Geddes Chris D, Parfenov Alex, Gryczynski Ignacy, Lakowicz Joseph R
Institute of Fluorescence and the Center for Fluorescence Spectroscopy, Medical Biotechnology Center, University of Maryland Biotechnology Institute, 725 West Lombard Street, Baltimore, Maryland 21201, and Center for Fluorescence Spectroscopy, Department of Biochemistry and Molecular Biology, University of Maryland at Baltimore, 725 West Lombard Street, Baltimore, Maryland 21201.
J Phys Chem B. 2003 Sep 18;107(37):9989-9993. doi: 10.1021/jp030290g.
Silver nanostructures deposited on glass showed luminescent blinking when excited at a high 442 nm irradiance. The irradiance required to photoactivate the silver, was dependent on the nature of the silver nanostructures. Silver fractal-like structures were found to be highly emissive, requiring only ≈30 W/cm(2) for photoactivation as compared to silver island films and spin-coated silver colloids, which required a significantly higher irradiance, > 100 W/cm(2), to observe similar luminescent emission. In contrast to our recent findings for gold colloids, foci with different color blinking were also observed, with an increase in luminescence intensity as a function of time. We place these findings in context with recent work from our laboratory which employs these silver nanostructures for applications in metal-enhanced fluorescence, a relatively new phenomenon in fluorescence, whereby metallic particles, colloids, and fractal-like structures can modify the intrinsic radiative decay rate of close proximity fluorescent species. These effects are a consequence of localized changes in photonic mode density around the fluorophores, and we can now report are typically observed at significantly lower illumination intensities as compared to those required to photoactivate silver. Subsequently, our findings strongly suggest that the enhanced fluorescence emission of fluorophores positioned in close proximity to metallic silver structures is not due to either intrinsic silver blinking, or indeed the silver luminescence pumping the fluorophore. Further, the intrinsic luminescence properties of silver reported here, suggest a new class of luminescence probes and labels.
沉积在玻璃上的银纳米结构在442 nm高辐照度激发下呈现发光闪烁现象。光激活银所需的辐照度取决于银纳米结构的性质。发现类银分形结构具有高发射性,与银岛膜和旋涂银胶体相比,光激活仅需约30 W/cm²,而银岛膜和旋涂银胶体需要显著更高的辐照度(>100 W/cm²)才能观察到类似的发光发射。与我们最近关于金胶体的发现不同,还观察到具有不同颜色闪烁的焦点,发光强度随时间增加。我们将这些发现与我们实验室最近的工作相结合,这些工作将这些银纳米结构应用于金属增强荧光,这是荧光领域中一种相对较新的现象,即金属颗粒、胶体和类分形结构可以改变近距离荧光物质的固有辐射衰减率。这些效应是荧光团周围光子模式密度局部变化的结果,并且我们现在可以报告,与光激活银所需的强度相比,通常在显著更低的光照强度下观察到这些效应。随后,我们的发现强烈表明,位于金属银结构附近的荧光团增强的荧光发射既不是由于银的固有闪烁,也不是由于银发光泵浦荧光团。此外,这里报道的银的固有发光特性表明了一类新的发光探针和标记物。