Long-lasting field-free alignment of large molecules inside helium nanodroplets

被引:48
作者
Chatterley, Adam S. [1 ]
Schouder, Constant [2 ]
Christiansen, Lars [1 ]
Shepperson, Benjamin [1 ]
Rasmussen, Mette Heidemann [1 ]
Stapelfeldt, Henrik [1 ]
机构
[1] Aarhus Univ, Dept Chem, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Dept Phys & Astron, DK-8000 Aarhus C, Denmark
基金
欧洲研究理事会;
关键词
LASER; DYNAMICS; COLD; SPECTROSCOPY; DIFFRACTION; DROPLETS;
D O I
10.1038/s41467-018-07995-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 oli-gomers. Our technique will enable molecular frame experiments, including ultrafast excited state dynamics, on a variety of large molecules and complexes.
引用
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页数:7
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