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Multiscale approach combining nonadiabatic dynamics with long-time radiative and non-radiative decay: Dissociative ionization of heavy rare-gas tetramers revisited

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    SYSNO ASEP0388544
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMultiscale approach combining nonadiabatic dynamics with long-time radiative and non-radiative decay: Dissociative ionization of heavy rare-gas tetramers revisited
    Author(s) Janeček, Ivan (UGN-S) RID
    Janča, T. (CZ)
    Naar, P. (CZ)
    Kalus, R. (CZ)
    Gadéa, F. X. (FR)
    Number of authors5
    Source TitleJournal of Chemical Physics. - : AIP Publishing - ISSN 0021-9606
    Roč. 138, č. 4 (2013), s. 1-12
    Number of pages12 s.
    Publication formOnline - E
    Languageeng - English
    CountryUS - United States
    Keywordsatomic clusters ; electromagnetic decays ; electron impact dissociation ; electron impact ionisation ; isomerism ; krypton ; nonradiative transitions ; xenon
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsED2.1.00/03.0082 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUGN-S - RVO:68145535
    UT WOS000314725900020
    DOI10.1063/1.4775804
    AnnotationA multiscale approach is proposed to address short-time nonadiabatic dynamics and long-time decay. We show the role of both radiative and non-radiative processes in cluster decay mechanisms on examples of rare-gas cluster fragmentation after electron impact ionization. Nonadiabatic molecular dynamics is used as an efficient tool for theoretical study on femto- and picosecond scales and a multiscale approach based on kinetic rates of radiative as well as non-radiative transitions, both considered as parallel reaction channels, is used for the analysis of the long-time system relaxation spanning times over microseconds to infinity.While the radiative processes are typically slow, the system relaxation through non-radiative electronic transitions connected with electron-nuclear interchange of energy may, on the other hand, significantly vary in kinetic rates according to kinetic couplings between relevant adiabatic states.
    WorkplaceInstitute of Geonics
    ContactLucie Gurková, lucie.gurkova@ugn.cas.cz, Tel.: 596 979 354
    Year of Publishing2013
    Electronic addresshttp://jcp.aip.org/resource/1/jcpsa6/v138/i4/p044303_s1?isAuthorized=no
Number of the records: 1  

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