Rinaldo Trotta

Nanomembrane Quantum‐Light‐Emitting Diodes Integrated onto Piezoelectric Actuators

We integrate resonant-cavity light-emitting diodes containing quantum dots onto substrates with giant piezoelectric response. Via strain, the energy of the photons emitted by the diode can be precisely controlled during electrical injection over a spectral range larger than 20 meV. Simultaneously, the exciton fine-structure-splitting and the biexciton binding energy can be tuned to the values required for entangled photon generation.

Highly Entangled Photons from Hybrid Piezoelectric-Semiconductor Quantum Dot Devices

Entanglement resources are key ingredients of future quantum technologies. If they could be efficiently integrated into a semiconductor platform, a new generation of devices could be envisioned, whose quantum-mechanical functionalities are controlled via the mature semiconductor technology. Epitaxial quantum dots (QDs) embedded in diodes would embody such ideal quantum devices, but a fine-structure splitting (FSS) between the bright exciton states lowers dramatically the degree of entanglement of the sources and hampers severely their real exploitation in the foreseen applications. In this work, we overcome this hurdle using strain-tunable optoelectronic devices, where any QD can be tuned for the emission of photon pairs featuring the highest degree of entanglement ever reported for QDs, with concurrence as high as 0.75 ± 0.02. Furthermore, we study the evolution of Bells parameters as a function of FSS and demonstrate for the first time that filtering-free violation of Bells inequalities requires the FSS to be smaller than 1 μeV. This upper limit for the FSS also sets the tuning range of exciton energies (∼1 meV) over which our device operates as an energy-tunable source of highly entangled photons. A moderate temporal filtering further increases the concurrence and the tunability of exciton energies up to 0.82 and 2 meV, respectively, though at the expense of 60% reduction of count rate.

Hydrogen-Bonded Organic Semiconductor Micro- And Nanocrystals: From Colloidal Syntheses to (Opto-)Electronic Devices

Organic pigments such as indigos, quinacridones, and phthalocyanines are widely produced industrially as colorants for everyday products as various as cosmetics and printing inks. Herein we introduce a general procedure to transform commercially available insoluble microcrystalline pigment powders into colloidal solutions of variously sized and shaped semiconductor micro- and nanocrystals. The synthesis is based on the transformation of the pigments into soluble dyes by introducing transient protecting groups on the secondary amine moieties, followed by controlled deprotection in solution. Three deprotection methods are demonstrated: thermal cleavage, acid-catalyzed deprotection, and amine-induced deprotection. During these processes, ligands are introduced to afford colloidal stability and to provide dedicated surface functionality and for size and shape control. The resulting micro- and nanocrystals exhibit a wide range of optical absorption and photoluminescence over spectral regions from the visible to the near-infrared. Due to excellent colloidal solubility offered by the ligands, the achieved organic nanocrystals are suitable for solution processing of (opto)electronic devices. As examples, phthalocyanine nanowire transistors as well as quinacridone nanocrystal photodetectors, with photoresponsivity values by far outperforming those of vacuum deposited reference samples, are demonstrated. The high responsivity is enabled by photoinduced charge transfer between the nanocrystals and the directly attached electron-accepting vitamin B2 ligands. The semiconducting nanocrystals described here offer a cheap, nontoxic, and environmentally friendly alternative to inorganic nanocrystals as well as a new paradigm for obtaining organic semiconductor materials from commercial colorants.

High yield and ultrafast sources of electrically triggered entangled-photon pairs based on strain-tunable quantum dots

Triggered sources of entangled photons play crucial roles in almost any existing protocol of quantum information science. The possibility to generate these non-classical states of light with high speed and using electrical pulses could revolutionize the field. Entangled-light-emitting-diodes (ELEDs) based on semiconductor quantum dots (QDs) are at present the only devices that can address this task 5. However, ELEDs are plagued by a source of randomness that hampers their practical exploitation in the foreseen applications: the very low probability (~10-2) of finding QDs with sufficiently small fine-structure-splitting for entangled-photon-generation. Here, we overcome this hurdle by introducing the first strain-tunable ELEDs (S-ELEDs) that exploit piezoelectric-induced strains to tune QDs for entangled-photon-generation. We demonstrate that up to 30% of the QDs in S-ELEDs emit polarization-entangled photon pairs with entanglement-fidelities as high as f+ = 0.83(5). Driven at the highest operation speed of 400 MHz ever reported so far, S-ELEDs emerge as unique devices for high-data rate entangled-photon applications.Triggered sources of entangled photon pairs are key components in most quantum communication protocols. For practical quantum applications, electrical triggering would allow the realization of compact and deterministic sources of entangled photons. Entangled-light-emitting-diodes based on semiconductor quantum dots are among the most promising sources that can potentially address this task. However, entangled-light-emitting-diodes are plagued by a source of randomness, which results in a very low probability of finding quantum dots with sufficiently small fine structure splitting for entangled-photon generation (∼10−2). Here we introduce strain-tunable entangled-light-emitting-diodes that exploit piezoelectric-induced strains to tune quantum dots for entangled-photon generation. We demonstrate that up to 30% of the quantum dots in strain-tunable entangled-light-emitting-diodes emit polarization-entangled photons. An entanglement fidelity as high as 0.83 is achieved with fast temporal post selection. Driven at high speed, that is 400 MHz, strain-tunable entangled-light-emitting-diodes emerge as promising devices for high data-rate quantum applications.

Wavelength-tunable sources of entangled photons interfaced with atomic vapours

The prospect of using the quantum nature of light for secure communication keeps spurring the search and investigation of suitable sources of entangled photons. A single semiconductor quantum dot is one of the most attractive, as it can generate indistinguishable entangled photons deterministically and is compatible with current photonic-integration technologies. However, the lack of control over the energy of the entangled photons is hampering the exploitation of dissimilar quantum dots in protocols requiring the teleportation of quantum entanglement over remote locations. Here we introduce quantum dot-based sources of polarization-entangled photons whose energy can be tuned via three-directional strain engineering without degrading the degree of entanglement of the photon pairs. As a test-bench for quantum communication, we interface quantum dots with clouds of atomic vapours, and we demonstrate slow-entangled photons from a single quantum emitter. These results pave the way towards the implementation of hybrid quantum networks where entanglement is distributed among distant parties using optoelectronic devices.

Highly indistinguishable and strongly entangled photons from symmetric GaAs quantum dots

The development of scalable sources of non-classical light is fundamental to unlocking the technological potential of quantum photonics. Semiconductor quantum dots are emerging as near-optimal sources of indistinguishable single photons. However, their performance as sources of entangled-photon pairs are still modest compared to parametric down converters. Photons emitted from conventional Stranski–Krastanov InGaAs quantum dots have shown non-optimal levels of entanglement and indistinguishability. For quantum networks, both criteria must be met simultaneously. Here, we show that this is possible with a system that has received limited attention so far: GaAs quantum dots. They can emit triggered polarization-entangled photons with high purity (g(2)(0) = 0.002±0.002), high indistinguishability (0.93±0.07 for 2 ns pulse separation) and high entanglement fidelity (0.94±0.01). Our results show that GaAs might be the material of choice for quantum-dot entanglement sources in future quantum technologies.

Photoreflectance and reflectance investigation of deuterium-irradiated GaAsN

The effect of deuterium irradiation on the optical and strain properties of GaAsN∕GaAs heterostructures was investigated by photoreflectance and reflectance techniques. The strain occurring in as-grown and deuterated GaAsN layers is monitored and measured by means of photoreflectance spectroscopy, highlighting the strain inversion after irradiation. By combining static and modulated reflectance results, evidence is given that the deuterium-induced recovery of the GaAs band gap as well as the strain inversion in GaAsN layers are accompanied by a 0.4%–0.8% reduction of the refractive index in the 1.31 and 1.55μm spectral windows of interest for fiber optic communications. These results anticipate a single step process to an in-plane confinement of carriers and photons.

Strain-induced tuning of the emission wavelength of high quality GaAs/AlGaAs quantum dots in the spectral range of the 87Rb D2 lines

Reversible biaxial strains are used for tuning the emission wavelengths of high quality GaAs/AlGaAs quantum dots (QDs) in the spectral range of the 87Rb D2 lines. The strain is transferred by integrating free standing (Al)GaAs nanomembranes, containing QDs, onto piezoelectric actuators. Narrow excitonic emission lines as sharp as 25 μeV are shown, and a tuning range larger than 5 nm is demonstrated. This range corresponds to an induced anisotropic biaxial strain of the order of 0.15%, as evaluated from the shift in the emission of the GaAs from the nanomembranes. The presented on-chip technology is potentially interesting for future quantum memories based on hybrid semiconductor-atomic interfaces.

Fabrication of site-controlled quantum dots by spatially selective incorporation of hydrogen in ga(asn)/gaas heterostructures

Full control over size, density, and positioning of semiconductor quantum dots (QDs) is desirable in numerous potential devices. This control is diffi cult to attain by bottom-up methods that rely on random self-assembly. [ 1 , 2 ] Conversely, a high number of processing and regrowth steps, a small density of nanostructures, and carrier depletion near surfaces are often drawbacks of top-down approaches. [ 3–5 ]

A Nanomembrane-Based Wavelength-Tunable High-Speed Single-Photon-Emitting Diode

We demonstrate an all-electrically operated wavelength-tunable on demand single-photon source for the first time. The device consists of a light-emitting diode in the form of a semiconductor nanomembrane containing self-assembled quantum dots integrated onto a piezoelectric crystal. Triggered single photons are generated via injection of ultrashort electrical pulses into the diode, while their energy can be precisely tuned over a broad range by varying the voltage applied to the piezoelectric crystal. High speed operation of this single-photon-emitting diode up to 0.8 GHz is demonstrated. These results represent an important step toward the realization of electrically driven sources of indistinguishable photons on demand.