کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
54810 | 47027 | 2013 | 8 صفحه PDF | دانلود رایگان |
A novel visible driven Mg–Zn–In ternary layered photocatalytic materials were synthesized, for the first time, by the isomorphous replacement of Zn for Mg in coprecipitation system. Scanning electron microscopy (SEM), X-ray diffraction (XRD) and N2 adsorption/desorption isothermal technique reveal that this ternary photocatalytic material possesses nano-sheet morphology and high crystallinity as well as hierarchy mesoporous structure. UV–vis spectroscopy confirms that the isomorphous replacement of Zn for Mg results in a significant red shift adsorption of the calcined Mg–Zn–In LDHs toward visible light region. The calcined Mg–Zn–In LDHs samples possess a high photocatalytic activity of 98% in degradation of an organic dye methylene blue (MB) under visible light irradiation, for which the possible photocatalytic mechanisms are discussed. Moreover, this ternary layered photocatalytic material exhibits satisfactory re-usability after three cycles and a strong structural “memory effect” even after calcined at temperature of 800 °C. The higher photocatalysis activity under visible light irradiation and facilitate synthesis process enable this ternary layered material to be a promising candidate in utilization of renewable energy for environmental remediation.
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► Mg–In–Zn ternary photocatalytic material possesses nano-sheet morphology, high crystallinity and hierarchy mesoporous structure.
► The isomorphous replacement of Zn2+ for Mg2+ can modify the nano-size and morphology of the ternary photocatalytic material.
► Ternary photocatalytic material demonstrates excellent photocatalytic activity in the degradation of methylene blue under visible light irradiation.
► This ternary layered photocatalytic material exhibits satisfactory re-usability.
► Strong structural “memory effect” was found on Mg–In–Zn ternary photocatalytic material even after calcined at temperature of 800 °C.
Journal: Catalysis Today - Volume 212, 1 September 2013, Pages 81–88