The ultrafast solvation and recombination dynamics of the hydrated electron
generated by two-photon ionization of water at 4.65 eV is studied by trans
ient absorption spectroscopy as a function of temperature in the range from
277 K to 355 K. The part of the spectral blue shift which is observed in t
he absorption spectrum of the hydrated electron after 1 ps is purely contin
uous and is accurately described by the well known analytical expression fo
r the temperature dependent absorption spectrum of the ground state hydrate
d electron. This indicates that thermal relaxation or more likely solvation
of the hydrated electron predominantly causes the blue shift. The survival
probability of the hydrated electron shows a strong temperature dependence
, which is satisfactory explained by the temperature dependent mobility and
reaction rates of the species involved in the recombination. This implies
that the average initial separation between the hydrated electron and the i
onization site of [r(0)]=1.0 +/- 0.1 nm does not depend significantly on th
e bulk water temperature. (C) 2000 American Institute of Physics. [S0021-96
06(00)50927-1].