Zhang Jian, Fu Yi, Lakowicz Joseph R
Center for Fluorescence Spectroscopy, University of Maryland School of Medicine, Department of Biochemistry and Molecular Biology, 725 West Lombard Street, Baltimore, MD 21201.
J Phys Chem C Nanomater Interfaces. 2009 Nov 12;113(45):19404-19410. doi: 10.1021/jp906742q.
In this paper we studied the metal-enhanced emission from long-lifetime lanthanide dyes that were encapsulated in the silver nanoshells. The metal nanoshells were synthesized with the silica spherical cores of 50 nm diameters and the silver shells of 5 - 60 nm. The optical properties of luminescent metal shells were performed on the either ensemble fluorescence spectroscopy or single particle imaging. The emission intensity from the encapsulated lanthanides was observed to enhance significantly by the metal nanoshell. The enhancement efficiency initially increased with the metal shell thickness and then decreased. The maximal enhancement occurred at the 20 - 30 nm thickness. The lifetime of encapsulated Eu(III) complexes was shorten dramatically indicating that they were coupled efficiently with the metal shells. The increased brightness and reduced lifetime of this core-shell structure demonstrate that the lanthanides are favorable for the single target molecule detections after encapsulating into the metal nanoshells.
在本文中,我们研究了封装在银纳米壳中的长寿命镧系染料的金属增强发射。金属纳米壳是用直径为50 nm的二氧化硅球形核和5 - 60 nm的银壳合成的。发光金属壳的光学性质通过整体荧光光谱或单颗粒成像来进行研究。观察到封装的镧系元素的发射强度被金属纳米壳显著增强。增强效率最初随着金属壳厚度的增加而增加,然后降低。最大增强发生在20 - 30 nm的厚度处。封装的Eu(III)配合物的寿命显著缩短,表明它们与金属壳有效耦合。这种核壳结构亮度的增加和寿命的缩短表明,镧系元素在封装到金属纳米壳中后有利于单目标分子的检测。