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Fluorescence studies of Rhodamine 6G functionalized silicon oxide nanostructures

机译:罗丹明6G功能化氧化硅纳米结构的荧光研究

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Selective anchoring of optically active molecules on nanostructured surfaces is a promising step towards the creation of nanoscale devices with new functionalities. Recently we have demonstrated the electrostatic attachment of charged fluorescent molecules on silicon oxide nanostructures prepared by atomic force microscopy (AFM) nanolithography via local anodic oxidation (LAO) of dodecyl-terminated silicon. In this paper we report on our findings from a more detailed optical investigation of the bound dye Rhodamine 6G. High sensitivity optical wide field microscopy as well as confocal laser microscopy have been used to characterize the Rhodamine fluorescence emission. A highly interesting question concerns the interaction between an emitter close to a silicon surface because mechanisms such as energy transfer and fluorescence quenching will occur which are still not fully understood. Since the oxide thickness can be varied during preparation continuously from 1 to ~5 nm, it is possible to investigate the fluorescence of the bound dye in close proximity to the underlying silicon. Using confocal laser microscopy we were also able to obtain optical spectra from the bound molecules. Together with the results from an analysis of their photochemical bleaching behaviour, we conjecture that some of the Rhodamine 6G molecules on the structure are interacting with the oxide, causing a spectral shift and differences in their photochemical properties.
机译:光学活性分子在纳米结构表面上的选择性锚固是朝着创建具有新功能的纳米级器件发展的有希望的一步。最近,我们已经证明了带电的荧光分子在通过原子力显微镜(AFM)纳米光刻技术通过十二烷基封端的硅的局部阳极氧化(LAO)制备的氧化硅纳米结构上的静电附着。在本文中,我们将从结合染料若丹明6G的更详细的光学研究中报告我们的发现。高灵敏度光学广域显微镜和共聚焦激光显微镜已被用来表征罗丹明的荧光发射。一个非常有趣的问题涉及到靠近硅表面的发射器之间的相互作用,因为会发生诸如能量转移和荧光猝灭之类的机制,而这些机制仍未被完全理解。由于在制备过程中氧化物的厚度可以在1到〜5 nm之间连续变化,因此有可能研究与下层硅紧密结合的染料的荧光。使用共聚焦激光显微镜,我们还能够从结合的分子获得光谱。连同对它们的光化学漂白行为的分析结果一起,我们推测该结构上的一些若丹明6G分子正在与氧化物相互作用,从而导致光谱移位和它们的光化学特性差异。

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