Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds

Numerous computations of the spectra of molecules are performed by mainstream methods based on the fundamental work by Lax [J. Chem. Phys. 20, 1752 (1952)] for smoothing a series of individual transitions represented by delta functions. There is an assumption that the linewidth of an individual rovi...

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Main Author: Peter Lebedev-Stepanov
Format: Article
Language:English
Published: AIP Publishing LLC 2021-03-01
Series:AIP Advances
Online Access:http://dx.doi.org/10.1063/5.0047044
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spelling doaj-fcfa6a429de14fb0afbf71d05519ba162021-04-02T15:45:27ZengAIP Publishing LLCAIP Advances2158-32262021-03-01113035115035115-1210.1063/5.0047044Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bondsPeter Lebedev-Stepanov0FSRC “Crystallography and Photonics” RAS, Leninskii Prospekt, 59, Moscow 119333, Russia and National Research Nuclear University MEPhI, Kashirskoye Shosse, 31, Moscow 115409, RussiaNumerous computations of the spectra of molecules are performed by mainstream methods based on the fundamental work by Lax [J. Chem. Phys. 20, 1752 (1952)] for smoothing a series of individual transitions represented by delta functions. There is an assumption that the linewidth of an individual rovibronic transition spectrum is many orders of magnitude smaller than the rovibronic bandwidth. However, the presence of rotational–vibrational structure in the molecular spectrum masks the broadening of each individual rovibronic transition. In this work, in the framework of harmonic approximation of potential energy surfaces, a new kind of contribution to homogenous broadening is considered to describe the optical spectrum of any single rovibronic transition. Its origin is in zero-point oscillations and thermal fluctuations around equilibrium positions of nuclei. Franck–Condon diagrams with slanting equidistant vibrational levels are proposed. Expressions of the spectral intensity of a single vibronic transition are derived from the first principles. This theory was used to estimate the broadening magnitude of the vibronic transition due to quantum uncertainty of nuclear coordinates of linear polymethine dyes with an extended π-electron system. It was shown that the calculated magnitude of the broadening is approximately two times smaller than the bandwidth observed in the experiment but it has the same order of magnitude. The value of such broadening depends on the environment that restricts the vibrational and rotational degrees of freedom of the molecule. It was demonstrated that an organic chromophore with an extended π-electron system can be considered to be a molecular optical parametric oscillator.http://dx.doi.org/10.1063/5.0047044
collection DOAJ
language English
format Article
sources DOAJ
author Peter Lebedev-Stepanov
spellingShingle Peter Lebedev-Stepanov
Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
AIP Advances
author_facet Peter Lebedev-Stepanov
author_sort Peter Lebedev-Stepanov
title Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
title_short Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
title_full Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
title_fullStr Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
title_full_unstemmed Parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
title_sort parametric broadening of the molecular vibronic band due to zero-point oscillations and thermal fluctuations of interatomic bonds
publisher AIP Publishing LLC
series AIP Advances
issn 2158-3226
publishDate 2021-03-01
description Numerous computations of the spectra of molecules are performed by mainstream methods based on the fundamental work by Lax [J. Chem. Phys. 20, 1752 (1952)] for smoothing a series of individual transitions represented by delta functions. There is an assumption that the linewidth of an individual rovibronic transition spectrum is many orders of magnitude smaller than the rovibronic bandwidth. However, the presence of rotational–vibrational structure in the molecular spectrum masks the broadening of each individual rovibronic transition. In this work, in the framework of harmonic approximation of potential energy surfaces, a new kind of contribution to homogenous broadening is considered to describe the optical spectrum of any single rovibronic transition. Its origin is in zero-point oscillations and thermal fluctuations around equilibrium positions of nuclei. Franck–Condon diagrams with slanting equidistant vibrational levels are proposed. Expressions of the spectral intensity of a single vibronic transition are derived from the first principles. This theory was used to estimate the broadening magnitude of the vibronic transition due to quantum uncertainty of nuclear coordinates of linear polymethine dyes with an extended π-electron system. It was shown that the calculated magnitude of the broadening is approximately two times smaller than the bandwidth observed in the experiment but it has the same order of magnitude. The value of such broadening depends on the environment that restricts the vibrational and rotational degrees of freedom of the molecule. It was demonstrated that an organic chromophore with an extended π-electron system can be considered to be a molecular optical parametric oscillator.
url http://dx.doi.org/10.1063/5.0047044
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