We show that by illuminating an InGaAs/GaAs self-assembled quantum dot with circularly polarized light, the nuclei of atoms constituting the dot can be driven into a bistable regime, in which either a threshold-like enhancement or reduction of the local nuclear field by up to 3 Tesla can be generated by varying the intensity of light. The excitation power threshold for such a nuclear spin "switch" is found to depend on both external magnetic and electric fields. The switch is shown to arise from the strong feedback of the nuclear spin polarization on the dynamics of spin transfer from electrons to the nuclei of the dot.The hyperfine interaction in solids [1] arises from the coupling between the magnetic dipole moments of nuclear and electron spins. It produces two dynamical effects: (i) inelastic relaxation of electron spin via the "flip-flop" process ( Fig.1a) and (ii) the Overhauser shift of the electron energy [2]. Recently, the hyperfine interaction in semiconductor quantum dots (QDs) has attracted close attention [3,4,5,6,7,8,9,10,11,12,13,14] fuelled by proposals for QD implementation in quantum information applications [15]. The full quantization of the electron states in QDs is beneficial for removing decoherence mechanisms present in extended systems [16,17]. However, the electron localization results in a stronger (than in a bulk material) overlap of its wave-function with a large number of nuclei (N ∼ 10 4 in small selfassembled InGaAs/GaAs dots and up to 10 5 ÷ 10 6 in electrostatically-defined GaAs QDs), and the resulting hyperfine interaction with nuclear spins has been found to dominate the decoherence [3,4,5,12,13,14] and life-time [9] of the electron spin at low temperatures.In this Letter, we report the observation of a pronounced bistable behaviour of nuclear spin polarisation, S, in optically pumped self-assembled InGaAs/GaAs dots. In our experiments, spin-polarized electrons are introduced one-by-one into an individual InGaAs dot at a rate w x (see Fig.1b) by the circularly polarized optical excitation of electron-hole pairs 120 meV above the lowest QD energy states. Due to hole spin-flip during its energy relaxation, both bright and dark excitons can form in the dot ground state. The former will quickly recombine radiatively with a rate w rec ≈ 10 9 sec −1 , whereas the dark exciton can recombine with simultaneous spin transfer to a nucleus via a spin "flip-flop" process (as in Fig.1a) at the rate w rec N p hf [12,18]. Here N is the number of nuclei interacting with the electron and p hf is the probability of a "flip-flop" process, which from our perturbation theory treatment is given by:(1) Here γ is the exciton life-time broadening, h hf is the strength of the hyperfine interaction of the electron with a single nucleus and E eZ is the electron Zeeman splitting. E eZ is strongly dependent on the effective nuclear magnetic field B N generated by the nuclei. This provides a feedback mechanism between the spin transfer rate and the degree of nuclear polarization (B N ∝ S) in the dot [19]. Th...
Efficient infrared light emitters integrated on the mature Si technology platform could lead to on-chip optical interconnects as deemed necessary for future generations of ultrafast processors as well as to nanoanalytical functionality. Toward this goal, we demonstrate the use of GaAs-based nanowires as building blocks for the emission of light with micrometer wavelength that are monolithically integrated on Si substrates. Free-standing (In,Ga)As/GaAs coaxial multishell nanowires were grown catalyst-free on Si(111) by molecular beam epitaxy. The emission properties of single radial quantum wells were studied by cathodoluminescence spectroscopy and correlated with the growth kinetics. Controlling the surface diffusivity of In adatoms along the NW side-walls, we improved the spatial homogeneity of the chemical composition along the nanowire axis and thus obtained a narrow emission spectrum. Finally, we fabricated a light-emitting diode consisting of approximately 10(5) nanowires contacted in parallel through the Si substrate. Room-temperature electroluminescence at 985 nm was demonstrated, proving the great potential of this technology.
We report direct evidence for the control of the oscillator strength of the exciton state in a single quantum dot by the application of a vertical electric field. This is achieved through the study of the radiative lifetime of a single InGaN-GaN quantum dot in a p-i-n diode structure. Our results are in good quantitative agreement with theoretical predictions from an atomistic tight-binding model. Furthermore, the increase of the overlap between the electron and hole wave functions due to the applied field is shown experimentally to increase the attractive Coulomb interaction leading to a change in the sign of the biexcitonic binding energy.
The authors report on the generation of single photons in the blue spectral region from a single InGaN∕GaN quantum dot. The collection efficiency was enhanced by embedding the quantum dot layer in the middle of a low-Q microcavity. The microphotoluminescence is observed to be approximately ten times stronger than typical InGaN quantum dot emission without a cavity. The measurements were performed using nonlinear excitation spectroscopy in order to suppress the background emission from the underlying wetting layer.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.