Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2nr31241g
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dc.titlePlasmon enhanced upconversion luminescence of NaYF 4:Yb, Er@SiO 2@Ag core-shell nanocomposites for cell imaging
dc.contributor.authorYuan, P.
dc.contributor.authorLee, Y.H.
dc.contributor.authorGnanasammandhan, M.K.
dc.contributor.authorGuan, Z.
dc.contributor.authorZhang, Y.
dc.contributor.authorXu, Q.-H.
dc.date.accessioned2014-10-08T09:46:47Z
dc.date.available2014-10-08T09:46:47Z
dc.date.issued2012-08-21
dc.identifier.citationYuan, P., Lee, Y.H., Gnanasammandhan, M.K., Guan, Z., Zhang, Y., Xu, Q.-H. (2012-08-21). Plasmon enhanced upconversion luminescence of NaYF 4:Yb, Er@SiO 2@Ag core-shell nanocomposites for cell imaging. Nanoscale 4 (16) : 5132-5137. ScholarBank@NUS Repository. https://doi.org/10.1039/c2nr31241g
dc.identifier.issn20403364
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/88038
dc.description.abstractNaYF 4:Yb,Er@SiO 2@Ag core-shell nanocomposites were prepared to investigate metal-enhanced upconversion luminescence. Two sizes (15 and 30 nm) of Ag nanoparticles were used. The emission intensity of the upconversion nanocrystals was found to be strongly modulated by the presence of Ag nanoparticles (NPs) on the outer shell layer of the nanocomposites. The extent of modulation depended on the separation distance between Ag NPs and upconversion nanocrystals. The optimum upconversion luminescence enhancement was observed at a separation distance of 10 nm for Ag NPs with two different sizes (15 and 30 nm). A maximum upconversion luminescence enhancement of 14.4-fold was observed when 15 nm Ag nanoparticles were used and 10.8-fold was observed when 30 nm Ag NPs were used. The separation distance dependent emission intensity is ascribed to the competition between energy transfer and enhanced radiative decay rates. The biocompatibility of the nanocomposites was significantly improved by surface modification with DNA. The biological imaging capabilities of these nanocomposites were demonstrated using B16F0 cells. © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2nr31241g
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1039/c2nr31241g
dc.description.sourcetitleNanoscale
dc.description.volume4
dc.description.issue16
dc.description.page5132-5137
dc.identifier.isiut000306855500042
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