Laser-Induced Electron Symmetry Restoration in Oriented Molecules Made Simple

被引:7
|
作者
Liu, ChunMei [1 ]
Manz, Jorn [2 ,3 ,4 ]
Tremblay, Jean Christophe [5 ]
机构
[1] Nanjing Univ Posts & Telecommun, Coll Sci, Nanjing 210023, Peoples R China
[2] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
[3] Shanxi Univ, Inst Laser Spect, State Key Lab Quantum Opt & Quantum Opt Devices, Taiyuan 030006, Peoples R China
[4] Shanxi Univ, Collaborat Innovat Ctr Extreme Opt, Taiyuan 030006, Peoples R China
[5] Univ Lorraine, Lab Phys & Chim Theor, CNRS, F-57070 Metz, France
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2021年 / 12卷 / 18期
基金
中国国家自然科学基金;
关键词
OPEN-SOURCE FRAMEWORK; CHARGE MIGRATION; DYNAMICS; IONIZATION; BREAKING; DENSITY; PULSES;
D O I
10.1021/acs.jpclett.1c00645
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
Electron symmetry determines many important properties of molecules, from selection rules for photoelectron spectroscopy to symmetry selection rules for chemical reactions. The original electron symmetry is broken if a laser pulse changes the initial state, typically the ground state g, to a superposition of g and an excited state e with different irreducible representations (IRREPs). Quantum dynamics simulations for two examples, the oriented benzene and LiCN molecules, show that the original electron symmetry can be restored by means of a reoptimized pi-laser pulse which transfers the component in the excited state e to another state e', or to several others with the same IRREP as the ground state. This method lends itself to much easier experimental applications than all previous ones because it allows the healing of electron symmetry immediately, without any attosecond constraint on the timing of the second pulse.
引用
收藏
页码:4421 / 4427
页数:7
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