We extend a method proposed by Seidner et al. J. Chem. Phys. 103, 3998 (1995) to extract directional terms from a time-dependent molecular polarization to obtain time-resolved four-wave-mixing (FWM) signals. Instead of employing perturbation theory, the total polarization induced in the molecular sample by the interaction with several femtosecond laser pulses is determined by solving the time-dependent Schrödinger equation for the nuclear dynamics in coupled electronic states numerically exact. Repeating the calculation for several combinations of relative phases of the involved fields leads to a linear system of equations for the contributions emitted in different directions. Gas-phase I2 molecules serve as a numerical example.
Description
Non-perturbative wave-packet calculations of time-resolved four-wave-mixing signals | SpringerLink
%0 Journal Article
%1 Meyer2000
%A Meyer, S.
%A Engel, V.
%D 2000
%J Applied Physics B
%K myown
%N 3
%P 293--297
%R 10.1007/s003400000342
%T Non-perturbative wave-packet calculations of time-resolved four-wave-mixing signals
%U http://dx.doi.org/10.1007/s003400000342
%V 71
%X We extend a method proposed by Seidner et al. J. Chem. Phys. 103, 3998 (1995) to extract directional terms from a time-dependent molecular polarization to obtain time-resolved four-wave-mixing (FWM) signals. Instead of employing perturbation theory, the total polarization induced in the molecular sample by the interaction with several femtosecond laser pulses is determined by solving the time-dependent Schrödinger equation for the nuclear dynamics in coupled electronic states numerically exact. Repeating the calculation for several combinations of relative phases of the involved fields leads to a linear system of equations for the contributions emitted in different directions. Gas-phase I2 molecules serve as a numerical example.
@article{Meyer2000,
abstract = {We extend a method proposed by Seidner et al. [J. Chem. Phys. 103, 3998 (1995)] to extract directional terms from a time-dependent molecular polarization to obtain time-resolved four-wave-mixing (FWM) signals. Instead of employing perturbation theory, the total polarization induced in the molecular sample by the interaction with several femtosecond laser pulses is determined by solving the time-dependent Schr{\"o}dinger equation for the nuclear dynamics in coupled electronic states numerically exact. Repeating the calculation for several combinations of relative phases of the involved fields leads to a linear system of equations for the contributions emitted in different directions. Gas-phase I2 molecules serve as a numerical example.},
added-at = {2017-07-03T08:00:24.000+0200},
author = {Meyer, S. and Engel, V.},
biburl = {https://www.bibsonomy.org/bibtex/2da64371185e467e9211fcbb8f389744b/ak-engel-uniwue},
day = 01,
description = {Non-perturbative wave-packet calculations of time-resolved four-wave-mixing signals | SpringerLink},
doi = {10.1007/s003400000342},
interhash = {ae6ccacd9050bfc1587802bb148fa01b},
intrahash = {da64371185e467e9211fcbb8f389744b},
issn = {1432-0649},
journal = {Applied Physics B},
keywords = {myown},
month = sep,
number = 3,
pages = {293--297},
timestamp = {2017-07-03T08:00:24.000+0200},
title = {Non-perturbative wave-packet calculations of time-resolved four-wave-mixing signals},
url = {http://dx.doi.org/10.1007/s003400000342},
volume = 71,
year = 2000
}