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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...

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Detalles Bibliográficos
Autores principales: Zhang, Jian, Li, Zhipeng, Yang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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
Descripción
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.