The electric field of a laser pulse exerts a force on charged particles whi
ch can be on the order of (or exceed) the forces that bind electrons to ato
ms, molecules, solids or that bind atoms together in molecules or solids. W
ith modern laser technology, this force can be applied with almost 1 fs, 1
mu m precision.
Even if the field is lower than the field required to ionize atoms or molec
ules, large nonresonant Stark shifts can be achieved. The Stark shift gives
us a means to control molecules. The dependence of the Stark shift with re
spect to the intensity profile of the laser focus determines the spatial fo
rce exerted on the molecule. The dependence of the Stark shift on the orien
tation of the molecule with respect to the laser polarization determines th
e torque exerted on the molecule. Through these forces we can control posit
ion, orientation, and linear and/or angular velocity.
The Stark shift also depends on the internuclear co-ordinates, giving us so
me degree of control over the structure of the potential energy surface in
molecules. The ability to control these basic forces with precision depends
on our ability to control optical pulses. Progress towards producing high
power pulses with almost arbitrary time-dependent infrared fields will be d
iscussed.
In even stronger fields, where ionization occurs, the shifting and mixing o
f states becomes extreme. Measurement in this complex spectroscopic environ
ment is difficult. Intuition based on perturbation theory is of limited val
ue. Yet strong field probing allows us to supply a lot of electronic energy
to a molecule very rapidly and to localize measurements in space and time.
We illustrate molecular alignment and strong field probing together in one
experiment where we study femtosecond dissociative ionization.