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Dielectric Nanoparticles Coated upon Silver Hollow Nanosphere as an Integrated Design to Reinforce SERS Detection of Trace Ampicillin in Milk Solution

机译:介电纳米粒子涂层银中空纳米作为综合设计,以加强SERs检测乳液溶液中的痕量氨苄青霉素

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Surface-enhanced Raman scattering (SERS) technique is competent to trace detection of target species, down to the single molecule level. The detection sensitivity is presumably degraded by the presence of non-specific binding molecules that occupy a SERS-active site (or hot spot) on the substrate surface. In this study, a silver hollow nano-sphere (Ag HNS) with cavity has been particularly designed, followed by depositing dielectric nanoparticles (Di NPs) upon Ag HNS. In the integrated nanostructures, Di NPs/Ag HNS were furthermore confirmed by cutting through the cross sections using the Focused Ion Beam (FIB) technique, which provides the Scanning Electron Microscope (SEM) with Energy-dispersive Spectroscope (EDS) mode for identifying the distribution of Di NPs upon Ag HNS. The results have indicated that Di NPs/Ag HNS exhibits small diameter of cavity, and among Di NPs in this study, Al2O3 with lower dielectric constant provides a much higher SERS enhancement factor (e.g., ~6.2 × 107). In this study, to detect trace amounts (e.g., 0.01 ppm) of Ampicillin in water or milk solution, Al2O3 NPs/Ag HNS was found to be more efficient and less influenced by non-specific binding molecules in milk. A substrate with integrated plasmonic and dielectric components was designed to increase the adsorption of target species and to repulse non-specific binding molecules from SERS-active sites.
机译:表面增强的拉曼散射(SERS)技术是追踪靶物种的追踪,降至单一分子水平。通过存在在基板表面上占据SERS-活性位点(或热点)的非特异性结合分子的存在可能降解检测灵敏度。在该研究中,特别设计了一种具有腔的银中空纳米球(Ag HnS),然后在Ag HNS上沉积介电纳米颗粒(DI NPS)。在集成的纳米结构中,通过使用聚焦离子束(FIB)技术通过横截面切割横截面来证实DI NPS / AG HNS,其为扫描电子显微镜(SEM)提供能量 - 分散光谱仪(EDS)模式来识别AG HNS对DI NPS的分布。结果表明,DI NPS / AG HNS表现出小的腔直径,并且在该研究的DI NP中,具有较低介电常数的AL2O3提供了更高的SERs增强因子(例如,〜6.2×107)。在该研究中,为了检测水或乳溶液中的氨苄青霉素的痕量(例如,0.01ppm),发现Al 2 O 3 NPS / Ag HNS在牛奶中的非特异性结合分子的影响更有效且较低。设计具有集成等离子体和介电部件的基板,以增加目标物种的吸附并从SERS-活性位点拒绝非特异性结合分子。

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