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Far-field optical nanoscopy

机译:远场光学显微镜

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In 1873, Ernst Abbe discovered that the resolution of focusing (‘far-field’) optical microscopy is limited to d = λ/(2nsinα ) > 200 nm, with nsinα denoting the numerical aperture of the lens and λ the wavelength of light. While the diffraction barrier has prompted the invention of electron, scanning probe, and x-ray microscopy, in the life sciences 80% of all microscopy studies are still performed with lens-based (fluorescence) microscopy. The reason is that the 3D-imaging of the interior of (live) cells requires the use of focused visible light. Hence, besides being a fascinating physics endeavor, the development of a far-field light microscope with nanoscale resolution would facilitate observing the molecular processes of life.
机译:1873年,恩斯特·阿贝(Ernst Abbe)发现,聚焦(“远场”)光学显微镜的分辨率限制为d =λ/(2nsinα)> 200 nm,其中nsinα表示透镜的数值孔径,而λ表示光的波长。尽管衍射屏障已促进了电子,扫描探针和X射线显微镜技术的发明,但在生命科学中,所有显微镜研究中的80%仍使用基于透镜的(荧光)显微镜进行。原因是(活)细胞内部的3D成像需要使用聚焦的可见光。因此,除了进行引人入胜的物理研究外,开发具有纳米级分辨率的远场光学显微镜还将有助于观察生命的分子过程。

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