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  • Title: Visible-Light-Driven Photocatalytic Activity of SnO2-ZnO Quantum Dots Anchored on g-C3N4 Nanosheets for Photocatalytic Pollutant Degradation and H2 Production.
    Author: Vattikuti SVP, Reddy PAK, Shim J, Byon C.
    Journal: ACS Omega; 2018 Jul 31; 3(7):7587-7602. PubMed ID: 31458911.
    Abstract:
    A zero-dimensional/two-dimensional heterostructure consists of binary SnO2-ZnO quantum dots (QDs) deposited on the surface of graphitic carbon nitride (g-C3N4) nanosheets. The so-called SnO2-ZnO QDs/g-C3N4 hybrid was successfully synthesized via an in situ co-pyrolysis approach to achieve efficient photoactivity for the degradation of pollutants and production of hydrogen (H2) under visible-light irradiation. High-resolution transmission electron microscopy images show the close contacts between SnO2-ZnO QDs with the g-C3N4 in the ternary SnO2-ZnO QDs/g-C3N4 hybrid. The optimized hybrid shows excellent photocatalytic efficiency, achieving 99% rhodamine B dye degradation in 60 min under visible-light irradiation. The enriched charge-carrier separation and transportation in the SnO2-ZnO QDs/g-C3N4 hybrid was determined based on electrochemical impedance and photocurrent analyses. This remarkable photoactivity is ascribed to the "smart" heterostructure, which yields numerous benefits, such as visible-light-driven fast electron and hole transfer, due to the strong interaction between the SnO2-ZnO QDs with the g-C3N4 matrix. In addition, the SnO2-ZnO QDs/g-C3N4 hybrid demonstrated a high rate of hydrogen production (13 673.61 μmol g-1), which is 1.06 and 2.27 times higher than that of the binary ZnO/g-C3N4 hybrid (12 785.54 μmol g-1) and pristine g-C3N4 photocatalyst (6017.72 μmol g-1). The synergistic effect of increased visible absorption and diminished recombination results in enhanced performance of the as-synthesized tin oxide- and zinc oxide-modified g-C3N4. We conclude that the present ternary SnO2-ZnO QDs/g-C3N4 hybrid is a promising electrode material for H2 production and photoelectrochemical cells.
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