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Cubic Silver Nanoparticles Fixed on TiO2 Nanotubes as Simple and Efficient Substrates for Surface Enhanced Raman Scattering

机译:固定在TiO2纳米管上的立方银纳米颗粒作为用于表面增强拉曼散射的简单高效基材

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摘要

In this work we show that ordered freestanding titanium oxide nanotubes (TiO NT) may be used as substrates for the simple and efficient immobilization of anisotropic plasmonic nanoparticles. This is important because anisotropic plasmonic nanostructures usually give greater spectral enhancement than spherical nanoparticles. The size of the pores in a layer of titanium oxide nanotubes can be easily fitted to the size of many silver plasmonic nanoparticles highly active in SERS (surface-enhanced Raman scattering) spectroscopy (for example, silver nanocubes with an edge length of ca. 45 nm), and hence, the plasmonic nanoparticles deposited can be strongly anchored in such a titanium oxide substrate. The tubular morphology of the TiO substrate used allows a specific arrangement of the silver plasmonic nanoparticles that may create many so-called SERS hot spots. The SERS activity of a layer of cubic Ag nanoparticles (AgCNPs) deposited on a tubular TiO substrate (AgCNPs@TiO NT) is about eight times higher than that of the standard electrochemically nanostructured surface of a silver electrode (produced by oxidation reduction cycling). Furthermore, a super hydrophilic character of the TiO nanotubes surface allows for a uniform distribution of AgCNPs, which are deposited from an aqueous suspension. The new AgCNPs@TiO NT hybrid layer ensures a good reproducibility of SERS measurements and exhibits a higher temporal stability of the achievable total SERS enhancement factor—one that is far better than standard SERS silver substrates. To characterize the morphology and chemical composition of such evidently improved SERS platforms thus received, we applied microscopic techniques (SEM, and scanning transmission electron microscopy (STEM)) and surface analytical techniques (Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS)).
机译:在这项工作中,我们表明有序的独立式氧化钛纳米管(TiO NT)可以用作简单有效地固定各向异性等离子体纳米颗粒的基质。这很重要,因为各向异性的等离子体纳米结构通常比球形纳米颗粒具有更大的光谱增强。氧化钛纳米管层中孔的大小可以轻松地与许多在SERS(表面增强拉曼散射)光谱中具有高活性的银等离激元纳米粒子的大小相适应(例如,边缘长度约为45的银纳米立方)因此,所沉积的等离子体纳米颗粒可以牢固地锚定在这种钛氧化物基底中。所使用的TiO衬底的管状形态允许特定的银等离子体纳米颗粒排列,这可能会产生许多所谓的SERS热点。沉积在管状TiO基底(AgCNPs @ TiO NT)上的立方Ag纳米颗粒(AgCNPs)层的SERS活性比银电极的标准电化学纳米结构表面(通过氧化还原循环生产)的SERS活性高约八倍。此外,TiO纳米管表面的超亲水特性允许从水性悬浮液中沉积的AgCNP均匀分布。新的AgCNPs @ TiO NT杂化层确保了SERS测量的良好再现性,并且可实现的总SERS增强因子具有更高的时间稳定性-远优于标准SERS银衬底。为了表征由此获得的这种明显改善的SERS平台的形态和化学成分,我们应用了显微镜技术(SEM和扫描透射电子显微镜(STEM))和表面分析技术(俄歇电子能谱(AES)和X射线光电子能谱( XPS))。

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