I. Pastirk et al., Control and characterization of intramolecular dynamics with chirped femtosecond three-pulse four-wave mixing, J PHYS CH A, 103(49), 1999, pp. 10226-10236
Experimental control and characterization of intramolecular dynamics are de
monstrated with chirped femtosecond three-pulse four-wave mixing (FWM). The
two-dimensional (spectrally dispersed and time-resolved) three-pulse FWM s
ignal is shown to contain important information about the population and co
herence of the electronic and vibrational states of the system. The experim
ents are carried out on gas-phase I-2 and the degenerate laser pulses are r
esonant with the X (ground) to B (excited) electronic transition. In the ab
sence of laser chirp, control over population and coherence transfer is dem
onstrated by selecting specific pulse sequences. When chirped lasers are us
ed to manipulate the optical phases of the pulses, the two-dimensional data
demonstrate the transfer of coherence between the ground and excited state
s. Positive chirps are also shown to enhance the signal intensity, particul
arly for bluer wavelengths. A theoretical model based on the multilevel den
sity matrix formalism in the perturbation limit is developed to simulate th
e data. The model takes into account two vibrational levels in the ground a
nd the excited states, as well as different pulse sequences and laser chirp
values. The analytical solution allows us to predict particular pulse sequ
ences that control the final electronic state of the population. In a simil
ar manner, the theory allows us to find critical chirp values that control
the transfer of vibrational coherence between the two electronic states. Wa
ve packet calculations are used to illustrate the process that leads to the
observation of ground-state dynamics. All the calculations are found to be
in excellent agreement with the experimental data. The ability to control
population and coherence transfer in molecular systems is of great importan
ce in the quest for controlling the outcome of laser-initiated chemical rea
ctions.