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      Enhanced Photoreduction Activity of Carbon Dioxide over Co3O4/CeO2Catalysts under Visible Light Irradiation

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      International Journal of Photoenergy
      Hindawi Limited

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          Abstract

          A series of new two semiconductor catalysts, Co 3O 4/CeO 2, were prepared by glycine-nitrate combustion method for photocatalytic reduction of carbon dioxide to produce methanol and ethanol under visible light ( λ > 400 nm) irradiation. The catalysts were characterized by BET, UV-vis spectra, XRD, SEM, PL, and XPS and the results indicated that the catalyst with 5 wt.% of Co 3O 4has the highest yield among all kinds of tests with the methanol yield of 1.52 μmol·g −1·h −1and the ethanol yield of 4.75 μmol·g −1·h −1, which are about 2.34 and 1.71 times as large as those of CeO 2. However, methanol and ethanol can hardly be detected for Co 3O 4under the same condition because of its too narrow band gap. The improvement of the photoreduction activity of Co 3O 4doped CeO 2was caused by the separation of electron-hole pairs of Co 3O 4/CeO 2and charge transfer between Co 3O 4and CeO 2, mimicking the Z-scheme in photosynthesis.

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          Most cited references43

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          Reduced graphene oxide for catalytic oxidation of aqueous organic pollutants.

          We discovered that chemically reduced graphene oxide, with an I(D)/I(G) >1.4 (defective to graphite) can effectively activate peroxymonosulfate (PMS) to produce active sulfate radicals. The produced sulfate radicals (SO(4)(•-)) are powerful oxidizing species with a high oxidative potential (2.5-3.1 vs 2.7 V of hydroxyl radicals), and can effectively decompose various aqueous contaminants. Graphene demonstrated a higher activity than several carbon allotropes, such as activated carbon (AC), graphite powder (GP), graphene oxide (GO), and multiwall carbon nanotube (MWCNT). Kinetic study of graphene catalyzed activation of PMS was carried out. It was shown that graphene catalysis is superior to that on transition metal oxide (Co(3)O(4)) in degradation of phenol, 2,4-dichlorophenol (DCP) and a dye (methylene blue, MB) in water, therefore providing a novel strategy for environmental remediation.
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            Efficient photocatalytic degradation of phenol over Co3O4/BiVO4 composite under visible light irradiation.

            Co3O4/BiVO4 composite photocatalyst with a p-n heterojunction semiconductor structure has been synthesized by the impregnation method. The physical and photophysical properties of the composite photocatalyst have been characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transimission electron microscopy (TEM), BET surface area, and UV-visible diffuse reflectance spectra. Co is present as p-type Co3O4 and disperses on the surface of n-type BiVO4 to constitute a heterojunction composite. The photocatalyst exhibits enhanced photocatalytic activity for phenol degradation under visible light irradiation. The highest efficiency is observed when calcined at 300 degrees C with 0.8 wt % cobalt content. On the basis of the calculated energy band positions and PL spectra, the mechanism of enhanced photocatalytic activity has been discussed.
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              Effect of graphitic carbon nitride microstructures on the activity and selectivity of photocatalytic CO2 reduction under visible light

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                Author and article information

                Journal
                International Journal of Photoenergy
                International Journal of Photoenergy
                Hindawi Limited
                1110-662X
                1687-529X
                2015
                2015
                : 2015
                :
                : 1-11
                Article
                10.1155/2015/230808
                3c57f8b9-97c2-4cb8-9c88-b01e8c3c737e
                © 2015

                http://creativecommons.org/licenses/by/3.0/

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