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Register a new userMulti-harmonic Quantum Dot Optomechanics in fused LiNbO$_3$-(Al)GaAs hybrids
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We fabricated an acousto-optic semiconductor hybrid device for strong optomechanical coupling of individual quantum emitters and a surface acoustic wave. Our device comprises a surface acoustic wave chip made from highly piezoelectric LiNbO$_3$ and a GaAs-based semiconductor membrane with an embedded layer of quantum dots. Employing multi-harmonic transducers, we generated sound waves on LiNbO$_3$ over a wide range of radio frequencies. We monitored their coupling to and propagation across the semiconductor membrane both in the electrical and optical domain. We demonstrate enhanced optomechanical tuning of the embedded quantum dots with increasing frequencies. This effect was verified by finite element modelling of our device geometry and attributed to an increased localization of the acoustic field within the semiconductor membrane. For moderately high acoustic frequencies, our simulations predict strong optomechanical coupling making our hybrid device ideally suited for applications in semiconductor based quantum acoustics.
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A hybrid device comprising a (Al)GaAs quantum dot heterostructure and a LiNbO$_3$ surface acoustic wave resonator is fabricated by heterointegration. High acoustic quality factors $Q>4000$ are demonstrated for an operation frequency $fapprox 300$ MHz. The measured large quality factor-frequency products $Qtimes f>10^{12}$ ensures the suppression of decoherence due to thermal noise for temperatures exceeding $T>50,mathrm{K}$. Frequency and position dependent optomechanical coupling of single quantum dots and the resonator modes is observed.
The optomechanical coupling of quantum dots and flexural mechanical modes is studied in suspended nanophononic strings. The investigated devices are designed and monolithically fabricated on an (Al)GaAs heterostructure. Radio frequency elastic waves with frequencies ranging between $f$=250 MHz to 400 MHz are generated as Rayleigh surface acoustic waves on the unpatterned substrate and injected as Lamb waves in the nanophononic string. Quantum dots inside the nanophononic string exhibit a 15-fold enhanced optomechanical modulation compared to those dynamically strained by the Rayleigh surface acoustic wave. Detailed finite element simulations of the phononic mode spectrum of the nanophononic string confirm, that the observed modulation arises from valence band deformation potential coupling via shear strain. The corresponding optomechanical coupling parameter is quantified to $0.15 mathrm{meV nm^{-1}}$. This value exceeds that reported for vibrating nanorods by approximately one order of magnitude at 100 times higher frequencies. Using this value, a derive vertical displacements in the range of 10 nm is deduced from the experimentally observed modulation. The results represent an important step towards the creation of large scale optomechanical circuits interfacing single optically active quantum dots with optical and mechanical waves.
Self-organized semiconductor quantum dots represent almost ideal two-level systems, which have strong potential to applications in photonic quantum technologies. For instance, they can act as emitters in close-to-ideal quantum light sources. Coupled quantum dot systems with significantly increased functionality are potentially of even stronger interest since they can be used to host ultra-stable singlet-triplet spin qubits for efficient spin-photon interfaces and for a deterministic photonic 2D cluster-state generation. We realize an advanced quantum dot molecule (QDM) device and demonstrate excellent optical properties. The device includes electrically controllable QDMs based on stacked quantum dots in a pin-diode structure. The QDMs are deterministically integrated into a photonic structure with a circular Bragg grating using in-situ electron beam lithography. We measure a photon extraction efficiency of up to (24$pm$4)% in good agreement with numerical simulations. The coupling character of the QDMs is clearly demonstrated by bias voltage dependent spectroscopy that also controls the orbital couplings of the QDMs and their charge state in quantitative agreement with theory. The QDM devices show excellent single-photon emission properties with a multi-photon suppression of $g^{(2)}(0) = (3.9 pm 0.5) cdot 10^{-3}$. These metrics make the developed QDM devices attractive building blocks for use in future photonic quantum networks using advanced nanophotonic hardware.
Charge-transfer excitons possessing long radiative lifetime and net permanent dipole moment are highly appealing for quantum dot (QD) based energy harvesting and photodetecting devices, in which the efficiency of charge separation after photo-excitation limits the device performance. Herein, using a hybrid time-dependent density functional theory, we have demonstrated that the prevailing rule of selecting materials with staggered type-II band alignment for realization of charge-transfer exciton breaks down in epitaxially fused QD molecules. The excitonic many-body effects are found to be significant and distinct depending on the exciton nature, causing unexpected reverse ordering of exciton states. Strikingly, twisting QD molecule appears as an effective means of modulating the orbital spatial localization towards charge separation that is mandatory for a charge-transfer exciton. Meanwhile, it manifests the intra-energy-level splitting that counterbalances the distinct many-body effects felt by excitons of different nature, thus ensuring the successful generation of energetically favourable charge-transfer exciton in both homodimer and heterodimer QD molecules. Our study extends the realm of twistroincs into zero-dimensional materials, and provides a genuine route of manipulating the exciton nature in QD molecules.
A coupled quantum dot--nanocavity system in the weak coupling regime of cavity quantumelectrodynamics is dynamically tuned in and out of resonance by the coherent elastic field of a $f_{rm SAW}simeq800,mathrm{MHz}$ surface acoustic wave. When the system is brought to resonance by the sound wave, light-matter interaction is strongly increased by the Purcell effect. This leads to a precisely timed single photon emission as confirmed by the second order photon correlation function $g^{(2)}$. All relevant frequencies of our experiment are faithfully identified in the Fourier transform of $g^{(2)}$, demonstrating high fidelity regulation of the stream of single photons emitted by the system.
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