Ionic conduction and thermal nature of synthetic Cu3BiS3.

  • MIZOTA Tadato
    Department of Advanced Materials Science and Engineering, Faculty of Engineering, Yamaguchi University
  • INOUE Atsushi
    Department of Advanced Materials Science and Engineering, Faculty of Engineering, Yamaguchi University
  • YAMADA Takao
    Department of Advanced Materials Science and Engineering, Faculty of Engineering, Yamaguchi University
  • NAKATSUKA Akihiko
    Department of Advanced Materials Science and Engineering, Faculty of Engineering, Yamaguchi University
  • NAKAYAMA Noriaki
    Department of Advanced Materials Science and Engineering, Faculty of Engineering, Yamaguchi University

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Abstract

Cu3BiS3 has been synthesized to clarify the thermal nature related to the ionic conduction. Heating and cooling measurements by the DSC showed reversible nature as a whole, except for a little hysteresis on temperature of the first order transition around 100–110°C. Resistivity decreased steeply from room temperature to about 77–90°C, above which the material showed good ionic conductivity. In cooling process, however, the resistivity did not recover the original value until room temperature. Several days are necessary to get back the initial resistivity at room temperature. The irreversible nature on conductivity will be explained by the existence, at least partially, of the metastable and electrolytic state on cooling to the room temperature. The reversible profiles in DSC and TMDSC indicates that the first order transition has essentially little or no effect to the conversion to the solid electrolyte. Temperature modulated DSC data were correlated well to heat capacity profiles obtained so far from the adiabatic calorimety and DSC-data.

Journal

  • Mineralogical Journal

    Mineralogical Journal 20 (2), 81-90, 1998

    Japan Association of Mineralogical Sciences

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Details 詳細情報について

  • CRID
    1390282681521822720
  • NII Article ID
    10008773156
  • NII Book ID
    AA00739590
  • DOI
    10.2465/minerj.20.81
  • ISSN
    18814174
    05442540
  • Text Lang
    en
  • Data Source
    • JaLC
    • Crossref
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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