The photoelectron spectra of C60 ionized using a 790 nm laser with pulse durations varying from 25 fs to 5 ps have been determined. For 25 fs pulses, in the absence of fragmentation, the ionization mechanism is direct multiphoton ionization with clear observation of above threshold ionization. As the pulse duration is increased, this becomes dominated by a statistical ionization due to equilibration among the electronic degrees of freedom. For pulse durations on the order of a ps coupling to the vibrational degrees of freedom occurs and the well-known phenomenon of delayed (&mgr;s) ionization is observed.

Thermionic emission is discussed as a long time (microseconds) decay mode of energy-rich large molecules, metallic and metcar clusters, and fullerenes. We review what is known and consider the many experiments, systems, and theoretical and computational studies that still need to be done. We conclude with a wish list for future work. Particular attention is given to the experimental signatures, such as the dependence on the mode of energy acquisition, and theoretical indications of a not-quite-statistical delayed ionization and to the competition of electron emission with other decay modes, such as fragmentation or radiative cooling. Coupling of the electronic and nuclear modes can be a bottleneck and quite long time-delayed ionization can be observed, as in the decay of high Rydberg states probed by ZEKE spectroscopy, before the onset of complete energy partitioning.

Rydberg series of C60 are reported for the first time. The Rydberg states are seen in photoelectron spectra using ultrashort pulsed-laser excitation, where the excited states formed are ionized with one further photon from the same laser pulse. The structure is observed for pulse durations as short as 100 fs with indications of residual structure for even shorter pulse excitation. The production mechanism is discussed and the Rydberg states are modeled by analytically solving the Schrödinger equation with a simple jelliumlike potential for C60.

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We have calculated the electric field enhancement factor for a metallic cylinder with a hemispherical end-cap in a plane capacitor geometry paying particular attention to the dependence of the field enhancement factor on the anode distance. In addition, we have investigated the angular dependence of the local field at the end-cap. The numerical results, which cover a range of different ratios of cylinder lengths and anode distances, can be fitted with simple functional expressions which provide a useful scaling for calculations of field emission currents from closed cap carbon nanotubes or nanowires.