The photodissociation of ozone trapped at high dilution in solid argon has
been reinvestigated at different temperatures and various photon flux, comb
ining irradiation at 266 nm and infrared spectroscopy. In argon, recombinat
ion of O+O-2 is a major pathway and the weak decrease of ozone is due to ca
ge exit of oxygen atoms which is dependent of the temperature and of the in
itial photon flux. Kinetic curves are well fitted by a double exponential e
xpression and a model based upon two different cage exit pathways is propos
ed. (C) 1999 American Institute of Physics. [S0021-9606(99)01316-1].