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arXiv:1505.04118 · Journal of Modern Optics

Multimode Raman light-atom interface in warm atomic ensemble as multiple three-mode quantum operations

Michal P. Parniak, Daniel Pęcak, Wojciech Wasilewski

Published Dec 27, 2015• 4 citations
arXivHTMLPDF

Abstract

We analyse the properties of a Raman quantum light-atom interface in long atomic ensemble and its applications as a quantum memory or two-mode squeezed state generator. We consider the weak-coupling regime and include both Stokes and anti-Stokes scattering and the effects of Doppler broadening in buffer gas assuming frequent velocity-averaging collisions. We find the Green functions describing multimode transformation from input to output fields of photons and atomic excitations. Proper mode basis is found via singular value decomposition for short interaction times. It reveals that triples of modes are coupled by a transformation equivalent to a combination of two beamsplitters and a two-mode squeezing operation. We analyse the possible transformations on an example of warm rubidium-87 vapour. The model we present bridges the gap between the Stokes only and anti-Stokes only interactions providing simple, universal description in a temporally and longitudinally multimode situation. Our results also provide an easy way to find an evolution of the states in a Schrödinger picture thus facilitating understanding and design.

DOI
10.1080/09500340.2015.1125538

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We analyse the properties of a Raman quantum light-atom interface in long atomic ensemble and its applications as a quantum memory or two-mode squeezed state generator. We consider the weak-coupling regime and include both Stokes and anti-Stokes scattering and the effects of Doppler broadening in buffer gas assuming frequent velocity-averaging collisions. We find the Green functions describing multimode transformation from input to output fields of photons and atomic excitations. Proper mode basis is found via singular value decomposition for short interaction times. It reveals that triples of modes are coupled by a transformation equivalent to a combination of two beamsplitters and a two-mode squeezing operation. We analyse the possible transformations on an example of warm rubidium-87 vapour. The model we present bridges the gap between the Stokes only and anti-Stokes only interactions providing simple, universal description in a temporally and longitudinally multimode situation. Our results also provide an easy way to find an evolution of the states in a Schrödinger picture thus facilitating understanding and design.
We present an experimental demonstration of the Hamiltonian manipulation in light-atom interface in Raman-type warm rubidium-87 vapor atomic memory. By adjusting the detuning of the driving beam we varied the relative contributions of the Stokes and anti-Stokes scattering to the process of four-wave mixing which reads out a spatially multimode state of atomic memory. We measured the temporal evolution of the readout fields and the spatial intensity correlations between write-in and readout as a function of detuning with the use of an intensified camera. The correlation maps enabled us to resolve between the anti-Stokes and the Stokes scattering and to quantify their contributions. Our experimental results agree quantitatively with a simple, plane-wave theoretical model we provide. They allow for a simple interpretation of the coaction of the anti-Stokes and the Stokes scattering at the readout stage. The Stokes contribution yields additional, adjustable gain at the readout stage, albeit with inevitable extra noise. Here we provide a simple and useful framework to trace it and the results can be utilized in the existing atomic memories setups. Furthermore, the shown Hamiltonian manipulation offers a broad range of atom-light interfaces readily applicable in current and future quantum protocols with atomic ensembles.
We apply collective Raman scattering to create, store and retrieve spatially multimode light in warm rubidium-87 vapors. The light is created in a spontaneous Stokes scattering process. This is accompanied by the creation of counterpart collective excitations in the atomic ensemble - the spin waves. After a certain storage time we coherently convert the spin waves into the light in deterministic anti-Stokes scattering. The whole process can be regarded as a delayed four-wave mixing which produces pairs of correlated, delayed random images. Storage of higher order spatial modes up to microseconds is possible owing to usage of a buffer gas. We study the performance of the Raman scattering, storage and retrieval of collective excitations focusing on spatial effects and the influence of decoherence caused by diffusion of rubidium atoms in different buffer gases. We quantify the number of modes created and retrieved by analyzing statistical correlations of intensity fluctuations between portions of the light scattered in the far field.
We analyze quantum entanglement of Stokes light and atomic electronic polarization excited during single-pass, linear-regime, stimulated Raman scattering in terms of optical wave-packet modes, and atomic-ensemble spatial modes. The output of this process is confirmed to be decomposable into multiple discrete, Bosonic mode pairs, each pair undergoing independent evolution into a two-mode squeezed state. For this we extend the Bloch-Messiah reduction theorem, previously known for discrete linear systems [S. L. Braunstein, Phys. Rev. A 71, 055801 (2005)]. We present typical mode functions in the case of one-dimensional scattering in an atomic vapor. We find that in the absence of dispersion, one mode pair dominates the process, leading to a simple interpretation of entanglement in this continuous-variable system. However, many mode pairs are excited in the presence of dispersion-induced temporal walkoff of the Stokes, as witnessed by the photon-count statistics. We also consider the readout of the stored atomic polarization using the anti-Stokes scattering process. We prove that the readout process can also be decomposed into multiple mode pairs, each pair undergoing independent evolution analogous to a beam-splitter transformation. We show that this process can have unit efficiency under realistic experimental conditions. The shape of the output light wave packet can be predicted. In the case of unit readout efficiency it contains only excitations originating from a specified atomic excitation mode.
A theoretical model describing the Raman scattering process in atomic vapors is constructed. The treatment investigates the low-excitation regime suitable for modern experimental applications. Despite the incorporated decoherence effects (possibly mode dependent) it allows for a direct separation of the time evolution from the spatial degrees of freedom. The impact of noise on the temporal properties of the process is examined. The model is applied in two experimentally relevant situations of ultracold and room-temperature atoms. The spatial eigenmodes of the Stokes photons and their coupling to atomic excitations are computed. Similarly, dynamics and the waveform of the collective atomic state are derived for quantum memory implementations.
We analyse a novel squeezing and entangling mechanism which is due to correlated Stokes and anti-Stokes photon forward scattering in a multi-level atom vapour. We develop a full quantum model for an alkali atomic vapour including quantized collective atomic states which predicts high degree of squeezing for attainable experimental conditions. Following the proposal we present an experimental demonstration of 3.5 dB pulsed frequency nondegenerate squeezed (quadrature entangled) state of light using room temperature caesium vapour. The source is very robust and requires only a few milliwatts of laser power. The squeezed state is generated in the same spatial mode as the local oscillator and in a single temporal mode. The two entangled modes are separated by twice the Zeeman frequency of the vapour which can be widely tuned. The narrow-band squeezed light generated near an atomic resonance can be directly used for atom-based quantum information protocols. Its single temporal mode characteristics make it a promising resource for quantum information processing.