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Plasmonic nano-protrusions: hierarchical nanostructures for single-molecule Raman spectroscopy

机译:等离子体纳米突起:单分子拉曼光谱的分层纳米结构

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Classical methods for enhancing the electromagnetic field from substrates for spectroscopic applications, such as surface-enhanced Raman spectroscopy (SERS), have involved the generation of hotspots through directed self-assembly of nanoparticles or by patterning nanoscale features using expensive nanolithography techniques. A novel large-area, cost-effective soft lithographic technique involving glancing angle deposition (GLAD) of silver on polymer gratings is reported here. This method produces hierarchical nanostructures with high enhancement factors capable of analyzing single-molecule SERS. The uniform ordered and patterned nanostructures provide extraordinary field enhancements that serve as excitatory hotspots and are herein interrogated by SERS. The high spatial homogeneity of the Raman signal and signal enhancement over a large area from a self-assembled monolayer (SAM) of 2-naphthalenethiol demonstrated the uniformity of the hotspots. The enhancement was shown to have a critical dependence on the underlying nanostructure via the surface energy landscape and GLAD angles for a fixed deposition thickness, as evidenced by atomic force microscopy and scanning electron microscopy surface analysis of the substrate. The nanostructured surface leads to an extremely concentrated electromagnetic field at sharp nanoscale peaks, here referred to as 'nano-protrusions', due to the coupling of surface plasmon resonance (SPR) with localized SPR. These nano-protrusions act as hotspots which provide Raman enhancement factors as high as 10(8) over a comparable SAM on silver. Comparison of our substrate with the commercial substrate Klarite (TM) shows higher signal enhancement and minimal signal variation with hotspot spatial distribution. By using the proper plasmon resonance angle corresponding to the laser source wavelength, further enhancement in signal intensity can be achieved. Single-molecule Raman spectra for rhodamine 6G are obtained from the best SERS substrate (a GL
机译:用于增强来自基板的电磁场的典型方法,例如表面增强拉曼光谱(SERS),通过纳米颗粒的定向自组装或通过使用昂贵的纳米线程技术进行图案化纳米级特征来产生热点的产生。这里据报道了一种新的大面积,涉及瞥亮角沉积(高兴)银在聚合物光栅上的大面积沉积(高兴)。该方法产生具有高增强因子的分层纳米结构,能够分析单分子SERS。均匀的有序和图案化的纳米结构提供了非凡的现场增强功能,其用作兴奋热点,在此通过SERS询问。拉曼信号的高空间均匀性和来自2-萘硫醇的自组装单层(SAM)的大面积上的信号增强证明了热点的均匀性。由于原子力显微镜显微镜和扫描电子显微镜表面分析和扫描基材的扫描电子显微镜表面分析,所示的增强通过表面能景观和用于固定沉积厚度的高档角度对底层纳米结构具有临界依赖性。纳米结构表面导致尖锐的纳米级峰值的极其浓缩的电磁场,这里被称为“纳米突起”,由于表面等离子体共振(SPR)与局部SPR的耦合。这些纳米突起充当热点,其在银上的可比较的Sam上提供高达10(8)的拉曼增强因子。与商业基板Klarite(TM)的基板的比较显示了具有热点空间分布的更高的信号增强和最小的信号变化。通过使用对应于激光源波长对应的适当的等离子体共振角,可以实现信号强度的进一步增强。用于罗丹明6G的单分子拉曼光谱从最好的SERS衬底获得(A GL

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