Photoelectron angular distributions from resonant two-photon ionisation of adiabatically aligned naphthalene and aniline molecules

被引:3
作者
Arlt, Jacqueline [1 ]
Singh, Dhirendra P. [2 ]
Thompson, James O. F. [2 ]
Chatterley, Adam S. [1 ]
Hockett, Paul [3 ]
Stapelfeldt, Henrik [1 ]
Reid, Katharine L. [2 ]
机构
[1] Aarhus Univ, Dept Chem, DK-8000 Aarhus C, Denmark
[2] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[3] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON, Canada
基金
欧盟地平线“2020”; 英国工程与自然科学研究理事会;
关键词
Photoelectron; images; multiphoton ionisation; strong-field alignment; PHOTOIONIZATION; DYNAMICS; VALENCE; S-1;
D O I
10.1080/00268976.2020.1836411
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photoelectron images have been measured following the ionisation of aligned distributions of gas phase naphthalene and aniline molecules. Alignment in the adiabatic regime was achieved by interaction with a 100 ps infrared laser pulse, with ionisation achieved in a two-photon resonant scheme using a low intensity UV pulse of similar to 6 ps duration. The resulting images are found to exhibit anisotropy that increases when the alignment pulse is present, with the aniline PADs peaking along the polarisation vector of the ionising light and the naphthalene PADs developing a characteristic four-lobed structure. Photoelectron angular distributions (PADs) that result from the ionisation of unaligned and fully aligned distributions of molecules are calculated using the ePolyScat ab initio suite and converted into two-dimensional photoelectron images. In the case of naphthalene excellent agreement is observed between experiment and the simulation for the fully aligned distribution, showing that the alignment step allows us to probe the molecular frame, but in the case of aniline it is clear that additional processes occur following the one-photon resonant step.
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页数:13
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