We report results on photocarrier transport in colloidal TiO2 films wi
th the aim of elucidating the fundamental features of the transport ki
netics. We find the transport process in these films to be dispersive.
Typical tripping lifetimes are of the order of microseconds and mobil
ity lifetime products several 10(-11) Cm2 V-1. The transport propertie
s are markedly improved when deep trap states are saturated by excess
carriers. We show that trapping lifetimes can be altered over several
orders of magnitude. Recombination is studied in Schottky barrier type
samples under double injection conditions. We find the recombination
lifetime to decrease when the injection level is raised, indicative of
bimolecular kinetics. Typical recombination times are in the range 10
mus to 1 ms. It is concluded from this study that specific operation
conditions can result in transport properties greatly different from t
hose near equilibrium. Recent success in using these films in photovol
taic applications may be due to the improved transport properties unde
r high carrier injection.