BiOBr and BiOCl decorated on TiO2 QDs: Impressively increased photocatalytic performance for the degradation of pollutants under visible light |
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Affiliation: | 1. Department of Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil, Iran;2. Nanoscience and Nanotechnology Research Group, Mineral and Drinking Waters Research Group, University of Mohaghegh Ardabili, Ardabil, Iran;3. Department of Organic and Inorganic Chemistry, Institute of Chemical Research “Andrés M. del Río” (IQAR), Universidad de Alcalá, Campus Universitario, 28805 Alcalá de Henares, Madrid, Spain |
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Abstract: | BiOBr and BiOCl were decorated on TiO2 QDs through n-p-p heterojunctions by a simple strategy and they were applied for degradation of three organic dyes upon visible illumination. The obtained photocatalysts were analyzed via XRD, FESEM, EDX, UV–vis DRS, PL, BET, TEM, HRTEM, FT-IR, EIS, XPS, and transient photocurrent measurements. The TiO2 QDs/BiOBr/BiOCl nanocomposite with 20% wt. of BiOBr and 30% wt. of BiOCl displayed superior photoability in the degradation of methylene blue, rhodamine B, and fuchsine, which was almost 34.5, 176, and 78.7-times larger than TiO2 and 27.8, 13.5, and 51.5-folds greater than TiO2 QDs, respectively. The results show that the construction of intimate n-p-p heterojunctions between BiOBr, TiO2 QDs, and BiOCl counterparts leads to enhanced visible-light harvesting and improved charge separation, resulted efficiently increased photocatalytic activity. The trapping results proved that h+, •O2−, and OH• species have considerable effects on the degradation reaction. We think that the improved efficiency of the ternary TiO2 QDS/BiOBr/BiOCl photocatalyst is a splendid alternative for the removal of toxic contaminants from wastewater. |
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Keywords: | Visible-light-driven photocatalysis n-p-p Heterojunction photocatalyst Wastewater treatment |
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