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Register a new userInterfacing GHz-bandwidth heralded single photons with a room-temperature Raman quantum memory
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Added by
Patrick Michelberger
Publication date
2014
fields
Physics
and research's language is
English
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Photonics is a promising platform for quantum technologies. However, photon sources and two-photon gates currently only operate probabilistically. Large-scale photonic processing will therefore be impossible without a multiplexing strategy to actively select successful events. High time-bandwidth-product quantum memories - devices that store and retrieve single photons on-demand - provide an efficient remedy via active synchronisation. Here we interface a GHz-bandwidth heralded single-photon source and a room-temperature Raman memory with a time-bandwidth product exceeding 1000. We store heralded single photons and observe a clear influence of the input photon statistics on the retrieved light, which agrees with our theoretical model. The preservation of the stored fields statistics is limited by four-wave-mixing noise, which we identify as the key remaining challenge in the development of practical memories for scalable photonic information processing.
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Narrowband single photons that couple well to atomic ensembles could prove essential for future quantum networks, but the efficient generation of such photons remains an outstanding challenge. We realize a spatially-multiplexed heralded source of single photons that are inherently compatible with the commonly employed D2 line of rubidium. Our source is based on four-wave mixing in hot rubidium vapor, requiring no laser cooling or optical cavities, and generates single photons with high rate and low noise. We use Hong-Ou-Mandel interference to verify the indistinguishability of the photons generated in two different (multiplexed) channels. We further demonstrate a five-fold tunability of the photons temporal width. The experimental results are well reproduced by a theoretical model.
Optically induced ultrafast switching of single photons is demonstrated by rotating the photon polarization via the Kerr effect in a commercially available single mode fiber. A switching efficiency of 97% is achieved with a $sim1.7$,ps switching time, and signal-to-noise ratio of $sim800$. Preservation of the quantum state is confirmed by measuring no significant increase in the second-order autocorrelation function $g^{(2)}(0)$. These values are attained with only nanojoule level pump energies that are produced by a laser oscillator with 80,MHz repetition rate. The results highlight a simple switching device capable of both high-bandwidth operations and preservation of single-photon properties for applications in photonic quantum processing and ultrafast time-gating or switching.
Broadband quantum memories hold great promise as multiplexing elements in future photonic quantum information protocols. Alkali vapour Raman memories combine high-bandwidth storage, on-demand read-out, and operation at room temperature without collisional fluorescence noise. However, previous implementations have required large control pulse energies and suffered from four-wave mixing noise. Here we present a Raman memory where the storage interaction is enhanced by a low-finesse birefringent cavity tuned into simultaneous resonance with the signal and control fields, dramatically reducing the energy required to drive the memory. By engineering anti-resonance for the anti-Stokes field, we also suppress the four-wave mixing noise and report the lowest unconditional noise floor yet achieved in a Raman-type warm vapour memory, $(15pm2)times10^{-3}$ photons per pulse, with a total efficiency of $(9.5pm0.5)$%.
Single photon emitters are indispensable to photonic quantum technologies. Here we demonstrate waveform-controlled high-purity single photons from room-temperature colloidal quantum dots. The purity of the single photons does not vary with the excitation power, thereby allowing the generation rate to be increased without compromising the single-photon quality.
We perform experimental quantum polarimetry using a heralded single photon to analyze the optical activity of linearly polarized light traversing a chiral medium. Three kinds of estimators are considered to estimate the concentrations of sucrose solutions from measuring the rotation angle of the linear polarization of the output photons. Through repetition of independent and identical measurements performed for each individual scheme and different concentration sucrose solutions, we compare the estimation uncertainty among the three schemes. The results are also compared to classical benchmarks for which a coherent state of light is taken into account. The quantum enhancement in the estimation uncertainty is evaluated and the impact of experimental and technical imperfections is discussed. In this work, we lay out a route for future applications relying on quantum polarimetry.
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