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Breaking Abbe's diffraction limit with harmonic deactivation microscopy
DOI:10.1126/sciadv.adp3056.png)
摘要
En 中文
Nonlinear optical microscopy provides elegant means for label-free imaging of biological samples and condensed matter systems. The widespread areas of application could even be increased if resolution was improved, which the famous Abbe diffraction limit now restrains. Super-resolution techniques can break the diffraction limit but most rely on fluorescent labeling. This makes them incompatible with (sub)femtosecond temporal resolution and applications that demand the absence of labeling. Here, we introduce harmonic deactivation microscopy (HADES) for breaking the diffraction limit in nonfluorescent samples. By controlling the harmonic generation process on the quantum level with a second donut-shaped pulse, we confine the third-harmonic generation to three times below the original focus size of a scanning microscope. We demonstrate that resolution improvement by deactivation is more efficient for higher harmonic orders and only limited by the maximum applicable deactivation-pulse fluence. This provides a route toward sub-100-nanometer resolution in a regular nonlinear microscope.
Keyword:
FLUORESCENCE MICROSCOPY
MULTIELECTRON DYNAMICS
GENERATION
RESOLUTION
MODULATION
RADIATION
MIGRATION
COHERENT
CELLS
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期刊
IF:
12.5
论文数:
2.1W
被引数:
18.1W
机构
引用论文
Nonlinear structured-illumination microscopy: Wide-field fluorescence imaging with theoretically unlimited resolution非线性结构照明显微镜: 理论上无限分辨率的宽场荧光成像
Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM)通过随机光学重建显微镜 (STORM) 进行亚衍射极限成像
NATURE METHODS
IF32.1

