Fluorescence enhancement of europium complexes by core-shell Ag@SiO2 nanoparticles

被引:16
|
作者
Zhang, Hai-Xia [1 ]
Lin, Xue-Mei [1 ]
Wang, Ai-Ling [1 ]
Zhao, Yong-Liang [1 ]
Chu, Hai-Bin [1 ]
机构
[1] Inner Mongolia Univ, Coll Chem & Chem Engn, Hohhot 010021, Peoples R China
基金
中国国家自然科学基金;
关键词
Europium complex; Halobenzoic acid; Ag@SiO2 core-shell nanoparticles; Metal-enhanced fluorescence; CRYSTAL-STRUCTURE; DISTANCE; FLUOROPHORES; INTENSITY; EMISSION;
D O I
10.1016/j.saa.2015.07.022
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Three kinds of core-shell Ag@SiO2 nanoparticles with shell thickness of around 10, 15, and 25 nm, respectively, have been prepared by modified Stober method and used for fluorescence enhancement. Six kinds of europium complexes with halobenzoic acid have been synthesized. Elemental analysis and lanthanide coordination titration show that the complexes have the compositions of Eu(p-XBA)(3 center dot)H2O and Eu(o-XBA)(3)center dot 2H(2)O (X= F, Cl, Br). The fluorescence spectra investigation indicates that the introduction of Ag@SiO2 nanoparticles into the europium complexes' solution can significantly enhance the fluorescence intensities of the complexes. The sequence of enhancement factors for halobenzoic acid complexes with different halogen atoms is F < Cl < Br, and the fluorescence enhancement factors increase as the excitation wavelength of complexes increase. When the thickness of the SiO2 shell is 25 nm, the fluorescence intensity of the europium complexes can reach a maximum enhancement factor of 5.1. The fluorescence enhancement mechanism may be the metal-enhanced fluorescence resulting from surface plasmon resonance of nanoparticles. And the nanoparticles near the complexes can effectively prevent complexes from the interaction with the solvent molecules, leading to a decrease of nonradiative energy transfer and the suppression of luminescence quench. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:716 / 722
页数:7
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