Co3O4 nanoparticles decorated Ag3PO4 tetrapods as an efficient visible-light-driven heterojunction photocatalyst
[Display omitted] •Ag3PO4 tetrapods were synthesized via a precipitation method.•Co3O4/Ag3PO4 photocatalysts were synthesized via an impregnation method.•Co3O4/Ag3PO4 composites showed superior photocatalytic activity and stability.•The mechanism of the high performance was proposed as well. Novel A...
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Published in | Applied catalysis. B, Environmental Vol. 181; pp. 707 - 715 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.02.2016
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•Ag3PO4 tetrapods were synthesized via a precipitation method.•Co3O4/Ag3PO4 photocatalysts were synthesized via an impregnation method.•Co3O4/Ag3PO4 composites showed superior photocatalytic activity and stability.•The mechanism of the high performance was proposed as well.
Novel Ag3PO4 tetrapods with exposed {111} facets were synthesized via a facile precipitation method, and then Co3O4 nanoparticles were decorated on the surface of Ag3PO4 tetrapods using an impregnation method. On top of the superior photocatalytic performance of highly reactive {111} facets of Ag3PO4 tetrapods, the Co3O4/Ag3PO4 heterostructured photocatalyst exhibited further improved efficiency in photodegrading methyl blue (MB) under visible light irradiation (>400nm). In addition, the Co3O4 content and calcination temperature had significant impacts on the photocatalytic activities of the samples. The highest efficiency was observed on the 2.0wt% Co3O4/Ag3PO4 heterojunction calcined at 673K. The improved photocatalytic performance could be mainly attributed to accelerated electron-hole separation by p–n junctions in Co3O4/Ag3PO4 heterojunction, and the enhanced structural stabilities may be due to the protection of insoluble Co3O4 and the effect of Ag0 on the surface of Ag3PO4. Moreover, h+ played the major role in the MB decolorization. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2015.08.045 |