4.6 Article

Morphology-Controlled Synthesis of ZnO Nanostructures for Caffeine Degradation and Escherichia coli Inactivation in Water

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CATALYSTS
卷 11, 期 1, 页码 -

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MDPI
DOI: 10.3390/catal11010063

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zinc oxide; nanosphere; nanorod; nanopetal; photocatalytic; antibacterial; caffeine; reactive oxygen species (ROS); degradation; pathogen

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The morphology of nanoparticles strongly influences their photocatalytic and antibacterial activities. Different shapes of ZnO nanoparticles can be obtained by varying the type of solvent used, affecting the generation of reactive oxygen species and metal ions, which ultimately determines their effectiveness. ZnO nanospheres showed the highest activity in degrading caffeine and killing E. coli among the tested nanostructures.
Photocatalytic and antibacterial activity of nanoparticles are strongly governed by their morphology. By varying the type of solvent used, one can obtain different shapes of ZnO nanoparticles and tune the amount of reactive oxygen species (ROS) and metal ion (Zn2+) generation, which in turn dictates their activity. ZnO nanostructures were fabricated via facile wet chemical method by varying the type of solvents. Solar light assisted photocatalytic degradation of caffeine and antibacterial activity against E. coli were examined in presence ZnO nanostructures. In addition to an elaborate nanoparticle characterization, adsorption and kinetic experiments were performed to determine the ability of nanostructures to degrade caffeine. Zone of inhibition, time kill assay and electron microscopy imaging were carried out to assess the antibacterial activity. Experimental findings indicate that ZnO nanospheres generated maximum ROS and Zn2+ ions followed by ZnO nanopetals and ZnO nanorods. As a result, ZnO nanospheres exhibited highest degradation of caffeine as well as killing of E. coli. While ROS is mainly responsible for the photocatalytic activity of nanostructures, their antibacterial activity is mostly due to the combination of ROS, metal ion, physical attrition and cell internalization.

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