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Spectroscopic Imaging in the Near Field with an Apertureless Solid Immersion Lens Microscope

机译:无孔固态浸没透镜显微镜在近场中的光谱成像

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To achieve high lateral resolution in microscopy, we exploit the localized electromagnetic field of a Solid Immersion Lens (SIL). The lens is mounted on a cantilever of a Scanning Probe Microscope (SPM) to allow a dynamic scan with constant tip-sample force. This unit can be integrated into a micro fluorescence (Zeiss UMSP) or Raman spectrometer (Renishaw) to allow spectroscopy and spectrally resolved imaging in the near field. Three methods can be applied with a lateral resolution of less than 30 nm: 1) Reflectance-SNOM: the sample is imaged by illuminating the surface through the SIL and detecting the reflected near-field. 2) Photon-tunneling-SNOM: the contrast is generated by the ability of the photons to tunnel through the energy barrier into the substrate. 3) Fluorescence- SNOM: the chromophore is excited and the fluorescence light is collected by the SIL. The collection efficiency for the fluorescence is increased by a factor of 10 due to the high refractive index of the SIL compared to conventional methods.
机译:为了在显微镜下获得较高的横向分辨率,我们利用了固态浸没透镜(SIL)的局部电磁场。镜头安装在扫描探针显微镜(SPM)的悬臂上,以恒定的尖端采样力进行动态扫描。该单元可以集成到微荧光(Zeiss UMSP)或拉曼光谱仪(Renishaw)中,以在近场中进行光谱和光谱分辨成像。可以使用横向分辨率小于30 nm的三种方法:1)反射SNOM:通过SIL照射表面并检测反射的近场来对样品成像。 2)光子隧道SNOM:通过光子穿过能垒进入衬底的能力产生对比度。 3)荧光-SNOM:发色团被激发,荧光被SIL收集。与传统方法相比,由于SIL的高折射率,荧光的收集效率提高了10倍。

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