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SPIE Quantum Technologies

On-demand single-photon source based on thermal rubidium (Conference Presentation)

Fabian Ripka, Harald Kübler, Robert Löw

Published May 29, 2018• 0 citations
Publisher

Abstract

Photonic quantum devices based on atomic vapors at room temperature combine the advantages of atomic vapors being intrinsically reproducable as well as semiconductor-based concepts being scalable and integrable. One key device in the field of quantum information are on-demand single-photon sources. Comparable to similar realizations using cold atoms [1], it has been supposed to realize room-temperature single-photon sources by combining the two effects of four-wave mixing and Rydberg blockade [2]. Driving the four-wave mixing cycles in a pulsed manner, single photons are generated on demand. The essential conditions of coherence [3,4] and sufficient Rydberg-Rydberg interaction strengths [5] have already been demonstrated. Up to now, the third condition has been missing: That is performing the excitation cycles in a low-dimensional geometry in order to obtain an excitation blockade of the whole volume by only one Rydberg excitation. We realize this spatial confinement in transversal direction by focusing one of the excitation beams by means of a high-NA lens, and in longitudinal direction by using vapor cells of about one micrometer inner thickness (“µ-cells”). In order to deal with reasonable numbers of atoms in such a small volume, we exploit the fact that in thermal equilibrium there are large numbers of adsorbed atoms on the glass surface. We can easily photo-desorb them shortly before the four-wave mixing cycles and increase by this the optical thickness in the excitation volume by one order of magnitude. By means of these techniques we are now able to generate single photons at 780nm. With a Rydberg blockade radius of 1.0µm and a cell thickness of 1.2µm, we observe pure anti-bunching in the light statistics of the coherent emission field, deviating with a significance of three standard deviations from Poisson-type statistics. We obtain generation efficiencies of currently up to 5% per four-wave mixing cycle, depending on experimental parameters. We systematically investigate the disappearance of the anti-bunching by increasing the cell thickness. The results are also compared to measurements at smaller blockade radii. This technique can be further improved by investigating different Rydberg states or different multi-level schemes which allow exploiting the latest developments in laser research. [1] Y. O. Dudin et al., Science 336, 6083 (2012) [2] M. M. Müller et al., PRA 87, 053412 (2013) [3] B. Huber et al., PRL 107, 243001 (2011) [4] B. Huber et al., PRA 90, 053806 (2014) [5] T. Baluktsian et al., PRL 110, 123001 (2013)

DOI
10.1117/12.2309776

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Photonic quantum devices based on atomic vapors at room temperature combine the advantages of atomic vapors being intrinsically reproducable as well as semiconductor-based concepts being scalable and integrable. One key device in the field of quantum information are on-demand single-photon sources. Comparable to similar realizations using cold atoms [1], it has been supposed to realize room-temperature single-photon sources by combining the two effects of four-wave mixing and Rydberg blockade [2]. Driving the four-wave mixing cycles in a pulsed manner, single photons are generated on demand. The essential conditions of coherence [3,4] and sufficient Rydberg-Rydberg interaction strengths [5] have already been demonstrated. Up to now, the third condition has been missing: That is performing the excitation cycles in a low-dimensional geometry in order to obtain an excitation blockade of the whole volume by only one Rydberg excitation. We realize this spatial confinement in transversal direction by focusing one of the excitation beams by means of a high-NA lens, and in longitudinal direction by using vapor cells of about one micrometer inner thickness (“µ-cells”). In order to deal with reasonable numbers of atoms in such a small volume, we exploit the fact that in thermal equilibrium there are large numbers of adsorbed atoms on the glass surface. We can easily photo-desorb them shortly before the four-wave mixing cycles and increase by this the optical thickness in the excitation volume by one order of magnitude. By means of these techniques we are now able to generate single photons at 780nm. With a Rydberg blockade radius of 1.0µm and a cell thickness of 1.2µm, we observe pure anti-bunching in the light statistics of the coherent emission field, deviating with a significance of three standard deviations from Poisson-type statistics. We obtain generation efficiencies of currently up to 5% per four-wave mixing cycle, depending on experimental parameters. We systematically investigate the disappearance of the anti-bunching by increasing the cell thickness. The results are also compared to measurements at smaller blockade radii. This technique can be further improved by investigating different Rydberg states or different multi-level schemes which allow exploiting the latest developments in laser research. [1] Y. O. Dudin et al., Science 336, 6083 (2012) [2] M. M. Müller et al., PRA 87, 053412 (2013) [3] B. Huber et al., PRL 107, 243001 (2011) [4] B. Huber et al., PRA 90, 053806 (2014) [5] T. Baluktsian et al., PRL 110, 123001 (2013)
We present an optimal protocol to implement a room-temperature Rydberg single-photon source within an experimental setup based on micro cells filled with thermal vapor. The optimization of a pulsed four wave mixing scheme allows us to double the effective Rydberg blockade radius as compared to a simple Gaussian pulse scheme, releasing some of the constraints on the geometry of the micro cells. The performance of the optimized protocol is improved by about 70% with respect to the standard protocol.
Single photon source is a non-classical light field with anti-bunching effect, which has a potential applications in the research of fundamental physics problems, quantum precision measurement, quantum communication, quantum computing, etc. The strong interaction between highly excited Rydberg atoms presents an excitation blockade effect. In a dense Rydberg atomic ensemble, the excitation of more than one Rydberg atom within a blockade volume is suppressed, where the interactions of Rydberg atoms shift the atomic states out of resonance with an excitation laser. We consider here the generation of single photon source by using a four-wave mixing scheme in a room-temperature atomic vapor cell. In a homemade micrometer-sized atomic vapor cell, one-dimensional size is smaller than the radius of Rydberg blockade and the other two-dimensional size is limited by the size of focused laser beam. The blockade radius is on the order of a few micrometers, depending on the Rydberg atom states. An excitation blockade effect can be used to realize single photon source in thermal cesium vapor microcells. The micron cesium-cell is used to spatially localize atomic groups, which results in the atomic decoherence time on the order of microseconds or even nanoseconds. This requires a high-power pulsed laser to prepare the Rydberg atomic state at a nanosecond scale. Four-photon excitation schemes with narrow linewidth lasers are also used experimentally. The cesium-Rydberg state can usually be excited by the lasers with optical wavelengths 852 and 509 nm, respectively. The laser system is well-stabilized so that the detuning is small compared with the spontaneous linewidth of Rydberg state, while the laser power and temporal mode need to be specified for ns-time coherence in thermal cesium vapor microcells. The 852 nm laser can be achieved by modulating the continuous laser beam with the help of an electro-optic intensity modulator (EOIM). While this remains a technical challenge for 509 nm laser with ns-laser pulse. There is no EOIM to generate the ns-laser pulse with high power. We demonstrate a novel generation method of 509 nm laser system. In our experiments, a 1018 nm fiber laser is used to produce a continuous laser with a typical linewidth of ～8 kHz and power of 10 mW. The nanosecond pulse is generated with the help of an electro-optic intensity modulator (EOIM) by modifying the continuous laser beam. The peak power of modulated optical pulse is amplified to 4600 W by using a homemade fiber amplifier. The output beam of 1018 nm is then injected into a periodically poled lithium-niobate (PPLN) to generate the second harmonics laser of 509 nm. The typical peak power of 509 nm reaches 173 W by optimizing PPLN phase matching parameters. The pulse repetition frequency of the 509 nm laser can be continuously tuned in a range of 300 kHz–100 MHz, and the pulse width can be continuously tuned in a range of 1–100 ns. Peak power fluctuation of the pulses is about 1.3%. The power 509 nm laser with optimized pulse parameters can be used to excite the cesium atom with GHz bandwidth. Meanwhile the two seed source lasers is well established experimentally, which allows alternating pulses with a different wavelength. This is an essential capability for realizing a single photon source through four-wave mixing.
Photons are good candidates for carrying quantum information because they are very stable particles: they interact weakly with the medium and barely with each other. However, this has drawbacks when you want to process the information because, in this case, it is preferable to have photon-photon interactions. For example, for applications in quantum repeaters, such interactions would allow deterministic Bell state measurements, increasing the entanglement distribution rate between two remote nodes. Getting two photons to interact with each other efficiently requires mapping them into a nonlinear medium at the single-photon level, that is, a medium that reacts differently when it interacts with a single photon than when it does with two. Such strong nonlinearity has been demonstrated with Rydberg atoms, which are atoms excited to a state with a high principal quantum number. In this thesis we have performed nonlinear quantum optics experiments using an ensemble of cold Rydberg atoms, where we have studied the properties of the quantum light emitted by these atoms. First, we demonstrated nonlinearities at the single-photon level. To reach this stage, we made several improvements to the previous experimental setup available in the group, of which the implementation of a dipole trap was especially relevant. We evidence quantum nonlinearity by measuring photon antibunching for the transmitted light after interacting with the Rydberg state under electromagnetically induced transparency (EIT). We also showed the generation of single photons on-demand after storing weak coherent states of light pulses as collective Rydberg excitations. Then, we studied the variation of the light statistic throughout the output pulse after propagating through the medium as Rydberg polaritons, which are superposition states of light and Rydberg excitations. We showed that the properties at the beginning and the end of the pulse were different from those of the steady state. In particular, the light detected after the input pulse was abruptly turned off gave much stronger suppression of two-photon events. Then, we investigated how to exploit this effect to generate single photons on demand. To do this, we analyzed the quality of the single photons detected at the end of the pulse as a function of the detection probability and compared the results with those obtained by storing the input pulse as collective Rydberg excitations. We showed that the photons were generated more efficiently when increasing the detection window at the cost of deteriorating the single photons statistics. Finally, we investigated the indistinguishability of the photons emitted by our Rydberg atomic ensemble, a crucial property for using Rydberg atoms as nodes in quantum networks. We also compared the single photons generated after storage under EIT conditions with those obtained using a two-photon Raman excitation to the Rydberg state. We measured the indistinguishability by making them interfere with weak coherent states of light in a Hong-Ou-Mandel experiment. And we showed that, although we obtained better photon statistics under EIT conditions, the indistinguishability from those obtained with Raman excitation was significantly higher.
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 simultaneously observe a fully single-mode (spectral, temporal, spatial, and polarization) efficiency up to 0.098(2), a detector-background-subtracted g ( 2 ) = 5.0 ( 1.6 ) × 10 − 4 , and indistinguishability of 0.980(7), at an average photon production rate of 1.18 ( 2 ) × 10 4 s − 1 . All of these make this system promising for scalable quantum information applications. Furthermore, we investigate the effects of contaminant Rydberg excitations on the source efficiency and observed single-mode efficiencies up to 0.18(2) for lower photon rates. Finally, recognizing that many quantum information protocols require a single photon in a fully single mode, we introduce metrics that take into account all degrees of freedom to benchmark the performance of on-demand sources.
An ensemble of rubidium atoms can be excited with lasers such that it evolves into an entangled state with just one collective excitation within the Rydberg-blockade radius. The decay of this state leads to the emission of a single antibunched photon. For a hot vapor of rubidium atoms in a microcell, we numerically study the feasibility of such a single-photon source under different experimental conditions like the atomic density distribution and the choice of electronic states addressed by the lasers. For the excitation process with three rectangular lasers pulses, we simulate the coherent dynamics of the system in a truncated Hilbert space. We investigate the radiative behavior of the moving rubidium atoms and optimize the laser pulse sequence accordingly. We find that the collective decay of the single excitation leads to a fast and directed photon emission and further that a pulse sequence similar to a spin echo increases the directionality of the photon. Finally, we analyze the residual double excitations and find that they do not exhibit these collective decay properties and play only a minor deleterious role.