Stark Effect in Color Centers of Alkali Halides

Abstract
The stark effect of the F center in NaCl, NaBr, KCl, KBr, KI, and RbCl, the M center in KCl, and the Z1 center in KCl: Sr was measured using an ac electric field. The fractional change of the absorption coefficient, Δαα, at the peak of the F band, normalized to a Lorentz local field of 200 kV/cm, was found to be approximately 2×105 for NaCl and NaBr, 11×105 for RbCl, and 17×105 for KCl, KBr, and KI. The value of Δαα at the peak of the M band in KCl was (3.9±0.4)×105 for an applied electric field of 97 kV/cm. A measurement of the change in the absorption coefficient, Δα, versus photon energy produced a nonsymmetrical curve. This indicates that the effect observed was not the linear Stark effect, and thus provides additional evidence that Seitz's model is incorrect. The absorption coefficient increased at energies lower than the M band, corresponding to a decrease in the absorption coefficient of the M band. The effect is attributed to the mixing of two nondegenerate energy levels of opposite parity. The optical transition to the level of lower energy is normally forbidden. The Z1 center in KCl: Sr did not exhibit a detectable Stark effect. It was determined, however, that Δαα<8×106 for an applied electric field of 97 kV/cm. If the Z1 possesses a permanent dipole moment, the difference between the expectation values of dipole moment in the ground state and excited state is less than 1.0×1020 cgs unit.

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