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Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes

[Image: see text] This work reports the development of a fast and simple route for the synthesis of ZnO sea urchin (SU) nanostructures by the formation and assembly of ZnO nanorods under favorable growth conditions in an aqueous solution. The thermal treatment of a basic zinc acetate solution in eth...

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Autores principales: Kiriarachchi, Hiran D., Abouzeid, Khaled M., Bo, Longli, El-Shall, M. Samy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714608/
https://www.ncbi.nlm.nih.gov/pubmed/31497719
http://dx.doi.org/10.1021/acsomega.9b01772
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author Kiriarachchi, Hiran D.
Abouzeid, Khaled M.
Bo, Longli
El-Shall, M. Samy
author_facet Kiriarachchi, Hiran D.
Abouzeid, Khaled M.
Bo, Longli
El-Shall, M. Samy
author_sort Kiriarachchi, Hiran D.
collection PubMed
description [Image: see text] This work reports the development of a fast and simple route for the synthesis of ZnO sea urchin (SU) nanostructures by the formation and assembly of ZnO nanorods under favorable growth conditions in an aqueous solution. The thermal treatment of a basic zinc acetate solution in ethanol results in the formation of aggregated seed clusters consisting of small ZnO nanorods, which were then grown in a precursor solution containing Zn(NO(3))(2)·6H(2)O and hexamethylenetetramine to assemble the SU structures from the anisotropic ZnO nanorods on the surface of the seed clusters. Each ZnO nanoparticle in the aggregated seed clusters grew sequentially into a ZnO nanorod, and the nanorods were concentric to the core of the clusters yielding the unique SU-like shape. In the presence of a capping agent such as cetyl trimethyl ammonium bromide (CTAB), the aggregated seed clusters were not formed, and the growth of the CTAB-capped ZnO nanorods resulted in separated rods with average aspect ratios of ∼10. The SU ZnO nanostructures exhibit a hexagonal wurtzite crystal structure and higher specific surface area (26.9 m(2)/g) than the CTAB-capped nanorods (17.7 m(2)/g). The SU ZnO nanostructures show superior photocatalytic efficiency for the degradation of three common organic dyes compared to the ZnO nanorods. The removal efficiencies of indigo carmine, methylene blue, and rhodamine B by the SU nanostructures were 99, 86, and 96%, respectively, after 1 h of UV irradiation. Therefore, the ZnO SU structures have the potential to be a versatile photocatalyst for the photodegradation of organic dyes in industrial wastewater.
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spelling pubmed-67146082019-09-06 Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes Kiriarachchi, Hiran D. Abouzeid, Khaled M. Bo, Longli El-Shall, M. Samy ACS Omega [Image: see text] This work reports the development of a fast and simple route for the synthesis of ZnO sea urchin (SU) nanostructures by the formation and assembly of ZnO nanorods under favorable growth conditions in an aqueous solution. The thermal treatment of a basic zinc acetate solution in ethanol results in the formation of aggregated seed clusters consisting of small ZnO nanorods, which were then grown in a precursor solution containing Zn(NO(3))(2)·6H(2)O and hexamethylenetetramine to assemble the SU structures from the anisotropic ZnO nanorods on the surface of the seed clusters. Each ZnO nanoparticle in the aggregated seed clusters grew sequentially into a ZnO nanorod, and the nanorods were concentric to the core of the clusters yielding the unique SU-like shape. In the presence of a capping agent such as cetyl trimethyl ammonium bromide (CTAB), the aggregated seed clusters were not formed, and the growth of the CTAB-capped ZnO nanorods resulted in separated rods with average aspect ratios of ∼10. The SU ZnO nanostructures exhibit a hexagonal wurtzite crystal structure and higher specific surface area (26.9 m(2)/g) than the CTAB-capped nanorods (17.7 m(2)/g). The SU ZnO nanostructures show superior photocatalytic efficiency for the degradation of three common organic dyes compared to the ZnO nanorods. The removal efficiencies of indigo carmine, methylene blue, and rhodamine B by the SU nanostructures were 99, 86, and 96%, respectively, after 1 h of UV irradiation. Therefore, the ZnO SU structures have the potential to be a versatile photocatalyst for the photodegradation of organic dyes in industrial wastewater. American Chemical Society 2019-08-14 /pmc/articles/PMC6714608/ /pubmed/31497719 http://dx.doi.org/10.1021/acsomega.9b01772 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Kiriarachchi, Hiran D.
Abouzeid, Khaled M.
Bo, Longli
El-Shall, M. Samy
Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes
title Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes
title_full Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes
title_fullStr Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes
title_full_unstemmed Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes
title_short Growth Mechanism of Sea Urchin ZnO Nanostructures in Aqueous Solutions and Their Photocatalytic Activity for the Degradation of Organic Dyes
title_sort growth mechanism of sea urchin zno nanostructures in aqueous solutions and their photocatalytic activity for the degradation of organic dyes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714608/
https://www.ncbi.nlm.nih.gov/pubmed/31497719
http://dx.doi.org/10.1021/acsomega.9b01772
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