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- W2801720487 abstract "MoS2/Ag3PO4 heterojunction photocatalysts have attracted great attention in dye degradation and water oxidation, in which Z-scheme plays a critical role in the catalytic performance as a result of energy band structure alignment between MoS2 and Ag3PO4. Creating metal sites at composite interfaces as recombination centers of photo-generated electrons from conduction band (CB) of Ag3PO4 and holes from valence band (VB) of MoS2 is an effective strategy to enhance the charge separation efficiency and photocatalytic performance. Strong coupled MoS2/Ag dots/Ag3PO4 ternary heterojunction photocatalysts were fabricated by one-pot precipitation method, in which highly dispersed Ag dots are located at the MoS2/Ag3PO4 interfaces and MoS2 is bonded with PO43- in the form of Mo-O-P. The fabricated MoS2/Ag dots/Ag3PO4 photocatalyst presents a 2.8-fold enhancement of photocatalytic activity of water oxidation compared to that of pristine Ag3PO4, which is achieved for the first time. The great enhancement of photocatalytic performance can be ascribed to the improved Z scheme mechanism with strongly coupled MoS2/Ag dots/Ag3PO4 ternary interfaces, in which highly dispersed Ag dots serve as efficient recombination centers resulting in the improved separation of photo-generated holes and electrons of Ag3PO4 as well as photocatalytic activity of oxygen evolution." @default.
- W2801720487 created "2018-05-17" @default.
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- W2801720487 date "2018-08-01" @default.
- W2801720487 modified "2023-10-17" @default.
- W2801720487 title "In situ synthesized MoS2/Ag dots/Ag3PO4 Z-scheme photocatalysts with ultrahigh activity for oxygen evolution under visible light irradiation" @default.
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- W2801720487 doi "https://doi.org/10.1016/j.apsusc.2018.04.149" @default.
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