Comparison Study on Antimicrobial and Photocatalytic Activity of Different Shaped ZnO Nanoparticles

ZnO nanoparticles (ZnO NPs) were synthesized through surfactant free non-hydrolytic organic phase method in which zinc acetate and zinc acetylacetonate were selected as precursors. Structural and size analysis of the as-prepared nanoparticles performed on X-ray diffractometer, transmission electron...

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Bibliographic Details
Published inSolid state phenomena Vol. 288; pp. 87 - 97
Main Authors Tsogoo, Ariunzaya, Batmandakh, Solongo, Tsedev, Ninjbadgar, Gibaud, Alain, Dashzeveg, Rentsenmyadag, Bilegsaikhan, Arvin, Daniel, Philippe, Ganbold, Erdene Ochir
Format Journal Article
LanguageEnglish
Published Zurich Trans Tech Publications Ltd 15.03.2019
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Summary:ZnO nanoparticles (ZnO NPs) were synthesized through surfactant free non-hydrolytic organic phase method in which zinc acetate and zinc acetylacetonate were selected as precursors. Structural and size analysis of the as-prepared nanoparticles performed on X-ray diffractometer, transmission electron microscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy showed that the obtained nanoparticles were crystalline particles with all reflections matching to wurtzite. TEM images revealed that ZnO NPs from synthesis in which zinc acetate involved as precursor had a shape of sphere while zinc acetylacetonate resulted in rod-shaped nanoparticles. Reaction rates from catalytic activity test performed on Methylene Blue dye (MB) were found to be 2.99×10-2 min-1 and 1.98×10-2 min-1 for spherical and rod-shaped ZnO NPs, respectively. Antibacterial activity experiments shows rod-shaped ZnO NPs almost completely (99.75%) inhibited the growth of Escherichia Coli while only around 6.5% was survived after treatment of spherical ZnO NPs under same conditions.
Bibliography:Selected, peer reviewed papers from the 7th International Conference on Materials Science (ICMS 2018), June 20 - 22, 2018, Erenhot, China
ISSN:1012-0394
1662-9779
1662-9779
DOI:10.4028/www.scientific.net/SSP.288.87