Semiconductor quantum dots coherently driven by pulsed laser are fundamental physical systems which allow studying the dynamical properties of confined quantum states. These systems are attractive candidates for a solid-state qubit, which open the possibility for several investigations in quantum-information processing. In this work we study the effects of a specific decoherence process, the spontaneous emission of excitonic states, in a quantum dot molecule. We model our system considering a three-level Hamiltonian and solve the corresponding master equation in the Lindblad form. Our results show that the spontaneous emission associated with the direct exciton helps to build up a robust indirect exciton state. This robustness against decoherence allows potential applications in quantum memories and quantum gate architectures. We further investigate several regimes of physical parameters, showing that this process is easily controlled by tuning of external fields.
Semiconductor quantum dots coherently driven by pulsed laser are fundamental physical systems which allow studying the dynamical properties of confined quantum states. These systems are attractive candidates for a solid-state qubit, which open the possibility for several investigations in quantum-information processing. In this work we study the effects of a specific decoherence process, the spontaneous emission of excitonic states, in a quantum dot molecule. We model our system considering a three-level Hamiltonian and solve the corresponding master equation in the Lindblad form. Our results show that the spontaneous emission associated with the direct exciton helps to build up a robust indirect exciton state. This robustness against decoherence allows potential applications in quantum memories and quantum gate architectures. We further investigate several regimes of physical parameters, showing that this process is easily controlled by tuning of external fields.
Quantum dots are attractive due to their potential technological applications and the opportunity they provide for study of fundamental physics in the mesoscopic scale. This dissertation studies optically controlled spins in quantum dots in connection to quantum information processing. The physical realization of the quantum bit (qubit) consists of the two spin states of an extra electron confined in a quantum dot. Spin rotations are performed optically, by use of an intermediate charged exciton (trion) state. The two spin states and the trion form a Lambda-type system. The merits of this system for quantum information processing include integrability into a solid-state device, long spin coherence time, and fast and focused optical control. In this dissertation, we study the optical decay mechanisms of the trion state in the quantum dot. Using a master-equation approach, we derive microscopically the optical decay of the three- level system and find a novel term, the so-called spontaneously generated coherence (SGC). The latter, though predicted more than a decade ago for atomic Lambda-systems satisfying certain conditions, had not been detected yet in any system. We found that in quantum dots, these conditions can be satisfied. We present the experiment which, in collaboration with our theory, constituted the first measurement of SGC. We establish the unification of SGC, polarization entanglement, and two- pathway decay. By keeping track of the spontaneously emitted photon dynamics, we find the conditions on the couplings that determine which effect will take place. We have thus placed SGC in a more quantum informational framework, characterizing it as lack of entanglement between the emitted photon and the three-level system. We develop a theory of ultrafast optical single-qubit rotations by use of 2pi pulses, which have the two-fold advantage of minimal trion excitation and negligible spin precession. The analytically solvable hyperbolic secant pulses of Rosen and Zener for the two-level system are investigated in the context of the three-level system. Ultrafast rotations about the quantum dot growth direction are designed, the angle of spin rotation is expressed analytically, and the fidelity is studied by simulations. Adaptive feedback loops are employed to correct for unintended dynamics
We propose an optoelectronic scheme to define and manipulate an indirect neutral exciton qubit within a quantum dot molecule. We demonstrate coherent dynamics of indirect excitons resilient against decoherence effects, including direct exciton spontaneous recombination. For molecules with large interdot separation, the exciton dressed spectrum yields an often overlooked avoided crossing between spatially indirect exciton states. Effective two-level system Hamiltonians are extracted by Feshbach projection over the multilevel exciton configurations. An adiabatic manipulation of the qubit states is devised using time-dependent electric field sweeps. The exciton dynamics yields the necessary conditions for qubit initialization and near unitary rotations in the picosecond time scale, driven by the system internal dynamics. Despite the strong influence of laser excitation, charge tunneling, and interdot dipole-dipole interactions, the effective relaxation time of indirect excitons is much longer than the direct exciton spontaneous recombination time, rendering indirect excitons as potential elemental qubits in more complex schemes.
Semiconductor Quantum dots are potentially an attractive source of non-classical light. They can confine bound electron-hole pairs, excitons, in all three spatial dimensions giving them discrete optical emission energies, much like the electronic states in atomic systems. The semiconductor nature of the system allows quantum dots to be integrated into complicated device structures including optical cavities [1] and electrical injection [2]. The radiative exciton emission from a semiconductor quantum dot can provide the simplest form of quantum light, a single photon source [2]. The finite re-excitation time following the radiative decay of an exciton in a quantum dot prevents the dot from emitting more than one photon if excited with a short optical or electronic pulse. In a similar fashion excitation of the biexciton state, consisting of two electrons and holes, in the quantum dot results in the emission of a pair of photons at the energy of the biexciton and exciton transitions. The biexciton state was, in fact, proposed as a possible source of polarisation-entangled photons in 2000 by Benson et al. [3] as it consists of two polarisation-correlated decay paths which could potentially be indistinguishable. The condition of indistinguishability is fundamental to the generation of entangled photons and is, in general, not true of the two decay paths from the biexciton state in a quantum dot; physical anisotropy causes the intermediate exciton states to hybridise and separate in energy providing ‘which-path’ information about the route taken through the biexciton decay. We demonstrate how the splitting between the intermediate exciton states in a single InAs quantum dot can be controlled by growth [4], rapid thermal annealing [5] and the application of an external magnetic field [6]. Each of these three techniques can be used to make the intermediate exciton states degenerate allowing the biexciton decay to produce singe pairs of entangled photons triggered by short laser pulses [7,8]. Entangled photon pair sources are essential for applications such as entanglement based quantum key distribution, and optical quantum computing. For these applications it is important that no more than one entangled photon pair is generated in a cycle, a requirement met by our quantum dot source which is not possible with traditional methods for generating entangled pairs of photons. Entanglement also enables quantum interferometry and metrology, the basis of image resolution beyond that possible with equivalent classical light. Biphoton interferometry using entangled emission from the biexciton decay reveals fringes with half the period of classical light [9], and less that that of the laser. In addition, interferometry suggests that this type of entangled light source is not limited by decoherence, we fine the biphoton is surprising robust against dephasing, in stark contrast to the devastating effect of decoherence upon single photons emitted by similar structures.
Semiconductor quantum dots tightly confine excited electron-hole pairs, called excitons, resulting in discrete energy levels similar to those of single atoms. Transition energies in the visible or near-infrared make quantum dots suitable for many applications in quantum optics and quantum information science, but to take advantage of all the properties of quantum dot emission, it is necessary to excite them coherently which has been a great challenge due to background scattering of the excitation laser. This dissertation presents the first coherent control of a single quantum dot with observation of its resonance fluorescence and decoherence phenomena. Strong continuous-wave excitation causes the dot to undergo several Rabi oscillations before emitting. These are visible as oscillations in the first- and second-order correlation functions of the emission, and the quantum dot states are "dressed", resulting in a Mollow triplet in the emission spectrum. Some resonantly excited dots, in addition to resonance fluorescence, also emit light from excited states several meV higher in energy. Such up-conversion fits existing theories of decoherence but has never been directly observed before. The up-conversion intensity is shown to be described well by a fairly simple three-level model with single-phonon absorption. The coherent phenomena of resonance fluorescence and the decoherence due to up-conversion paint a dual picture of single quantum dots wherein they can sometimes be treated as an ideal two-level system, but their interactions with the host crystal can lead to many complex behaviors.
Currently there is strong interest in realizing implementations of quantum computation and quantum cryptography in a solid state environment. One of the systems that are actively studied are semiconductor quantum dots (QDs). Due to their discrete energy level structure, they are often called artificial atoms, and they attract immediately interest of quantum information science since they allow to mimic the design developed for atomic physics systems such as ions in traps or atoms in cavities. However, despite of the similarities, one has to keep in main that any elementary excitation in a QD has a generic many-body character. An essential building block of a quantum processor is a quantum gate which entangles the states of two quantum bits. Recently it has been proposed that a pair of vertically aligned QDs could be used as an optically driven quantum gate: The quantum bits are individual carriers either on dot zero or dot one. The different dot indices play the same role as a "spin," therefore we term them "isospin." Quantum mechanical tunneling between the dots rotates the "isospin" and leads to superposition of two quantum dot states. The quantum gate is built when two different particles, an electron and a hole, are created optically. The two particles form entangled isospin states. The entanglement can be controlled by application of an electric field along the heterostructure growth direction. Here we present spectroscopic studies on single quantum dot molecules (QDMs) with different vertical separation between the dots that support the feasibility of this proposal. The comparison of the evolution of the excitonic recombination spectrum with the results of calculations allows us to demonstrate coherent tunneling of electrons and holes across the separating barrier and the formation of entangled exciton states. For a given barrier width, we find only small variations of the tunneling induced splitting between the entangled states demonstrating a good homogeneity within the obtained QDM ensembles.