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Enhanced photocatalytic degradation of methyl orange using Ag/Sn-doped CeO2 nanocomposite
Cerium oxide (CeO 2 ) has attracted much attention in recent years because of its unique physiochemical properties in photocatalysis. Herein, pure CeO 2 and Sn-doped CeO 2 (Sn–CO) nanoparticles were synthesized by a simple hydrothermal method. In addition, the Sn-doped CeO 2 sample was composited wi...
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Published in: | Journal of materials science. Materials in electronics 2019-03, Vol.30 (6), p.6116-6126 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Cerium oxide (CeO
2
) has attracted much attention in recent years because of its unique physiochemical properties in photocatalysis. Herein, pure CeO
2
and Sn-doped CeO
2
(Sn–CO) nanoparticles were synthesized by a simple hydrothermal method. In addition, the Sn-doped CeO
2
sample was composited with Ag nanoparticles by a chemical precipitation method to prepare Ag/Sn–CO nanocomposite. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS) and UV-visible absorption spectroscopy. Furthermore, the photocatalytic activity of the as-prepared cerium oxide-based samples was evaluated using the degradation of methyl orange (MO) under ultraviolet and visible light irradiation. It was found that photocatalytic activity of the pure CeO
2
nanoparticles was enhanced through Sn doping and surface sensitization with Ag. The enhanced photocatalytic performance of the Sn-doped CeO
2
sample can be ascribed mainly to a decrease in its band gap energy. Moreover, the improved photocatalytic activity of the Ag/Sn–CO nanocomposite compared to that of the Sn–CO sample is due to its localized surface plasmon resonance (LSPR) effect. The Ag/Sn–CO sample exhibited an efficient photocatalytic characteristic for degrading MO under visible light irradiation with a high degradation rate of 99% after 45 min. The responsible mechanism for the enhancement of photocatalytic activity of cerium oxide was discussed. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-019-00913-0 |