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  • Articles: DFG German National Licenses  (3)
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  • Articles: DFG German National Licenses  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 8773-8779 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The optical absorption of size-selected helium cluster ions was studied via photofragmentation spectroscopy. Absorption cross sections were measured for He+n (n=3, 4, 10, 21, and 30). A broad absorption peak was found, which for He+3 is centered at ≈5.3 eV, and which with increasing cluster size shifts slightly to the red. In addition, the kinetic energy release to the ionized and neutral photofragments was measured by a time-of-flight technique for cluster sizes between n=3 and 10. From the energy balance the total binding energy of the He+3 trimer ion was determined to be 2.6±0.15 eV. The results further indicate that a charged linear trimer acts as a core molecule for the sizes n=4–7. For n(approximately-greater-than)7, an additional isomer with a tetramer core is identified. The results are compared with recent ab initio calculations. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 3450-3462 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The velocities of neutral and charged photofragments of the rare gas trimers He+3, Ar+3, and Xe+3 have been examined in a comprehensive study for photon energies ranging from 1.5 to 6 eV. For this purpose, a novel time-of-flight technique has been applied which allows the simultaneous examination of both neutral and charged fragments. The general fragmentation pattern of all three species was that of a linear trimer with a parallel transition moment and a totally repulsive excited state: In the course of the dissociation, two of the particles gain high velocities in opposite directions, while the third particle (the middle particle of the linear trimer) only obtains a small velocity. The positive charge generally localizes on one of the fast outer particles, as can be expected from the symmetry properties of the excited state. For Ar+3 and Xe+3, however, also localization of the charge on the slow particle can be observed. This effect strongly depends on the energy of the absorbed photon, and can be quenched by decreasing the vibrational excitation of the trimer. Comparison of the results with new potential energy surface calculations indicate that mainly spin–orbit coupling induced conical intersections are responsible for this charge redistribution phenomenon. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 2513-2518 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ionized rare gas clusters Ar4+ and Xe4+ have been studied by photofragmentation. Center-of-mass velocities of the neutral and ionized photofragments have been measured for photon energies between 1.6 and 4.4 eV. In almost all of the examined photon energy region, both clusters exhibit fragment velocity distributions which show that they consist of a linear ionized trimer with an additional atom loosely attached to its side. For the lowest photon energies, however, fragmentation patterns are observed which can only be explained by a linear tetramer structure. This demonstrates that stable linear isomers of the ionized rare gas tetramers exist. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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