Duncan G. England

Entangling macroscopic diamonds at room temperature.

Optical pulses are used to quantum mechanically entangle two diamonds several centimeters apart. Quantum entanglement in the motion of macroscopic solid bodies has implications both for quantum technologies and foundational studies of the boundary between the quantum and classical worlds. Entanglement is usually fragile in room-temperature solids, owing to strong interactions both internally and with the noisy environment. We generated motional entanglement between vibrational states of two spatially separated, millimeter-sized diamonds at room temperature. By measuring strong nonclassical correlations between Raman-scattered photons, we showed that the quantum state of the diamonds has positive concurrence with 98% probability. Our results show that entanglement can persist in the classical context of moving macroscopic solids in ambient conditions.

Quantum memories: emerging applications and recent advances

Quantum light–matter interfaces are at the heart of photonic quantum technologies. Quantum memories for photons, where non-classical states of photons are mapped onto stationary matter states and preserved for subsequent retrieval, are technical realizations enabled by exquisite control over interactions between light and matter. The ability of quantum memories to synchronize probabilistic events makes them a key component in quantum repeaters and quantum computation based on linear optics. This critical feature has motivated many groups to dedicate theoretical and experimental research to develop quantum memory devices. In recent years, exciting new applications, and more advanced developments of quantum memories, have proliferated. In this review, we outline some of the emerging applications of quantum memories in optical signal processing, quantum computation and non-linear optics. We review recent experimental and theoretical developments, and their impacts on more advanced photonic quantum technologies based on quantum memories.

Multi-pulse addressing of a Raman quantum memory: Configurable beam splitting and efficient readout

We address an optical quantum memory with multiple pulses, enabling unit efficiency readout and programmable beam splitting. The resulting coherent processor with built-in storage is universal for scalable photonic quantum information processing.

Interfacing GHz-bandwidth heralded single photons with a warm vapour Raman memory

Broadband quantum memories, used as temporal multiplexers, are a key component in photonic quantum information processing, as they make repeat-until-success strategies scalable. We demonstrate a prototype system, operating on-demand, by interfacing a warm vapour, high time-bandwidth-product Raman memory with a travelling wave spontaneous parametric down-conversion source. We store single photons and observe a clear influence of the input photon statistics on the retrieved light, which we find currently to be limited by noise. We develop a theoretical model that identifies four-wave mixing as the sole important noise source and point towards practical solutions for noise-free operation.

Storage and retrieval of THz-bandwidth single photons using a room-temperature diamond quantum memory.

We report the storage and retrieval of single photons, via a quantum memory, in the optical phonons of a room-temperature bulk diamond. The THz-bandwidth heralded photons are generated by spontaneous parametric down-conversion and mapped to phonons via a Raman transition, stored for a variable delay, and released on demand. The second-order correlation of the memory output is g((2))(0)=0.65±0.07, demonstrating a preservation of nonclassical photon statistics throughout storage and retrieval. The memory is low noise, high speed and broadly tunable; it therefore promises to be a versatile light-matter interface for local quantum processing applications.

Toward quantum processing in molecules: a THz-bandwidth coherent memory for light.

The unusual features of quantum mechanics are enabling the development of technologies not possible with classical physics. These devices utilize nonclassical phenomena in the states of atoms, ions, and solid-state media as the basis for many prototypes. Here we investigate molecular states as a distinct alternative. We demonstrate a memory for light based on storing photons in the vibrations of hydrogen molecules. The THz-bandwidth molecular memory is used to store 100-fs pulses for durations up to ~1 ns, enabling ~10(4) operational time bins. The results demonstrate the promise of molecules for constructing compact ultrafast quantum photonic technologies.

High-fidelity polarization storage in a gigahertz bandwidth quantum memory

We demonstrate a dual-rail optical Raman memory inside a polarization interferometer; this enables us to store polarization-encoded information at GHz bandwidths in a room-temperature atomic ensemble. By performing full process tomography on the system, we measure up to 97 ± 1% process fidelity for the storage and retrieval process. At longer storage times, the process fidelity remains high, despite a loss of efficiency. The fidelity is 86 ± 4% for 1.5 μs storage time, which is 5000 times the pulse duration. Hence, high fidelity is combined with a large time-bandwidth product. This high performance, with an experimentally simple setup, demonstrates the suitability of the Raman memory for integration into large-scale quantum networks.

Frequency and bandwidth conversion of single photons in a room-temperature diamond quantum memory.

The spectral manipulation of photons is essential for linking components in a quantum network. Large frequency shifts are needed for conversion between optical and telecommunication frequencies, while smaller shifts are useful for frequency-multiplexing quantum systems, in the same way that wavelength division multiplexing is used in classical communications. Here we demonstrate frequency and bandwidth conversion of single photons in a room-temperature diamond quantum memory. Heralded 723.5 nm photons, with 4.1 nm bandwidth, are stored as optical phonons in the diamond via a Raman transition. Upon retrieval from the diamond memory, the spectral shape of the photons is determined by a tunable read pulse through the reverse Raman transition. We report central frequency tunability over 4.2 times the input bandwidth, and bandwidth modulation between 0.5 and 1.9 times the input bandwidth. Our results demonstrate the potential for diamond, and Raman memories in general, as an integrated platform for photon storage and spectral conversion.Kent A.G. Fisher,1 Duncan G. England,2 Jean-Philippe W. MacLean,1 Philip J. Bustard,2 Kevin J. Resch,1 and Benjamin J. Sussman2, 3 Institute for Quantum Computing and Department of Physics & Astronomy, University of Waterloo, 200 University Avenue West, Waterloo, Ontario N2L 3G1, Canada National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, K1A 0R6, Canada Physics Department, University of Ottawa, 150 Louis Pasteur, Ottawa, Ontario, K1N 6N5, Canada (Dated: September 21, 2015)

Pump-probe study of the formation of rubidium molecules by ultrafast photoassociation of ultracold atoms

An experimental pump-probe study of the photoassociative creation of translationally ultracold rubidium molecules is presented together with numerical simulations of the process. The formation of loosely bound excited-state dimers is observed as a first step toward a fully coherent pump-dump approach to the stabilization of

Efficient Raman generation in a waveguide: A route to ultrafast quantum random number generation

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