We
performed a time-resolved spectroscopy experiment on the dissociation
of oxygen molecules after the interaction with intense extreme-ultraviolet
(XUV) light from the free-electron laser in Hamburg at Deutsches Elektronen-Synchrotron.
Using an XUV-pump/XUV-probe transient-absorption geometry with a split-and-delay
unit, we observe the onset of electronic transitions in the O
2+
cation near 50 eV photon energy, marking the end of
the progression from a molecule to two isolated atoms. We observe
two different time scales of 290 ± 53 and 180 ± 76 fs
for the emergence of different ionic transitions, indicating different
dissociation pathways taken by the departing oxygen atoms. With regard
to the emerging opportunities of tuning the central frequencies of
pump and probe pulses and of increasing the probe–pulse bandwidth,
future pump–probe transient-absorption experiments are expected
to provide a detailed view of the coupled nuclear and electronic dynamics
during molecular dissociation.