Abstract
The kinetics of excitons localized by statistic potential fluctuations have been studied in CdS1–xSex ternary alloys under quasi-stationary excitation conditions and have been time resolved after picosecond-pulse excitation. In luminescence experiments we observe the filling of the band tail with rising excitation intensity. The reduction of carrier density with time by recombination leads to a red shift of the luminescence band after picosecond-pulse excitation. Bleaching of absorption of the localized states is found in pump–probe experiments. Its dynamics depend on the localization depth of the excitons and on the pump-pulse energy. Using higher excitation intensities, we observe stimulated emission in luminescence, correlated with significant changes in the behavior of the absorption bleaching. The possible origin of the stimulated emission situated in the spectral region of localized states is discussed.
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