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Pb9(PO4)6/Ag3PO4 photocatalysts with different amounts of Pb9(PO4)6 were successfully synthesised 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 , the main active oxygen species.
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Guo et al. (2017) studied this question.
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