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Large-Scale Plasmonic nanoCones Array For Spectroscopy Detection

机译:用于光谱检测的大规模等离子体纳米锥阵列

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摘要

Advanced optical materials or interfaces are gaining attention for diagnostic applications. However, the achievement of large device interface as well as facile surface functionalization largely impairs their wide use. The present work is aimed to address different innovative aspects related to the fabrication of large-area 3D plasmonic arrays, their direct and easy functionalization with capture elements, and their spectroscopic verifications through enhanced Raman and enhanced fluorescence techniques. In detail, we have investigated the effect of a Au-based nanoCone array, fabricated by means of direct nanoimprint technique over large area (mm(2)), on protein capturing and on the enhancement in optical signal. A selective functionalization of gold surfaces was proposed by using a peptide (AuPi3) previously selected by phage display. In this regard, two different sequences, labeled with fluorescein and biotin, were chemisorbed on metallic surfaces. The presence of Au nanoCones array consents an enhancement in electric field on the apex of cone, enabling the detection of molecules. We have witnessed around 12-fold increase in fluorescence intensity and SERS enhancement factor around 1.75 × 10(5) with respect to the flat gold surface. Furthermore, a sharp decrease in fluorescence lifetime over nanoCones confirms the increase in radiative emission (i.e., an increase in photonics density at the apex of cones).
机译:先进的光学材料或界面在诊断应用中正受到关注。但是,大型设备接口的实现以及容易的表面功能化大大损害了它们的广泛使用。本工作旨在解决与大面积3D等离子体阵列的制造有关的不同创新方面,它们具有捕获元件的直接和简便功能,以及通过增强拉曼和增强荧光技术进行光谱验证。详细地,我们已经研究了通过直接纳米压印技术在大面积(mm(2))上制造的基于Au的nanoCone阵列对蛋白质捕获和光信号增强的影响。通过使用预先通过噬菌体展示选择的肽(AuPi3)提出了金表面的选择性功能化。在这方面,标记为荧光素和生物素的两个不同序列被化学吸附在金属表面上。 Au nanoCones阵列的存在可以增强视锥细胞顶端的电场,从而可以检测分子。我们已经看到,相对于平坦的金表面,荧光强度和SERS增强因子大约增加了12倍,大约为1.75×10(5)。此外,与nanoCones相比,荧光寿命的急剧下降证实了辐射发射的增加(即,在圆锥体顶点处的光子密度的增加)。

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