论文标题
等离子体热点与Shurikens的耦合,用于基于SERS的映体识别
Coupling of Plasmonic Hot Spots with Shurikens for Superchiral SERS-based Enantiomer Recognition
论文作者
论文摘要
对映异构体的检测是药物开发以及环境和食品质量监测的一个具有挑战性的问题,传统的光学检测方法遭受了低信号和敏感性的影响。表面增强的拉曼散射(SER)在对映体歧视中的应用是分析光学活性小有机或大生物分子的强大方法。在这项工作中,对于对映选择性感应,我们提出了支撑手性的近场分布的一次性手性等离子体shuriken的耦合,SERS活跃的银纳米簇。由于血浆耦合在光学活性分析物的SERS响应中存在显着差异。这是通过数值模拟来假设并确认的,这是银色颗粒受到表面上产生的超手杆病场或实现额外极化的探针分子激发的结果。发现血浆耦合现象对shuriken几何形状,银纳米结构层参数和SERS激发波长的轻微变化极为敏感。设计的结构能够在几分钟内使用公共拉曼光谱仪在纳摩尔范围内的浓度和探针生物分子手性的浓度区分半胱氨酸对映异构体。一次性等离子底物与特定近场极化的组合可以使SERS对映异构体歧视是使用标准拉曼光谱仪的常用技术。
Detection of enantiomers is a challenging problem in drug development as well as environmental and food quality monitoring where traditional optical detection methods suffer from low signals and sensitivity. Application of surface enhanced Raman scattering (SERS) for enantiomeric discrimination is a powerful approach for the analysis of optically active small organic or large biomolecules. In this work, for enantio-selective sensing we proposed the coupling of disposable chiral plasmonic shurikens supporting the chiral near-field distribution with SERS active silver nanoclusters. As a result of the plasmonic coupling significant difference in SERS response of optically active analytes is observed. This is hypothesized and confirmed by numerical simulations to be a consequence of the silver particles being excited by superchiral fields generated at the surface or the probe molecules achieving additional polarization. The plasmon coupling phenomena was found to be extremely sensitive to slight variations in shuriken geometry, silver nanostructured layer parameters, and SERS excitation wavelength(s). Designed structures were able to discriminate cysteine enantiomers at concentrations in the nanomolar range and probe biomolecular chirality, using a common Raman spectrometer within several minutes. The combination of disposable plasmonic substrates with specific near-field polarization can make the SERS enantiomer discrimination a commonly available technique using standard Raman spectrometers.