拉曼光谱
荧光
光子上转换
光谱学
激发态
荧光寿命成像显微镜
等离子体子
材料科学
荧光光谱法
相干反斯托克斯拉曼光谱
化学成像
共振拉曼光谱
光电子学
拉曼散射
核磁共振
光学
发光
物理
原子物理学
高光谱成像
计算机科学
人工智能
量子力学
作者
Hanqing Xiong,Lixue Shi,Lu Wei,Yihui Shen,Rong Long,Zhilun Zhao,Wei Min
出处
期刊:Nature Photonics
[Nature Portfolio]
日期:2019-04-01
卷期号:13 (6): 412-417
被引量:108
标识
DOI:10.1038/s41566-019-0396-4
摘要
Powerful optical tools have revolutionized science and technology. The prevalent fluorescence detection offers superb sensitivity down to single molecules but lacks sufficient chemical information1-3. In contrast, Raman-based vibrational spectroscopy provides exquisite chemical specificity about molecular structure, dynamics and coupling, but is notoriously insensitive3-5. Here we report a hybrid technique of Stimulated Raman Excited Fluorescence (SREF) that integrates superb detection sensitivity and fine chemical specificity. Through stimulated Raman pumping to an intermediate vibrational eigenstate followed by an upconversion to an electronic fluorescent state, SREF encodes vibrational resonance into the excitation spectrum of fluorescence emission. By harnessing narrow vibrational linewidth, we demonstrated multiplexed SREF imaging in cells, breaking the "color barrier" of fluorescence. By leveraging superb sensitivity of SREF, we achieved all-far-field single-molecule Raman spectroscopy and imaging without plasmonic enhancement, a long-sought-after goal in photonics. Thus, through merging Raman and fluorescence spectroscopy, SERF would be a valuable tool for chemistry and biology.
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