We report a photoluminescence study of excitons localized by interface fluctuations in a narrow GaAs͞AlGaAs quantum well. This type of structure provides a valuable system for the optical study of quantum dots. By reducing the area of the sample studied down to the optical near-field regime, only a few dots are probed. With resonant excitation we measure the excited-state spectra of single quantum dots. Many of the spectral lines are linearly polarized with a fine structure splitting of 20 -50 meV. These optical properties are consistent with the characteristic asymmetry of the interface fluctuations. PACS numbers: 78.55.Cr, 71.35.Cc In this Letter we describe the polarization dependence of the optical spectra of single naturally formed GaAs quantum dots. Most previous optical studies of quantum dots (QDs) have probed large ensembles which have led to inhomogeneous broadening of the spectral features. However, recently several groups have shown that it is possible to study single QDs with photoluminescence (PL) either by reducing the size of the sample, [1] by cathodoluminescence [2,3], or by reducing the size of the laser spot on the sample through microscopic [4,5] or optical near-field techniques [6]. Here we use a similar technique whereby we combine high spatial and spectral resolution optics with excitation spectroscopy to study in detail the spectrum of a single QD [7]. With improved resolution we are able to resolve the spectral lines and to study the polarization dependence of the PL spectrum of an individual QD. We often find that the PL is linearly polarized along the (110) crystal axes and observe a fine structure splitting in each of the spectral lines. These results are analogous to the early days of atomic spectroscopy as improvements in techniques allowed the observation of fine structure splittings in the optical spectra. However, the physical phenomena responsible for the effects presented here are unique to the quantized condensed matter system.The QDs we have studied were formed naturally by interface steps in narrow quantum wells [4][5][6][7]. Specifically, the electrons and holes become localized into QDs in regions of the quantum well that are a monolayer wider than the surrounding region and, therefore, have a slightly smaller confinement energy. These well width fluctuations arise from monolayer-high islands at the interfaces which are randomly formed on the growth-interrupted surface by the migration of the cations to step edges. By interrupting the growth these islands can grow to diameters larger than the exciton Bohr diameter (20 nm). A scanning tunneling microscope image of a growth-interrupted GaAs surface grown under similar conditions as our quantum dot sample is shown in Fig. 1. Large monolayer-high islands of varying lateral sizes are evident, and the islands tend to be elongated along the [110] crystal axis. Thus we intuitively expect that the optical properties associated with the localized excitons will reflect this characteristic interface structure. In fact, as we will...

An asymmetric pair of coupled InAs quantum dots is tuned into resonance by applying an electric field so that a single hole forms a coherent molecular wave function. The optical spectrum shows a rich pattern of level anticrossings and crossings that can be understood as a superposition of charge and spin configurations of the two dots. Coulomb interactions shift the molecular resonance of the optically excited state (charged exciton) with respect to the ground state (single charge), enabling light-induced coupling of the quantum dots. This result demonstrates the possibility of optically coupling quantum dots for application in quantum information processing.

Picosecond optical excitation was used to coherently control the excitation in a single quantum dot on a time scale that is short compared with the time scale for loss of quantum coherence. The excitonic wave function was manipulated by controlling the optical phase of the two-pulse sequence through timing and polarization. Wave function engineering techniques, developed in atomic and molecular systems, were used to monitor and control a nonstationary quantum mechanical state composed of a superposition of eigenstates. The results extend the concept of coherent control in semiconductors to the limit of a single quantum system in a zero-dimensional quantum dot.

Quantum dots are typically formed from large groupings of atoms and thus may be expected to have appreciable many-body behavior under intense optical excitation. Nonetheless, they are known to exhibit discrete energy levels due to quantum confinement effects. We show that, like single-atom or single-molecule two- and three-level quantum systems, single semiconductor quantum dots can also exhibit interference phenomena when driven simultaneously by two optical fields. Probe absorption spectra are obtained that exhibit Autler-Townes splitting when the optical fields drive coupled transitions and complex Mollow-related structure, including gain without population inversion, when they drive the same transition. Our results open the way for the demonstration of numerous quantum level-based applications, such as quantum dot lasers, optical modulators, and quantum logic devices.