Abstract
Ag3PO4/TiO2 nanotube (TNT) heterojunctions were fabricated via a facile in situ growth method. Hemispherical Ag3PO4 nanocrystals were uniformly grown on the TNT surface, and their size was confined to 5-10 nm. A joint area was distinctly observed between the Ag3PO4 nanocrystals and TNT, indicating the formation of a Ag3PO4/TNT heterojunction. Compared with pure Ag3PO4, the Ag3PO4/TNT heterojunction possesses more active sites, less bulk defects, more efficient electron-hole separation, as well as better dye adsorption properties, and thus exhibits a significantly elevated photocatalytic activity for Rhodamine B (RhB) degradation. The study of the reactive species demonstrates that the photocatalytic degradation of RhB over the Ag3PO4/TNT heterojunction is primarily driven by both photogenerated h(+) and ˙OH radicals. This easily-fabricated Ag3PO4/TNT heterojunction with promising photocatalytic activity may find potential applications in energy and environmental related areas.
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