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Multifunctional Fe3O4@SiO2-Au Satellite Structured SERS Probe for Charge Selective Detection of Food Dyes

机译:多功能Fe3O4 @ SiO2-Au卫星结构SERS探针用于食品染料的电荷选择性检测

摘要

Nanofabrication of multifunctional surface-enhanced Raman scattering (SERS) substrates is strongly desirable but currently remains a challenge. The motivation of this study was to design such a substrate, a versatile core satellite Fe3O4@SiO2 Au (FA) hetero-nanostructure, and demonstrate its use for charge selective detection of food dye molecules as an exemplary application. Our experimental results and three-dimensional finite difference time domain (FDTD) simulation suggest that tuning the Au nanoparticle (NP) gap to sub-10 nm, which could be readily accomplished, substantially enhanced the Ronan signals. Further layer-by-layer deposition of a charged polyelectrolyte on this magnetic SERS substrate induced active adsorption and selective detection of food dye molecules of opposite charge on the substrates. Molecular dynamics (MD) simulations suggest that the selective SERS enhancement could be attributed to the high affinity and close contact (within a 20 angstrom range) between the substrate and molecules. Density function theory (DFT) calculations confirm the charge transfer from food dye molecules to Au NPs -via the polyelectrolytes. This multifunctional SERS platform provides easy separation and selective detection of charged molecules from complex chemical mixtures.
机译:多功能表面增强拉曼散射(SERS)基板的纳米加工是非常需要的,但是目前仍然是一个挑战。这项研究的动机是设计这样的基质,一种多功能的人造卫星Fe3O4 @ SiO2 Au(FA)杂纳米结构,并证明其作为示例性应用可用于食品染料分子的电荷选择性检测。我们的实验结果和三维有限差分时域(FDTD)模拟表明,将金纳米粒子(NP)的间隙调节至10 nm以下很容易实现,从而显着增强了Ronan信号。带电的聚电解质在此磁性SERS基底上的进一步逐层沉积可导致主动吸附并选择性检测基底上带相反电荷的食用染料分子。分子动力学(MD)模拟表明,选择性SERS增强可能归因于底物与分子之间的高亲和力和紧密接触(在20埃范围内)。密度函数理论(DFT)的计算证实了食用染料分子通过聚电解质将电荷转移到Au NP上。该多功能SERS平台可轻松分离和选择性检测复杂化学混合物中的带电分子。

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