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Facile Fabrication of Flower-Like BiOI/BiOCOOH p-n Heterojunctions for Highly Efficient Visible-Light-Driven Photocatalytic Removal of Harmful Antibiotics.

ABSTRACT: Novel heterojunction photocatalysts with remarkable photocatalytic capabilities and durability for degrading recalcitrant contaminants are extremely desired; however, their development still remains quite challenging. In this study, a series of flower-like BiOI/BiOCOOH p-n heterojunctions were fabricated via a controlled in situ anion-exchange process. During the process, BiOI formation and even deposition on BiOCOOH microspheres with tight interfacial contact were realized. As expected, BiOI/BiOCOOH heterojunctions revealed remarkable enhancements in photocatalytic antibiotic degradation capacities under visible light irradiation compared with pristine BiOI and BiOCOOH. The best-performing BiOI/BiOCOOH heterojunction (i.e., IBOCH-2) showed much improved photocatalytic CIP degradation efficiency of approximately 81- and 3.9-fold greater than those of bare BiOI and BiOCOOH, respectively. The eminent photocatalytic performances were due not only to the enhanced capability in harvesting photon energies in visible light regions, but also the accelerated separation of electrons and holes boosted by the p-n heterojunction. Active species trapping tests demonstrated that superoxide free radicals (•O2-) and photo-generated holes (h+) were major active species for CIP degradation. Recycling experiments verified the good durability of BIBO-2 over four runs. The facile in situ synthesis route and excellent performance endow flower-like BiOI/BiOCOOH heterojunctions with a promising potential for actual environmental remediation.

SUBMITTER: Li S

PROVIDER: S-EPMC6915482 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Facile Fabrication of Flower-Like BiOI/BiOCOOH p-n Heterojunctions for Highly Efficient Visible-Light-Driven Photocatalytic Removal of Harmful Antibiotics.

Li Shijie S Xue Bing B Wang Chunchun C Jiang Wei W Hu Shiwei S Liu Yanping Y Wang Hengwei H Liu Jianshe J

Nanomaterials (Basel, Switzerland) 20191106 11

Novel heterojunction photocatalysts with remarkable photocatalytic capabilities and durability for degrading recalcitrant contaminants are extremely desired; however, their development still remains quite challenging. In this study, a series of flower-like BiOI/BiOCOOH p-n heterojunctions were fabricated via a controlled in situ anion-exchange process. During the process, BiOI formation and even deposition on BiOCOOH microspheres with tight interfacial contact were realized. As expected, BiOI/Bi ...[more]

PMID: 31698760

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Project description:Graphitic carbon nitride (g-C₃N₄) and titanium dioxide (TiO₂) were chosen as a model system to investigate photocatalytic abilities of heterojunction system under UV and visible light conditions. The use of g-C₃N₄ has been shown to be effective in the reduction in recombination through the interaction between the two interfaces of TiO₂ and g-C₃N₄. A simple method of preparing g-C₃N₄ through the pyrolysis of melamine was employed, which was then added to undoped TiO₂ material to form the g-C₃N₄-TiO₂ system. These materials were then fully characterized by X-ray diffraction (XRD), Brunauer Emmett Teller (BET), and various spectroscopic techniques including Raman, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), diffuse absorbance, and photoluminescence analysis. Photocatalysis studies were conducted using the model dye, rhodamine 6G utilizing visible and UV light irradiation. Raman spectroscopy confirmed that a composite of the materials was formed as opposed to a mixture of the two. Using XPS analysis, a shift in the nitrogen peak to that indicative of substitutional nitrogen was detected for all doped samples. This is then mirrored in the diffuse absorbance results, which show a clear decrease in band gap values for these samples, showing the effective band gap alteration achieved through this preparation process. When g-C₃N₄-TiO₂ samples were analyzed under visible light irradiation, no significant improvement was observed compared that of pure TiO₂. However, under UV light irradiation conditions, the photocatalytic ability of the doped samples exhibited an increased reactivity when compared to the undoped TiO₂ (0.130 min-1), with 4% g-C₃N₄-TiO₂ (0.187 min-1), showing a 43.9% increase in reactivity. Further doping to 8% g-C₃N₄-TiO₂ lead to a decrease in reactivity against rhodamine 6G. BET analysis determined that the surface area of the 4% and 8% g-C₃N₄-TiO₂ samples were very similar, with values of 29.4 and 28.5 m²/g, respectively, suggesting that the actual surface area is not a contributing factor. This could be due to an overloading of the system with covering of the active sites resulting in a lower reaction rate. XPS analysis showed that surface hydroxyl radicals and oxygen vacancies are not being formed throughout this preparation. Therefore, it can be suggested that the increased photocatalytic reaction rates are due to successful interfacial interactions with the g-C₃N₄-doped TiO₂ systems.

Dataset Information

Facile Fabrication of Flower-Like BiOI/BiOCOOH p-n Heterojunctions for Highly Efficient Visible-Light-Driven Photocatalytic Removal of Harmful Antibiotics.

Publications

Facile Fabrication of Flower-Like BiOI/BiOCOOH p-n Heterojunctions for Highly Efficient Visible-Light-Driven Photocatalytic Removal of Harmful Antibiotics.

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