Abstract.
(C60) m Na n clusters are produced in a tandem laser vaporization source and analyzed by photoionization and photofragmentation time-of-flight mass spectroscopy. At low sodium coverage, the special behavior of (C60) m=1,2Na n clusters \((n\leq 6m)\) is consistent with a significant electron transfer from the first six adsorbed atoms towards each of the C60 fullerenes and an ionic-like bonding in this size range. However, the stability of the (C60)Na3 + cation is found much more pronounced than the one of (C60)Na7 + predicted to be a magic size under the hypothesis of a full charge transfer from the metal atoms to the C60 molecule. When more sodium atoms are present, metal-metal bonds tend to become preponderant and control the cluster properties. Relative to the number of sodium atoms, an odd-even alternation in their stability is explained by the high dissociation rates for even-numbered clusters. The even clusters evaporate neutral sodium atoms whereas odd ones prefer to evaporate Na2 molecules. The hypotheses for the growth of a sodium droplet that does not wet the fullerene surface or for the formation of a concentric metallic layer are discussed in the light of this study.
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Received: 7 May 2003, Published online: 17 July 2003
PACS:
36.40.Qv Stability and fragmentation of clusters - 36.40.Mr Spectroscopy and geometrical structure of clusters
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Pellarin, M., Cottancin, E., Lermé, J. et al. Photodissociation and photoionization of sodium coated C \(_\mathsf{60}\) clusters. Eur. Phys. J. D 25, 31–40 (2003). https://doi.org/10.1140/epjd/e2003-00216-4
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DOI: https://doi.org/10.1140/epjd/e2003-00216-4