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Analysis of femtosecond Raman-induced polarization spectroscopy (RIPS) in N2 and CO2 by fitting and scaling laws

✍ Scribed by Bruno Lavorel; Olivier Faucher; Mike Morgen; Roland Chaux


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
115 KB
Volume
31
Category
Article
ISSN
0377-0486

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✦ Synopsis


Raman-induced polarization spectroscopy (RIPS) experiments were conducted at room temperature and pressures below 2 atm in pure N 2 and CO 2 . Both homodyne and optically heterodyne detection were used. Calculations of the signal as a function of the pump-probe delay were performed taking into account the pulse duration of the laser, the rotational dependence of the dephasing rates and the small instantaneous electronic Kerr effect. The observed decay and shape of the rotational quantum beats are in good agreement with the calculations. Several sets of linewidth coefficients corresponding to the diagonal part of the collisional-rotational relaxation matrix were used. This matrix was choosen among available models derived from wavenumber domain studies (fitting and scaling laws). The energy-corrected sudden model derived from extensive wavenumber domain studies reproduces the experimental data well. A comparison between different models is discussed.