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双金属 Al-Au 杂化二聚体的波长相关光力成像。

Wavelength-Dependent Optical Force Imaging of Bimetallic Al-Au Heterodimers.

出版信息

Nano Lett. 2018 Mar 14;18(3):2040-2046. doi: 10.1021/acs.nanolett.8b00020. Epub 2018 Feb 15.

Abstract

Many important applications of nanometer-scale metallic complexes arise from the light-induced, near-field interactions between their component structures. Here we examine the near-field interactions in bimetallic Al-Au plasmonic nanodisk heterodimers, where the coupling between the primitive plasmons of nanostructures composed of two different metals is studied. Understanding the correlations between nanoparticle morphology and near-field optical properties, particularly for nanostructures composed of two different metals, requires spectrally resolved near-field spatial information. An ideal tool for such investigations is the recently developed photoinduced force microscopy, where the electromagnetic forces between an optically excited plasmonic nanostructure and an adjacent scanning nanoscale tip are measured. Using this approach, we visualize the wavelength-dependent near-field interactions in these bimetallic heterodimers. This system provides a prime example of the diabatic, antenna-reactor picture of plasmon coupling where for a given wavelength the more resonant primitive "driving" plasmon induces a response, the "forced" plasmon, in the off-resonant component. We critically examine spectrally resolved tip-nanostructure forces, comparing experiment with theory, for tips and nanoscale structures of realistic dimensions relative to frequently used approximations for tip geometries. The contrasting effects of dielectric versus metallic tips on acquired spectral force profiles are also examined.

摘要

许多纳米级金属配合物的重要应用源于其组成结构之间光诱导的近场相互作用。在这里,我们研究了由两种不同金属组成的纳米结构的原始等离子体之间的耦合,即双金属 Al-Au 等离子体纳米盘杂化二聚体中的近场相互作用。为了理解纳米颗粒形态和近场光学性质之间的相关性,特别是对于由两种不同金属组成的纳米结构,需要具有光谱分辨的近场空间信息。一种理想的研究工具是最近开发的光致动力显微镜,它可以测量光学激发的等离子体纳米结构与相邻的扫描纳米级尖端之间的电磁力。使用这种方法,我们可以可视化这些双金属杂化二聚体中的波长相关近场相互作用。该系统提供了等离子体耦合的非绝热天线-反应体模型的一个极好示例,其中对于给定的波长,更共振的原始“驱动”等离子体在非共振组件中诱导响应,即“强迫”等离子体。我们对光谱分辨的尖端-纳米结构力进行了严格的检查,将实验与理论进行了比较,考虑了相对于经常使用的尖端几何形状近似值的实际尺寸的尖端和纳米结构。还研究了介电和金属尖端对获得的光谱力曲线的对比影响。

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