Summary form only given. In the excitonic ac Stark shift in quantum wells the excitonic absorption line is blueshifted by shining on the sample an intense laser pulse, whose frequency is lower than the exciton transition frequency. The effect is bigger when the laser spectrum approaches the resonance with the excitonic absorption. But if the laser and excitonic absorption spectra sensibly overlap, a great amount of electronic population is excited and consequently the Coulomb nonlinearities due to the interaction between excited carries or excitons dramatically increase. One prominent effect under these conditions is the excitation- induced dephasing which can destroy the coherence of the electronic system and therefore the coupling between excitons and light, which is inherently coherent. Some evidence for the resonant Stark effect was already reported, but the direct observation of the spectral splitting was still missing. This observation demonstrates that the coherent exciton light coupling in semiconductors can be strong enough to survive the fast dephasing, and that therefore an efficient ultrafast manipulation of the exciton absorption in the coherent transient is possible. In order to magnify the ac Stark effect and its visibility a special sample was designed: a single In/sub 0.04/Ga/sub 0.96/As quantum well is grown on the top of an AlAs/AlGaAs distributed Bragg reflector; two /spl lambda//2 spacers separate the quantum well from the mirror and from the air. In this configuration the light field incident on the sample and the one reflected by the mirror constructively interfere at the quantum well position, giving a high effective absorption.
Absorption spectra of strained InGaAs/InP quantum wells exhibit a single, unusually large exciton feature. 60% quenching is obtained for 4.3 mW Nd:YAG effective pump power at a wavelength of 1.064 mu m. A simple two-level formula fits well the behaviour at the exciton peak, and absorption spectra are reasonably approximated by a standard two-dimensional exciton model. Saturation intensities calculated with these techniques range around 200 W cm-2. Finally the Kramers-Kronig relations are used to calculate the associated refractive index change.
We perform femtosecond spectrally resolved pump-probe differential reflectivity measurements on excitons in GaAs quantum wells in both coherent and incoherent regimes. The spectral signal is nonzero and oscillatory at $\ensuremath{-}\mathrm{ve}$ delay up to a few ps indicating persistent coherence between excitonic polarization induced by the probe pulse and the delayed pump pulse. The signal for small
+ve and $\ensuremath{-}\mathrm{ve}$ delay $(\ensuremath{\tau})$ shows modulation caused by quantum beats due to coexcitation of heavy and light hole excitons. The rise of the signal with $\ensuremath{\tau}$ for $\ensuremath{\tau}<0$ is rather nonexponential and is sensitive to detuning of the detection energy with respect to the exciton energy. The signal decay with $\ensuremath{\tau}$ for small
+ve $\ensuremath{\tau}$ shows dependence on pump-probe relative polarization. The excitonic reflectivity shows a large reduction caused by excitonic absorption saturation for both
+ve and $\ensuremath{-}\mathrm{ve}$ $\ensuremath{\tau}$ when the pump pulse intensity is increased to large values. To compare the experimental results with theory, we obtain an expression for the PPDR signal in terms of the third order excitonic polarization. This has an additional term not considered earlier to describe pump-probe experiments. The calculations are performed using optical Bloch equations, modified to incorporate exciton inhomogeneous broadening, quantum beats, and many body effects such as local field, excitation induced energy shift, and dephasing. These effects are found essential in explaining the observed PPDR spectral data. The delay dependence of the signal near the exciton energy is mainly controlled by inhomogeneous broadening for $\ensuremath{-}\mathrm{ve}$ $\ensuremath{\tau}.$ The signal decay for large
+ve $\ensuremath{\tau}$ has an exponential behavior determined by the lifetime of incoherent excitons. Experiments for collinear polarization reveal an additional exponential component for small
+ve delay. Theoretically, this is found to be related to exciton dephasing and is present only when many body effects are included.
Summary form only given. Ultrafast dephasing of excitons in semiconductor quantum wells is important because it presents insight into fundamental interactions and possible coherent control of optical properties. Standard measurement techniques include time- and frequency-domain four-wave mixing, resonant Rayleigh scattering, and Faraday rotation. We report on a new time-resolved technique based on reflective probing of pump-induced transient linear birefringence. This has various advantages, including sensitivity, applicability to opaque as-grown samples, ease of implementation, and freedom from superimposed signals.
Recently, coherent control of exciton populations has been demonstrated through terahertz, reflection, and four-wave-mixing experiments. However, the most direct probe of exciton population control is the absorption, which has been lacking in previous studies. In this report, we probe the time evolution of exciton population directly through a transmission experiment. In particular, using upconversion technique with both narrow (spectrally broad) and broad (spectrally narrow) pulses, we can obtain both the temporal and the spectral information. The main thrust of our report is that when phase controlled, the second pulse can be either greatly enhanced or completely destroyed by gaining energy from exciton or giving all of its energy to the system, respectively.