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Solvothermal synthesis of ZnO spheres: Tuning the structure and morphology from nano- to micro-meter range and its impact on their photocatalytic activity

Nano- and micro-sized ZnO spheres were fabricated via a simple solvothermal synthesis using two different precursors, while diethanolamine was used to control the morphology. The applied solvent composition, precursor ratio and solvothermal treatment temperature were mathematically correlated with t...

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Bibliographic Details
Published in:Catalysis today 2022-08, Vol.397-399, p.16-27
Main Authors: Kovács, Zoltán, Molnár, Csanád, Gyulavári, Tamás, Magyari, Klára, Tóth, Zsejke-Réka, Baia, Lucian, Pap, Zsolt, Hernádi, Klara
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Language:English
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Summary:Nano- and micro-sized ZnO spheres were fabricated via a simple solvothermal synthesis using two different precursors, while diethanolamine was used to control the morphology. The applied solvent composition, precursor ratio and solvothermal treatment temperature were mathematically correlated with the diameter of spheres. The crystallite size could be easily controlled by adjusting the temperature, providing flexibility during synthesis. The photocatalytic activity and its dependence on the unique morphology were investigated via the decomposition of phenol model pollutant. It was revealed that the surface proprieties were more defining than the secondary particle size in this regard. A surprising synergic effect was observed between the ratio of exposed crystallographic planes of (100) and (002) and crystallite size upon the activity, while the size of the spheres shows little influence. The presented method enables the flexible design of ZnO photocatalysts with spherical morphology in a tunable size range. [Display omitted] •Spherical ZnO with tunable morphology were synthesized using different precursors.•Diameter and crystallite size can be tuned by mixing the two precursors.•Morphology tuning does not affect significantly photocatalytic activity.•Crystallite size and (100), (200) crystal facet relate to activity predominantly.
ISSN:0920-5861
1873-4308
DOI:10.1016/j.cattod.2022.03.004