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One-step synthesis of highly-branched gold nanostructures and its application in fabrication of SERS-active substrates

机译:高枝金纳米结构的一步合成及其在SERS-活性基材的制造中的应用

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In this paper, we reported a simple one-step synthesis of highly-branched gold nanostructures (HGNs) in high yields. The reduction of HAuClsub4/sub was accomplished by dopamine hydrochloride in the reaction system. By varying the amount of dopamine hydrochloride, HAuClsub4/sub and the reaction temperature, we managed to tune the size of the HGNs from 200 to 600 nm. Systematic analysis revealed that the optical properties and surface-enhanced Raman scattering (SERS) activities of the HGNs were highly dependent on their morphology and size. In terms of their SERS activities, it was found that the HGNs synthesized at 60 °C with 2.0 mL dopamine hydrochloride (53 mM), 0.4 mL HAuClsub4/sub (50 mM) exhibited the largest SERS enhancement. When the HGNs were assembled onto the silicon wafers, outstanding SERS efficiency was obtained with a detection limit of 5×10sup-10/sup M of 4-mercaptobenzoic acid (4-MBA) and the analytical enhancement factor (AEF) was calculated to be 7×10sup7/sup. Besides, the 3-aminopropyltriethoxysilane (APTES)-functionalized substrates with the HGNs displayed remarkable signal reproducibility with relative standard deviation (RSD) of 3.57%. All these results demonstrated that the SERS-active substrates held great promise to be applied in trace-level molecule detection in the future.
机译:在本文中,我们报道了高产率高屈服的金纳米结构(HGNS)的简单一步合成。 HauCl 4 的还原是通过反应体系中的多巴胺盐酸盐完成的。通过改变盐酸多巴胺的量,HauCl 4 和反应温度,我们设法将HGNS的大小从200到600 nm调整。系统分析显示,HGNS的光学性质和表面增强拉曼散射(SERS)活性高度依赖于其形态和大小。就其SERS的活动而言,发现在60℃下合成的HGN在2.0mL多巴胺盐酸盐(53mm),0.4mL HauCl 4 (50mm)上表现出最大的SERs增强。当HGNS组装到硅晶片上时,获得优异的SER效率,检测限为5×10 -10米的4-巯基苯甲酸(4-MBA)和分析增强因子(AEF)计算为7×10 7 。此外,3-氨基丙基三乙氧基硅烷(APTES) - 官能化基材,具有HGNS的相对标准偏差(RSD)显示出显着的信号再现性,为3.57%。所有这些结果表明,SERS-活跃的基材在未来核对痕量分子检测中持久承诺。

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