Transient photoconductivity in thin-film NbxTi1-xO2 and TiO2 was studied as
a function of temperature, light intensity, illumination time, and ambient
composition in a time range of 10(-2)-10(7) s. Both excitation and relaxat
ion transients were slow and followed a nonexponential rate law. A conducti
vity model predominantly involving hole capture by O-2(-) at the surface is
proposed. It was possible to use a Laplace transform method to determine t
he free electron density and the photoinduced change in the surface barrier
caused by hole capture at the surface. In argon, both the oxygen adsorptio
n rate and the rate at which excess electrons reach the surface may contrib
ute to the decay whereas only the latter may be important in air.