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  Highly efficient double ionization of mixed alkali dimers by intermolecular Coulombic decay

LaForge, A. C., Shcherbinin, M., Stienkemeier, F., Richter, R., Moshammer, R., Pfeifer, T., et al. (2019). Highly efficient double ionization of mixed alkali dimers by intermolecular Coulombic decay. Nature Physics, 15, 247-250. doi:10.1038/s41567-018-0376-5.

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1812.07652.pdf (Preprint), 366KB
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https://doi.org/10.1038/s41567-018-0376-5 (Verlagsversion)
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 Urheber:
LaForge, A. C., Autor
Shcherbinin, M., Autor
Stienkemeier, F., Autor
Richter, R., Autor
Moshammer, R.1, Autor           
Pfeifer, T.1, Autor           
Mudrich, M., Autor
Affiliations:
1Division Prof. Dr. Thomas Pfeifer, MPI for Nuclear Physics, Max Planck Society, ou_2025284              

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Schlagwörter: Physics, Atomic and Molecular Clusters, physics.atm-clus
 Zusammenfassung: As opposed to purely molecular systems where electron dynamics proceed only
through intramolecular processes, weakly bound complexes such as He droplets
offer an environment where local excitations can interact with neighbouring
embedded molecules leading to new intermolecular relaxation mechanisms. Here,
we report on a new decay mechanism leading to the double ionization of alkali
dimers attached to He droplets by intermolecular energy transfer. From the
electron spectra, the process is similar to the well-known shake-off mechanism
observed in double Auger decay and single-photon double ionization, however, in
this case, the process is dominant, occurring with efficiencies equal to, or
greater than, single ionization by energy transfer. Although an alkali dimer
attached to a He droplet is a model case, the decay mechanism is relevant for
any system where the excitation energy of one constituent exceeds the double
ionization potential of another neighbouring molecule. The process is, in
particular, relevant for biological systems, where radicals and slow electrons
are known to cause radiation damage

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 Datum: 2019-01-07
 Publikationsstatus: Online veröffentlicht
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Titel: Nature Physics
  Andere : Nat. Phys.
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: London : Nature Pub. Group
Seiten: - Band / Heft: 15 Artikelnummer: - Start- / Endseite: 247 - 250 Identifikator: ISSN: 1745-2473
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000025850