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Controlled Assembly of Gold Nanostructures on a Solid Substrate via Imidazole Directed Hydrogen Bonding for High Performance Surface Enhance Raman Scattering Sensing of Hypochlorous Acid

机译:通过咪唑定向氢键控制固体表面上金纳米结构的组装,以实现次氯酸的高性能表面增强拉曼散射传感

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摘要

Here, we report an efficient and facile method for constructing plasmonic gold nanostructures with controlled morphology on a Si wafer and its use as a surface enhanced Raman scattering (SERS) reporting system for specific detection of HClO. To achieve this substrate, the core gold nanoparticles (AuNPs, similar to 100 nm) with a monolayer of 4-mercaptoimidazole (MI) ligands were covalently linked to a thiol-derived Si wafer (MI-AuNPs@SH-Si). Taking advantage of the intermolecular NH...N hydrogen bond (HB) provided by the neighboring imidazole moiety, multiple satellite AuNPs (similar to 12 nm) decorated with both MI and a Raman reporter are assembled around the core MI-AuNPs at pH 5.0. The uniform morphology of the AuNP-based nanostructures on the Si wafer offer a high density of hot spots with good SERS performance for detecting HClO. The fast oxidation of the imidazole moieties by HClO causes HB destruction and therefore separation of the satellite AuNPs from the core AuNPs, which gives rise to SERS signal damping of the chip that is employed for HClO analysis. This simple and cost-effective method is highly selective for HClO over common interferences and several reactive oxygen/nitrogen species, and enabled rapid analysis at concentrations as low as 1.2 mu mol L-1. The present approach is applied to analyze water and human serum samples with satisfactory results.
机译:在这里,我们报告了一种高效且简便的方法,用于在Si晶片上构建具有可控形态的等离子体金纳米结构,并将其用作表面增强拉曼散射(SERS)报告系统,用于HClO的特异性检测。为了获得该基底,将具有4-巯基咪唑(MI)配体单层的核心金纳米颗粒(AuNP,类似于100 nm)共价连接至硫醇衍生的硅片(MI-AuNPs @ SH-Si)。利用相邻咪唑部分提供的分子间NH ... N氢键(HB),在pH 5.0时,用MI和拉曼报道分子修饰的多个卫星AuNP(类似于12 nm)组装在核心MI-AuNP周围。 Si晶片上基于AuNP的纳米结构的均匀形态提供了高密度的热点,并具有良好的SERS性能以检测HClO。 HClO对咪唑部分的快速氧化会导致HB破坏,从而使卫星AuNP与核心AuNP分离,这会导致用于HClO分析的芯片的SERS信号衰减。这种简单且具有成本效益的方法对HClO具有较高的选择性,优于常见的干扰物和多种活性氧/氮,可在低至1.2μmol的L-1浓度下快速分析。本方法用于分析水和人血清样品,结果令人满意。

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