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arXiv:1505.04071 · Physical Review B

Atomic clouds as spectrally selective and tunable delay lines for single photons from quantum dots

Johannes S. Wildmann, Rinaldo Trotta, Javier Martín‐Sánchez, Eugenio Zallo, Mark O'Steen, Oliver G. Schmidt, Armando Rastelli

Published Dec 21, 2015• 28 citations
arXivHTMLPDF

Abstract

For the first time, it is experimentally shown that a cloud of cesium (Cs) atoms can be used as a spectrally selective and tunable delay line for single photons emitted by semiconductor quantum dots. This delay line -- significant slowing down of photons separated in frequency by only a few gigahertz -- may represent the missing ingredient for the demonstration of a time-reordering scheme for entangled photon generation, and it could play a key role in future quantum networks and quantum communication.

DOI
10.1103/physrevb.92.235306

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For the first time, it is experimentally shown that a cloud of cesium (Cs) atoms can be used as a spectrally selective and tunable delay line for single photons emitted by semiconductor quantum dots. This delay line -- significant slowing down of photons separated in frequency by only a few gigahertz -- may represent the missing ingredient for the demonstration of a time-reordering scheme for entangled photon generation, and it could play a key role in future quantum networks and quantum communication.
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Future quantum networks will need flying qubits and stationary nodes. As for the generation of single photons which may act as flying qubits, resonantly excited single-semiconductor quantum dots are ideal in terms of their on-demand single-photon emission, indistinguishability, and brightness. Atomic systems can effectively act as mediators for photon–photon interactions, storage media, or building blocks for stationary qubits. Here, we hybridize these two systems and investigate the non-classical interference of spectral Lorentzian-shaped photons, fine-tuned between the cesium (Cs)-D1 hyperfine resonances. The temporal delay in the dispersive hot atomic cesium vapor amounts up to 50 times the photons’ initial width and reveals beats on the single quanta. The photons’ indistinguishability is preserved even after atomic-enabled delay. This proves that the interaction with the Cs vapor conserves the photons’ coherence. The role of spectral diffusion in the solid-state emitter is studied in single- and two-photon experiments in light of the strong frequency dependence of the atomic medium. Our results pave the way for efficient hybrid interfaces between quantum dots and hot atomic vapors as storage media in future quantum networks.
In forthcoming quantum networks various quantum systems might be involved to accomplish individual tasks, including storage of quantum states, quantum logic operations, error correction, or entanglement distillation. An interface between a single photon emitter and a potential photon storage could provide one fundamental building block of such a hybrid quantum system. Semiconductor quantum dots (QD) and atomic vapors have already been brought together by single photon spectroscopy of cesium and rubidium [1,2], narrow filtering of QD resonance fluorescence in cesium [3], slowing down QD photons by dispersion between the 6.8 GHz hyperfine-split rubidium D2transitions [4] and in the middle of the four cesium D1 transitions [5] (at around 5.0 GHz in Fig. 1 b).In our experiment the neutrally charged excitonic transition of a strain-tunable InGaAs QD is pumped either resonantly or non-resonantly by a pulsed laser. The QD emission is set between two cesium D1 transitions at 894 nm, which are hyperfine-split only by 1.2 GHz, with a very strong dispersion compared to preceding studies [4,5]. This allows for delay times of a few nanoseconds even at low optical densities, resulting in a propagation velocity at the order of 1/20 of the vacuum speed of light. Such a single photon - atom interface might lay the foundations for a low-loss quantum memory in a future hybrid quantum network.
Hybrid interfaces between distinct quantum systems play a major role in the implementation of quantum networks. Quantum states have to be stored in memories to synchronize the photon arrival times for entanglement swapping by projective measurements in quantum repeaters or for entanglement purification. Here, we analyze the distortion of a single-photon wave packet propagating through a dispersive and absorptive medium with high spectral resolution. Single photons are generated from a single In(Ga)As quantum dot with its excitonic transition precisely set relative to the Cesium D1 transition. The delay of spectral components of the single-photon wave packet with almost Fourier-limited width is investigated in detail with a 200 MHz narrow-band monolithic Fabry-Pérot resonator. Reflecting the excited state hyperfine structure of Cesium, “slow light” and “fast light” behavior is observed. As a step towards room-temperature alkali vapor memories, quantum dot photons are delayed for 5 ns by strong dispersion between the two 1.17 GHz hyperfine-split excited state transitions. Based on optical pumping on the hyperfine-split ground states, we propose a simple, all-optically controllable delay for synchronization of heralded narrow-band photons in a quantum network.
Abstract Hybrid interfaces between distinct quantum systems play a major role in the implementation of quantum networks. Quantum states have to be stored in memories to synchronize the photon arrival times for entanglement swapping by projective measurements in quantum repeaters or for entanglement purification. Here, we analyze the distortion of a single-photon wave packet propagating through a dispersive and absorptive medium with high spectral resolution. Single photons are generated from a single In(Ga)As quantum dot with its excitonic transition precisely set relative to the Cesium D1 transition. The delay of spectral components of the single-photon wave packet with almost Fourier-limited width is investigated in detail with a 200 MHz narrow-band monolithic Fabry-Pérot resonator. Reflecting the excited state hyperfine structure of Cesium, “slow light” and “fast light” behavior is observed. As a step towards room-temperature alkali vapor memories, quantum dot photons are delayed for 5 ns by strong dispersion between the two 1.17 GHz hyperfine-split excited state transitions. Based on optical pumping on the hyperfine-split ground states, we propose a simple, all-optically controllable delay for synchronization of heralded narrow-band photons in a quantum network.
Hybrid interfaces between distinct quantum systems play a major role in the implementation of quantum networks. Quantum states have to be stored in memories to synchronize the photon arrival times for entanglement swapping by projective measurements in quantum repeaters or for entanglement purification. Here, we analyze the distortion of a single-photon wave packet propagating through a dispersive and absorptive medium with high spectral resolution. Single photons are generated from a single In(Ga)As quantum dot with its excitonic transition precisely set relative to the Cesium D1 transition. The delay of spectral components of the single-photon wave packet with almost Fourier-limited width is investigated in detail with a 200 MHz narrow-band monolithic Fabry-Pérot resonator. Reflecting the excited state hyperfine structure of Cesium, “slow light” and “fast light” behavior is observed. As a step towards room-temperature alkali vapor memories, quantum dot photons are delayed for 5 ns by strong dispersion between the two 1.17 GHz hyperfine-split excited state transitions. Based on optical pumping on the hyperfine-split ground states, we propose a simple, all-optically controllable delay for synchronization of heralded narrow-band photons in a quantum network.