Abstract
Pb9(PO4)6/Ag3PO4 photocatalysts with different amounts of Pb9(PO4)6 were successfully synthesized by the ion exchange method. The catalysts were characterized by X-ray diffractometry (XRD), High resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Brunauer- Emmett-Teller (BET), Fourier transform infrared spectrometry (FT-IS), and ultraviolet-visible (UV-vis) spectroscopy. All Pb9(PO4)6/Ag3PO4 photocatalysts show much higher photocatalytic activities than pure Ag3PO4 under visible light irradiation in the methyl-orange (MO) decomposition. Especially, the 3.0 wt% Pb9(PO4)6/Ag3PO4 photocatalyst shows the highest photoactivity and also high stability after five cycles. The MO degradation rate during each cycle is almost maintained at 97%. Photo-electrochemical measurement of photocatalysts verified that the enhancing photocatalytic activity was resulted from the electron-hole pair high separation. The photocatalytic activity enhancement of Pb9(PO4)6/Ag3PO4 is closely related to •OH, the main active oxygen species.
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