Charge Resonance Enhanced Ionization of CO2 Probed by Laser Coulomb Explosion Imaging

dc.citation.doi10.1103/PhysRevLett.107.063201
dc.citation.issn0031-9007
dc.citation.issue6
dc.citation.jtitlePhysical Review Letters
dc.citation.volume107
dc.contributor.authorBocharova, Irina
dc.contributor.authorKarimi, Reza
dc.contributor.authorPenka, Emmanuel F.
dc.contributor.authorBrichta, Jean-Paul
dc.contributor.authorLassonde, Philippe
dc.contributor.authorFu, Xiquan
dc.contributor.authorKieffer, Jean-Claude
dc.contributor.authorBandrauk, André D.
dc.contributor.authorLitvinyuk, Igor
dc.contributor.authorSanderson, Joseph
dc.contributor.authorLégaré, François
dc.date.accessioned2023-12-07T18:56:12Z
dc.date.available2023-12-07T18:56:12Z
dc.date.issued2011-08-02
dc.date.published2011-08-02
dc.description.abstractThe process by which a molecule in an intense laser field ionizes more efficiently as its bond length increases towards a critical distance Rc is known as charge resonance enhanced ionization (CREI). We make a series of measurements of this process for CO2, by varying pulse duration from 7 to 200 fs, in order to identify the charge states and time scales involved. We find that for the 4+ and higher charge states, 100 fs is the time scale required to reach the critical geometry ⟨RCO⟩≈2.1 Å and ⟨θOCO⟩≈163° (equilibrium CO2 geometry is ⟨RCO⟩≈1.16 Å and ⟨θOCO⟩≈172°). The CO3+2 molecule, however, appears always to begin dissociation from closer than 1.7 Å indicating that dynamics on charge states lower than 3+ is not sufficient to initiate CREI. Finally, we make quantum ab initio calculations of ionization rates for CO2 and identify the electronic states responsible for CREI.
dc.identifier.urihttps://hdl.handle.net/2097/43839
dc.relation.urihttps://link.aps.org/doi/10.1103/PhysRevLett.107.063201
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dc.titleCharge Resonance Enhanced Ionization of CO2 Probed by Laser Coulomb Explosion Imaging
dc.typeText

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