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The effect of resonance excitation of atoms on cross sections of atomic collisions

S. M. Bortsaǐkin, L. P. Kudrin, Yu. V. Mikhaǐlova

Published Jan 1, 1971• 0 citations
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Broadening of a two-photon resonance in a zinc atom in collisions with CO2, CO, and NO molecules

Petr A. Bokhan, Dm. E. Zakrevsky, Nikolai V. Fateev

The broadening of a two-photon resonance is studied experimentally at the 4 s 1 S 0 −6 s 3 S 1 transition in a zinc atom upon absorption of two waves with a small detuning from an intermediate state in collisions with CO 2 , CO, and NO molecules. The measured absolute values of broadening cross sections greatly exceed gas-kinetic cross sections and are (9.4±2.4, 6.5±1.6, and 3.9±1.0)×10 − 14 cm 2 for CO 2 , CO, and NO, respectively. Anomalously large rate constants and cross sections obtained in experiments are explained by the efficient resonance quenching of the excited states of zinc atoms in collisions with molecules accompanied by transfer of the energy of excited atoms to vibrational-rotational degrees of freedom of molecules.

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Inelastic Collisions between Excited Alkali Atoms and Molecules. II. The Quenching of Sodium Resonance Radiation by N2 , H2 , HD, and D2

B P Kibble, G. H. Copley, L. Krause

The cross sections for quenching collisions between excited sodium atoms and ${\mathrm{N}}_{2}$, ${\mathrm{H}}_{2}$, HD, and ${\mathrm{D}}_{2}$ molecules in their electronic ground states have been determined using a delayed-coincidence method. The sodium atoms in mixtures with the gases were excited with 20-nsec pulses of NaD radiation, and the delays between the exciting and fluorescent pulses were measured with a time-to-pulse-height converter. The resulting pulse-height spectra, which were accummulated in a 400-channel kicksorter, yielded the effective lifetimes ${\ensuremath{\tau}}^{\ensuremath{'}}$ of the sodium resonance state, which are shorter than the natural lifetime $\ensuremath{\tau}$ because of the nonradiative decay induced in collisions with the molecules. The cross sections for collisions with ${\mathrm{N}}_{2}$, ${\mathrm{H}}_{2}$, HD, and ${\mathrm{D}}_{2}$, obtained from an analysis of the dependence of ${\ensuremath{\tau}}^{\ensuremath{'}}$ on the gas pressures, are 30.4\ifmmode\pm\else\textpm\fi{}1.2, 16.2\ifmmode\pm\else\textpm\fi{}0.3, 11.6\ifmmode\pm\else\textpm\fi{}0.4, and 9.8\ifmmode\pm\else\textpm\fi{}0.3 ${\mathrm{\AA{}}}^{2}$, respectively.

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Excitation Transfer in Atomic Collisions

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Resonance transfer of excitation in the collision of identical atoms

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•Nov 11, 1974•0 citations

Probing Scattering Resonances in (Ultra)Cold Inelastic NO–He Collisions

Jolijn Onvlee, Ad van der Avoird, Gerrit C. Groenenboom +1 more

We theoretically study inelastic collisions between NO radicals and He atoms at low collision energies, focusing on the occurrence of scattering resonances. We specifically investigate de-excitation of rotationally excited NO radicals (X (2)Π1/2, v = 0, j = 3/2, f) at collision energies ranging from 10(-3) to 20 cm(-1) and compute integral and differential cross sections using quantum mechanical close-coupling calculations. Although unconventional, we show that the measurement of rotational de-excitation cross sections brings several advantages to experiments that aim to study rotational energy transfer at temperatures approaching zero kelvin. We analyze the nature and partial wave composition of the quasi-bound states associated with each individual resonance and compute the scattering wave functions. The differential cross sections contain the partial wave fingerprints of the scattering process and are found to change drastically as the collision energy is varied over the resonances. The prospects for measuring these differential cross sections in inelastic de-excitation collisions at low energies are discussed.

The Journal of Physical Chemistry A•Jan 13, 2016•12 citations
The broadening of a two-photon resonance is studied experimentally at the 4 s 1 S 0 −6 s 3 S 1 transition in a zinc atom upon absorption of two waves with a small detuning from an intermediate state in collisions with CO 2 , CO, and NO molecules. The measured absolute values of broadening cross sections greatly exceed gas-kinetic cross sections and are (9.4±2.4, 6.5±1.6, and 3.9±1.0)×10 − 14 cm 2 for CO 2 , CO, and NO, respectively. Anomalously large rate constants and cross sections obtained in experiments are explained by the efficient resonance quenching of the excited states of zinc atoms in collisions with molecules accompanied by transfer of the energy of excited atoms to vibrational-rotational degrees of freedom of molecules.
The cross sections for quenching collisions between excited sodium atoms and N2{\mathrm{N}}_{2}N2​, H2{\mathrm{H}}_{2}H2​, HD, and D2{\mathrm{D}}_{2}D2​ molecules in their electronic ground states have been determined using a delayed-coincidence method. The sodium atoms in mixtures with the gases were excited with 20-nsec pulses of NaD radiation, and the delays between the exciting and fluorescent pulses were measured with a time-to-pulse-height converter. The resulting pulse-height spectra, which were accummulated in a 400-channel kicksorter, yielded the effective lifetimes ${\ensuremath{\tau}}^{\ensuremath{'}}$ of the sodium resonance state, which are shorter than the natural lifetime $\ensuremath{\tau}$ because of the nonradiative decay induced in collisions with the molecules. The cross sections for collisions with N2{\mathrm{N}}_{2}N2​, H2{\mathrm{H}}_{2}H2​, HD, and D2{\mathrm{D}}_{2}D2​, obtained from an analysis of the dependence of ${\ensuremath{\tau}}^{\ensuremath{'}}$ on the gas pressures, are 30.4\ifmmode\pm\else\textpm\fi{}1.2, 16.2\ifmmode\pm\else\textpm\fi{}0.3, 11.6\ifmmode\pm\else\textpm\fi{}0.4, and 9.8\ifmmode\pm\else\textpm\fi{}0.3 A˚2{\mathrm{\AA{}}}^{2}A˚2, respectively.
We theoretically study inelastic collisions between NO radicals and He atoms at low collision energies, focusing on the occurrence of scattering resonances. We specifically investigate de-excitation of rotationally excited NO radicals (X (2)Π1/2, v = 0, j = 3/2, f) at collision energies ranging from 10(-3) to 20 cm(-1) and compute integral and differential cross sections using quantum mechanical close-coupling calculations. Although unconventional, we show that the measurement of rotational de-excitation cross sections brings several advantages to experiments that aim to study rotational energy transfer at temperatures approaching zero kelvin. We analyze the nature and partial wave composition of the quasi-bound states associated with each individual resonance and compute the scattering wave functions. The differential cross sections contain the partial wave fingerprints of the scattering process and are found to change drastically as the collision energy is varied over the resonances. The prospects for measuring these differential cross sections in inelastic de-excitation collisions at low energies are discussed.