Department of Bio & Nano Chemistry, Kookmin University, Seoul 136-702, Republic of Korea.
Phys Chem Chem Phys. 2014 Mar 21;16(11):5312-8. doi: 10.1039/c3cp54870h.
We present time-gated femtosecond stimulated Raman spectroscopy (fSRS) under the pre-resonance Raman conditions of diethylthiatricarbocyanine (DTTC) iodide. A 'pseudo emission-free' condition is achieved by delivering the probe beam ahead of the pump beam. Regeneratively amplified pulse trains are employed to create an angle-geometry (non-collimated) mixing between the pump and probe beams, leading to highly sensitive measurement of the stimulated Raman gain. Time-integrated spectroscopy allows for a more quantitative distinction between the contributions of stimulated Raman scattering and stimulated emission. We successfully obtain a highly sensitive (signal-to-noise ratio >100) stimulated Raman spectrum under the optimized conditions, which compares favourably to results obtained using two-dimensional correlation spectroscopy (2DCOS). Given the optical pre-resonance of ∼0.1 eV, the background signals mostly originate from the stimulated emission of excited electrons and are significantly reduced by partial overlapping of the pump and probe beams; a genuine fSRS spectral profile is obtained for a temporal delay of ∼0.2 ps between the two beams.
我们展示了在二乙基噻二嗪菁碘化物(DTTC)的预共振拉曼条件下的时间门控飞秒受激拉曼光谱(fSRS)。通过在泵浦光束之前传输探针光束,可以实现“伪无发射”条件。再生放大脉冲串用于在泵浦和探针光束之间创建角几何(非准直)混合,从而实现对受激拉曼增益的高灵敏度测量。时间积分光谱学允许更定量地区分受激拉曼散射和受激辐射的贡献。在优化条件下,我们成功获得了高灵敏度(信噪比>100)的受激拉曼光谱,这与使用二维相关光谱学(2DCOS)获得的结果相当。考虑到约 0.1 eV 的光学预共振,背景信号主要源自受激电子发射,并且通过泵浦和探针光束的部分重叠显著减少;当两束之间的时间延迟约为 0.2 ps 时,获得了真正的 fSRS 光谱轮廓。