• DocumentCode
    2367127
  • Title

    Preparation of nano-powders of p-type transparent conductive copper aluminum oxide by co-precipitation method

  • Author

    Lu, Hsin-Chun ; Lu, Jo-Ling ; Chu, Chun-Lung ; Lai, Chi-You ; Wu, Gwo-mei

  • Author_Institution
    Dept. of Chem. Eng. & Mater. Eng., Chang Gung Univ., Taoyuan
  • fYear
    2008
  • fDate
    24-27 March 2008
  • Firstpage
    485
  • Lastpage
    488
  • Abstract
    Nano-powders of p-type transparent conductive copper aluminum oxide (CAO) have been successfully synthesized by co-precipitation method. By adding sodium hydroxide into the mixed solution of copper chloride and aluminum chloride, co-precipitate precursors of CAO with particle size around 50-60 nm were produced After washing, filtering, and drying of the co-precipitates, nano-powders of CuAlO2 were produced when the dried co-precipitate precursors were calcined at temperature above 1100degC. By aging at pH = 3.5 for six hours and co-precipitating at pH = 8.0, the atomic ratio of Cu/Al of the nano-powders can be maintained throughout the synthesis. After calcining at 12000 in air for 4 hours, the CAO co-precipitate precursors totally transformed into nano-powders of CuAlO2 with crystal size around 64 nm. Continued calcining at 1200degC above 4 hours led to the decomposition of CuAlO2 into nano-powders of CuAl2O4 and volatile CuO with no significant change in crystal size. Finally, it was found that by calcining under inert atmosphere, the decomposition of CuAlO2 could be suppressed at the expense of decreasing its crystallinity.
  • Keywords
    copper compounds; nanoparticles; precipitation; CuAlO2; coprecipitate precursors; coprecipitation method; nanopowder preparation; p-type transparent conductive copper aluminum oxide; sodium hydroxide; Aluminum oxide; Copper; Nanoelectronics;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Nanoelectronics Conference, 2008. INEC 2008. 2nd IEEE International
  • Conference_Location
    Shanghai
  • Print_ISBN
    978-1-4244-1572-4
  • Electronic_ISBN
    978-1-4244-1573-1
  • Type

    conf

  • DOI
    10.1109/INEC.2008.4585533
  • Filename
    4585533