Core/Shell ZnO/TiO<sub>2</sub>, SiO<sub>2</sub>/TiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub>, and Al<sub>1.9</sub>Co<sub>0.1</sub>O<sub>3</sub>/TiO<sub>2</sub> Nanoparticles for the Photodecomposition of Brilliant Blue E-4BA
The synthesis and characterization of ZnO/TiO<sub>2</sub>, SiO<sub>2</sub>/TiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub>, and Al<sub>1.9</sub>Co<sub>0.1</sub>O<sub>3</sub>/TiO&l...
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| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2024-10-01
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| Series: | Inorganics |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2304-6740/12/11/281 |
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| Summary: | The synthesis and characterization of ZnO/TiO<sub>2</sub>, SiO<sub>2</sub>/TiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub>, and Al<sub>1.9</sub>Co<sub>0.1</sub>O<sub>3</sub>/TiO<sub>2</sub> core/shell nanoparticles (NPs) is reported. The NPs were used for photocatalytic degradation of brilliant blue E-4BA under UV and visible light irradiation, monitored by high-performance liquid chromatography and UV-vis absorption spectroscopy. The size of the NPs ranged from 10 to 30 nm for the core and an additional 3 nm for the TiO<sub>2</sub> shell. Al<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub> and Al<sub>1.9</sub>Co<sub>0.1</sub>O<sub>3</sub>/TiO<sub>2</sub> showed superior degradation under UV and visible light compared to ZnO/TiO<sub>2</sub> and SiO<sub>2</sub>/TiO<sub>2</sub> with complete photodecomposition of 20 ppm dye in 20 min using a 10 mg/100 mL photocatalyst. The “Co-doped” Al<sub>1.9</sub>Co<sub>0.1</sub>O<sub>3</sub>/TiO<sub>2</sub> NPs show the best performance under visible light irradiation, which is due to increased absorption in the visible range. DFT-calculated band structure calculations confirm the generation of additional electronic levels in the band gap of γ-Al<sub>2</sub>O<sub>3</sub> through Co<sup>3+</sup> ions. This indicates that Co-doping enhances the generation of electron–hole pairs after visible light irradiation. |
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| ISSN: | 2304-6740 |