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On the vibrational temperature of metal cluster beams: A time-resolved thermionic emission study

J. Chem. Phys. 99, 4174 (1993); doi:10.1063/1.466114

Issue Date: 1 September 1993

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Bruce A. Collings, Andreas H. Amrein, David M. Rayner, and Peter A. Hackett
Steacie Institute for Molecular Sciences, National Research Council of Canada, Ottawa, Ontario K1A 0R6, Canada
Delayed ionization rates for small niobium clusters are measured as a function of the cluster size, the laser wavelength, the number of photons absorbed, and the initial internal energy content of the cluster. It is shown, for the first time, that vibrational excitation of the clusters modulates their rate of delayed ionization. An analysis of the rate of ionization in terms of the total energy content of the cluster establishes unequivocally that delayed ionization is a statistically determined, unimolecular, activated process. It is shown that the rate of delayed ionization can be used to gauge the initial vibrational energy content of the cluster. Quantitative analysis of this effect establishes, for the first time, a thermometry for metal cluster beams. Thermal rate parameters, activation energies, and ``Arrhenius factors'' are presented for delayed ionization of a series of niobium clusters Nbn, n=5, 6, 7, 8, 9, 11, 12, and 13. The activation energies are lower than the corresponding ionization potentials by ~1 eV. The ``Arrhenius factors'' are all in the range 1011 s−1. These parameters highlight the differences between delayed ionization and photoionization of clusters and draw attention to the need for an adequate theory of unimolecular processes in clusters taking into account both nonadiabatic effects and the important effects arising from the fluxionality of the cluster at high internal energies. The Journal of Chemical Physics is copyrighted by The American Institute of Physics.
History: Received 1 April 1993; accepted 25 May 1993
Permalink: http://link.aip.org/link/?JCPSA6/99/4174/1
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KEYWORDS and PACS

Keywords
PACS
  • 36.40.+d
    Studies of special atoms and molecules Atomic and molecular clusters
  • 79.40.+z
    Electron and ion emission by liquids and solids; impact phenomena Thermionic emission
  • YEAR: 1993

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ISSN:
0021-9606 (print)   1089-7690 (online)
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REFERENCES (26)

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  1. S. J. Riley, in NATO ASI Series, Series C, edited by D. R. Salahub and N. Russo (Kluwer, Dordrecht, 1992), Vol. 378 and references therein.
  2. J. P. Butcher, in NATO ASI Series, Series C, edited by P. Jena, S. N. Khanna, and B. K. Rao (Kluwer, Dordrecht, 1992), Vol. 374, p. 721.
  3. G. C. Nieman, E. K. Parks, S. C. Richtsmeier, K. Liu, L. G. Probo, and S. J. Riley, High. Temp. Sci. 22, 115 (1986).
  4. A. Amrein, R. Simpson, and P. A. Hackett, J. Chem. Phys. 95, 1781 (1991).
  5. A. Amrein, R. Simpson, and P. A. Hackett, J. Chem. Phys. 94, 4663 (1991).
  6. T. Leisner, K. Athanassenas, O. Kandler, D. Kreisle, E. Rechnagel, and O. Echt, Z. Phys. D 20, 127 (1991).
  7. T. Leisner, K. Athanassenas, O. Echt, D. Kreisle, and E. Rechnagel, in NATO ASI Series, Series C, edited by P. Jena, S. N. Khanna, and B. K. Rao (Kluwer, Dordrecht, 1992), Vol. 374, p. 235.
  8. S. Maruyama, M. Y. Lee, R. E. Haufler, Y. Chai, and R. E. Smalley, Z. Phys. D 19, 409 (1991).
  9. E. E. B. Cambell, G. Ulmer, and I. V. Hertel, Phys. Rev. Lett. 67, 1981 (1991).
  10. P. Wurz and K. R. Lykke, J. Chem. Phys. 95, 7008 (1991).
  11. G. Walder and O. Echt, in Clusters and Fullerenes, edited by V. Kumar, T. P. Martin, and E. Tosatti (to be published).
  12. P. M. St. John and R. L. Whetten, Chem. Phys. Lett. 196, 330 (1992).
  13. J. S. Blakemore, Solid State Physics (Cambridge University, Cambridge, 1985).
  14. D. Hales, L. Lian, and P. B. Armentrout, Int. J. Mass Spectrom. Ion Proc. 102, 269 (1990).
  15. M. B. Knickelbein and S. Yang, J. Chem. Phys. 93, 5760 (1990).
  16. C. E. Klots, Chem. Phys. Lett. 186, 73 (1991).
  17. C. E. Klots, J. Chem. Phys. 90, 4470 (1989).
  18. C. E. Klots, J. Chem. Phys. 93, 2513 (1990).
  19. C. E. Klots, Z. Phys. D 20, 105 (1991).
  20. D. Proch and T. Trickl, Rev. Sci. Instrum. 60, 713 (1989).
  21. S. Maruyama, L. R. Anderson, and R. E. Smalley, Rev. Sci. Instrum. 61, 3683 (1990).
  22. M. F. Jarrold and J. E. Bower, J. Chem. Phys. 87, 5728 (1987).
  23. J. P. Bucher, D. C. Douglass, and L. A. Bloomfield, Phys. Rev. Lett. 66, 3052 (1991).
  24. P. J. Robinson and K. A. Holbrooke, Unimolecular Reactions (Wiley-Interscience, New York, 1972).
  25. W. Forst, Theory of Unimolecular Reactions (Academic, New York, 1973).
  26. L. Goodwin and D. Salahub, Phys. Rev. A 47, R774 (1993).

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