钻石针中的颜色中心的光动态
Elena Filonenko1, Polina Kuzhir1, Sergei Malykhin1
1Department of Physics and Mathematics, Faculty of Science, Forestry and Technology, University of Eastern Finland, Joensuu, Finland.
Nanotechnology
|March 25, 2025
概括
单晶钻石针表现出来自各种颜色中心的独特光特性. 389nm中心显示了长时间的衰变时间,对量子应用有益.
科学领域:
- 材料科学 材料科学 材料科学
- 量子光学是一种量子光学.
- 固态物理 固态物理
背景情况:
- 钻石中的颜色中心对量子技术具有前景.
- 单晶钻石针 (SCDNs) 为研究这些中心提供了一个独特的平台.
研究的目的:
- 为了研究SCDN中颜色中心的光特性.
- 描述它们的电子结构和发光寿命.
主要方法:
- 稳态和时间分辨率光发光 (PL) 谱学.
- 在室温下进行PL激发光谱.
- 已识别的颜色中心的终身测量.
主要成果:
- 在389nm,468nm,575nm (NV0),637nm (NV-) 和738nm (SiV-) 处识别了零声波线的颜色中心.
- 室温PL激发揭示了复杂的电子结构.
- 389 nm 的中心呈现出最长的衰变时间 (~30 ns).
结论:
- SCDN托管了各种颜色中心,具有可调的光.
- 389nm中心的长寿命有利于量子连贯性和效率.
- SCDN显示出下一代光子和量子设备的巨大潜力.
相关概念视频
Protein Dynamics in Living Cells
2.0K
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...
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...
2.0K
Fluorescence and Phosphorescence: Instrumentation
505
Fluorometers and spectrofluorometers are two types of instruments used for measuring molecular fluorescence. These instruments differ in how they select excitation and emission wavelengths and the type of light sources they utilize. Fluorometers use absorption interference filters to choose excitation and emission wavelengths. The excitation source in a fluorometer is typically a low-pressure mercury vapor lamp that emits intense lines distributed throughout the ultraviolet and visible regions.
505
Super-resolution Fluorescence Microscopy
6.8K
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...
6.8K


