Laser-induced oxygen molecule desorption from crystalline (110)and com
pressed-powder rutile TiO2 surfaces is investigated by time-of-flight
distributions and desorption signal dependencies oil laser fluence. A
double-component distribution of desorbed O-2 molecules (a fast one an
d a slow one) justifies validity of both photoelectronic and thermo-ac
tivation mechanisms. The defected surfaces characterized by the more i
ntensive oxygen escape supporting the desorption flow formation via th
e surface defect sites. (C) 1998 Elsevier Science B.V.