• DocumentCode
    2469120
  • Title

    Investigation of olivine LiFePO4 cathode substitutted by magnesium at Li-site and Fe-site for secondary lithium ion batteries

  • Author

    Wu, Chuan ; Bai, Ying ; Wei, Yuan-yuan ; Wu, Feng ; Zhong, Yu

  • Author_Institution
    School of Chemical Engineering and the Environment, Beijing Institute of Technology, China
  • fYear
    2011
  • fDate
    24-26 June 2011
  • Firstpage
    6072
  • Lastpage
    6075
  • Abstract
    Mg-substituted olivine LiFePO4 at Li-site and Fe-site, namely, Li0.98FeMg0.02PO4/C, LiFe0.98Mg0.02PO4/C and Li0.99Fe0.99Mg0.02PO4/C, were synthesize via a two-step method with pre-heating. X-ray diffraction (XRD) patterns indicate all of the samples have pure olivine structures. Scanning electron microscopy (SEM) imply that the Li-site doping will lead to an anomalistic apparent morphology with a particle size in the range of 1–2µm; while the Fe-site doping will promote a spherelike morphology with a smaller particle size. At the current density of 0.2mA/cm2, the initial specific discharge capacity of Li0.98FeMg0.02PO4/C, LiFe0.98Mg0.02PO4/C and Li0.99Fe0.99Mg0.02PO4/C are 106mAh/g, 123mAh/g and 112mAh/g, respectively. The cyclic voltammetry (CV) curves and the electrochemical impedance spectroscopy (EIS) profiles indicate that LiFe0.98Mg0.02PO4/C has the best reversibility and the smallest charge transfer resistance, which are in favor of the good electrochemical performances.
  • Keywords
    Batteries; Cathodes; Doping; Iron; Materials; X-ray scattering; cathode; doping; electrochemical performance; lithium ion battery; metal-site; olivine LiFePO4;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Remote Sensing, Environment and Transportation Engineering (RSETE), 2011 International Conference on
  • Conference_Location
    Nanjing, China
  • Print_ISBN
    978-1-4244-9172-8
  • Type

    conf

  • DOI
    10.1109/RSETE.2011.5965740
  • Filename
    5965740