4.6 Article

Highly flexible self-standing film electrode composed of mesoporous rutile TiO2/C nanofibers for lithium-ion batteries

Journal

ELECTROCHIMICA ACTA
Volume 85, Issue -, Pages 636-643

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2012.08.126

Keywords

Film electrode; Lithium ion battery; Rutile TiO2; Electrospinning; Nanofiber

Funding

  1. National Science Foundation for Distinguished Young Scholars of China [51025209]
  2. National Nature Science Foundation of China [21103089]
  3. Key Projects in Nature Science Foundation of Jiangsu Province [BK2011030]

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There is increasing interest in flexible, safe, high-power thin-film lithium-ion batteries which can be applied to various modern devices. Although TiO2 in rutile phase is highly attractive as an anode material of lithium-ion batteries for its high thermal stability and theoretical capacity of 336 mA h g(-1) and low price, its inflexibility and sluggish lithium intercalation kinetics of bulk phase strongly limit its practical application for particular in thin-film electrode. Here we show a simple way to prepare highly flexible self-standing thin-film electrodes composed of mesoporous rutile TiO2/C nanofibers with low carbon content (<15 wt.%) by electrospinning technique with outstanding electrochemical performance, which can be applied directly as electrodes of lithium-ion batteries without the further use of any additive and binder. The atmosphere during calcination plays a critical role in determining the flexible nature of thin film and particle size of TiO2 in as-fabricated nanofibers. Big size (10 cm x 4cm), flexible thin film is obtained after heat treatment under 10%H-2-Ar at 900 degrees C for 3 h. After optimization, the diameter of fibers can reach as small as similar to 110nm, and the as-prepared rutile TiO2 films show high initial electrochemical activity with the first discharge capacity as high as 388 mA hg(-1). What is more, very stable reversible capacities of similar to 122, 92, and 70 mA h g(-1) are achieved respectively at 1,5 and 10C rates with negligible decay rate within 100 cycling times. (C) 2012 Elsevier Ltd. All rights reserved.

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