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三维和时序表面增强拉曼散射热点矩阵。

Three-dimensional and time-ordered surface-enhanced Raman scattering hotspot matrix.

机构信息

Institute of Intelligent Machines, Chinese Academy of Sciences , Hefei 230031, China.

出版信息

J Am Chem Soc. 2014 Apr 9;136(14):5332-41. doi: 10.1021/ja501951v. Epub 2014 Mar 28.

Abstract

The "fixed" or "flexible" design of plasmonic hotspots is a frontier area of research in the field of surface-enhanced Raman scattering (SERS). Most reported SERS hotspots have been shown to exist in zero-dimensional point-like, one-dimensional linear, or two-dimensional planar geometries. Here, we demonstrate a novel three-dimensional (3D) hotspot matrix that can hold hotspots between every two adjacent particles in 3D space, simply achieved by evaporating a droplet of citrate-Ag sols on a fluorosilylated silicon wafer. In situ synchrotron-radiation small-angle X-ray scattering (SR-SAXS), combined with dark-field microscopy and in situ micro-UV, was employed to explore the evolution of the 3D geometry and plasmonic properties of Ag nanoparticles in a single droplet. In such a droplet, there is a distinct 3D geometry with minimal polydispersity of particle size and maximal uniformity of interparticle distance, significantly different from the dry state. According to theoretical simulations, the liquid adhesive force promotes a closely packed assembly of particles, and the interparticle distance is not fixed but can be balanced in a small range by the interplay of the van der Waals attraction and electrostatic repulsion experienced by a particle. The "trapping well" for immobilizing particles in 3D space can result in a large number of hotspots in a 3D geometry. Both theoretical and experimental results demonstrate that the 3D hotspots are predictable and time-ordered in the absence of any sample manipulation. Use of the matrix not only produces giant Raman enhancement at least 2 orders of magnitude larger than that of dried substrates, but also provides the structural basis for trapping molecules. Even a single molecule of resonant dye can generate a large SERS signal. With a portable Raman spectrometer, the detection capability is also greatly improved for various analytes with different natures, including pesticides and drugs. This 3D hotspot matrix overcomes the long-standing limitations of SERS for the ultrasensitive characterization of various substrates and analytes and promises to transform SERS into a practical analytical technique.

摘要

等离子体热点的“固定”或“灵活”设计是表面增强拉曼散射(SERS)领域的一个前沿研究领域。大多数报道的 SERS 热点都存在于零维点状、一维线性或二维平面几何形状中。在这里,我们展示了一种新颖的三维(3D)热点矩阵,通过在氟硅化硅片上蒸发柠檬酸银溶胶液滴,可以在 3D 空间中保持每两个相邻颗粒之间的热点。结合同步辐射小角 X 射线散射(SR-SAXS)、暗场显微镜和原位微紫外光谱,我们探索了单个液滴中 Ag 纳米颗粒的 3D 几何形状和等离子体特性的演变。在这样的液滴中,存在明显的 3D 几何形状,颗粒尺寸的多分散性最小,颗粒间距离的均匀性最大,与干燥状态显著不同。根据理论模拟,液体粘合力促进了颗粒的紧密组装,颗粒间的距离不是固定的,而是可以通过一个颗粒所经历的范德华吸引力和静电排斥力的相互作用在小范围内平衡。在 3D 空间中固定颗粒的“陷阱井”可以导致大量的 3D 几何热点。理论和实验结果均表明,在没有任何样品处理的情况下,3D 热点是可预测和有序的。使用该矩阵不仅可以产生比干燥基底大至少 2 个数量级的巨大拉曼增强,而且为捕获分子提供了结构基础。即使是单个共振染料分子也可以产生大的 SERS 信号。使用便携式拉曼光谱仪,对各种不同性质的分析物,包括农药和药物,也大大提高了检测能力。这种 3D 热点矩阵克服了 SERS 对各种基底和分析物的超灵敏特性的长期限制,并有望将 SERS 转化为一种实用的分析技术。

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