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  • 1
    ISSN: 1434-6079
    Keywords: 36.40
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Stoichiometric and non-stoichiometric, positive and negative oxygen cluster ions (n up to 70) have been produced in a crossed neutral beam/electron beam ion source. The abundance and stability of the ions formed have been analyzed with a double focussing sector field mass spectrometer in a series of experiments. Positive and negative ion mass spectra observed exhibit distinct abundance anomalies, however, at different cluster sizes. Abundance maxima and minima correlate with correspondingly small and large metastable fractions of (O2) n + and (O2) n − ions, respectively. (O2) n + ions may also lose up top=(n−1) monomers by collision induced dissociation with monotonously decreasing probability with increasingp. Metastable fractions determined for (O2) n − ions produced with appr. zero eV electrons are in general larger than those for ions produced with appr. 7 eV electrons. (O2) n − ions are also observed to decay via autodetachment, with lifetimes increasing with increasing cluster size. Finally, here we were able to prove that an apparent loss of the monomer fragment O (and higher homologues) observed in the metastable time regime is due to ordinary metastable monomer evaporation in the acceleration region. Moreover, we will also present here some new data and interpretation concerning the electron attachment cross section function for O2 clusters.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-6079
    Keywords: 36.40 ; 33.40.Hp ; 32.30.Bv
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A new metastable decay reaction of ArnO+ cluster ions produced by the electron impact ionization of argonoxygen clusters has been discovered, leading to the evaporation of more than two monomers in the metastable time regime. It is estimated that an energy of approx. 1 eV has to be released from the intramolecular to intermolecular modes prior to this metastable decay. In contrast to previously observed excimer-induced fragmentation of pure argon cluster ions, it has been concluded that the localized metastable state of an ionic rather than a neutral species is involved in the fragmentation. A reaction mechanism involving an electronic transition from the a2Π ArO+* (O(3P)-Ar+(2P)) excited state to the X4Σ− ArO+ (O+(4S)-Ar(1S)) ground state of the ArO+ complex ion within the cluster and subsequent release of considerable amount of vibrational energy to cluster modes is suggested to account for the observed fragmentation. Based on these measurements, a lifetime of approx. 2 µsis proposed for the excited state a2Π ArO+*.
    Type of Medium: Electronic Resource
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