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Well Controlling of Plasmonic Features of Gold Nanoparticles on Macro Porous Silicon Substrate by HF Acid Concentration

机译:用HF酸浓度很好地控制大孔硅基底上金纳米粒子的等离子体特征。

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摘要

In this work, we fabricated an efficient macroporous silicon/gold nanoparticles (macro psi/AuNPs) hybrid structure and how well controlling of plasmonic features on macro psi/AuNPs employs them for highly sensitive detection of the very low concentration of cyanine (Cy) dyes molecules. Macro-PSi was synthesized on n-type Si wafer with 3–10 Ω. cm resistivity and 100 orientation using Photo Electro Chemical Etching (PECE) process with630 nm illumination wavelength and 30 mW/cm2 illumination intensity. The macroPSi /AuNPs hybrid structure substrates were prepared by simple and quick dipping process of macroPSi in tetrachloroauric gold solution HAuCl4 with different concentrations of (10−2  M, 10−2 M diluted in 2.9  M of HF, 5 × 10−3 M, and 5 × 10−3 M diluted in 2.9 M of HF). Efficient surface-enhanced Raman scattering (SERS) signals was obtained from macroPSi/AuNPs substrates for Cy dye concentration of about 10−6 and 10−10 M. The detection method is dependent on a nanoparticles sizes process through controlling the concentration in a HAuCl4 solution. Higher SERS signal was found for sample with lower salt concentration of 5 × 10−3 M diluted in HF. The enhancement factors (EF) of Raman’s signal increased four orders of magnitude by diluting the salt concentration. The values of EF in the range of 0.8 × 103−0.72 × 107 were obtained by controlling the salt concentration from 10−2 to 5 × 10−3 diluted in HF acid.
机译:在这项工作中,我们制造了一种高效的大孔硅/金纳米颗粒(macro psi / AuNPs)杂化结构,以及如何很好地控制宏观psi / AuNPs上的等离激元特征如何利用它们对非常低浓度的花青(Cy)染料进行高灵敏度检测分子。 Macro-PSi在3-10Ω的n型Si晶片上合成。使用光电化学蚀刻(PECE)工艺在630 nm的电阻率和100取向下实现了630 nm的照射波长和30 mW / cm 2 的照射强度。 macroPSi / AuNPs杂化结构底物是通过将macroPSi简单快速地浸入具有不同浓度(10 -2 M,10 −2 M的四氯金金溶液HAuCl4中制备的在2.9 M HF中稀释5×10 −3 M和在2.9 M HF中稀释5×10 −3 M)。从macroPSi / AuNPs底物获得有效的表面增强拉曼散射(SERS)信号,用于Cy染料浓度约为10 -6 和10 -10 M。检测方法为通过控制HAuCl4溶液中的浓度,取决于纳米颗粒的大小。对于在HF中稀释的5 of×10 -3 M盐浓度较低的样品,发现其SERS信号较高。拉曼信号的增强因子(EF)通过稀释盐浓度而增加了四个数量级。通过控制盐浓度从10 -2 到0.8 to×10 3 − 0.72×10 7 ,可以得到EF值。用HF酸稀释5××10 10 -3

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