• DocumentCode
    1921111
  • Title

    Hydrothermal synthesis and rate capacity studies of Li3V2(PO4)3 cathode material

  • Author

    Tang, Yan ; Zhong, Benghe ; Guo, Xiaodong ; Zhao, Haochuan ; Song, Yang ; Liu, Heng

  • Author_Institution
    Coll. of Chem. Eng., Sichuan Univ., Chengdu, China
  • Volume
    1
  • fYear
    2011
  • fDate
    20-22 May 2011
  • Firstpage
    690
  • Lastpage
    693
  • Abstract
    The Li3V2(PO4)3 cathode material was obtained by a hydrothermal process, using citric acid as reduction agent. During the calcination process, citric acid and glucose were both used as the carbon sources. The structure, morphology, and electrochemical performance of the synthesized materials were studied by XRD, SEM, charge-discharge tests and cycle voltammetry. The results showed that both of the two samples are monoclinic structure and no impure phase is detected. The sample using glucose as carbon source has smaller particle size and better electrochemical performance, it exhibited an initial discharge capacity of 136.76 mAh/g under 0.1C rate in the voltage range of 3.0-4.5 V; the highest discharge capacity at 10C, 20C and 30C were as high as 119.01, 105.35 and 87.69 mAh/g, respectively, indicating good rate capacity.
  • Keywords
    X-ray diffraction; calcination; electrochemical electrodes; liquid phase deposition; lithium compounds; particle size; scanning electron microscopy; vanadium compounds; voltammetry (chemical analysis); Li3V2(PO4)3; SEM; XRD; calcination process; carbon source; cathode material; charge-discharge test; citric acid; cycle voltammetry; discharge capacity; electrochemical performance; hydrothermal process; hydrothermal rate capacity; hydrothermal synthesis; monoclinic structure; phase detection; reduction agent; synthesized material; Li3V2(PO4)3; carbon sources; cathode material; hydrothermal; lithium ion batteries; vacuum distillation;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Materials for Renewable Energy & Environment (ICMREE), 2011 International Conference on
  • Conference_Location
    Shanghai
  • Print_ISBN
    978-1-61284-749-8
  • Type

    conf

  • DOI
    10.1109/ICMREE.2011.5930903
  • Filename
    5930903