金

  1. Ministry of Higher Education of the Government of Malaysia
  2. Australian Research Council (ARC) [LP0775456]
  3. Australian Research Council [LP0775456] Funding Source: Australian Research Council

向作者/读者索取更多资源

Nanostructured alpha-Fe2O3 was synthesised by a simple molten salt process using FeCl2 center dot 4H(2)O as a starting material and LiNO3-LiOH center dot H2O-H2O2 as a eutectic mixture at 300 degrees C. To synthesise alpha-Fe2O3/C composite, both alpha-Fe2O3 and malic acid were dispersed together in toluene, where malic acid was used as a carbon source. The morphology and microstructure of both compounds were confirmed by X-ray diffraction, Raman spectroscopy and transmission electron microscopy. Electrochemical testing, including constant current charge-discharge and cyclic voltammetry (CV), was carried out. The alpha-Fe2O3/C composite anode exhibited much better electrochemical performance than the bare alpha-Fe2O3. The discharge capacities of the composite were measured to be 2112 mAh g(-1) at C/2 after 100 cycles and 584 mAh g(-1) at 20 C after 10 cycles. The superior electrochemical performance of alpha-Fe2O3/C composite can be mainly attributed to the combined effects of the nanostructure, the carbon layering on the alpha-Fe2O3 nanoparticles, and the porous ultra-fine carbon matrix, where the three factors would contribute to provide high electronic conductivity, reduce the traverse time of electrons and lithium-ions, and could also prevent high volume expansion of the anode film during cycling. Our results indicate that the prepared alpha-Fe2O3/C nanocomposite is a very promising anode material for Li-ion power batteries. (C) 2010 Elsevier Ltd. All rights reserved.

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