期刊
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
卷 179, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpcs.2023.111374
关键词
Semiconductor; Self-doping; Composite; Photocatalysis
This study aims to fabricate self-doped Ti3+-TiO2 microspheres and dye sensitized self-doped Ti3+-TiO2 composites with high surface areas and visible-light absorption for highly enhanced photocatalytic tetracycline degradation under visible-light irradiation. The experimental results showed that the obtained Ti3+-TiO2 microspheres showed enhanced visible-light capture capacity and a larger surface area. Besides, the obtained Eosin Y/Ti3+-TiO2 composites showed efficient visible-light absorption and highly boosted photocatalytic performance towards tetracycline degradation. The highest rate constant for Eosin Y/Ti3+-TiO2-9% composite reached as high as 0.06657 min-1, approximately 8.09 times that of commercial TiO2, strongly demonstrating the significant roles of dye sensitization. Finally, a reasonable dye sensitization visible-light photocatalytic mechanism was suggested.
Strong visible-light absorption and high surface areas contribute to high-perform semiconductor photocatalysis. This work aims to fabricate self-doped Ti3+-TiO2 microspheres and dye sensitized self-doped Ti3+-TiO2 composites with high surface areas and visible-light absorption via one-pot solvothermal strategy for highly enhanced photocatalytic tetracycline degradation under visible-light irradiation. The experimental results showed that the obtained Ti3+-TiO2 microspheres showed enhanced visible-light capture capacity and a larger surface area of 204.9 m2 g � 1. Besides, the obtained Eosin Y/Ti3+-TiO2 composites showed efficient visible-light absorption and highly boosted photocatalytic performance towards tetracycline degradation. The highest rate constant for Eosin Y/Ti3+-TiO2-9% composite reached as high as 0.06657 min-1, approximately 8.09 times that of commercial TiO2, strongly demonstrating the significant roles of dye sensitization. Finally, a reasonable dyesensitization visible-light photocatalytic mechanism was suggested.
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