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Topical Meeting on Optical Bistability (OB)

Low Power Optical Bistability Near Bound Excitons in Cadmium Sulfide

M. Dagenais, H. G. Winful

Published Jan 1, 1983• 0 citations
Publisher

Abstract

The I2 bound exciton in cadmium sulfide has a giant oscillator strength of 6. It decays mostly radiatively in 500 psec. Such a large oscillator strength leads to a very large transition dipole moment and to very large nonlinear effects off-resonance. At 2K, this sytem saturates like an inhomogeneously broadened system for intensities up to 30 times the saturation intensity. The transition linewidth is 7.5 GHz. In a tight focusing geometry, only 3.6 μW is required to see the onset of saturation. This corresponds to a measured saturation intensity of about 60 W/cm2. The linear absorption coefficient right at the resonance peak was measured to be 3.2 x 103 cm-1. At higher temperatures, the transition linewidth broadens and the line becomes more and more homogeneously broadened because of phonon interaction. At intensities above 50 times the saturation intensity, the absorption coefficient stops decreasing and then starts increasing. At these high intensities, thermal effects appear to play a significant role in shifting the free and bound exciton resonances toward lower energies. At intensities less than 20 times the saturation intensity, thermal effects are believed to be insignificant in our saturation measurements.

DOI
10.1364/obi.1983.fb2

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The I2 bound exciton in cadmium sulfide has a giant oscillator strength of 6. It decays mostly radiatively in 500 psec. Such a large oscillator strength leads to a very large transition dipole moment and to very large nonlinear effects off-resonance. At 2K, this sytem saturates like an inhomogeneously broadened system for intensities up to 30 times the saturation intensity. The transition linewidth is 7.5 GHz. In a tight focusing geometry, only 3.6 μW is required to see the onset of saturation. This corresponds to a measured saturation intensity of about 60 W/cm2. The linear absorption coefficient right at the resonance peak was measured to be 3.2 x 103 cm-1. At higher temperatures, the transition linewidth broadens and the line becomes more and more homogeneously broadened because of phonon interaction. At intensities above 50 times the saturation intensity, the absorption coefficient stops decreasing and then starts increasing. At these high intensities, thermal effects appear to play a significant role in shifting the free and bound exciton resonances toward lower energies. At intensities less than 20 times the saturation intensity, thermal effects are believed to be insignificant in our saturation measurements.
Very large nonlinearities are observed in the vicinity of a bound exciton resonance in cadmium sulfide. Power levels of the order of 8 μW are sufficient for saturating the bound exciton resonance in a tight focusing geometry. In a more loosely focused geometry, power levels of the order of 250 μW are sufficient for saturating the bound exciton resonance and for observing optical bistability. Transverse effects are found to play a very important role. For all our measurements, no thermal contributions to the nonlinearity were observed. Since thermal effects are not playing a role and since the studied bound excitons decay radiatively in 500 psec, we infer subnanosecond switchoff and cycling times.
Optical bistability caused by thermal heating is observed when the CdS crystal is excited near the I2 bound exciton absorption line [1]. Impact ionization of free and bound excitons occurs in the crystal upon its illumination in electric field. The probability of impact ionization depends in a threshold way on exciton and free carrier concentration. At a certain field dependent carrier concentratiοn avalanche occurs, the electric current therewith increases the crystal temperature by 5-20 K [2] which is followed by a red I2 shift. The shift leads to an increase in absorption, carrier density and current. Therefore, feedback results from impact ionization current heating the crystal (Fig. 1).