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相关概念视频

Overview of Electron Microscopy01:25

Overview of Electron Microscopy

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The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
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Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
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Transmission electron microscopy (TEM) can be used to determine the 3D structure of biological samples with the help of techniques such as electron microscope tomography and single-particle reconstruction. While single-particle reconstruction can examine macromolecules and macromolecular complexes in vitro conditions only, tomography permits the study of cell components or small cells in vivo.
Electron Tomography
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A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
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Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
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相关实验视频

Updated: Oct 30, 2025

Laser-induced Breakdown Spectroscopy: A New Approach for Nanoparticle's Mapping and Quantification in Organ Tissue
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具有微电子伏特能量分辨率的单分子激光纳米光谱

Hiroshi Imada1,2, Miyabi Imai-Imada3, Kuniyuki Miwa3,4

  • 1Surface and Interface Science Laboratory, RIKEN, Wako, Saitama 351-0198, Japan. himada@riken.jp ykim@riken.jp.

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|July 2, 2021
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概括

研究人员开发了一种单分子光谱技术,以精确控制和描述分子量子状态. 这种方法可以通过高精度调节能量水平来设计新的能量转换分子系统.

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科学领域:

  • 量子化学
  • 光谱学
  • 纳米技术

背景情况:

  • 精确描述激发状态对于能量转换至关重要.
  • 目前的方法在单个分子水平上缺乏所需的分辨率.

研究的目的:

  • 开发具有高能量和空间分辨率的单分子光谱方法.
  • 使分子量子状态的状态选择性表征和调整成为可能.

主要方法:

  • 使用激光驱动的纳米腔等离子体来诱导分子发光.
  • 使用扫描道显微镜进行亚分子空间分辨率.
  • 使用斯塔克效应和等离子激励合来调节能量水平.

主要成果:

  • 实现了微电子伏特能分辨率和亚分子空间分辨率.
  • 证明了单个电子和振动量子状态的状态选择性表征.
  • 在道结口成功调整了分子能量水平.

结论:

  • 开发的纳米探测器在单分子量子状态上提供了前所未有的控制.
  • 这种技术为设计具有量身定制的能量转换功能的分子系统铺平了道路.