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Acta Physica Sinica

852-nm triggered single-photon source based on trapping and manipulation of a single cesium atom confined in a microscopic optical dipole trap

Liu Bei, Jin Gang, Jun He, Junmin Wang

Published Jan 1, 2016• 0 citations
Publisher

Abstract

Single-atom-based single-photon source has several advantages, such as narrow bandwidth, wavelength matching with the absorption line of the same atomic ensemble, and insensitivity to the environment disturbing, and it is very important not only for basic researches in quantum optic field but also for applications in quantum information processing. In this paper, we report the generation of a 10-MHz-repetition-rate triggered single-photon source at 852 nm based on a trapped single cesium atom in a far-off-resonance microscopic optical dipole trap (FORT). To generate an optical dipole trap, a far-red-detuned 1064 nm laser beam is tightly focused by using a high numerical aperture lens, a typical trap depth is 2 mK and trap waist is 2.3 m. To obtain a maximum probability of pulsed excitation, the frequency of the pulsed laser should be resonant with the atomic energy levels and the trapped single atom must be excited with a -pulse. However, the interaction between the FORT laser and the atoms causes AC Stark shifts of the atomic energy levels. Thus, in order to demonstrate the resonant pulsed excitation, it is important to calculate and measure the shift of 6S1/2|Fg=4,mF=+4-6P3/2|Fe=5,mF=+5 cyclical transition in the FORT. For a two-level system, the probability of pulsed excitation can be described by Rabi oscillations with a characteristic Rabi frequency . With an optimized time sequence, we experimentally demonstrate the Rabi oscillation between the ground state and the excited state, and the peak power of -pulse laser is about 1.25 mW. We also measure the temporal envelope of single photons after a -pulse excitation. A gated pulsed excitation and cooling technique are used to reduce the possibility that atoms are heated by -pulse laser. The typical trapping lifetime of single cesium atom is extended from~108 ups to~2536 ms. The corresponding number of excitations is improved from 108 to 360000. The second-order intensity correlations of the emitted single-photon are characterized by implementing Hanbury Brown-Twiss setup. The statistics shows a strong anti-bunching with a value of 0.09 for the second-order correlation at zero delay. In the future, we will perform a Hong-Ou-Mandel two-photon interference experiment to analyze the indistinguishability of the single photons. We will also trap single atoms in a magic-wavelength optical dipole trap where the ground and the excited states have the same shift.

DOI
10.7498/aps.65.233701

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•Jan 1, 2005•1 citation
Single-atom-based single-photon source has several advantages, such as narrow bandwidth, wavelength matching with the absorption line of the same atomic ensemble, and insensitivity to the environment disturbing, and it is very important not only for basic researches in quantum optic field but also for applications in quantum information processing. In this paper, we report the generation of a 10-MHz-repetition-rate triggered single-photon source at 852 nm based on a trapped single cesium atom in a far-off-resonance microscopic optical dipole trap (FORT). To generate an optical dipole trap, a far-red-detuned 1064 nm laser beam is tightly focused by using a high numerical aperture lens, a typical trap depth is 2 mK and trap waist is 2.3 m. To obtain a maximum probability of pulsed excitation, the frequency of the pulsed laser should be resonant with the atomic energy levels and the trapped single atom must be excited with a -pulse. However, the interaction between the FORT laser and the atoms causes AC Stark shifts of the atomic energy levels. Thus, in order to demonstrate the resonant pulsed excitation, it is important to calculate and measure the shift of 6S1/2|Fg=4,mF=+4-6P3/2|Fe=5,mF=+5 cyclical transition in the FORT. For a two-level system, the probability of pulsed excitation can be described by Rabi oscillations with a characteristic Rabi frequency . With an optimized time sequence, we experimentally demonstrate the Rabi oscillation between the ground state and the excited state, and the peak power of -pulse laser is about 1.25 mW. We also measure the temporal envelope of single photons after a -pulse excitation. A gated pulsed excitation and cooling technique are used to reduce the possibility that atoms are heated by -pulse laser. The typical trapping lifetime of single cesium atom is extended from108 ups to2536 ms. The corresponding number of excitations is improved from 108 to 360000. The second-order intensity correlations of the emitted single-photon are characterized by implementing Hanbury Brown-Twiss setup. The statistics shows a strong anti-bunching with a value of 0.09 for the second-order correlation at zero delay. In the future, we will perform a Hong-Ou-Mandel two-photon interference experiment to analyze the indistinguishability of the single photons. We will also trap single atoms in a magic-wavelength optical dipole trap where the ground and the excited states have the same shift.
We investigate single-cesium-atom heating owing to the momentum accumulation process induced by the resonant pulsed excitation in a microscopic optical dipole trap formed by a strongly focused 1064-nm laser beam. The heating depends on the trap frequency, which restricts the maximum repetition rate of the pulsed excitation. We experimentally verify the heating of a single atom and then demonstrate how to suppress it with an optimized pulsed excitation and cooling method. The typical trap lifetime of a single cesium atom is extended from $108\ifmmode\pm\else\textpm\fi{}6\phantom{\rule{0.16em}{0ex}}\ensuremath{\mu}\mathrm{s}$ to $2536\ifmmode\pm\else\textpm\fi{}31\phantom{\rule{0.16em}{0ex}}\mathrm{ms}$, and the corresponding number of excitations increases from $\ensuremath{\sim}108$ to $\ensuremath{\sim}360\phantom{\rule{0.16em}{0ex}}000$. In applying this faster cooling method, we use the trapped single cesium atom as a triggered single-photon source at an excitation repetition rate of 10 MHz. The second-order intensity correlations of the emitted single photons are characterized by implementing a Hanbury Brown and Twiss setup, and a clear antibunching effect has been observed.
Atoms trapped in magic-wavelength optical tweezer will have the same light shift for the desired ground and excited states. In this case the position-dependence differential light shift of the desired transition can be eliminated. For cesium 6S_1/2 (Fg = 4, mF = +4) - 6P_3/2 (Fe = 5, mF = +5) cycling transition (852 nm), the magic wavelength was calculated theoretically for a linearly-polarized optical tweezer, and also it was verified experimentally to be 937.6 nm. We have demonstrated 852-nm triggered single-photon sources based on single cesium atom trapped in linearly-polarized optical tweezers implemented by using of 1064-nm and 937.6-nm lasers, respectively. The photon statistics were characterized by using of the Hanbury Brown - Twiss (HBT) scheme based on Si single-photon detectors (SSPDs). Strong anti-bunching effect [g^2(t=0) = 0.09] was recognized, and it shown perfectly the single-photon characters. The Hong-Ou-Mandel (HOM) two-photon interference measurements based on SSPDs were employed to evaluate the photon indistinguishability. Our preliminary experimental results indicated that the indistinguishability of single photons has been improved ~ 20% for the case of magic-wavelength optical tweezer. References: [1] Phys. Rev. A 94 (2016) 013409; [2] Appl. Phys. Express 9 (2016) 072702; [3] Opt. Express 25 (2017) p.15861
This work deals with the cooling and trapping of single cesium (Cs) atoms in a large-magnetic-gradient magneto-optical trap (MOT) and the confinement of single Cs atoms in a far-off-resonance optical dipole trap (FORT). The experiment setup is based on two large-numerical-aperture lens assemblies which allow us to strongly focus a 1064-nm TEM00-mode Gaussian laser beam to a 1/e2 radius of ~ 2.3 μm to form a microscopic FORT for isolating single atom with environment and to efficiently collect the laser-induced-fluorescence photons emitted by single atoms for detecting and recognizing single atom’s internal state. We have tried both of “bottom-up” and “top-down” loading schemes to confine single atoms in the microscopic FORT. In the “bottom-up” scheme, we have successfully prepared single Cs atoms in the MOT and transferred it into FORT with a probability of almost 100%. In the “top-down” scheme, we have achieved ~ 74% of single atom loading probability in the FORT using light-assisted collisions induced by blue detuning laser and with prepared many Cs atoms in the MOT. The relaxation time in hyperfine level of ground state of trapped single Cs atom is measured to be ~5.4 s. To coherently manipulate atomic quantum bits (qubit) encoded in the clock states (mF = 0 states in Fg = 3 and 4 hyperfine levels) of single Cs atom via the two-photon simulated Raman adiabatic passage (STIRAP), we have prepared two phase-locked laser beams with a frequency difference of ~ 9.192 GHz by optically injecting an 852-nm master laser to lock the +1-order sideband of a 9-GHz current-modulated slave diode laser. The two phase-locked laser beams are used to drive STIRAP process in the Λ-type three-level system consists of Cs |6S1/2 Fg = 4, mF = 0> and |6S1/2 Fg = 3, mF = 0< long-lived clock states and Cs |6S1/2 Fe = 4, mF = +1 > excited state with the single-photon detuning of ~ -20 GHz. Rabi flopping experiments are in progress.
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.
Two-photon Raman process (TPRP) is an important technique in controlling the atomic internal states. It plays an important role in quantum manipulation and quantum information process. A reliable Raman laser for specific atom is the first step to demonstrate TPRP and quantum manipulation of an atom. In this paper, we theoretically analyze the two-photon Raman process regarding to Cesium “clock states” |6S1/2, F=4, mF=0 and |6S1/2, F=3, mF=0, and we obtain the dependences of the corresponding Rabi frequency on one-and two-photon detunings and one-photon Rabi frequencies in a realistic multi-level Cesium atom system. We find that to obtain an atom state flopping efficiency of 0.99 the Raman laser power fluctuation should be controlled to be smaller than 3.2%. We also report our simple experimental Raman laser system for TPRP of Cesium atom based on a fiber waveguide phase modulator. The phase modulator is driven by a 4.6 GHz microwave source and the two first-order sidebands with a frequency difference of 9.19 GHz are filtered out by a Fabry-Pérot cavity with a finesse of 48. After an amplitude-modulator-based intensity stabilization system, a total power of 73 μupW with a fluctuation of 2.2% within 90 min is obtained. By applying this Raman laser to a single Cesium atom trapped in a micrometer size far-off resonant trap (FORT), we obtain Raman spectra between Cesium “clock states” |6S1/2, F=4, mF=0 and |6S1/2, F=3, mF=0. The discrepancy between the two-photon resonance frequency and the defined clock frequency 9.192631770 GHz is due to the differential Stark shifts by FORT beam and Raman beams as well as the inaccuracy of the microwave source. By varying the Raman pulse length we also show the corresponding Rabi flopping with a rate of 153 kHz, which is consistent with the theoretical calculation. The obtained state transfer efficiency of 0.75 is much smaller than theoretical expectation 0.99, which is mainly limited by the state initialization efficiency. The Raman laser system reported in this paper is simple and reliable to realize and it provides a reliable method to manipulate the Cesium internal state. Moreover it could also be easily extended to other system for quantum manipulation of other species of atom.
We present recent results on the coherent control of an optical transition in a single rubidium atom, trapped in an optical tweezer. We excite the atom using resonant light pulses that are short (4 ns) compared with the lifetime of the excited state (26 ns). By varying the intensity of the laser pulses, we can observe an adjustable number of Rabi oscillations, followed by free decay once the light is switched off. To generate the pulses we have developed a novel laser system based on frequency doubling a telecoms laser diode at 1560 nm. By setting the laser intensity to make a pi-pulse, we use this coherent control to make a high quality triggered source of single photons. We obtain an average single photon rate of 9600 s-1 at the detector. Measurements of the second-order temporal correlation function show almost perfect antibunching at zero delay. In addition, we present preliminary results on the use of Raman transitions to couple the two hyperfine levels of the ground state of our trapped atom. This will allow us to prepare and control a qubit formed by two hyperfine sub-levels.