Several ways to electronically synchronize
different
types of amplified
femtosecond laser systems are presented based on a single freely programmable
electronics hardware: arbitrary-detuning asynchronous optical sampling
(ADASOPS), as well as actively locking two femtosecond laser oscillators,
albeit not necessarily to the same round-trip frequency. They allow
us to rapidly probe a very wide range of timescales, from picoseconds
to potentially seconds, in a single transient absorption experiment
without the need to move any delay stage. Experiments become possible
that address a largely unexplored aspect of many photochemical reactions,
in particular in the context of photo-catalysis as well as photoactive
proteins, where an initial femtosecond trigger very often initiates
a long-lasting cascade of follow-up processes. The approach is very
versatile and allows us to synchronize very different lasers, such
as a Ti:Sa amplifier and a 100 kHz Yb-laser system. The jitter of
the synchronization, and therewith the time-resolution in the transient
experiment, lies in the range from 1 to 3 ps, depending on the method.
For illustration, transient IR measurements of the excited state solvation
and decay of a metal carbonyl complex as well as the full reaction
cycle of bacteriorhodopsin are shown. The pros and cons of the various
methods are discussed, with regard to the scientific question one
might want to address, and also with regard to the laser systems that
might be already existent in a laser lab.