• DocumentCode
    2940971
  • Title

    Controlled Synthesis of ZnO Microcrystals by a Simple Microwave Reaction Method

  • Author

    Chen, Lifei ; Wei, Yu

  • Author_Institution
    Sch. of Urban Dev. & Environ. Eng., Shanghai Second Polytech. Univ., Shanghai, China
  • fYear
    2010
  • fDate
    19-21 June 2010
  • Firstpage
    1
  • Lastpage
    4
  • Abstract
    A simple microwave reaction method without using additives was employed to synthesize ZnO microcrystals with controllable morphology. Zinc acetate dehydrate was selected as reactants and ethylene glycol-water was solvents. Peanutlike ZnO built up by short nanorods, multi-sphere aggregations, spherelike microcrystals covered by ZnO nanoparticles, and spinous morphology mixed with flake like ZnO were obtained only by change of power and time of microwave reaction. The products were characterized by means of scanning electron microscopy (SEM), X-ray powder diffraction, and UV/Vis spectrophotometer. X-ray diffraction pattern suggests that the ZnO crystals are pure hexagonal phase.
  • Keywords
    II-VI semiconductors; X-ray diffraction; aggregation; crystal growth from solution; crystal morphology; microwave heating; nanofabrication; nanoparticles; nanorods; scanning electron microscopy; semiconductor growth; ultraviolet spectra; visible spectra; wide band gap semiconductors; zinc compounds; SEM; UV-Vis spectrophotometer; X-ray powder diffraction; ZnO; controllable morphology; controlled synthesis; ethylene glycol-water; hexagonal phase; microcrystals; multisphere aggregation; nanoparticles; nanorods; simple microwave reaction method; solvents; zinc acetate dehydrate; Electromagnetic heating; Microwave ovens; Microwave theory and techniques; Morphology; Nanostructures; Scanning electron microscopy; Shape control; X-ray diffraction; X-ray scattering; Zinc oxide;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Photonics and Optoelectronic (SOPO), 2010 Symposium on
  • Conference_Location
    Chengdu
  • Print_ISBN
    978-1-4244-4963-7
  • Electronic_ISBN
    978-1-4244-4964-4
  • Type

    conf

  • DOI
    10.1109/SOPO.2010.5504391
  • Filename
    5504391