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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 80 (1996), S. 4990-4996 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Epitaxial growth of C60 was found in vapor-deposited crystals on the KI (001) cleavage surface. C60 molecules deposited on the KI surface, which was preheated at 400 °C, then kept at 195 °C during deposition, crystallized in the face-centered cubic form with two types of morphologies. Truncated pyramidal crystals epitaxially grew along the KI 〈110〉 directions, taking its C60 (001) face parallel to the KI (001) surface. This epitaxial nucleation occurred at a corner of the crossing steps along the KI 〈100〉 directions which were caused by thermal etching of the KI surface. Molecular mechanics and dynamics calculations revealed that a three-dimensional (2×2) commensurate lattice matching between the C60 {100} planes and the KI {100} faces at the step corner attributed to the epitaxial nucleation of the pyramidal crystal, in spite of the lower stability of the monolayer interaction of the C60 (001) face with the KI (001) surface. On the other hand, platelike crystals grew, with the C60 (111) face parallel to the KI (001) surface. A stable monolayer nucleation of the close-packed C60 (111) face made this two-dimensional growth of the platelike crystals possible to occur on the (001) terrace of the etched KI surface. © 1996 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 116 (2002), S. 7673-7684 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have clarified the dynamics and mechanism of CH4 dissociative chemisorption processes on a cesiated Pt(111) surface by means of molecular beam scattering techniques. A comparison is made of similar processes on a Pt(111) surface. It is found that the CH4 molecules with enough energy to overcome the activation barrier for dissociation can no longer dissociate on a cesiated surface of Pt(111). Time-of-flight and angular intensity distribution measurements of the reflected CH4 molecules have revealed a similarity in inelastic collision dynamics both on the Pt(111) and the cesiated Pt(111) surfaces. Even a low concentration of the Cs layer as 0.06 of coverage is found to modify the surface electronic structure such that the activation barrier is enhanced as a result of an increased Pauli repulsive potential component in the potential energy surface. It is also found from time-of-flight measurements that direct dissociation is the only pass way and precursor mediated dissociation is not possible both on the Pt(111) and the cesiated Pt(111) surfaces in our experimental conditions. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2016-06-23
    Description: To understand the interaction between fast plasma flow and perpendicular magnetic field, we have investigated the behavior of a one-dimensional fast plasma flow in a perpendicular magnetic field by a laboratory-scale experiment using a pulsed-power discharge. The velocity of the plasma flow generated by a tapered cone plasma focus device is about 30 km/s, and the magnetic Reynolds number is estimated to be 8.8. After flow through the perpendicular magnetic field, the accelerated ions are measured by an ion collector. To clarify the behavior of the accelerated ions and the electromagnetic fields, numerical simulations based on an electromagnetic hybrid particle-in-cell method have been carried out. The results show that the behavior of the accelerated ions corresponds qualitatively to the experimental results. Faster ions in the plasma flow are accelerated by the induced electromagnetic fields modulated with the plasma flow.
    Print ISSN: 1070-664X
    Electronic ISSN: 1089-7674
    Topics: Physics
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