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最热的几何结构和吸附参数如何影响吸附在不同尺寸纳米胶体金颗粒上的亚甲基蓝分子的表面增强拉曼散射(SERRS)光谱?

How hottest geometries and adsorptive parameters influence the SER(R)S spectra of Methylene Blue molecules adsorbed on nanocolloidal gold particles of varied sizes?

作者信息

Roy Sannak Dutta, Ghosh Manash, Chowdhury Joydeep

机构信息

Department of Physics, Sammilani Mahavidyalaya, Baghajatin Station, E.M. Bypass, Kolkata 700094, India.

Department of Spectroscopy, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Dec 5;151:796-806. doi: 10.1016/j.saa.2015.06.125. Epub 2015 Jul 7.

Abstract

The SER(R)S spectra of Methylene Blue (MB) molecule adsorbed on gold nanocolloidal particles (AuNCs) have been investigated. The adsorptive parameters of the molecule adsorbed on AuNCs have been evaluated with the aid of Fluorescence Spectroscopy study. Fluorescence spectroscopic studies have been further applied to understand the concentration of probe molecule actually adsorbed on AuNC surfaces. Gigantic enhancements ∼10(6)-10(16) orders of magnitude have been recorded for the enhanced Raman bands in the SER(R)S spectra. Three-dimensional Finite Difference Time Domain (3D-FDTD) simulations studies have been carried out to predict the distributions of electric fields around the possible nanoaggregated hot geometries considered to be responsible for the huge enhancements of SER(R)S bands of the MB molecule.

摘要

对吸附在金纳米胶体颗粒(AuNCs)上的亚甲基蓝(MB)分子的表面增强共振拉曼散射(SER(R)S)光谱进行了研究。借助荧光光谱研究评估了吸附在AuNCs上的分子的吸附参数。进一步应用荧光光谱研究来了解实际吸附在AuNC表面的探针分子的浓度。在SER(R)S光谱中,增强的拉曼带记录到了约10(6)-10(16)个数量级的巨大增强。进行了三维时域有限差分(3D-FDTD)模拟研究,以预测被认为是导致MB分子SER(R)S带巨大增强的可能纳米聚集热几何结构周围的电场分布。

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