Frontiera Renee R, Henry Anne-Isabelle, Gruenke Natalie L, Van Duyne Richard P
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
J Phys Chem Lett. 2011 May 19;2(10):1199-203. doi: 10.1021/jz200498z. Epub 2011 Apr 29.
Surface-enhanced Raman spectroscopy (SERS) and femtosecond stimulated Raman spectroscopy (FSRS) have revolutionized the Raman spectroscopy field. SERS provides spectroscopic detection of single molecules, and FSRS enables the acquisition of Raman spectra on the ultrafast time scale of molecular motion. Here, we present the first successful combination of these two techniques, demonstrating surface-enhanced femtosecond stimulated Raman spectroscopy (SE-FSRS) using gold nanoantennas with embedded reporter molecules. Using a picosecond Raman and femtosecond probe pulse, the time- and ensemble-averaged enhancement factor is estimated to be in the range of 10(4)-10(6). We report the line shapes, power dependence, and magnitude of the SE-FSRS signal and discuss contributions to sample degradation on the minute time scale. With these first successful proof-of-principle experiments, time-resolved SE-FSRS techniques can now be rationally attempted with the goals of investigating the dynamics of plasmonic materials as well as examining the contributions of environmental heterogeneities by probing more homogeneous molecular subsets.
表面增强拉曼光谱(SERS)和飞秒受激拉曼光谱(FSRS)彻底改变了拉曼光谱领域。SERS提供单分子的光谱检测,而FSRS能够在分子运动的超快时间尺度上获取拉曼光谱。在此,我们展示了这两种技术的首次成功结合,即使用嵌入报告分子的金纳米天线演示表面增强飞秒受激拉曼光谱(SE-FSRS)。使用皮秒拉曼和飞秒探测脉冲,时间平均和系综平均增强因子估计在10^4 - 10^6范围内。我们报告了SE-FSRS信号的线形、功率依赖性和幅度,并讨论了在微小时间尺度上对样品降解的影响。通过这些首次成功的原理验证实验,现在可以合理尝试时间分辨SE-FSRS技术,目标是研究等离子体材料的动力学以及通过探测更均匀的分子子集来研究环境不均匀性的影响。