Allodi Marco A, Finneran Ian A, Blake Geoffrey A
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
J Chem Phys. 2015 Dec 21;143(23):234204. doi: 10.1063/1.4938165.
We report the first coherent excitation of intramolecular vibrational modes via the nonlinear interaction of a TeraHertz (THz) light field with molecular liquids. A terahertz-terahertz-Raman pulse sequence prepares the coherences with a broadband, high-energy, (sub)picosecond terahertz pulse, that are then measured in a terahertz Kerr effect spectrometer via phase-sensitive, heterodyne detection with an optical pulse. The spectrometer reported here has broader terahertz frequency coverage, and an increased sensitivity relative to previously reported terahertz Kerr effect experiments. Vibrational coherences are observed in liquid diiodomethane at 3.66 THz (122 cm(-1)), and in carbon tetrachloride at 6.50 THz (217 cm(-1)), in exact agreement with literature values of those intramolecular modes. This work opens the door to 2D spectroscopies, nonlinear in terahertz field, that can study the dynamics of condensed-phase molecular systems, as well as coherent control at terahertz frequencies.
我们报道了通过太赫兹(THz)光场与分子液体的非线性相互作用对分子内振动模式进行的首次相干激发。太赫兹-太赫兹-拉曼脉冲序列利用宽带、高能、(亚)皮秒太赫兹脉冲制备相干性,然后通过与光脉冲的相敏外差检测在太赫兹克尔效应光谱仪中进行测量。这里报道的光谱仪具有更宽的太赫兹频率覆盖范围,并且相对于先前报道的太赫兹克尔效应实验具有更高的灵敏度。在液态二碘甲烷中于3.66太赫兹(122厘米⁻¹)处以及在四氯化碳中于6.50太赫兹(217厘米⁻¹)处观察到了振动相干性,这与那些分子内模式的文献值完全一致。这项工作为二维光谱学打开了大门,这种光谱学在太赫兹场中是非线性的,可以研究凝聚相分子系统的动力学以及太赫兹频率下的相干控制。