Formation of electronic coherences in conical intersection-mediated dynamics

被引:17
作者
Neville, Simon P. [1 ]
Stolow, Albert [1 ,2 ,3 ,4 ]
Schuurman, Michael S. [1 ,2 ]
机构
[1] Natl Res Council Canada, 100 Sussex Dr, Ottawa, ON K1A 0R6, Canada
[2] Univ Ottawa, Dept Chem & Biomol Sci, 150 Louis Pasteur, Ottawa, ON K1N 6N5, Canada
[3] Univ Ottawa, Dept Phys, 150 Louis Pasteur, Ottawa, ON K1N 6N5, Canada
[4] Univ Ottawa Natl Res Council Joint Ctr Extreme Ph, Ottawa, ON K1A 0R6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
conical intersections; electronic coherences; non-adiabatic dynamics; quantum dynamics; MOLECULAR-DYNAMICS; SPECTROSCOPY;
D O I
10.1088/1361-6455/ac5460
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We consider the formation of vibrationally-induced transient electronic coherences driven by conical intersection (CI)-mediated population transfer between two electronic states. By invoking fundamental symmetry arguments, we identify several important factors which modulate the magnitude of these electronic coherences. We consider the sub-cases where the two electronic states have either the same or different Abelian point group symmetry at the Franck-Condon geometry. For the different symmetry case, due to the inherent symmetry of the molecular Hamiltonian, significant electronic coherences are unlikely to form. In contrast, for electronic states of the same symmetry, large magnitude electronic coherences can form. However, the magnitude of these coherences is highly dependent on the topography of the CI. These results offer a guide to experimental studies of electronic coherences which may (or may not) be induced by nuclear motion in the vicinity of a CI, as well as to ab initio simulations which are employed to simulate them.
引用
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页数:12
相关论文
共 45 条
[1]   POTENTIAL-ENERGY SURFACES NEAR INTERSECTIONS [J].
ATCHITY, GJ ;
XANTHEAS, SS ;
RUEDENBERG, K .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (03) :1862-1876
[2]   Ab initio multiple spawning:: Photochemistry from first principles quantum molecular dynamics [J].
Ben-Nun, M ;
Quenneville, J ;
Martínez, TJ .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (22) :5161-5175
[3]   Monitoring molecular nonadiabatic dynamics with femtosecond X-ray diffraction [J].
Bennett, Kochise ;
Kowalewski, Markus ;
Rouxel, Jeremy R. ;
Mukamel, Shaul .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (26) :6538-6547
[4]   Ultrafast X-ray Transient Absorption Spectroscopy of Gas-Phase Photochemical Reactions: A New Universal Probe of Photoinduced Molecular Dynamics [J].
Bhattacherjee, Aditi ;
Leone, Stephen R. .
ACCOUNTS OF CHEMICAL RESEARCH, 2018, 51 (12) :3203-3211
[5]   Stimulated X-ray Resonant Raman Spectroscopy of Conical Intersections in Thiophenol [J].
Cho, Daeheum ;
Rouxel, Jeremy R. ;
Mukamel, Shaul .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2020, 11 (11) :4292-4297
[6]  
Domcke W., 2004, Advanced Series in Physical Chemistry
[7]   Role of Conical Intersections in Molecular Spectroscopy and Photoinduced Chemical Dynamics [J].
Domcke, Wolfgang ;
Yarkony, David R. .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, VOL 63, 2012, 63 :325-352
[8]   A combination of Kohn-Sham density functional theory and multi-reference configuration interaction methods [J].
Grimme, S ;
Waletzke, M .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (13) :5645-5655
[9]  
Herzberg, 1967, ELECT SPECTRA ELECT
[10]  
Herzberg G, 1933, Z PHYS CHEM B-CHEM E, V21, P410