Regarding an experimental measurement of proton kinetic energy spectra of H
-2(+) with a chirped pulse [L. J. Frasinski, J. H. Posthumus, J. Plumridge,
and K. Golding, Phys. Rev. Lett. 83, 3625 (1999)], we present a nonperturb
ative, time-dependent calculation for the photodissociation of H-2(+) in in
tense laser fields by combining three numerical techniques. The results sho
w a finer kinetic-energy distribution structure of a proton due to the intr
apulse pump-dump mechanism between two electronic states as the pulse durat
ion and intensity change. Higher-energy peaks are also suppressed by freque
ncy chirping of the laser field. The dissociation probabilities show that a
positively chirped pulse is always more efficient for population inversion
than no chirping or negatively chirped pulses, and a slight coordinate shi
ft of the initial state could result in a significant increase of dissociat
ion probability.