Abstract
The burning kinetics of closely spaced equidistant holes in impurity absorption spectra of glasses and polymers is theoretically studied in an alternating electric field (alternating in the magnitude, sign, and direction). The height of barriers between wells of the burnt multiwell spectral hole depends on the shape of the distribution of impurity molecules over the Stark dipole moments. Centrally symmetric impurity molecules are considered whose Stark moment is determined exclusively by the interaction with matrix molecules. Model calculations performed for different hypothetical distribution functions of Stark moments yield substantially different kinetics. Therefore, the method described allows one to verify experimentally various hypotheses about the nature of matrix-induced Stark moments.
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