• Title of article

    Structural and Optical Properties of Bismuth-doped ZnO Nanoparticles Synthesized by Co-precipitation

  • Author/Authors

    Sermsrithong, C Physics and General Science Program - Faculty of Science and Technology - Nakhon Ratchasima Rajabhat University, Bangkok, Thailand , Jaidaew, P Physics and General Science Program - Faculty of Science and Technology - Nakhon Ratchasima Rajabhat University, Bangkok, Thailand , Promjantuk, C Physics and General Science Program - Faculty of Science and Technology - Nakhon Ratchasima Rajabhat University, Bangkok, Thailand , Buabthong, P Physics and General Science Program - Faculty of Science and Technology - Nakhon Ratchasima Rajabhat University, Bangkok, Thailand

  • Pages
    6
  • From page
    2344
  • To page
    2349
  • Abstract
    Bismuth-doped zinc oxide (ZnO) nanoparticles can serve as efficient photocatalysts for various reactions. Herein, we synthesized and discussed the growth mechanisms of Bi-doped ZnO nanoflakes using co-precipitation with Bi concentrations ranging from 0 to 3 %. The resulting ZnO were hexagonal nanosheets with diameters ranging from 80 nm (ZnO) to 200 nm (ZnO: Bi 3%). The dominant crystal structure matches hexagonal wurtzite with a small presence of Bi2O3 diffraction peaks. The estimated crystallite sizes range from ~ 33 nm to ~ 45 nm, indicating multiple crystalline regions in each nanoflake. Nevertheless, as sheet resistance monotonically decreases with the Bi concentration, the higher number of grain boundaries likely has a lower effect on the conductivity compared to an increase in free carriers and larger grain size in the samples with higher Bi concentration. The bandgap decreases from ~ 3.13 eV to ~ 2.96 eV, likely due to the shrinkage effect from electron-electron or electron-impurity interaction that lowers the conduction band of ZnO.
  • Keywords
    Zinc Oxide Nanoparticles , Bismuth-doped ZnO , Co-precipitation , Photo-catalyst
  • Journal title
    International Journal of Engineering
  • Serial Year
    2022
  • Record number

    2731918