Publications by authors named "Duncan England"

Strongly driven nonlinear optical processes such as spontaneous parametric down-conversion and spontaneous four-wave mixing can produce multiphoton nonclassical beams of light which have applications in quantum information processing and sensing. In contrast to the low-gain regime, new physical effects arise in a high-gain regime due to the interactions between the nonclassical light and the strong pump driving the nonlinear process. Here, we describe and experimentally observe a gain-induced group delay between the multiphoton pulses generated in a high-gain type-II spontaneous parametric down-conversion source.

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We propose a quantum information processing platform that utilizes the ultrafast time-bin encoding of photons. This approach offers a pathway to scalability by leveraging the inherent phase stability of collinear temporal interferometric networks at the femtosecond-to-picosecond timescale. The proposed architecture encodes information in ultrafast temporal bins processed using optically induced nonlinearities and birefringent materials while keeping photons in a single spatial mode.

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Holography is an established technique for measuring the wavefront of optical signals through interferometric combination with a reference wave. Conventionally the integration time of a hologram is limited by the interferometer coherence time, thus making it challenging to prepare holograms of remote objects, especially using weak illumination. Here, we circumvent this limitation by using intensity correlation interferometry.

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As first demonstrated by Hanbury Brown and Twiss, it is possible to observe interference between independent light sources by measuring correlations in their intensities rather than their amplitudes. In this work, we apply this concept of intensity interferometry to holography. We combine a signal beam with a reference and measure their intensity cross-correlations using a time-tagging single-photon camera.

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Hyperspectral imaging (HSI) has a wide range of applications from environmental monitoring to biotechnology. Conventional snapshot HSI techniques generally require a trade-off between spatial and spectral resolution and are thus limited in their ability to achieve high resolutions in both simultaneously. Most techniques are also resource inefficient with most of the photons lost through spectral filtering.

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We show a simple yet effective method that can be used to characterize the per pixel quantum efficiency and temporal resolution of a single photon event camera for quantum imaging applications. Utilizing photon pairs generated through spontaneous parametric down-conversion, the detection efficiency of each pixel, and the temporal resolution of the system, are extracted through coincidence measurements. We use this method to evaluate the TPX3CAM, with appended image intensifier, and measure an average efficiency of [Formula: see text]% and a temporal resolution of 7.

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We propose a quantum memory protocol based on trapping photons in a fiber-integrated cavity, comprised of a birefringent fiber with dichroic reflective end facets. Photons are switched into resonance with the fiber cavity by intracavity Bragg-scattering frequency translation, driven by ancillary control pulses. After the storage delay, photons are switched out of resonance with the cavity, again by intracavity frequency translation.

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In this work we demonstrate spectral-temporal correlation measurements of the Hong-Ou-Mandel (HOM) interference effect with the use of a spectrometer based on a photon-counting camera. This setup allows us to take, within seconds, spectral temporal correlation measurements on entangled photon sources with sub-nanometer spectral resolution and nanosecond timing resolution. Through post processing, we can observe the HOM behaviour for any number of spectral filters of any shape and width at any wavelength over the observable spectral range.

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Wavelength-tunable, time-locked pairs of ultrafast pulses are crucial in modern-day time-resolved measurements. We demonstrate a simple means of generating configurable optical pulse sequences: sub-picosecond pulses are carved out from a continuous wave laser via pump-induced optical Kerr switching in 10 cm of a commercial single-mode fiber. By introducing dispersion to the pump, the near transform-limited switched pulse duration is tuned between 305-570 fs.

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We examine the propagation of optical beams possessing different polarization states and spatial modes through the Ottawa River in Canada. A Shack-Hartmann wavefront sensor is used to record the distorted beam's wavefront. The turbulence in the underwater channel is analysed, and associated Zernike coefficients are obtained in real-time.

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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 ∼1.7  ps switching time and signal-to-noise ratio of ∼800.

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Photon pair sources have wide ranging applications in a variety of quantum photonic experiments and protocols. Many of these protocols require well controlled spectral correlations between the two output photons. However, due to low cross-sections, measuring the joint spectral properties of photon pair sources has historically been a challenging and time-consuming task.

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Optical quantum memories are an important component of future optical and hybrid quantum technologies. Raman schemes are strong candidates for use with ultrashort optical pulses due to their broad bandwidth; however, the elimination of deleterious four-wave mixing noise from Raman memories is critical for practical applications. Here, we demonstrate a quantum memory using the rotational states of hydrogen molecules at room temperature.

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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.

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Quantum interference of single photons is a fundamental aspect of many photonic quantum processing and communication protocols. Interference requires that the multiple pathways through an interferometer be temporally indistinguishable to within the coherence time of the photon. In this Letter, we use a diamond quantum memory to demonstrate interference between quantum pathways, initially temporally separated by many multiples of the optical coherence time.

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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.

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Quantum photonics offers much promise for the development of new technologies. The ability to control the interaction of light and matter at the level of single quantum excitations is a prerequisite for the construction of potentially powerful devices. Here we use the rotational levels of a room temperature ensemble of hydrogen molecules to couple two distinct optical modes at the single photon level using femtosecond pulses with 2 THz bandwidth.

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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.

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Random number sequences are a critical resource in modern information processing systems, with applications in cryptography, numerical simulation, and data sampling. We introduce a quantum random number generator based on the measurement of pulse energy quantum fluctuations in Stokes light generated by spontaneously-initiated stimulated Raman scattering. Bright Stokes pulse energy fluctuations up to five times the mean energy are measured with fast photodiodes and converted to unbiased random binary strings.

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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.

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The dynamics of the excited state during the photoassociation of cold molecules from cold rubidium atoms is studied in a series of pump-probe experiments. Dipole transitions similar to those of the atoms are observed in the molecular signal. While such behaviour is characteristic of the long-range molecules, the photoassociation of bound molecules is confirmed in additional experiments.

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