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Sustainable visible-light-driven Z-scheme porous Zn3(VO4)2/g-C3N4 heterostructure toward highly photoredox pollutant and mechanism insight
• ZV-CN heterostructure was first constructed via impregnation–calcination method.• Proposed Z-scheme mechanism elaborates the high-efficiency charge carrier transfer.• ZV-CN hybrid possesses higher redox ability than ZOV-CN system.• The nanocomposite preserves excellent photostability and reusabili...
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Published in: | Journal of the Taiwan Institute of Chemical Engineers 2017-09, Vol.78, p.517-529 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | • ZV-CN heterostructure was first constructed via impregnation–calcination method.• Proposed Z-scheme mechanism elaborates the high-efficiency charge carrier transfer.• ZV-CN hybrid possesses higher redox ability than ZOV-CN system.• The nanocomposite preserves excellent photostability and reusability.
A simple impregnation–calcination method has been proposed to produce excellent photocatalytic Z-scheme Zn3(VO4)2 porous nanoflower/g-C3N4 nanosheet (ZV-CN) heterostructure photocatalyst. The optical, morphological and photocatalytical properties were investigated in details. Interestingly, after coupling Zn3(VO4)2 with g-C3N4, the hybrids exhibited the extended spectral response and obviously enhanced photocatalytic MB dye mineralization activity. Particularly, the high stable and reusable 5-ZV-CN photocatalyst possessed excellent photocatalytic performance (95.45%) for MB degradation as compared to g-C3N4 (57.66%) and Zn3(VO4)2 (36.71%), which could be attributed to the drastically improved separation efficiency of photoinduced carries, the stronger oxidation and reduction ability via direct Z-scheme transfer as well as the porous surfaces. This present work provides a new kind of g-C3N4 based Z-scheme heterojunctions with high photocatalytic activity.
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ISSN: | 1876-1070 1876-1089 |
DOI: | 10.1016/j.jtice.2017.06.032 |