Vibronic mean-field and perturbation theory for Jahn-Teller and pseudo-Jahn-Teller molecules

被引:0
作者
Changala, P. Bryan [1 ]
机构
[1] Ctr Astrophys Harvard & Smithsonian, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
Vibrational self-consistent field theory; non-adiabatic interactions; Jahn-Teller effect; symmetry breaking; SELF-CONSISTENT-FIELD; WAVE-FUNCTIONS; DYNAMICS; SYSTEMS; SPECTROSCOPY; ENERGIES; STATES;
D O I
10.1080/00268976.2021.1962556
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
A generalisation of vibrational mean-field theory is developed for non-adiabatic Jahn-Teller and pseudo-Jahn-Teller molecules with coupled vibrational and electronic degrees of freedom treated within a quasi-diabatic framework. Solutions to the vibronic self-consistent field equations of motion generate qualitatively correct zeroth-order vibronic wavefunctions even in the strong coupling limit. These serve as an efficient basis for further perturbative or variational corrections. Particular attention is paid to complications arising in multi-mode Jahn-Teller systems, where the degenerate ground state exhibits artificial symmetry-breaking in the mean-field approximation. This effect is shown to behave like a second-order phase transition, with the symmetry of finite-temperature mean-field solutions restored above a critical temperature.
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页数:14
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共 76 条
[11]   Vibrational self-consistent field method for many-mode systems: A new approach and application to the vibrations of CO adsorbed on Cu(100) [J].
Carter, S ;
Culik, SJ ;
Bowman, JM .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (24) :10458-10469
[12]   A simple quasi-diabatization scheme suitable for spectroscopic problems based on one-electron properties of interacting states [J].
Cave, Robert J. ;
Stanton, John F. .
JOURNAL OF CHEMICAL PHYSICS, 2016, 144 (05)
[13]   Block diagonalization of the equation-of-motion coupled cluster effective Hamiltonian: Treatment of diabatic potential constants and triple excitations [J].
Cave, Robert J. ;
Stanton, John F. .
JOURNAL OF CHEMICAL PHYSICS, 2014, 140 (21)
[14]  
Changala P.B., 2021, NITROGEN VERSION 2 0 NITROGEN VERSION 2 0
[15]   Ab initio effective rotational and rovibrational Hamiltonians for non-rigid systems via curvilinear second order vibrational Moller-Plesset perturbation theory [J].
Changala, P. Bryan ;
Baraban, Joshua H. .
JOURNAL OF CHEMICAL PHYSICS, 2016, 145 (17)
[16]   Vibrational coupled cluster theory [J].
Christiansen, O .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (05) :2149-2159
[17]   Moller-Plesset perturbation theory for vibrational wave functions [J].
Christiansen, O .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (12) :5773-5781
[18]   INVESTIGATIONS OF SELF-CONSISTENT FIELD, SCF CI AND VIRTUAL STATE CONFIGURATION-INTERACTION VIBRATIONAL ENERGIES FOR A MODEL 3-MODE SYSTEM [J].
CHRISTOFFEL, KM ;
BOWMAN, JM .
CHEMICAL PHYSICS LETTERS, 1982, 85 (02) :220-224
[19]   Jet cooled cavity ringdown spectroscopy of the A2E" ← X2A2′ transition of the NO3 radical [J].
Codd, Terrance ;
Chen, Ming-Wei ;
Roudjane, Mourad ;
Stanton, John F. ;
Miller, Terry A. .
JOURNAL OF CHEMICAL PHYSICS, 2015, 142 (18)
[20]   Coupling electrons and vibrations in molecular quantum chemistry [J].
Dresselhaus, Thomas ;
Bungey, Callum B. A. ;
Knowles, Peter J. ;
Manby, Frederick R. .
JOURNAL OF CHEMICAL PHYSICS, 2020, 153 (21)