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Electric-dipole-momentum sensitive Coulomb explosion in doubly ionized CO dimer and trimer: An environmental effect at molecular-scale

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F25%3A43931709" target="_blank" >RIV/60461373:22340/25:43931709 - isvavai.cz</a>

  • Result on the web

    <a href="https://pubs.aip.org/aip/jcp/article/162/5/054302/3333267/Electric-dipole-momentum-sensitive-Coulomb" target="_blank" >https://pubs.aip.org/aip/jcp/article/162/5/054302/3333267/Electric-dipole-momentum-sensitive-Coulomb</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1063/5.0244051" target="_blank" >10.1063/5.0244051</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Electric-dipole-momentum sensitive Coulomb explosion in doubly ionized CO dimer and trimer: An environmental effect at molecular-scale

  • Original language description

    Molecular clusters are aggregates of molecules weakly bound by the van der Waals force between molecules. Removing one electron from each constitutive molecule results in van der Waals bond cleavages through Coulomb explosion. This provides an ideal prototype to further study the environmental effects played by one fragmented ion on the other one at the molecular scale. Here, we report an experimental measurement of the two-body Coulomb explosion of (CO)22+ and (CO)22+, produced in a 40 keV Ar2+ double-electron capture collision with a CO dimer and trimer. Accurate reaction pathways are identified with the advanced ion-ion coincidence and momentum-imaging techniques. The measured kinetic energy release deviates from the calculated results based on the reciprocal of internuclear distance (i.e., Coulomb interaction only) and which, therefore, requires the inclusion of rotational energy of CO+ initiated by molecular electric-dipole momentum. Molecular dynamics simulations reveal that the separation defining the rotational energy takes place within a few hundred fs after the onset of dissociation. This molecular-scale environmental effect significantly brings calculations and measurements of the kinetic energy release into agreement. © 2025 Author(s).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    <a href="/en/project/GA23-07066S" target="_blank" >GA23-07066S: Time-dependent simulations for time-resolved electronic spectroscopies</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    JOURNAL OF CHEMICAL PHYSICS

  • ISSN

    0021-9606

  • e-ISSN

  • Volume of the periodical

    162

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    054302

  • UT code for WoS article

    001413934600009

  • EID of the result in the Scopus database

    2-s2.0-85217847267