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  • American Institute of Physics  (21)
  • American Institute of Physics (AIP)  (16)
  • Oxford University Press  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 254-261 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: In this paper both deuterium saturation measurements and gas-phase kinetic measurements of chemisorption of H2, D2, N2, CD4, CH4, C2H4, and C2H6 on neutral palladium clusters are reported. Saturation studies with D2 show that small palladium clusters can bind up to three deuterium atoms per palladium atom in the cluster, in contast to H/M ratios near unity typically reported for metal surfaces. In addition, the small palladium clusters exhibit pronounced discontinuities in deuterium uptake which may be indicative of structural transformations or selective desorption of deuterium. From the kinetic studies we find that, in general, the rate constants for a given size cluster towards different reagents tend to order as D2, H2〉N2〉C2H4〉CD4, CH4, C2H6. The shape of the reactivity pattern with the different reagents varies strongly with cluster size for clusters containing less than 25 atoms. Finally, an inverse hydrogen isotope effect is observed for both hydrogen and methane, i.e., the D2 and CD4 rate constants are significantly larger than those of H2 and CH4, respectively.
    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 96 (1992), S. 4102-4105 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Zero electron kinetic energy (ZEKE) spectroscopy and photodetachment cross section measurements have been carried out on Au−6. The transition frequencies of ZEKE peaks and resonance peaks are nearly identical, consistent with the proposal that the excited negative ion of Au6 has a geometry quite similar to that of neutral Au6, and supporting the picture of the resonances as weakly bound "surface states.'' From these studies the 0–0 transition frequency between Au−6 and Au6 is measured to be 16 541±17 cm−1, and the vibrational frequencies for the neutral Au6 ground state, the Au−6 ground state, and the (Au−6)* anion excited electronic state are 107, 73, and 107 cm−1, respectively. Lastly, we observe evidence for a previously unreported resonance transition to the excited anion which we suggest is the 0–0 transition of Au−6 to (Au−6)*.
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  • 3
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Well-defined librational excitations have been observed at energies of 2–3 meV in the low temperature ordered phase of solid C60. These relatively high energies imply a stiff orientational potential below the transition. The sharpness of the peaks indicates that this potential does not depend strongly on the axis of the angular displacement. The modes soften and broaden as the temperature approaches that of the orientational melting transition which occurs when the librational amplitude is a considerable fraction of nearest-neighbor interatomic angles.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 8395-8396 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 854-858 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: This paper reports the observation of autodetaching resonances in photoelectron spectroscopy of Au−2 according to the process Au−2 +hν(large-closed-square)(Au−2)*(large-closed-square)Au2 +e−. They appear as sharp features superimposed upon a nearly constant signal associated with direct photodetachment process from Au−2 :Au−2 +hν(large-closed-square)Au2+e−. By altering the cluster expansion conditions, the dimer anion temperature can be varied. This leads to changes in the linewidth and relative intensities of the resonances and allows ground state and hot band transitions to be identified. The resonances correspond to electronic transitions to a long-lived excited state of Au−2 with a significantly lower vibrational frequency (128±2 cm−1) than that of the neutral ground state (190.9 cm−1), or even the anion ground state (149 cm−1). It decays via electronic autodetachment in a two-electron process similar to autoionization of neutral atoms.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 1201-1202 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 5943-5947 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The gas-phase reaction of positively charged niobium cluster ions Nb+x with normal and perdeuterobenzene has been studied using a fast-flow reactor and direct ion sampling techniques. Chemisorption of benzene onto the ion is facile, with the rate being essentially independent of x. However, both the resulting product distributions, consisting of species NbxC6H+m and NbxC6D+m with m=0,2,4,6, and the relative product yields not only display a dramatic dependence on cluster size, but are also remarkably similar to those previously observed for neutral Nbx using gentle, low-fluence, single-photon 6.42 eV photoionization. Direct observation of products with m≤6 indicates that both chemical dehydrogenation of benzene and desorption of hydrogen from the cluster ions must occur in the fast-flow reactor. Further, the relative yield of dehydrogenated products is found to increase substantially with increase in cluster "temperature.'' Complete dehydrogenation of benzene to m=0 is also found to occur for niobium cluster oxides NbxO+ containing 5–14 Nb atoms. The present results are discussed in terms of the mechanism of the dehydrogenation process, as well as with respect to their relevance in determining "true'' parent product distributions formed in reactions of the corresponding neutral clusters.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 88 (1988), S. 3555-3560 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The effect of charge state on niobium cluster chemisorption kinetics is explored via measurement of the relative rates of D2 activation by Nb−x, Nbx, and Nb+x containing up to 28 atoms. The presence of the + or − charge is found to have only a minor effect on rate for the majority of the clusters, with the reactivity of the ions being generally within a factor of 2.5 of the corresponding neutrals. The excess charge does, however, have a profund influence on reaction rate for a number of clusters in the 7≤x≤16 size range, which may be indicative of the importance of cluster electronic structure in the chemisorption process. Kinetic data for Nb9, Nb12, and Nb+12 are found to deviate significantly from the expected pseudo-first-order behavior, suggesting the existence of structural isomers for these species. The anomalous behavior for Nb9 and Nb12 was not observed in previous neutral Nbx chemisorption studies. The maximum uptake of D2 by niobium clusters is found to be essentially independent of charge state, but varies strongly with x, consistent with the presence of a high barrier to D–D bond activation for certain of the clusters.
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 57 (1985), S. 3829-3829 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report the first measurements of the magnetic moments of isolated metal atom clusters. In particular we have measured the magnetic moments of iron atom clusters ranging in size from 2 to 15 atoms and for aluminum atom clusters Al2 and Al3 and their corresponding mono-oxides Al2O, Al3O. We produce a supersonic beam of metal atom clusters by pulsed laser vaporization of a metal substrate within the narrow throat of a pulsed nozzle. The clusters are passed through a Stern–Gerlach magnet and the spatial profile of the magnetic deflection pattern is measured using UV laser photoionization combined with time-of-flight mass analysis of the resulting photoions. The magnetic moments of the iron clusters are found to increase linearly with the number of atoms in the cluster consistent with a net spin per atom of about 3.0 μB compared to the bulk value of 2.2 μB. These observations are consistent with theoretical predictions of the magnetic moments of iron clusters of 4, 9, and 15 atoms. For Al2 we observe Stern–Gerlach behavior and for Al3 we measure a maximum moment of approximately 1/3 μB. The implication of these findings regarding the electronic and structural properties of small metal clusters will be discussed.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 5046-5048 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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