• Title of article

    Advanced surface and microstructural characterization of natural graphite anodes for lithium ion batteries

  • Author/Authors

    Gallego، نويسنده , , Nidia C. and Contescu، نويسنده , , Cristian I. and Meyer III، نويسنده , , Harry M. and Howe، نويسنده , , Jane Y. and Meisner، نويسنده , , Roberta A. and Payzant، نويسنده , , E. Andrew and Lance، نويسنده , , Michael J. and Yoon، نويسنده , , Sang Y. and Denlinger، نويسنده , , Matthew and Wood III، نويسنده , , David L.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2014
  • Pages
    9
  • From page
    393
  • To page
    401
  • Abstract
    Natural graphite powders were subjected to a series of thermal treatments to improve the anode irreversible capacity loss and capacity retention during long-term cycling of lithium-ion batteries. A baseline thermal treatment in inert Ar or N2 atmosphere was compared to cases with a proprietary additive to the furnace gas. This additive substantially altered the surface chemistry of the uncoated natural graphite powders and resulted in significantly improved long-term cycling performance of the lithium ion batteries over the commercial, carbon-coated natural graphite baseline. Different heat-treatment temperatures were investigated ranging from 950 to 2900 °C to achieve the desired long-term cycling performance with a significantly reduced thermal budget. A detailed summary of the characterization data is also presented, which includes X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, and temperature-programmed desorption-mass spectroscopy. Characterization data was correlated to the observed capacity fade improvements over the course of long-term cycling at high charge–discharge rates in full lithium-ion cells. It is believed that the long-term performance improvements are a result of forming a more stable solid electrolyte interface (SEI) layer on the anode graphite surfaces, which is directly related to the surface chemistry modifications imparted by the proprietary gas environment during thermal treatment.
  • Journal title
    Carbon
  • Serial Year
    2014
  • Journal title
    Carbon
  • Record number

    1927495