Photocatalytic activity enhancement for removal of dye molecules based on plasmonic Ag grafted TiO2 nanocubes under visible light driven
Introduction: Finding a novel photocatalyst for photocatalytic degradation operating in the wavelength range from UV to visible light has been considered a great potential for environmental remediation. Herein, TiO2 nanocubics (NCs) decorated Ag nanoparticles (NPs) with various concentrations were d...
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Published in | Science and Technology Development Journal Vol. 23; no. 4; pp. 743 - 751 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
08.11.2020
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Online Access | Get full text |
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Summary: | Introduction: Finding a novel photocatalyst for photocatalytic degradation operating in the wavelength range from UV to visible light has been considered a great potential for environmental remediation. Herein, TiO2 nanocubics (NCs) decorated Ag nanoparticles (NPs) with various concentrations were developed.
Methods: The crystal structure, morphological and chemical characteristics of prepared photocatalysts were thoroughly analyzed by a series of main analyses (X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), and UVVis spectra).
Results: The results revealed that a significantly promoting visible-light photocatalytic behavior of TiO2NCs@Ag photocatalyst was observed. The photocatalytic methyl orange (MO) degradation of the as-synthesized Ag anchored TiO2NCs photocatalyst (85% and 62% under UV light and visible light, respectively) exhibited outstanding photocatalytic efficacy compared with pristine TiO2 NCs. The achieved results could be assigned to the synergistic effects between TiO2NCs and Ag- NPs, leading to enhanced charge carrier separation and improved absorption ability in visible-light response.
Conclusion: This work facilitates designing and developing high-efficiency heterostructure photocatalysts for practical works related to environmental deterioration. |
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ISSN: | 1859-0128 |
DOI: | 10.32508/stdj.v23i4.2455 |