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Register a new userOn-demand indistinguishable single photons from an efficient and pure source based on a Rydberg ensemble
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Added by
Dalia P Ornelas Huerta
Publication date
2020
fields
Physics
and research's language is
English
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Single photons coupled to atomic systems have shown to be a promising platform for developing quantum technologies. Yet a bright on-demand, highly pure and highly indistinguishable single-photon source compatible with atomic platforms is lacking. In this work, we demonstrate such a source based on a strongly interacting Rydberg system. The large optical nonlinearities in a blockaded Rydberg ensemble convert coherent light into a single-collective excitation that can be coherently retrieved as a quantum field. We observe a single-transverse-mode efficiency up to 0.18(2), $g^{(2)}=2.0(1.5)times10^{-4}$, and indistinguishability of 0.982(7), making this system promising for scalable quantum information applications. Accounting for losses, we infer a generation probability up to 0.40(4). Furthermore, we investigate the effects of contaminant Rydberg excitations on the source efficiency. Finally, we introduce metrics to benchmark the performance of on-demand single-photon sources.
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The first two decades of the 21st century have witnessed remarkable progress in harnessing the power of quantum mechanics, on-chip, enabled by the development in epitaxial semiconductor nanoscience with proof-of-principle demonstrations -- many tour-de force -- of quantum functionalities such as entanglement and teleportation amongst photon and matter qubits ---quintessential quantum phenomena that underpin the development of quantum technologies. A basic hindrance to such development however has been the absence of a platform of on-demand single photon sources (SPSs) with adequate spectral characteristics and arranged in spatially regular arrays necessary for their incorporation in surrounding light manipulation units to enable quantum networks. Here we report on the first spatially-ordered, scalable platform of deterministic, bright, spectrally highly uniform, pure, and indistinguishable SPSs. At 19.5K, and without Purcell enhancement, these SPSs exhibit emission purity ~99.2% and two-photon interference (TPI) indistinguishability ~57%. Oscillation behavior of the photon emission indicates that the photons originate from a coherent superposition of two excitonic states, revealing effectively a three-level electronic structure which can be exploited as potential two-frequency qubit generating energy entangled photons for teleportation. Time-dependent two photon interference (Hong-Ou Mandel interferometry) coincidence counts g(2)({tau}) near {tau}=0 show effectively zero count which, analyzed using the three-level model, reveals a highly encouraging dephasing time of ~0.58ns at ~20K. Such SPS arrays in a planarized structure open the pathway to creating interconnected quantum networks for application in communication, sensing, computing and more.
By using the zero-phonon line emission of an individual organic molecule, we realized a source of indistinguishable single photons in the near infrared. A Hong-Ou-Mandel interference experiment is performed and a two-photon coalescence probability of higher than 50% at 2 K is obtained. The contribution of the temperature-dependent dephasing processes to the two-photon interference contrast is studied. We show that the molecule delivers nearly ideal indistinguishable single photons at the lowest temperatures when the dephasing is nearly lifetime limited. This source is used to generate post-selected polarization-entangled photon pairs, as a test-bench for applications in quantum information.
We generate indistinguishable photons from a semiconductor diode containing a InAs/GaAs quantum dot. Using an all-electrical technique to populate and control a single-photon emitting state we filter-out dephasing by Stark-shifting the emission energy on timescales below the dephasing time of the state. Mixing consecutive photons on a beam-splitter we observe two-photon interference with a visibility of 64%.
We report on a fast, bandwidth-tunable single-photon source based on an epitaxial GaAs quantum dot. Exploiting spontaneous spin-flip Raman transitions, single photons at $780,$nm are generated on-demand with tailored temporal profiles of durations exceeding the intrinsic quantum dot lifetime by up to three orders of magnitude. Second-order correlation measurements show a low multi-photon emission probability ($g^{2}(0)sim,0.10-0.15$) at a generation rate up to $10,$MHz. We observe Raman photons with linewidths as low as $200,$MHz, narrow compared to the $1.1,$GHz linewidth measured in resonance fluorescence. The generation of such narrow-band single photons with controlled temporal shapes at the rubidium wavelength is a crucial step towards the development of an optimized hybrid semiconductor-atom interface.
We experimentally demonstrate that a non-classical state prepared in an atomic memory can be efficiently transferred to a single mode of free-propagating light. By retrieving on demand a single excitation from a cold atomic gas, we realize an efficient source of single photons prepared in a pure, fully controlled quantum state. We characterize this source using two detection methods, one based on photon-counting analysis, and the second using homodyne tomography to reconstruct the density matrix and Wigner function of the state. The latter technique allows us to completely determine the mode of the retrieved photon in its fine phase and amplitude details, and demonstrate its nonclassical field statistics by observing a negative Wigner function. We measure a photon retrieval efficiency up to 82% and an atomic memory coherence time of 900 ns. This setup is very well suited to study interactions between atomic excitations, and to use them in order to create and manipulate more sophisticated quantum states of light with a high degree of experimental control.
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