Dataset Information

Synthesis of Flower-Like AgI/BiOCOOH p-n Heterojunctions With Enhanced Visible-Light Photocatalytic Performance for the Removal of Toxic Pollutants.

ABSTRACT: In this study, flower-like AgI/BiOCOOH heterojunctions were constructed through a two-step procedure involving the solvothermal synthesis of BiOCOOH microflowers followed by AgI modification using a precipitation method. These novel photocatalysts were systematically examined by XRD, UV-vis DRS, SEM, TEM, EDS, and PL spectroscopy techniques. The AgI/BiOCOOH heterojunction were studied as a decent photocatalyst for the removal of the industrial dye (rhodamine B, and methyl blue) and antibiotic (tetracycline) under visible light. The AgI/BiOCOOH heterojunctions are much more active than bare BiOCOOH, and AgI, which could be ascribed to the improved separation of charge carriers, resulting from the formation of p-n heterojunction between two constituents. The holes (h⁺) and superoxide radical (•O 2 - ) were detected as the main active species responsible for the pollutant degradation. The results showed that a highly efficient visible-light-driven photocatalytic system was developed for the decomposition of toxic pollutants.

SUBMITTER: Li S

PROVIDER: S-EPMC6213583 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

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Synthesis of Flower-Like AgI/BiOCOOH p-n Heterojunctions With Enhanced Visible-Light Photocatalytic Performance for the Removal of Toxic Pollutants.

Li Shijie S Jiang Wei W Xu Kaibing K Hu Shiwei S Liu Yu Y Zhou Yingtang Y Liu Jianshe J

Frontiers in chemistry 20181026

In this study, flower-like AgI/BiOCOOH heterojunctions were constructed through a two-step procedure involving the solvothermal synthesis of BiOCOOH microflowers followed by AgI modification using a precipitation method. These novel photocatalysts were systematically examined by XRD, UV-vis DRS, SEM, TEM, EDS, and PL spectroscopy techniques. The AgI/BiOCOOH heterojunction were studied as a decent photocatalyst for the removal of the industrial dye (rhodamine B, and methyl blue) and antibiotic (t ...[more]

PMID: 30416996

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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

Synthesis of Flower-Like AgI/BiOCOOH p-n Heterojunctions With Enhanced Visible-Light Photocatalytic Performance for the Removal of Toxic Pollutants.

Publications

Synthesis of Flower-Like AgI/BiOCOOH p-n Heterojunctions With Enhanced Visible-Light Photocatalytic Performance for the Removal of Toxic Pollutants.

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