A theoretical study of the subpicosecond fragmentation of C60 clusters in
response to ultrafast laser pulses is presented. We simulate the laser
excitation and the consequent nonequilibrium relaxation dynamics of the
electronic and nuclear degrees of freedom. The first stages of the
nonequilibrium dynamics are dominated by a coherent breathing mode followed by
the cold ejection of single C atoms, in contrast to the dimer emission which
characterizes the thermal relaxation. We also determine the nonequilibrium
damage thresholds as a function of the pulse duration.Comment: 5 pages, 4 figures, submitted to Chem. Phys. Let