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arXiv:1212.2811 · Physical Review A

Room-temperature Rydberg single-photon source

Matthias M. Müller, A. Kölle, R. Löw, Tilman Pfau, Tommaso Calarco, Simone Montangero

Published May 24, 2013• 47 citations
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Abstract

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.

DOI
10.1103/physreva.87.053412

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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.
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 a pulsed four-wave mixing scheme via a Rydberg state to create, store, and retrieve collective Rydberg polaritons. The storage medium consists of a gas of thermal Rb atoms confined in a $220\ensuremath{-}\ensuremath{\mu}\mathrm{m}$-thick cell, which is heated above room temperature. The experimental sequence consists of a pulsed excitation of Rydberg polaritons via the D1{D}_{1}D1​ line, a variable delay or storage time, and a final retrieval pulse via the D2{D}_{2}D2​ line. The lifetime of the Rydberg polaritons is around 1.2 ns, almost entirely limited by the excitation bandwidth and the corresponding motional dephasing of the atoms. The presented scheme combined with a tightly confined atomic ensemble is a good candidate for a deterministic single-photon source, as soon as strong interactions in terms of a Rydberg blockade are added.
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.