Karpf Sebastian, Eibl Matthias, Wieser Wolfgang, Klein Thomas, Huber Robert
Lehrstuhl für BioMolekulare Optik, Fakultät für Physik, Ludwig-Maximilians-Universität München, Oettingenstreet 67, 80538 Munich, Germany.
Institut für Biomedizinische Optik, Universität zu Lübeck, Peter-Monnik-Weg 4, 23562 Lübeck, Germany.
Nat Commun. 2015 Apr 17;6:6784. doi: 10.1038/ncomms7784.
Raman sensing and microscopy are among the most specific optical technologies to identify the chemical compounds of unknown samples, and to enable label-free biomedical imaging. Here we present a method for stimulated Raman scattering spectroscopy and imaging with a time-encoded (TICO) Raman concept. We use continuous wave, rapidly wavelength-swept probe lasers and combine them with a short-duty-cycle actively modulated pump laser. Hence, we achieve high stimulated Raman gain signal levels, while still benefitting from the narrow linewidth and low noise of continuous wave operation. Our all-fibre TICO-Raman setup uses a Fourier domain mode-locked laser source to achieve a unique combination of high speed, broad spectral coverage (750-3,150 cm(-1)) and high resolution (0.5 cm(-1)). The Raman information is directly encoded and acquired in time. We demonstrate quantitative chemical analysis of a solvent mixture and hyperspectral Raman microscopy with molecular contrast of plant cells.
拉曼传感与显微镜技术是用于识别未知样品化学成分以及实现无标记生物医学成像的最具特异性的光学技术之一。在此,我们介绍一种采用时间编码(TICO)拉曼概念的受激拉曼散射光谱与成像方法。我们使用连续波、快速扫频的探测激光,并将其与占空比短的主动调制泵浦激光相结合。因此,我们在仍受益于连续波操作的窄线宽和低噪声的同时,实现了高受激拉曼增益信号水平。我们的全光纤TICO拉曼装置使用傅里叶域锁模激光源,以实现高速、宽光谱覆盖范围(750 - 3150 cm⁻¹)和高分辨率(0.5 cm⁻¹)的独特组合。拉曼信息直接在时间上进行编码和采集。我们展示了对溶剂混合物的定量化学分析以及具有植物细胞分子对比度的高光谱拉曼显微镜成像。