Xiong Hanqing, Shi Lixue, Wei Lu, Shen Yihui, Long Rong, Zhao Zhilun, Min Wei
Department of Chemistry, Columbia University, New York, NY 10027, USA.
Nat Photonics. 2019 Jun;13(6):412-417. doi: 10.1038/s41566-019-0396-4. Epub 2019 Apr 1.
Powerful optical tools have revolutionized science and technology. The prevalent fluorescence detection offers superb sensitivity down to single molecules but lacks sufficient chemical information. In contrast, Raman-based vibrational spectroscopy provides exquisite chemical specificity about molecular structure, dynamics and coupling, but is notoriously insensitive. 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.
强大的光学工具已经彻底改变了科学和技术。普遍使用的荧光检测技术具有极高的灵敏度,甚至能检测到单分子,但缺乏足够的化学信息。相比之下,基于拉曼的振动光谱能够提供有关分子结构、动力学和耦合的精确化学特异性,但灵敏度极低。在此,我们报告了一种受激拉曼激发荧光(SREF)的混合技术,该技术整合了极高的检测灵敏度和精细的化学特异性。通过受激拉曼泵浦到中间振动本征态,然后上转换到电子荧光态,SREF将振动共振编码到荧光发射的激发光谱中。利用窄振动线宽,我们在细胞中展示了多重SREF成像,打破了荧光的“颜色障碍”。通过利用SREF的超高灵敏度,我们实现了无需等离子体增强的全远场单分子拉曼光谱和成像,这是光子学领域长期追求的目标。因此,通过融合拉曼光谱和荧光光谱,SREF将成为化学和生物学领域的宝贵工具。