首页> 外文期刊>Journal of nanotechnology >Surface-Enhanced Raman Spectroscopy of Dye and Thiol Molecules Adsorbed on Triangular Silver Nanostructures: A Study of Near-Field Enhancement, Localization of Hot-Spots, and Passivation of Adsorbed Carbonaceous Species
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Surface-Enhanced Raman Spectroscopy of Dye and Thiol Molecules Adsorbed on Triangular Silver Nanostructures: A Study of Near-Field Enhancement, Localization of Hot-Spots, and Passivation of Adsorbed Carbonaceous Species

机译:三角形银纳米结构上吸附的染料和硫醇分子的表面增强拉曼光谱:近场增强,热点局部化和吸附的碳质物种钝化的研究

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摘要

Surface-enhanced Raman spectroscopy (SERS) of thiols and dye molecules adsorbed on triangular silver nanostructures was investigated. The SERS hot-spots are localized at the edges and corners of the silver triangular particles. AFM and SEM measurements permit to observe many small clusters formed at the edges of triangular particles fabricated by nanosphere lithography. Finite-element calculations show that near-field enhancements can reach values of more than 200 at visible wavelengths, in the gaps between small spherical particles and large triangular particles, although for the later no plasmon resonance was found at the wavelengths investigated. The regions near the particles showing strong near-field enhancement are well correlated with spatial localization of SERS hot-spots done by confocal microscopy. Silver nanostructures fabricated by thermal evaporation present strong and fast fluctuating SERS activity, due to amorphous carbon contamination. Thiols and dye molecules seem to be able to passivate the undesired SERS activity on fresh evaporated silver.
机译:研究了巯基和染料分子吸附在三角形银纳米结构上的表面增强拉曼光谱(SERS)。 SERS热点位于银色三角形粒子的边缘和角落。原子力显微镜(AFM)和扫描电镜(SEM)测量允许观察到许多小团簇,这些团簇是通过纳米球体光刻技术在三角形颗粒的边缘形成的。有限元计算表明,在较小的球形颗粒和较大的三角形颗粒之间的间隙中,在可见波长处,近场增强可以达到200多个值,尽管后来在所研究的波长处未发现等离子体激元共振。通过共聚焦显微镜观察,颗粒附近的区域显示出强的近场增强,与SERS热点的空间定位密切相关。由于无定形碳污染,通过热蒸发制备的银纳米结构呈现出强而快速的SERS活性波动。硫醇和染料分子似乎能够钝化新鲜蒸发银上不希望的SERS活性。

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