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Photoluminescence spectroscopy of YVO4:Eu3+ nanoparticles with aromatic linker molecules: A precursor to biomedical functionalization.

Authors :
Senty, T. R.
Yalamanchi, M.
Zhang, Y.
Cushing, S. K.
Seehra, M. S.
Shi, X.
Bristow, A. D.
Source :
Journal of Applied Physics; 2014, Vol. 115 Issue 16, p163107-1-163107-5, 5p, 1 Chart, 5 Graphs
Publication Year :
2014

Abstract

Photoluminescence spectra of YVO<subscript>4</subscript>:Eu<superscript>3+</superscript> nanoparticles are presented, with and without the attachment of organic molecules that are proposed for linking to biomolecules. YVO<subscript>4</subscript>:Eu<superscript>3+</superscript> nanoparticles with 5% dopant concentration were synthesized via wet chemical synthesis. X-ray diffraction and transmission electron microscopy show the expected wakefieldite structure of tetragonal particles with an average size of 17 nm. Fourier-transform infrared spectroscopy determines that metal-carboxylate coordination is successful in replacing native metal-hydroxyl bonds with three organic linkers, namely, benzoic acid, 3-nitro 4-chloro-benzoic acid, and 3,4-dihydroxybenzoic acid, in separate treatments. UV-excitation photoluminescence spectra show that the position and intensity of the dominant <superscript>5</superscript>D<subscript>0</subscript> - <superscript>7</superscript>F<subscript>2</subscript> electric-dipole transition at 619 nm are unaffected by the benzoic acid and 3-nitro 4-chloro-benzoic acid treatments. Attachment of 3,4-dihydroxybenzoic acid produces an order-of-magnitude quenching in the photoluminescence, due to the presence of high-frequency vibrational modes in the linker. Ratios of the dominant electric- and magnetic-dipole transitions confirm infrared measurements, which indicate that the bulk crystal of the nanoparticle is unchanged by all three treatments. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00218979
Volume :
115
Issue :
16
Database :
Complementary Index
Journal :
Journal of Applied Physics
Publication Type :
Academic Journal
Accession number :
95862446
Full Text :
https://doi.org/10.1063/1.4874179