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        Formation of intermediate band and low recombination rate in ZnO-BiVO4 heterostructured photocatalyst: Investigation based on experimental and theoretical studies

        Sonal Singh,Rishabh Sharma,Girdhar Joshi,Jitendra Kumar Pandey 한국화학공학회 2017 Korean Journal of Chemical Engineering Vol.34 No.2

        We present systematic investigations on the relationship between interface formation and enhanced photocatalytic activity of ZnO-BiVO4 nanocomposite based on experimental techniques supported by theoretical calculations. The interaction between ZnO (101) nanosheet and BiVO4 surface at the heterojunction was explored to study the charge transfer and separation mechanism responsible for enhanced photocatalytic response. XPS results and DFT computations mutually validate the reasonable existence of ZnO-BiVO4 interface. The nanocomposite photocatalytic activity, tested for various weight ratios, was found to be highest for ZnO-BiVO4 (1 : 1) under visible-light irradiation. Moreover, the percentage removal of MB was found to be greater than RhB for the same time duration. Steady state and time resolve photoluminescence were employed to understand the carrier lifetime and emissivity. Visible light driven high photoactivity exhibited by ZnO-BiVO4 (1 : 1) was ascribed to the formation of intermediate band and comparatively low recombination rate, which facilitates the separation of electron-hole pairs. Based on the theoretical outcome, we found that valence band maximum was occupied by Bi s orbital and conduction band minimum was occupied by Zn s orbital, which indicates the maximum electron transition from BiVO4 valence band to ZnO conduction band in ZnO-BiVO4 composite. These results demonstrated that heterojunction semiconductors are an effective strategy that can be successfully applied to develop photocatalysts that respond to visible light for organic pollutant degradation.

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        A review and recent developments on strategies to improve the photocatalytic elimination of organic dye pollutants by BiOX (X=Cl, Br, I, F) nanostructures

        Sonal Singh,Rishabh Sharma,Manika Khanuja 한국화학공학회 2018 Korean Journal of Chemical Engineering Vol.35 No.10

        The main environmental problems associated with water body pollution are typically those caused by the discharge of untreated effluents released by various industries. Wastewater from the textile dye industry is itself a large contributor and contains a huge number of complex components, a wide spectrum of organic pollutants with high concentration of biochemical oxygen demand (BOD)/chemical oxygen demand (COD) and other toxic elements. One of several potential techniques to degrade such reactive dyes before being discharged to water bodies is photocatalysis, and bismuth-based photocatalysts are rapidly gaining popularity in this direction. Bismuth oxyhalides, BiOX (X=Cl, Br, I, F), as a group of ternary compound semiconductors (V-VI-VII), have been explored extensively for their photocatalytic activity due to their unique crystal lattice with special layered structure in pure as well as modified form. With suitable band gap and band edge positions, which are a required condition for efficient water breakup and high photon absorption, BiOCl scores over other oxyhalides. Photocatalytic activity depends on many factors such as synthesis method, morphology, size, illumination type, dye choice among others. This paper gives a critical review on bismuth oxyhalides as a family on various aspects of modifications such as doping (with unique and interesting metals as well), morphology and synthesis parameters, polymer and carbon assisted composites in order to further enhance the photocatalytic efficiency in UV/visible region of solar spectrum.

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