Abstract
The observed nonexponential decay of the slow luminescence componet of Pb2+ and Tl+ centres in alkali halide crystals has been modelled. The model is based on the assumption that there is lattice relaxation on the same time scale as the slow-component decay time. This relaxation is taken to be a response to the Jahn-Teller local distortion of the Tl+ and Pb2+ luminescence centres. We successfully fit experimental data for the slow componet decay of KX:Pb2+ and KX:Tl+ (X = Cl, Br, I). An essential feature of the model is that the lattice relaxation causes a time-dependent coupling of the Jahn-Teller levels and it is found that the coupling strength systematically increases as the anion size increases.
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