Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Overview of Electron Microscopy01:25

Overview of Electron Microscopy

9.1K
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.
9.1K
Transmission Electron Microscopy01:15

Transmission Electron Microscopy

5.5K
In 1931, physicist Ernst Ruska—building on the idea that magnetic fields can direct an electron beam just as lenses can direct a beam of light in an optical microscope—developed the first prototype of the electron microscope. This development led to the development of the field of electron microscopy. In the transmission electron microscope (TEM), electrons are produced by a hot tungsten element and accelerated by a potential difference in an electron gun, which gives them up to 400...
5.5K
Protein Dynamics in Living Cells01:19

Protein Dynamics in Living Cells

2.1K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.1K
Scanning Electron Microscopy01:07

Scanning Electron Microscopy

4.2K
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.
Fundamental Principles
Accelerated...
4.2K
Photoluminescence: Fluorescence and Phosphorescence01:23

Photoluminescence: Fluorescence and Phosphorescence

2.1K
Photoluminescence is a process where a molecule absorbs light energy and re-emits it in the form of light. This phenomenon occurs when a substance absorbs photons, promoting its electrons to higher energy level excited states, followed by a relaxation process in which the electrons return to their original ground state energy levels and emit light. Photoluminescence is widely observed in various materials, including semiconductors, and organic and inorganic compounds.
A pair of electrons in a...
2.1K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Few-atom-thick silver films for enhanced nanoscale nonlinear optics.

Nature communications·2026
Same author

Probing picometre-scale interlayer deformations via hyperbolic polaritons.

Nature·2026
Same author

Mid-Infrared Sensing and Ultrafast Photoresponse in Silicon-Based Plasmonic Detectors.

ACS photonics·2026
Same author

Active steering of cathodoluminescence through a generalized Smith-Purcell effect.

Light, science & applications·2026
Same author

<i>Operando</i> Multimodal Electron Microscopy of Perovskite Nano-LEDs: Nanoscale Degradation and Recovery Behavior.

ACS nano·2026
Same author

Ultrafast Near-Field Dynamics in Silver Nanowires Driven by Few-Cycle Short-Wave Infrared Pulses.

ACS photonics·2026

相关实验视频

Updated: Jul 5, 2025

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F&#8722;
06:53

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F−

Published on: July 27, 2018

8.7K

电子在飞行中捕获光脉冲

Albert Polman1, F Javier García de Abajo2,3

  • 1Center for Nanophotonics, NWO Institute AMOLF, Amsterdam, Netherlands.

Science (New York, N.Y.)
|January 11, 2024
PubMed
概括

材料的超快探测是通过电子和光子之间的受控能量交换实现的. 这种相互作用使得在极高的速度下对材料特性有了前所未有的洞察力.

科学领域:

  • 物理
  • 材料科学

背景情况:

  • 对于技术进步至关重要.
  • 电子-光子相互作用是凝聚物质物理学中的基本过程.

研究的目的:

  • 研究电子光子能量交换的潜力,用于超快的材料分析.
  • 开发用于探测材料动态的新方法.

主要方法:

  • 使用5秒激光脉冲激发电子群体.
  • 使用先进的光谱技术来监测能量传输.

主要成果:

  • 在电子和光子之间证明了高效的能量传输.
  • 在五秒时间尺度上观察到材料性能的动态变化.

结论:

  • 电子光子能量交换为超快的材料表征提供了强大的工具.
  • 这种方法为研究材料中的短暂现象开辟了新的途径.

更多相关视频

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy
10:01

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy

Published on: May 1, 2017

14.0K
Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
10:35

Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals

Published on: May 29, 2018

8.7K

相关实验视频

Last Updated: Jul 5, 2025

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F&#8722;
06:53

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F−

Published on: July 27, 2018

8.7K
Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy
10:01

Flash-and-Freeze: A Novel Technique to Capture Membrane Dynamics with Electron Microscopy

Published on: May 1, 2017

14.0K
Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
10:35

Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals

Published on: May 29, 2018

8.7K