Electrochemical properties of natural graphite in the electrolyte solutions containing propylene carbonate and nonflammable organo-fluorine compounds for lithium-ion batteries

Bibliographic Information

Other Title
  • プロピレンカーボネートと不燃性有機フッ素化合物を含むリチウムイオン電池用電解液中における天然黒鉛の電気化学的性質

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Description

High improvement in the battery performances such as low temperature characteristics, thermal stability and high rate charge/discharge is urgently requested. Because EC-based solvents should be used for graphite anode, lithium-ion batteries currently used have difficulty for the use at low temperatures. In the present study, surface fluorination using F2, ClF3, NF3 and plasma-treatment was applied to natural graphite samples. Surface fluorination highly increased surface disorder in all fluorinated natural graphite samples, reducing the electrochemical decomposition of PC. Due to decrease in the decomposition of PC, first coulombic efficiencies increased by 10–20%.<br>High safety is one of the most important issues for the application of lithium-ion batteries to hybrid cars and electric vehicles because lithium-ion batteries use flammable organic solvents. Organo-fluorine compounds are new candidates since fluorine substitution of organic compounds reduce HOMO level, i.e. increases oxidation stability. In the present study, thermal and electrochemical oxidation stability of organo-fluorine compound-mixed electrolyte solutions was evaluated, and charge/discharge characteristics of natural graphite were investigated using fluorine compound-mixed electrolyte solutions. It was found that organo-fluorine compounds improved thermal and electrochemical oxidation stability of electrolyte solutions, and highly increased first coulombic efficiencies for graphite in PC-containing electrolyte solution.

Journal

  • TANSO

    TANSO 2010 (243), 135-136, 2010

    THE CARBON SOCIETY OF JAPAN

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Details 詳細情報について

  • CRID
    1390001204226263168
  • NII Article ID
    10026403746
  • NII Book ID
    AN00140335
  • DOI
    10.7209/tanso.2010.135
  • ISSN
    18845495
    03715345
  • Data Source
    • JaLC
    • Crossref
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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