Single-electron transistor spectroscopy of InGaAs self-assembled quantum dots

A single-electron transistor (SET) is used to detect tunneling of single electrons into individual InGaAs self-assembled quantum dots (QDs). By using an SET with a small island area and growing QDs with a low density we are able to distinguish and measure three QDs. The bias voltage at which resonant tunneling into the dots occurs can be shifted using a surface gate electrode. From the applied voltages at which we observe electrons tunneling, we are able to measure the electron addition energies of three QDs.     

Optical control of coherent interactions between electron spins in InGaAs quantum dots

Coherent interactions between spins in quantum dots are a key requirement for quantum gates. We have performed pump-probe experiments in which pulsed lasers emitting at different photon energies manipulate two distinct subsets of electron spins within an inhomogeneous InGaAs quantum dot ensemble. The spin dynamics are monitored through their precession about an external magnetic field. These measurements demonstrate spin precession phase shifts and modulations of the magnitude of one subset of oriented spins after optical orientation of the second subset. The observations are consistent with results from a model using a Heisenberg-like interaction with μeV strength.     

Exciton fine structure splitting of single InGaAs self-assembled quantum dots

We show how the resonant absorption of the ground state neutral exciton confined in a single InGaAs self-assembled quantum dot can be directly observed in an optical transmission experiment. A spectrum of the differential transmitted intensity is obtained by sweeping the exciton energy into resonance with laser photons exploiting the voltage induced Stark-shift. We describe the details of this experimental technique and some example results which exploit the 1 μeV spectral resolution. In addition to the fine structure splitting of the neutral exciton and an upper bound on the homogeneous linewidth at 4.2 K, we also determine the transition electric dipole moment.     

Coherent dynamics in InGaAs quantum dots and quantum dot molecules

We measure the dephasing time of the exciton ground state transition in InGaAs quantum dots (QD) and quantum dot molecules (QDM) using a sensitive four-wave mixing technique. In the QDs we find experimental evidence that the dephasing time is given only by the radiative lifetime at low temperatures. We demonstrate the tunability of the radiatively limited dephasing time from 400 ps up to 2 ns in a series of annealed QDs with increasing energy separation of 69–330 meV from the wetting layer continuum. Furthermore, the distribution of the fine-structure splitting δ₁ and of the biexciton binding energy δ_B is measured. δ₁ decreases from 96 to with increasing annealing temperature, indicating an improving circular symmetry of the in-plane confinement potential. The biexciton binding energy shows only a weak dependence on the confinement energy, which we attribute to a compensation between decreasing confinement and decreasing separation of electron and hole. In the QDM we measured the exciton dephasing as function of interdot barrier thickness in the temperature range from 5 to 60 K. At 5 K dephasing times of several hundred picoseconds are found. Moreover, a systematic dependence of the dephasing dynamics on the barrier thickness is observed, showing how the quantum mechanical coupling in the molecules affects the exciton lifetime and acoustic-phonon interaction.     

Excitonic energy shell structure of self-assembled InGaAs/GaAs quantum dots

Performing optical spectroscopy of highly homogeneous quantum dot arrays in ultrahigh magnetic fields, an unprecedently well resolved Fock-Darwin spectrum is observed. The existence of up to four degenerate electronic shells is demonstrated where the magnetic field lifts the initial degeneracies, which reappear when levels with different angular momenta come into resonance. The resulting level shifting and crossing pattern also show evidence of many-body effects such as the mixing of configurations and exciton condensation at the resonances.     

Generating entanglement and squeezed states of nuclear spins in quantum dots

We present a scheme for achieving coherent spin squeezing of nuclear spin states in semiconductor quantum dots. The nuclear polarization dependence of the electron spin resonance generates a unitary evolution that drives nuclear spins into a collective entangled state. The polarization dependence of the resonance generates an area-preserving, twisting dynamics that squeezes and stretches the nuclear spin Wigner distribution without the need for nuclear spin flips. Our estimates of squeezing times indicate that the entanglement threshold can be reached in current experiments.     

Electrically driven reverse overhauser pumping of nuclear spins in quantum dots

We propose a new mechanism for polarizing nuclear spins in quantum dots, based on periodic modulation of the hyperfine coupling by electric driving at the electron spin resonance frequency. Dynamical nuclear polarization results from resonant excitation rather than hyperfine relaxation mediated by a thermal bath, and thus is not subject to Overhauser-like detailed balance constraints. This allows polarization in the direction opposite to that expected from the Overhauser effect. Competition of the electrically driven and bath-assisted mechanisms can give rise to spatial modulation and sign reversal of polarization on a scale smaller than the electron confinement radius in the dot.     

Self-polarization and dynamical cooling of nuclear spins in double quantum dots

The spin-blockade regime of double quantum dots features coupled dynamics of electron and nuclear spins resulting from the hyperfine interaction. We explain observed nuclear self-polarization via a mechanism based on feedback of the Overhauser shift on electron energy levels, and propose to use the instability toward self-polarization as a vehicle for controlling the nuclear spin distribution. In the dynamics induced by a properly chosen time-dependent magnetic field, nuclear spin fluctuations can be suppressed significantly below the thermal level.     

Microscopic approach to many-exciton complexes in self-assembled InGaAs/GaAs quantum dots

We present a numerical calculation of many-exciton complexes in self-assembled InAs/GaAs quantum dots. We apply continuum elasticity theory and atomistic valence-force-field method to calculate strain distribution, and make use of various methods, ranging from a quasi-atomistic tight-binding approach to the single-band effective-mass approximation, to obtain single-particle energy levels. The effect of strain is incorporated by the deformation potential theory. We expand multiexciton states in the basis of Slater determinants and solve the many-body problem by the configuration-interaction method. The dynamics of multiexcitons is studied by solving the rate equations, from which the excitation–power dependence of emission spectrum is obtained. The emission spectra calculated by the microscopic tight-binding approach are found to be in good agreement with those obtained by the simple effective-mass method.     

State-filling and magneto-photoluminescence of excited states in InGaAs/GaAs self-assembled quantum dots

We present the first radiative lifetime measurements and magneto-photoluminescence results of excited states in InGaAs/GaAs semiconductor self-assembled quantum dots. By increasing the photo-excitation intensity, excited state interband transitions up ton= 5 can be observed in the emission spectrum. The dynamics of the interband transitions and the inter-sublevel relaxation in these zero-dimensional energy levels lead to state-filling of the lower-energy states, allowing the quasi-Fermi level to be raised by more than 200 meV due to the combined large inter-sublevel spacing and the low density of states. The decay time of each energy level obtained under various excitation conditions is used to evaluate the inter-sublevel thermalization time. Finally, the emission spectrum of the dots filled with an average of about eight excitons is measured in magnetic fields up to 13 Tesla. The dependences of the spectrum as a function of carrier density and magnetic field are compared to calculations and interpreted in terms of coherent many-exciton states and their destruction by the magnetic field.     

具有InAlAs浸润层的InGaAs量子点的制备和特性研究

采用自组装方法生长了一种新型的InGaAs量子点/InAlAs浸润层结构.通过选取合适的In组分 ，使InAlAs浸润层的能级与GaAs势垒相当，从而使浸润层的量子阱特征消失.通过低温光致 发光（PL）谱的测试分析得到InGaAs量子点/InAlAs浸润层在样品中的确切位置.变温PL谱的 研究显示，具有这种结构的量子点发光峰的半高全宽随温度上升出现展宽，这明显区别于普 通InGaAs量子点半高全宽变窄的行为.这是因为采用了InAlAs浸润层后，不仅增强了对InGaA s量子点的限制作用，同时切断了载流子的 关键词： InGaAs量子点 InAlAs浸润层 PL谱     

Electron dynamics in modulation p-doped InGaAs/GaAs quantum dots

We investigate the electron dynamics of p-type modulation doped and undoped InGaAs/GaAs quantum dots using up-conversion photoluminescence at low temperature and room temperature. The rise time of the p-doped sample is significantly shorter than that of the undoped at low temperature. With increasing to room temperature the undoped sample exhibits a decreased rise time whilst that of the doped sample does not change. A relaxation mechanism of electron-hole scattering is proposed in which the doped quantum dots exhibit an enhanced and temperature independent relaxation due to excess built-in holes in the valence band of the quantum dots. In contrast, the rise time of the undoped quantum dots decreases significantly at room temperature due to the large availability of holes in the ground state of the valence band. Furthermore, modulation p-doping results in a shorter lifetime due to the presence of excess defects.     

Voltage-selective bidirectional polarization and coherent rotation of nuclear spins in quantum dots

We propose and demonstrate that the nuclear spins of the host lattice in GaAs double quantum dots can be polarized in either of two opposite directions, parallel or antiparallel to an external magnetic field. The direction is selected by adjusting the dc voltage. This nuclear polarization manifests itself by repeated controlled electron-nuclear spin scattering in the Pauli spin-blockade state. Polarized nuclei are also controlled by means of nuclear magnetic resonance. This Letter confirms that the nuclear spins in quantum dots are long-lived quantum states with a coherence time of up to 1 ms, and may be a promising resource for quantum-information processing such as quantum memories for electron spin qubits.     

Polaron relaxation dynamics in InAs/GaAs self-assembled quantum dots

Polaron decay in n-type InAs quantum dots has been investigated using energy dependent, mid-infrared pump–probe spectroscopy. By studying samples with differing ground state to first excited state energy separations the relaxation time has been measured between 40 and 60 meV. The low-temperature decay time increases with increasing detuning between the pump energy and the optical phonon energy and is maximum (55 ps) at 56 meV. From the experimentally determined decay times we are able to extract a low-temperature optical phonon lifetime of 13 ps for InAs QDs. We find that the polaron decay time decreases by a factor of 2 at room temperature due to the reduction of the optical phonon lifetime.     

Size-dependent carrier dynamics in self-assembled CdTe/ZnTe quantum dots

We investigate size-dependent carrier dynamics in self-assembled CdTe/ZnTe quantum dots (QDs) grown using molecular beam epitaxy and atomic layer epitaxy. Photoluminescence (PL) spectra show that the excitonic peak corresponding to transitions from the ground electronic subband to ground heavy-hole band in CdTe/ZnTe QDs shifts to a lower energy with increasing ZnTe buffer thicknesses. This shift of the PL peak can be attributed to size variation of the CdTe QDs. In particular, carrier dynamics in CdTe QDs grown on various ZnTe buffer layer thicknesses is studied using time-resolved PL measurements. As a result, the decay time of CdTe QDs is shown to increase with increasing ZnTe buffer layer thicknesses due to the reduction of the exciton oscillator strength in the larger QDs.     

Dynamics of nuclear polarization in InGaAs quantum dots in a transverse magnetic field

The time-resolved Hanle effect is examined for negatively charged InGaAs/GaAs quantum dots. Experimental data are analyzed by using an original approach to separate behavior of the longitudinal and transverse components of nuclear polarization. This made it possible to determine the rise and decay times of each component of nuclear polarization and their dependence on transverse magnetic field strength. The rise and decay times of the longitudinal component of nuclear polarization (parallel to the applied field) were found to be almost equal (approximately 5 ms). An analysis of the transverse component of nuclear polarization shows that the corresponding rise and decay times differ widely and strongly depend on magnetic field strength, increasing from a few to tens of milliseconds with an applied field between 20 and 100 mT. Current phenomenological models fail to explain the observed behavior of nuclear polarization. To find an explanation, an adequate theory of spin dynamics should be developed for the nuclear spin system of a quantum dot under conditions of strong quadrupole splitting.     

Cracking self-assembled InAs quantum dots

We present a cross-sectional scanning tunneling microscopy (X-STM) investigation of InAs quantum dots in a GaAs matrix. The structures were grown by molecular beam epitaxy (MBE) at a low growth rate of 0.01 ML/s and consist of five layers of uncoupled quantum dot structures. Detailed STM images with atomic resolution show that the dots consist of an InGaAs alloy and that the indium content in the dot increases towards the top. The analysis of the height versus base-length relation obtained from cross-sectional images of the dots shows that the shape of the dots resembles that of a truncated pyramid and that the square base is oriented along the [010] and [100] directions. Using scanning tunneling spectroscopy (STS) we determined the onset for electron tunneling into the conduction and out of the valence band, both in the quantum dots and in the surrounding GaAs matrix. We found equal voltages for tunneling out of the valence band in GaAs or InGaAs whereas tunneling into GaAs occurred at higher voltages than in InGaAs.     

Intersublevel transitions in self-assembled quantum dots

Intersublevel transitions in semiconductor quantum dots are transitions of a charge carrier between quantum dot confined states. In InAs/GaAs self-assembled quantum dots, optically active intersublevel transitions occur in the mid-infrared spectral range. These transitions can provide a new insight on the physics of semiconductor quantum dots and offer new opportunities to develop mid-infrared devices. A key feature characterizing intersublevel transitions is the coupling of the confined carriers to phonons. We show that the effect of the strong coupling regime for the electron–optical phonon interaction and the formation of mixed electron–phonon quasi-particles called polarons drastically affect and control the dynamical properties of quantum dots. The engineering of quantum dot relaxation rates through phonon coupling opens the route to the realization of new devices like mid-infrared polaron lasers. We finally show that the measurement of intersublevel absorption is not limited to quantum dot ensembles and that the intersublevel ultrasmall absorption of a single quantum dot can be measured with a nanometer scale resolution by using phonon emission as a signature of the absorption. To cite this article: P. Boucaud et al., C. R. Physique 9 (2008).