State Key Laboratory of Precision Spectroscopy, East China Normal University, 200062, Shanghai, China.
AMOS and Department of Chemical and Biological Physics, Weizmann Institute of Science, 7610001, Rehovot, Israel.
Nat Commun. 2018 Dec 3;9(1):5134. doi: 10.1038/s41467-018-07567-2.
Orientation and alignment of molecules by ultrashort laser pulses is crucial for a variety of applications and has long been of interest in physics and chemistry, with the special emphasis on stereodynamics in chemical reactions and molecular orbitals imaging. As compared to the laser-induced molecular alignment, which has been extensively studied and demonstrated, achieving molecular orientation is a much more challenging task, especially in the case of asymmetric-top molecules. Here, we report the experimental demonstration of all-optical field-free three-dimensional orientation of asymmetric-top molecules by means of phase-locked cross-polarized two-color laser pulse. This approach is based on nonlinear optical mixing process caused by the off-diagonal elements of the molecular hyperpolarizability tensor. It is demonstrated on SO molecules and is applicable to a variety of complex nonlinear molecules.
通过超短激光脉冲对分子进行取向和调整对于各种应用至关重要,这在物理学和化学领域一直备受关注,特别是在化学反应的立体动力学和分子轨道成像方面。与已经得到广泛研究和证明的激光诱导分子取向相比,实现分子取向是一项更加具有挑战性的任务,特别是在非对称陀螺分子的情况下。在这里,我们通过锁相的交叉偏振双色激光脉冲实验演示了非对称陀螺分子的全光学无场三维取向。该方法基于分子超极化率张量的非对角元素引起的非线性光学混合过程。我们在 SO 分子上进行了演示,并且该方法适用于各种复杂的非线性分子。