光学
波长
红外线的
吸收(声学)
近场扫描光学显微镜
材料科学
分辨率(逻辑)
显微镜
显微镜
红外光谱学
化学成像
散射
红外显微镜
衍射
光学显微镜
光电子学
化学
物理
扫描电子显微镜
高光谱成像
遥感
有机化学
人工智能
计算机科学
地质学
出处
期刊:Nature
[Nature Portfolio]
日期:1999-05-01
卷期号:399 (6732): 134-137
被引量:891
摘要
Identification of chemical compounds by vibrational spectroscopy at infrared wavelengths requires macroscopic samples: the spatial resolution is diffraction-limited to a scale of about half the wavelength, or about five micrometres. The scanning near-field optical microscope1,2, however, can reveal sub-wavelength detail because it uses near-field probing rather than beam focusing. Here we demonstrate the use of the aperture-less approach to scanning near-field optical microscopy3,4,5,6 to obtain contrast in vibrational absorption on a scale of about 100 nanometres, about one-hundredth of a wavelength. We record infrared scattering from the tip of an atomic force microscope scanned over a composite polymer film. At the boundary between different polymers we observe contrast changes owing to changes in vibrational absorption. The contrast is strongly enhanced in the near field of the probe tip, which we interpret as evidence of surface-enhanced infrared absorption7. When extended to multi-wavelength operation, this approach should enable imaging of chemical composition at nanometre resolution.
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