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Register a new userAn AC Stark Gradient Echo Memory in Cold Atoms
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The burgeoning fields of quantum computing and quantum key distribution have created a demand for a quantum memory. The gradient echo memory scheme is a quantum memory candidate for light storage that can boast efficiencies approaching unity, as well as the flexibility to work with either two or three level atoms. The key to this scheme is the frequency gradient that is placed across the memory. Currently the three level implementation uses a Zeeman gradient and warm atoms. In this paper we model a new gradient creation mechanism - the ac Stark effect - to provide an improvement in the flexibility of gradient creation and field switching times. We propose this scheme in concert with a move to cold atoms (~1 mK). These temperatures would increase the storage times possible, and the small ensemble volumes would enable large ac Stark shifts with reasonable laser power. We find that memory bandwidths on the order of MHz can be produced with experimentally achievable laser powers and trapping volumes, with high precision in gradient creation and switching times on the order of nanoseconds possible. By looking at the different decoherence mechanisms present in this system we determine that coherence times on the order of 10s of milliseconds are possible, as are delay-bandwidth products of approximately 50 and efficiencies over 90%.
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Quantum memories are an integral component of quantum repeaters - devices that will allow the extension of quantum key distribution to communication ranges beyond that permissible by passive transmission. A quantum memory for this application needs to be highly efficient and have coherence times approaching a millisecond. Here we report on work towards this goal, with the development of a $^{87}$Rb magneto-optical trap with a peak optical depth of 1000 for the D2 $F=2 rightarrow F=3$ transition using spatial and temporal dark spots. With this purpose-built cold atomic ensemble to implement the gradient echo memory (GEM) scheme. Our data shows a memory efficiency of $80pm 2$% and coherence times up to 195 $mu$s, which is a factor of four greater than previous GEM experiments implemented in warm vapour cells.
We study the storage and retrieval of images in a hot atomic vapor using the gradient echo memory protocol. We demonstrate that this technique allows for the storage of multiple spatial modes. We study both spatial and temporal multiplexing by storing a sequence of two different images in the atomic vapor. The effect of atomic diffusion on the spatial resolution is discussed and characterized experimentally. For short storage time a normalized cross-correlation between a retrieved image and its input of 88 % is reported.
We show that portions of an image written into a gradient echo memory can be individually retrieved or erased on demand, an important step towards processing a spatially multiplexed quantum signal. Targeted retrieval is achieved by locally addressing the transverse plane of the storage medium, a warm 85Rb vapor, with a far-detuned control beam. Spatially addressable erasure is similarly implemented by imaging a bright beam tuned near the 85Rb D1 line in order to scatter photons and induce decoherence. Under our experimental conditions atomic diffusion is shown to impose an upper bound on the effective spatial capacity of the memory. The decoherence induced by the optical eraser is characterized and modeled as the response of a two level atom in the presence of a strong driving field.
We experimentally demonstrate a ring geometry all-fiber cavity system for cavity quantum electrodynamics with an ensemble of cold atoms. The fiber cavity contains a nanofiber section which mediates atom-light interactions through an evanescent field. We observe well-resolved, vacuum Rabi splitting of the cavity transmission spectrum in the weak driving limit due to a collective enhancement of the coupling rate by the ensemble of atoms within the evanescent field, and we present a simple theoretical model to describe this. In addition, we demonstrate a method to control and stabilize the resonant frequency of the cavity by utilizing the thermal properties of the nanofiber.
We investigate the effect of far-off-resonant trapping light on ultracold bosonic RbCs molecules. We use kHz-precision microwave spectroscopy to measure the differential AC Stark shifts between the ground and first excited rotational levels of the molecule with hyperfine-state resolution. We demonstrate through both experiment and theory that coupling between neighboring hyperfine states manifests in rich structure with many avoided crossings. This coupling may be tuned by rotating the polarization of the linearly polarized trapping light. A combination of spectroscopic and parametric heating measurements allows complete characterization of the molecular polarizability at a wavelength of 1550~nm in both the ground and first excited rotational states.
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