Two kinds of excitonic luminescence were investigated for the entire s
eries of solid solutions, AgBr1-xClx, (0 less than or equal to x less
than or equal to 1). The time-resolved spectra observed around 2.5 eV
after both pulsed high-power electron beam and N-2-laser irradiations
are analyzed in terms of the diffusion-controlled recombination of Fre
nkel defects Ag-i(0) and Ag2+Vc-. It is shown that the effective activ
ation energy of Ag-i(0) migration is a linear function of the composit
ion x; and predominantly two kinds of nearest neighbours contribute to
this process. The position of maximum of the excitonic molecule lumin
escence found in mixed monocrystals ana fibers reveals a distinctive d
ependence on the composition x. Its amplitude and half-width correlate
with the optical losses in fibers which could be used for their chara
cterization.