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Autoenhanced Raman Spectroscopy via Plasmonic Trapping for Molecular Sensing

机译:通过等离子阱的自动增强拉曼光谱技术进行分子传感

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As a label-free and sensitive biosensor, surface-enhanced Raman spectroscopy (SERS) is a rapidly emerging technique. However, because SERS spectra are obtained in the area of light excitation and the enhancement effect can be varied depending on the position of a substrate, it is important to match the enhanced area with an illuminated spot. Here, in order to overcome such difficulty, we demonstrated a new technique combining SERS with plasmonic trapping. By plasmonic trapping, we can collect gold nanoparticles (GNPs) in the middle of initially fabricated nanobowtie structures where a laser is excited. As a result of trapping GNPs, hot-spots are formed at that area. Because SERS is measured in the area irradiated by a laser, hot-spot can be simultaneously coincided with a detection site for SERS. By using this, we detected Rhodamine 6G to 100 pM. To further verify and improve the reproducibility of our technique, we also calculated the electric field distribution, trapping force and trapping potential.
机译:作为一种无标签且灵敏的生物传感器,表面增强拉曼光谱(SERS)是一项迅速兴起的技术。但是,由于在光激发的区域中获得了SERS光谱,并且可以根据基板的位​​置来改变增强效果,因此重要的是使增强区域与照明点匹配。在这里,为了克服这种困难,我们展示了一种将SERS与等离子体捕获结合的新技术。通过等离子体捕获,我们可以在最初制造的纳米领结结构的中间收集金纳米颗粒(GNP),在该结构中激光被激发。捕获GNP的结果是在该区域形成了热点。因为SERS是在激光照射的区域中测量的,所以热点可以与SERS的检测位置同时重合。通过使用它,我们检测到若丹明6G至100 pM。为了进一步验证和提高我们技术的可重复性,我们还计算了电场分布,俘获力和俘获电位。

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