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On-demand entangled photon pairs at telecom wavelengths are crucial for quantum communication, distributed quantum computing, and quantum-enhanced sensing and metrology. The O-band is particularly advantageous because of its minimal chromatic dispersion and transmission loss in optical fibers, making it well-suited for long-distance quantum networks. Site-controlled nanowire quantum dots have emerged as a promising platform for the on-demand generation of single and entangled photons, offering high extraction efficiency and the potential for scalable fabrication in large uniform arrays. However, their operation has been largely restricted to the visible and first near-infrared (NIR-I) windows. Here, we demonstrate an on-demand bright source of entangled photon pairs with high fidelity in the telecom O-band based on site-controlled nanowire quantum dots. We measure a fine-structure splitting of 4.6 $\mu$eV, verifying the suitability of the quantum dot for generating high-fidelity polarization-entangled photon pairs. Full quantum state tomography of the two-photon state generated by the biexciton\hyph exciton cascade reveals a maximum fidelity of $85.8\% \pm 1.1\%$ to the $\Phi^+$ Bell state, and a maximum concurrence of $75.1\% \pm 2.1\%$. We estimate the source efficiency at the first lens to be 12.5$\%$. This bright, scalable, and deterministic source of entangled photons in the telecom range represents a valuable step forward in advancing practical quantum applications at telecom wavelengths.

Coherent control of single photon sources is a key requirement for the advancement of photonic quantum technologies. Among them, nanowire-based quantum dot sources are popular due to their potential for on-chip hybrid integration. Here we demonstrate on-demand single-photon generation ($g^{(2)}(0)(X^{*}) =0.078$ and $g^{(2)}(0)(X)= 0.03$) from resonantly excited InAsP/InP nanowire quantum dots and observe Rabi oscillations in the dot emission, indicating successful coherent manipulation of the excitonic states in the nanowire. We also measure a low emission time jitter for resonant excitation as compared to above-band excitation. This work addresses the long-standing challenge of resonantly exciting nanowire-quantum dots. It paves the way for hybrid quantum photonic integration, enabling spin-photon entanglement and matter memories on-chip.

Surface acoustic waves (SAWs) are a powerful tool for controlling a wide range of quantum systems, particularly quantum dots (QDs) via their oscillating strain fields. The resulting energy modulation of these single photon sources can be harnessed to achieve spectral overlap between two QDs otherwise emitting at different wavelengths. In this study, we integrate InAsP/InP nanowire quantum dots onto a thin-film lithium niobate platform, a strong piezoelectric material, and embed them within Si$_{3}$N$_{4}$-loaded waveguides. We demonstrate emission wavelength modulation of 0.70 nm at 13 dBm with a single focused interdigital transducer (FIDT) operating at 400 MHz, and achieve twice this modulation by using two FIDTs as an acoustic cavity. Additionally, we bring two QDs with an initial wavelength difference of 0.5 nm into resonance using SAWs. This scalable strain-tuning approach represents a significant step towards producing indistinguishable single photons from remote emitters heterogeneously integrated on a single photonic chip, and paves the way for large scale on-chip quantum information processing using photonic platforms.

Single photon sources operating on-demand at telecom wavelengths are required in fiber-based quantum secure communication technologies. In this work we demonstrate single photon emission from position-controlled nanowire quantum dots emitting at {\lambda} > 1530 nm. Using above-band pulsed excitation, we obtain single photon purities of g(2)(0) = 0.062. These results represent an important step towards the scalable manufacture of high efficiency, high rate single photon emitters in the telecom C-band.

Hybrid quantum technologies aim to harness the best characteristics of multiple quantum systems, in a similar fashion that classical computers combine electronic, photonic, magnetic, and mechanical components. For example, quantum dots embedded in semiconductor nanowires can produce highly pure, deterministic, and indistinguishable single-photons with high repetition, while atomic ensembles offer robust photon storage capabilities and strong optical nonlinearities that can be controlled with single-photons. However, to successfully integrate quantum dots with atomic ensembles, one needs to carefully match the optical frequencies of these two platforms. Here, we propose and experimentally demonstrate simple, precise, reversible, broad-range, and local method for controlling the emission frequency of individual quantum dots embedded in tapered semiconductor nanowires and use it to interface with an atomic ensemble via single-photons matched to hyperfine transitions and slow-light regions of the cesium D1-line. Our approach allows linking together atomic and solid-state quantum systems and can potentially also be applied to other types of nanowire-embedded solid-state emitters, as well as to creating devices based on multiple solid-state emitters tuned to produce indistinguishable photons.

We demonstrate on-chip generation of indistinguishable photons based on a nanowire quantum dot. From a growth substrate containing arrays of positioned-controlled single dot nanowires, we select a single nanowire which is placed on a SiN waveguide fabricated on a Si-based chip. Coupling of the quantum dot emission to the SiN waveguide is via the evanescent mode in the tapered nanowire. Post-selected two-photon interference visibilities using continuous wave excitation above-band and into a p-shell of the dot were 100%, consistent with a single photon source having negligible multi-photon emission probability. Visibilities over the entire photon wavepacket, measured using pulsed excitation, were reduced by a factor of 5 when exciting quasi-resonantly and by a factor of 10 for above-band excitation. The role of excitation timing jitter, spectral diffusion and pure dephasing in limiting visibilities over the temporal extent of the photon is investigated using additional measurements of the coherence and linewidth of the emitted photons.

An on-demand source of bright entangled photon pairs is desirable for quantum key distribution (QKD) and quantum repeaters. The leading candidate to generate entangled photon pairs is based on spontaneous parametric down-conversion (SPDC) in a non-linear crystal. However, there exists a fundamental trade-off between entanglement fidelity and efficiency in SPDC sources due to multiphoton emission at high brightness, which limits the pair extraction efficiency to 0.1% when operating at near-unity fidelity. Quantum dots in photonic nanostructures can in principle overcome this trade-off; however, the quantum dots that have achieved entanglement fidelities on par with SPDC sources (99%) have poor pair extraction efficiencies of 0.01%. Here, we demonstrate a 65-fold increase in the pair extraction efficiency compared to quantum dots with equivalent peak fidelity from an InAsP quantum dot in a photonic nanowire waveguide. We measure a raw peak concurrence and fidelity of 95.3% $\pm$ 0.5% and 97.5% $\pm$ 0.8%, respectively. Finally, we show that an oscillating two-photon Bell state generated by a semiconductor quantum dot can be utilized to establish a secure key for QKD, alleviating the need to remove the quantum dot energy splitting of the intermediate exciton states in the biexciton-exciton cascade., Comment: 24 pages (7 main body, excluding references plus 14 supplemental information) and 4 main body figures

Quantum physics phenomena, entanglement and coherence, are crucial for quantum information protocols, but understanding these in systems with more than two parts is challenging due to increasing complexity. The W state, a multipartite entangled state, is notable for its robustness and benefits in quantum communication. Here, we generate an 8-mode on-demand single photon W states, using nanowire quantum dots and a silicon nitride photonic chip. We demonstrate a reliable, scalable technique for reconstructing W-state in photonic circuits using Fourier and real-space imaging, supported by the Gerchberg-Saxton phase retrieval algorithm. Additionally, we utilize an entanglement witness to distinguish between mixed and entangled states, thereby affirming the entangled nature of our generated state. The study provides a new imaging approach of assessing multipartite entanglement in W-states, paving the way for further progress in image processing and Fourier-space analysis techniques for complex quantum systems.

The integration of on-demand single photon sources in photonic circuits is a major prerequisite for on-chip quantum applications. Among the various high-quality sources, nanowire quantum dots can be efficiently coupled to optical waveguides because of their preferred emission direction along their growth direction. However, local tuning of the emission properties remains challenging. In this work, we transfer a nanowire quantum dot on a bulk lithium niobate substrate and show that its emission can be dynamically tuned by acousto-optical coupling with surface acoustic waves. The purity of the single photon source is preserved during the strain modulation. We further demonstrate that the transduction is maintained even with a SiO2 encapsulation layer deposited on top of the nanowire acting as the cladding of a photonic circuit. Based on these experimental findings and numerical simulations, we introduce a device architecture consisting of a nanowire quantum dot efficiently coupled to a thin film lithium niobate rib waveguide and strain-tunable by surface acoustic waves.

Single photon emitters are a key component for enabling the practical use of quantum key distribution protocols for secure communications. For long-haul optical networks it is imperative to use photons at wavelengths that are compatible with standard single mode fibers: 1.31 {\mu}m and 1.55 {\mu}m. We demonstrate high purity single photon emission at 1.31 {\mu}m using deterministically positioned InP photonic waveguide nanowires containing single InAsP quantum dot-in-a-rod structures. At 4 K the detected count rate in fiber was 1.9 Mcps under above-band pulsed laser excitation at 80 MHz corresponding to a single photon collection efficiency at the first lens of 25%. At this count rate, the probability of multiphoton emission is g(2)(0) = 0.021. We have also evaluated the performance of the source as a function of temperature. Multiphoton emission probability increases with temperature with values of 0.11, 0.34 and 0.57 at 77 K, 220 K and 300 K, respectively, which is attributed to an overlap of temperature-broadened excitonic emission lines. These results are a promising step towards scalably fabricating telecom single photon emitters that operate under relaxed cooling requirements.

We demonstrate that, even when employing above-band excitation, photons emitted from semiconductor quantum dots can have linewidths that approach their transform-limited values. This is accomplished by using quantum dots embedded in bottom-up photonic nanowires, an approach which mitigates several potential mechanisms that can result in linewidth broadening: (i) only a single quantum dot is present in each device, (ii) dot nucleation proceeds without the formation of a wetting layer, and (iii) the sidewalls of the photonic nanowire are comprised not of etched facets, but of epitaxially grown crystal planes. Using these structures we achieve linewidths of 2x the transform limit, unprecedented for above-band excitation. We also demonstrate a highly nonlinear dependence of the linewidth on both excitation power and temperature which can be described by an independent Boson model that considers both deformation and piezoelectric exciton-phonon coupling. We find that for sufficiently low excitation powers and temperatures, the observed excess broadening is not dominated by phonon dephasing, a surprising result considering the high phonon occupation that occurs with above-band excitation.

Achieving atomic resolution is the ultimate limit of magnetic resonance imaging (MRI), and attaining this capability offers enormous technological and scientific opportunities, from drug development to understanding the dynamics in interacting quantum systems. In this work, we present a new approach to nanoMRI utilizing nuclear magnetic resonance diffraction (NMRd) -- a method that extends NMR imaging to probe the structure of periodic spin systems. The realization of NMRd on the atomic scale would create a powerful new methodology for materials characterization utilizing the spectroscopic capabilities of NMR. We describe two experiments that realize NMRd measurement of $^{31}$P spins in an indium-phosphide (InP) nanowire with sub-\r{A}ngstrom precision. In the first experiment, we encode a nanometer-scale spatial modulation of the $z$-axis magnetization by periodically inverting the $^{31}$P spins, and detect the period and position of the modulation with a precision of $<0.8$ \r{A}. In the second experiment, we demonstrate an interferometric technique, utilizing NMRd, for detecting an \r{A}ngstrom-scale displacement of the InP sample with a precision of 0.07 \r{A}. The diffraction-based techniques developed in this work represent new measurement modalities in NMR for probing the structure and dynamics of spins on sub-\r{A}ngstrom length scales, and demonstrate the feasibility of crystallographic MRI measurements., Comment: Main text: 11 pages, 8 figures; supplemental material: 20 pages, 15 figures

We report on a platform for the production of single photon devices with a fabrication yield of 100%. The sources are based on InAsP quantum dots embedded within position-controlled bottom-up InP nanowires. Using optimized growth conditions, we produce large arrays of structures having highly uniform geometries. Collection efficiencies are as high as 83% and multiphoton emission probabilities as low as 0.6% with the distribution away from optimal values associated with the excitation of other charge complexes and re-excitation processes, respectively, inherent to the above-band excitation employed. Importantly, emission peak lineshapes have Lorentzian profiles indicating that linewidths are not limited by inhomogeneous broadening but rather pure dephasing, likely elastic carrier-phonon scattering due to a high phonon occupation. This work establishes nanowire-based devices as a viable route for the scalable fabrication of efficient single photon sources and provides a valuable resource for hybrid on-chip platforms currently being developed., Comment: 9 pages, 5 figures

We present a compact, fibre-coupled single photon source using gradient-index (GRIN) lenses and an InAsP semiconductor quantum dot embedded within an InP photonic nanowire waveguide. A GRIN lens assembly is used to collect photons close to the tip of the nanowire, coupling the light immediately into a single mode optical fibre. The system provides a stable, high brightness source of fibre-coupled single photons. Using pulsed excitation, we demonstrate on-demand operation with a single photon purity of 98.5% when exciting at saturation in a device with a source-fibre collection efficiency of 35% and an overall single photon collection efficiency of 10%. We also demonstrate "plug and play" operation using room temperature photoluminescence from the InP nanowire for room temperature alignment.

We study experimentally and theoretically the in-plane magnetic field dependence of the coupling between dots forming a vertically stacked double dot molecule. The InAsP molecule is grown epitaxially in an InP nanowire and interrogated optically at millikelvin temperatures. The strength of interdot tunneling, leading to the formation of the bonding-antibonding pair of molecular orbitals, is investigated by adjusting the sample geometry. For specific geometries, we show that the interdot coupling can be controlled in-situ using a magnetic field-mediated redistribution of interdot coupling strengths. This is an important milestone in the development of qubits required in future quantum information technologies., Comment: 5 pages, 3 figures

Resonant excitation of the biexciton state in an InAsP quantum dot by a phase-coherent pair of picosecond pulses allows preparing time-bin entangled pairs of photons via the biexciton-exciton cascade. We show that this scheme can be implemented for a dot embedded in an InP nanowire. The underlying physical mechanisms can be represented and quantitatively analyzed by an effective three-level open system master equation. Simulation parameters including decay and intensity dependent dephasing rates are extracted from experimental data, which in turn let us predict the resulting entanglement and optimal operating conditions.

Global quantum secure communication can be achieved using quantum key distribution (QKD) with orbiting satellites. Established techniques use attenuated lasers as weak coherent pulse (WCP) sources, with so-called decoy-state protocols, to generate the required single-photon-level pulses. While such approaches are elegant, they come at the expense of attainable final key due to inherent multi-photon emission, thereby constraining secure key generation over the high-loss, noisy channels expected for satellite transmissions. In this work we improve on this limitation by using true single-photon pulses generated from a semiconductor quantum dot (QD) embedded in a nanowire, possessing low multi-photon emission ($<10^{-6}$) and an extraction system efficiency of -15 dB (or 3.1%). Despite the limited efficiency, the key generated by the QD source is greater than that generated by a WCP source under identical repetition rate and link conditions representative of a satellite pass. We predict that with realistic improvements of the QD extraction efficiency to -4.0 dB (or 40%), the quantum-dot QKD protocol outperforms WCP-decoy-state QKD by almost an order of magnitude. Consequently, a QD source could allow generation of a secure key in conditions where a WCP source would simply fail, such as in the case of high channel losses. Our demonstration is the first specific use case that shows a clear benefit for QD-based single-photon sources in secure quantum communication, and has the potential to enhance the viability and efficiency of satellite-based QKD networks., Comment: 6 pages, 5 figures

Adiabatic operations are powerful tools for robust quantum control in numerous fields of physics, chemistry and quantum information science. The inherent robustness due to adiabaticity can, however, be impaired in applications requiring short evolution times. We present a single versatile gradient-based optimization protocol that combines adiabatic control with effective Hamiltonian engineering in order to design adiabatic operations tailored to the specific imperfections and resources of an experimental setup. The practicality of the protocol is demonstrated by engineering a fast, 2.3 Rabi cycle-long adiabatic inversion pulse for magnetic resonance with built-in robustness to Rabi field inhomogeneities and resonance offsets. The performance and robustness of the pulse is validated in a nanoscale force-detected magnetic resonance experiment on a solid-state sample, indicating an ensemble-averaged inversion accuracy of $\sim 99.997\%$. We further showcase the utility of our protocol by providing examples of adiabatic pulses robust to spin-spin interactions, parameter-selective operations and operations connecting arbitrary states, each motivated by experiments., Comment: Main text: 14 pages, 6 figures; supplemental material: 6 pages, 2 figures

Solid-state quantum emitters are excellent sources of on-demand indistinguishable or entangled photons and can host long-lived spin memories, crucial resources for photonic quantum information applications. However, their scalability remains an outstanding challenge. Here we present a scalable technique to multiplex streams of photons from multiple independent quantum dots, on-chip, into a fiber network for use off-chip. Multiplexing is achieved by incorporating a multi-core fiber into a confocal microscope and spatially matching the multiple foci, seven in this case, to quantum dots in an array of deterministically positioned nanowires. First, we report the coherent control of the emission of biexciton-exciton cascade from a single nanowire quantum dot under resonant two-photon excitation. Then, as a proof-of-principle demonstration, we perform parallel spectroscopy on the nanowire array to identify two nearly identical quantum dots at different positions which are subsequently tuned into resonance with an external magnetic field. Multiplexing of background-free single photons from these two quantum dots is then achieved. Our approach, applicable to all types of quantum emitters, can readily be scaled up to multiplex $>100$ quantum light sources, providing a breakthrough in hardware for photonic based quantum technologies. Immediate applications include quantum communication, quantum simulation, and quantum computation., Comment: 10 pages, 4 figures

An InAs-on-InP quantum dash buried heterostructure laser and silicon chip optimized for mutual integration by direct facet-to-facet coupling have achieved -1.2 dB coupling efficiency, with coupled laser RIN of -150 dB/Hz and 152 kHz linewidth.

A broad range of scientific and industrial disciplines require precise optical measurements at very low light levels. Single-photon detectors combining high efficiency and high time resolution are pivotal in such experiments. By using relatively thick films of NbTiN (8-11\,nm) and improving the pattern fidelity of the nano-structure of the superconducting nanowire single-photon detectors (SNSPD), we fabricated devices demonstrating superior performance over all previously reported detectors in the combination of efficiency and time resolution. Our findings prove that small variations in the nanowire width, in the order of a few nanometers, can lead to a significant penalty on their temporal response. Addressing these issues, we consistently achieved high time resolution (best device 7.7\,ps, other devices $\sim$10-16\,ps) simultaneously with high system detection efficiencies ($80-90\%$) in the wavelength range of 780-1000\,nm, as well as in the telecom bands (1310-1550\,nm). The use of thicker films allowed us to fabricate large-area multi-pixel devices with homogeneous pixel performance. We first fabricated and characterized a $100\times100\, \mu m^2$ 16-pixel detector and showed there was little variation among individual pixels. Additionally, to showcase the power of our platform, we fabricated and characterized 4-pixel multimode fiber-coupled detectors and carried out photon correlation experiments on a nanowire quantum dot resulting in $g^2(0)$ values lower than 0.04. The multi-pixel detectors alleviate the need for beamsplitters and can be used for higher order correlations with promising prospects not only in the field of quantum optics, but also in bio-imaging applications, such as fluorescence microscopy and positron emission tomography.

We demonstrate a method to monolithically integrate nanowire-based quantum dot single photon sources on-chip using evanescent coupling. By deterministically placing an appropriately tapered III-V nanowire waveguide, containing a single quantum dot, on top of a silicon-based ridge waveguide, the quantum dot emission can be transferred to the ridge waveguide with calculated efficiencies close to 100%. As the evanescent coupling is bidirectional, the source can be optically pumped in both free-space and through the ridge waveguide. The latter onfiguration provides a self-contained, all-fiber, single photon source suitable as a plug-and-play solution for applications requiring bright, on-demand single photons. Using InAsP quantum dots embedded in InP nanowire waveguides, we demonstrate coupling efficiencies to a SiN ridge waveguide of 74% with a single photon purity of 97%.

Integration of superconducting nanowire single photon detectors and quantum sources with photonic waveguides is crucial for realizing advanced quantum integrated circuits. However, scalability is hindered by stringent requirements on high performance detectors. Here we overcome the yield limitation by controlled coupling of photonic channels to pre-selected detectors based on measuring critical current, timing resolution, and detection efficiency. As a proof of concept of our approach, we demonstrate a hybrid on-chip full-transceiver consisting of a deterministically integrated detector coupled to a selected nanowire quantum dot through a filtering circuit made of a silicon nitride waveguide and a ring resonator filter, delivering 100 dB suppression of the excitation laser. In addition, we perform extensive testing of the detectors before and after integration in the photonic circuit and show that the high performance of the superconducting nanowire detectors, including timing jitter down to 23 $\pm$ 3 ps, is maintained. Our approach is fully compatible with wafer level automated testing in a cleanroom environment.

We present a quantum optics theory, numerical calculations, and experiments on coupled quantumdots in semiconductor nanowire waveguides. We first present an analytical Green function theory tocompute the emitted spectra of two coupled quantum dots, treated as point dipoles, fully accountingfor retardation effects, and demonstrate the signatures of coherent and incoherent coupling througha pronounced splitting of the uncoupled quantum dot resonances and modified spectral broadening.In the weak excitation regime, the classical Green functions used in models are verified and justifiedthrough full 3D solutions of Maxwell equations for nanowire waveguides, specifically using finite-difference time-domain techniques, showing how both waveguide modes and near-field evanescentmode coupling is important. The theory exploits an ensemble-based quantum description, and andan intuitive eigenmode-expansion based Maxwell theory. We then demonstrate how the molecularresonances (in the presence of coupling) take on the form of bright and dark (or quasi-dark) reso-nances, and study how these depend on the excitation and detection conditions. To go beyond theweak excitation regime, we also introduce a quantum master equation approach to model the non-linear spectra from an increasing incoherent pump field, which shows the role of the pump field onthe oscillator strengths and broadening of the molecular resonances, with and without pure dephas-ing. Next, we present experimental photoluminescence spectra for spatially-separated quantum dotmolecules (InAsP) in InP nanowires, which show clear signatures of pronounced splittings, thoughthey also highlight additional mechanisms that are not accounted for in the dipole-dipole couplingmodel. Two different approaches are taken to control the spatial separation of the quantum dotmolecules, and we discuss the advantages and disadvantages of each., Comment: 20 pages, 16 figures

Quantum dots are arguably the best interface between matter spin qubits and flying photonic qubits. Using quantum dot devices to produce joint spin-photonic states requires the electronic spin qubits to be stored for extended times. Therefore, the study of the coherence of spins of various quantum dot confined charge carriers is important both scientifically and technologically. In this study we report on spin relaxation measurements performed on five different forms of electronic spin qubits confined in the very same quantum dot. In particular, we use all optical techniques to measure the spin relaxation of the confined heavy hole and that of the dark exciton - a long lived electron-heavy hole pair with parallel spins. Our measured results for the spin relaxation of the electron, the heavy-hole, the dark exciton, the negative and the positive trions, in the absence of externally applied magnetic field, are in agreement with a central spin theory which attributes the dephasing of the carriers' spin to their hyperfine interactions with the nuclear spins of the atoms forming the quantum dots. We demonstrate that the heavy hole dephases much slower than the electron. We also show, both experimentally and theoretically, that the dark exciton dephases slower than the heavy hole, due to the electron-hole exchange interaction, which partially protects its spin state from dephasing., Comment: 12 pages, 5 figures, 1 table

We demonstrate an in-situ technique to tune the emission energy of semiconductor quantum dots. The technique is based on laser-induced atomic intermixing applied to nanowire quantum dots grown using a site-selective process that allows for the deterministic tuning of individual emitters. A tuning range of up to 15 meV is obtained with a precision limited by the laser exposure time. A distinct saturation of the energy shift is observed, which suggests an intermixing mechanism relying on grown-in defects that are subsequently removed from the semiconductor material during annealing. The ability to tune different emitters into resonance with each other will be required for fabricating remote quantum dot-based sources of indistinguishable photons for secure quantum networks.

We report on the site-selected growth of bright single InAsP quantum dots embedded within InP photonic nanowire waveguides emitting at telecom wavelengths. We demonstrate a dramatic dependence of the emission rate on both the emission wavelength and the nanowire diameter. With an appropriately designed waveguide, tailored to the emission wavelength of the dot, an increase in count rate by nearly two orders of magnitude (0.4kcps to 35kcps) is obtained for quantum dots emitting in the telecom O-band. Using emission-wavelength-optimised waveguides, we demonstrate bright, narrow linewidth emission from single InAsP quantum dots with an unprecedented tuning range from 880nm to 1550nm. These results pave the way towards efficient single photon sources at telecom wavelengths using deterministically grown InAsP/InP nanowire quantum dots.

Quantum states of light play a pivotal role in modern science[1] and future photonic applications[2]. While impressive progress has been made in their generation and manipulation with high fidelities, the common table-top approach is reaching its limits for practical quantum applications. Since the advent of integrated quantum nanophotonics[3] different material platforms based on III-V nanostructures-, color centers-, and nonlinear waveguides[4-8] as on-chip light sources have been investigated. Each platform has unique advantages and limitations in terms of source properties, optical circuit complexity, and scaling potentials. However, all implementations face major challenges with efficient and tunable filtering of individual quantum states[4], scalable integration and deterministic multiplexing of on-demand selected quantum emitters[9], and on-chip excitation-suppression[10]. Here we overcome all of these challenges with a novel hybrid and scalable nanofabrication approach to generate quantum light on-chip, where selected single III-V quantum emitters are positioned and deterministically integrated in a CMOS compatible circuit[11] with controlled on-chip filtering and excitation-suppression.Furthermore, we demonstrate novel on-chip quantum wavelength division multiplexing, showing tunable routing of single-photons. Our reconfigurable quantum photonic circuits with a foot print one million times smaller than similar table-top approaches, offering outstanding excitation suppression of more than 95 dB and efficient routing of single photons over a bandwidth of 40 nm, are essential to unleash integrated quantum optical technologies full potential., Comment: 30 pages, 10 figures

Producing advanced quantum states of light is a priority in quantum information technologies. While remarkable progress has been made on single photons and photon pairs, multipartite correlated photon states are usually produced in purely optical systems by post-selection or cascading, with extremely low efficiency and exponentially poor scaling. Multipartite states enable improved tests of the foundations of quantum mechanics as well as implementations of complex quantum optical networks and protocols. It would be favorable to directly generate these states using solid state systems, for better scaling, simpler handling, and the promise of reversible transfer of quantum information between stationary and flying qubits. Here we use the ground states of two optically active coupled quantum dots to directly produce photon triplets. The wavefunctions of photogenerated excitons localized in these ground states are correlated via molecular hybridization and Coulomb interactions. The formation of a triexciton leads to a triple cascade recombination and sequential emission of three photons with strong correlations. The quantum dot molecule is embedded in an epitaxially grown nanowire engineered for single-mode waveguiding and improved extraction efficiency at the emission wavelength. We record 65.62 photon triplets per minute, surpassing rates of all earlier reported sources, in spite of the moderate efficiency of our detectors. Our structure and data represent a breakthrough towards implementing multipartite photon entanglement and multi-qubit readout schemes in solid state devices, suitable for integrated quantum information processing., Comment: 27 pages, 3 figures

Global, secure quantum channels will require efficient distribution of entangled photons. Long distance, low-loss interconnects can only be realized using photons as quantum information carriers. However, a quantum light source combining both high qubit fidelity and on-demand bright emission has proven elusive. Here, we show a bright photonic nanostructure generating polarization-entangled photon-pairs that strongly violates Bell's inequality. A highly symmetric InAsP quantum dot generating entangled photons is encapsulated in a tapered nanowire waveguide to ensure directional emission and efficient light extraction. We collect $\sim$200 kHz entangled photon-pairs at the first lens under 80\,MHz pulsed excitation, which is a 20 times enhancement as compared to a bare quantum dot without a photonic nanostructure. The performed Bell test using the Clauser-Horne-Shimony-Holt inequality reveals a clear violation ($S_{\text{CHSH}}>2$) by up to 9.3 standard deviations. By using a novel quasi-resonant excitation scheme at the wurtzite InP nanowire resonance to reduce multi-photon emission, the entanglement fidelity ($F=0.817\,\pm\,0.002$) is further enhanced without temporal post-selection, allowing for the violation of Bell's inequality in the rectilinear-circular basis by 25 standard deviations. Our results on nanowire-based quantum light sources highlight their potential application in secure data communication utilizing measurement-device-independent quantum key distribution and quantum repeater protocols.