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Title: In situ decoration of plasmonic Au nanoparticles on graphene quantum dots-graphitic carbon nitride hybrid and evaluation of its visible light photocatalytic performance. Author: Rajender G, Choudhury B, Giri PK. Journal: Nanotechnology; 2017 Sep 27; 28(39):395703. PubMed ID: 28726671. Abstract: This work spotlights the development of a plasmonic photocatalyst showing surface plasmon induced enhanced visible light photocatalytic (PC) performance. Plasmonic Au nanoparticles (NPs) are decorated over the hybrid nanosystem of graphitic carbon nitride (GCN) and graphene quantum dots (GQD) by citrate reduction method. Surface plasmon resonance (SPR) induced enhancement of Raman G and 2D band intensity is encountered on excitation of the Plasmonic hybrid at 514.5 nm, which is near to the 532 nm absorption band of Au NPs. Time-resolved photoluminescence and XPS studies show charge transfer interaction between GQD-GCN and Au NPs. Plasmonic hybrid exhibits an enhanced PC activity over the other catalysts in the photodegradation of methylene blue (MB) under visible light illumination. Plasmonic photocatalyst displays more than 6 fold enhancement in the photodecomposition rate of MB over GQD and nearly 2 fold improvement over GCN and GQD-GCN. GQD-GCN absorbs mostly in the near visible region and can be photoexcited by visible light of wavelength ([Formula: see text]) < 460 nm. Plasmon activation in Au NPs decorated GQD-GCN could exploit the entire UV-visible light for photocatalysis. Furthermore, plasmonic Au act as antennas for accumulation and enhancement of localized electromagnetic field at the interface with GQD-GCN, and thereby promotes photogeneration of large numbers of carriers on GQD-GCN. The carriers are separated by charge transfer migration from hybrid to Au NPs. Finally, the carriers on the plasmonic Au nanostructures initiate MB degradation under visible light. Our results have shown that plasmon decoration is a suitable strategy to design a carbon based hybrid photocatalyst for solar energy conversion.[Abstract] [Full Text] [Related] [New Search]