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Multi-ionization of the Cl(2) molecule in the near-infrared femtosecond laser field
The multi-electron ionization and subsequent dissociation of the Cl(2) molecule in a near-infrared femtosecond laser field was investigated via the dc-sliced ion imaging technique. The single charged molecular ions, Cl(2)(+), dissociate from two excited states, (2)Π(u) and (2)Σ(g)(+), with the elect...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048264/ https://www.ncbi.nlm.nih.gov/pubmed/35492539 http://dx.doi.org/10.1039/c9ra06746a |
Sumario: | The multi-electron ionization and subsequent dissociation of the Cl(2) molecule in a near-infrared femtosecond laser field was investigated via the dc-sliced ion imaging technique. The single charged molecular ions, Cl(2)(+), dissociate from two excited states, (2)Π(u) and (2)Σ(g)(+), with the electrons ionized from the HOMO−1 and HOMO−2 orbital, respectively. For the multi-charged molecular ions, Cl(2)(n+) (n = 2–8), our results showed that the stretch of the inter-nuclear distance benefitted the ionization of the electrons to produce highly-charged molecular ions. In addition, compared with the traditional charge resonance enhanced ionization (CREI) model, the critical distance (R(c)) for the Cl(2) molecule in our experiment was a short range that depended on the charge state rather than a single point. |
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