Journal
OPTICAL MATERIALS
Volume 113, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.optmat.2021.110878
Keywords
Nanocomposite; Graphene oxide; Tin dioxide; Zinc hydroxystannate; Photocatalysis; Hydrothermal
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Funding
- Shahid Chamran University of Ahvaz
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ZnSn(OH)(6)/SnO2/rGO ternary nanocomposites were synthesized via a facile one-step hydrothermal route, showing excellent photocatalytic performance for efficient degradation of dyes. The synthesized nanocomposites exhibited superior photocatalytic activity, making them promising for dye degradation applications.
In this study, Zinc hydroxystannate/tin dioxide/reduced graphene oxide (ZnSn(OH)(6)/SnO2/rGO) ternary nanocomposites were synthesized via a facile one-step hydrothermal route by using graphene oxide, zinc nitrate hexahydrate, and tin (IV) chloride pentahydrate as the precursors. The crystal structure, morphology, and optical properties of ZnSn(OH)(6)/SnO2/rGO ternary nanocomposites were characterized by x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Raman spectroscopy and UV-vis spectroscopy, respectively. The results of XRD pattern revealed the formation of fcc perovskite ZnSn(OH)(6)(ZHS) and tetragonal SnO2 structure. The FESEM images displayed that the ZHS microcubes and SnO2 nanoparticles were distributed on the graphene sheets. The composites were used as photocatalyst for degradation of methylene blue (MB) molecules. The photocatalytic performance of the samples showed that the ZHS/SnO2/rGO nanocomposite exhibited a much higher photocatalytic activity than pure samples. The ternary nanocomposite synthesized at 160 degrees C with a graphene oxide concentration of 1 mg/mL has the ability to completely degradation MB in less than 60 min under UV radiation. The rate of hydroxyl radical (center dot OH) generated in the photocatalytic process was investigated using PL spectroscopy and coumarin (COU) as a probe molecule. Thus it can be intended that the mechanism of MB degradation by the as-synthesized nanocomposites followed indirect oxidation of the dye by center dot OH generated during the photocatalyst process.
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