RESUMO
The kinetic energy release distribution of neutral atoms emitted from photoexcited clusters Sr(+)(n) with n=4-15, has been obtained by time-of-flight velocity dispersion. The deduced temperature is plotted as a function of the excitation energy. For small sizes n<7 a general increase is observed. For cluster sizes larger than n=9, the deduced caloric curves first increase, and then show evidence of a plateau regime as excitation energy increases. This limiting temperature in neutral atom ejection is consistent with a bound cluster-vapor phase transition in a microcanonical system.
RESUMO
The fission of Sr(2+)(n) is studied from time-of-flight (TOF) measurements. The TOF acts both as a mass spectrometer and as a velocity dispersion analyzer. Evidence of the postfission ejection of a fast neutral atom is shown. It is explained assuming a strong deformation of the fissioning system at the transition state. The relaxation of the deformation energy into vibrations promotes the evaporation of the large fragment.
RESUMO
Experimental and theoretical studies of fission of doubly charged Li, Na, and K clusters in the low-fissility regime reveal the strong influence of electronic shell effects on the fission products. The electronic entropy controls the quenching of the shell effects and the competition between magic-fragment channels, leading to a transition from favored channels of higher mass symmetry to the asymmetric channel involving the trimer cation at elevated temperatures.
RESUMO
We present a combined theoretical and experimental study of charge transfer and dissociation in collisions of slow Li31(2+) clusters with Cs atoms. We provide a direct quantitative comparison between theory and experiment and show that good agreement is found only when the exact experimental time of flight and initial cluster temperature are taken into account in the theoretical modeling. We demonstrate the validity of the simple physical image that consists in explaining evaporation as resulting from a collisional energy deposit due to cluster electronic excitation during charge transfer.