Department of Chemistry, Aarhus University, 8000, Aarhus C, Denmark.
Department of Physics and Astronomy, Aarhus University, 8000, Aarhus C, Denmark.
Nat Commun. 2019 Jan 11;10(1):133. doi: 10.1038/s41467-018-07995-0.
Molecules with their axes sharply confined in space, available through laser-induced alignment methods, are essential for many current experiments, including ultrafast molecular imaging. For these applications the aligning laser field should ideally be turned-off, to avoid undesired perturbations, and the strong alignment should last long enough that reactions and dynamics can be mapped out. Presently, this is only possible for small, linear molecules and for times less than 1 picosecond. Here, we demonstrate strong, field-free alignment of large molecules inside helium nanodroplets, lasting >10 picoseconds. One-dimensional or three-dimensional alignment is created by a slowly switched-on laser pulse, made field-free through rapid pulse truncation, and retained thanks to the impeding effect of the helium environment on molecular rotation. The opportunities field-free aligned molecules open are illustrated by measuring the alignment-dependent strong-field ionization yield of dibromothiophene oligomers. Our technique will enable molecular frame experiments, including ultrafast excited state dynamics, on a variety of large molecules and complexes.
分子的轴在空间中被强烈限制,可通过激光诱导的对准方法获得,这对于许多当前的实验至关重要,包括超快分子成像。对于这些应用,理想情况下应关闭对准激光场,以避免不必要的干扰,并且强对准应持续足够长的时间,以便可以绘制出反应和动力学过程。目前,这仅适用于小的线性分子和小于 1 皮秒的时间。在这里,我们演示了氦纳米液滴内部大分子的强无场对准,持续时间>10 皮秒。通过缓慢开启的激光脉冲创建一维或三维对准,通过快速脉冲截断使其无场,并由于氦环境对分子旋转的阻碍作用而保持。通过测量二溴噻吩低聚物的强场离化产额的对准依赖性,说明了无场对准分子带来的机会。我们的技术将能够在各种大分子和复合物上进行分子框架实验,包括超快激发态动力学。