Luminescence Enhancement Mechanism of Lanthanide-Doped Hybrid Nanostructures Decorated by Silver Nanocrystals

被引:12
|
作者
He, E. J. [1 ,2 ]
Moskovits, M. [3 ]
Dong, J. [1 ]
Gao, W. [1 ]
Han, Q. Y. [1 ]
Zheng, H. R. [1 ]
Liu, N. [4 ]
机构
[1] Shaanxi Normal Univ, Sch Phys & Informat Technol, Xian 710119, Peoples R China
[2] Anhui Sci & Technol Univ, Dept Optoelect Technol, Fengyang 233100, Peoples R China
[3] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[4] Anhui Polytech Univ, Coll Mech & Automot Engn, Wuhu 241000, Peoples R China
基金
美国国家科学基金会;
关键词
Surface plasmon resonance; Luminescence enhancement; Ag nanoparticles; Hybrid nanostructures; Lanthanide; UP-CONVERSION LUMINESCENCE; GOLD NANOPARTICLES; OPTICAL-PROPERTIES; FLUORESCENCE; SURFACE; SCATTERING; SPHERES;
D O I
10.1007/s11468-014-9817-x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hybrid nanostructures composed of rare earth ion-doped lanthanum trifluoride nanocrystals deposited on silica nanospheres (LaF3:Yb3+, Er3+@SiO2) and decorated with varying quantities of silver nanoparticles (Ag NPs) were synthesized using a simple strategy. Down and upconversion luminescence spectra were recorded. The luminescence dynamics were also recorded following excitation ith a 532-nm pulse. Silver loading was found to have a significant effect both on the luminescence intensity and the luminescence decay rate, with the samples with the lowest silver content showing reduced luminescence intensity over silver-free samples, while the samples with large levels of silver loading showed significant luminescence enhancement. The results were successfully (and quantitatively) interpreted in terms of the competition between surface plasmon-induced field enhancement mediated by the Ag nanoparticles and nonradiative energy transfer from the luminescent ions to Ag nanoparticles. By combining the measured luminescence intensity with the luminescence decay rate determined from the dynamics measurements, and with the measured surface plasmon absorption spectra, one could obtain a quantitative and self-consistent understanding of the observed dependence of the green S-4(3/2)-> I-4(15/2) (similar to 540 nm) and red F-4(9/2)-> I-4(15/2) (similar to 650) emission bands on the Ag NP metal loading.
引用
收藏
页码:357 / 368
页数:12
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