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- W4224277270 abstract "Recently, there has been a significant interest in developing high-performance photocatalysts for removing organic pollutants from water environment. Herein, a ternary graphitic C 3 N 4 (g-C 3 N 4 )/Ag 3 PO 4 /AgBr composite photocatalyst is synthesized using an in-situ precipitation-anion-exchange process and characterized by several spectroscopic and microscopic techniques. During the photocatalytic reaction, X-ray photoelectron spectroscopy clearly illustrated the formation of metallic Ag on the g-C 3 N 4 /Ag 3 PO 4 /AgBr composite surface. The ternary composite photocatalyst demonstrated an increased photoactivity under visible light (>420 nm), achieving a complete decolorization of methyl orange (MO) in 5 min. The ternary g-C 3 N 4 /Ag 3 PO 4 /AgBr hybrid was also applied to the 2-chlorophenol degradation under visible light, further confirming its excellent photocatalytic activity. In addition, quenching experiments revealed that holes (h + ) and O 2 •– were the major attack species in the decolorization of MO. The enhanced photoactivity of g-C 3 N 4 /Ag 3 PO 4 /AgBr results from the efficient transfer/separation of photoinduced charges with the dual Z-scheme pathway and the charge recombination sites on the formed Ag particles. • Ternary g-C 3 N 4 /Ag 3 PO 4 /AgBr photocatalyst was synthesized. • Ag particles formed on the composite surface during photocatalytic reaction. • The ternary composite displays the excellent photocatalytic activity under visible light. • h + and O 2 . •– are major species for the methyl orange decolorization. • Efficient charge separation via dual Z-scheme mechanism with metallic Ag transit sites." @default.
- W4224277270 created "2022-04-26" @default.
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- W4224277270 date "2022-08-01" @default.
- W4224277270 modified "2023-10-03" @default.
- W4224277270 title "Dual Z-scheme heterojunction g-C3N4/Ag3PO4/AgBr photocatalyst with enhanced visible-light photocatalytic activity" @default.
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- W4224277270 doi "https://doi.org/10.1016/j.ceramint.2022.04.176" @default.
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