| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 50985 | Catalysis Communications | 2012 | 5 Pages |
Ag3PO4 nanoparticle of ~ 100 nm size was synthesized by an ion-exchange reaction between AgNO3 and Na3PO4 at ambient condition. The dark yellowish Ag3PO4 with a bandgap of 2.44 eV revealed significant visible-light absorption. Novel heterojunction structures of Ag3PO4/TiO2 were then fabricated by covering the surface of Ag3PO4 with polycrystalline TiO2 by sol–gel process. Under visible-light irradiation (λ ≥ 420 nm), 3/97 Ag3PO4/TiO2 (in wt.% ratio) showed remarkably high photocatalytic activity in removal of gaseous 2-propanol (IP) and in evolution of CO2. Its photocatalytic behavior seemed to be caused by the inter-semiconductor hole-transfer between the valence band (VB) of Ag3PO4 and TiO2.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Ag3PO4/TiO2 was formed by covering the surface of Ag3PO4 nanoparticle with TiO2. ► Ag3PO4/TiO2 exhibits notable visible-light catalytic activity in evolving CO2 from 2-propanol. ► Visible-light photocatalytic activity is based on the hole-transfer between Ag3PO4 and TiO2.
