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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. We demonstrate storage of quantum-level THz-bandwidth coherent states for a lifetime up to 16 cavity round trips, or 200ns, and a maximum overall efficiency of 73%., Comment: 7 pages, 5 figures

In this work we investigate quantum-enhanced target detection in the presence of large background noise using multidimensional quantum correlations between photon pairs generated through spontaneous parametric down-conversion. Until now similar experiments have only utilized one of the photon pairs' many degrees of freedom such as temporal correlations and photon number correlations. Here, we utilized both temporal and spectral correlations of the photon pairs and achieved over an order of magnitude reduction to the background noise and in turn significant reduction to data acquisition time when compared to utilizing only temporal modes. We believe this work represents an important step in realizing a practical, real-time quantum-enhanced target detection system. The demonstrated technique will also be of importance in many other quantum sensing applications and quantum communications., 9 pages, 7 figures

At the fundamental level, quantum communication is ultimately limited by noise. For instance, quantum signals cannot be amplified without the introduction of noise in the amplified states. Furthermore, photon loss reduces the signal-to-noise ratio, accentuating the effect of noise. Thus, most of the efforts in quantum communications have been directed towards overcoming noise to achieve longer communication distances, larger secret key rates, or to operate in noisier environmental conditions. Here, we propose and experimentally demonstrate a platform for quantum communication based on ultrafast optical techniques. In particular, our scheme enables the experimental realization of high-rates and quantum signal filtering approaching a single spectro-temporal mode, resulting in a dramatic reduction in channel noise. By experimentally realizing a 1-ps optically induced temporal gate, we show that ultrafast time filtering can result in an improvement in noise tolerance by a factor of up to 1200 compared to a 2-ns electronic filter enabling daytime quantum key distribution or quantum communication in bright fibers., 11 pages, 9 figures

We describe a simple multivariate technique of likelihood ratios for improved discrimination of signal and background in multi-dimensional quantum target detection. The technique combines two independent variables, time difference and summed energy, of a photon pair from the spontaneous parametric down-conversion source into an optimal discriminant. The discriminant performance was studied in experimental data and in Monte-Carlo modelling with clear improvement shown compared to previous techniques. As novel detectors become available, we expect this type of multivariate analysis to become increasingly important in multi-dimensional quantum optics., The following article has been published by Applied Physics Letters. It can be found at https://aip.scitation.org/doi/10.1063/5.0012429

In order to enhance LIDAR performance metrics such as target detection sensitivity, noise resilience and ranging accuracy, we exploit the strong temporal correlation within the photon pairs generated in continuous-wave pumped semiconductor waveguides. The enhancement attained through the use of such non-classical sources is measured and compared to a corresponding target detection scheme based on simple photon-counting detection. The performances of both schemes are quantified by the estimation uncertainty and Fisher information of the probe photon transmission, which is a widely adopted sensing figure of merit. The target detection experiments are conducted with high probe channel loss (\(\simeq 1-5\times10^{-5}\)) and formidable environment noise up to 36 dB stronger than the detected probe power of \(1.64\times 10^{-5}\) pW. The experimental result shows significant advantages offered by the enhanced scheme with up to 26.3 dB higher performance in terms of estimation uncertainty, which is equivalent to a reduction of target detection time by a factor of 430 or 146 (21.6 dB) times more resilience to noise. We also experimentally demonstrated ranging with these non-classical photon pairs generated with continuous-wave pump in the presence of strong noise and loss, achieving \(\approx\)5 cm distance resolution that is limited by the temporal resolution of the detectors.

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. Our setup also offers great versatility in that it is capable of operating at a wide spectral range from the visible to the near infrared and does not require a pulsed pump laser for timing purposes. This work offers the ability to gain large amounts of spectral and temporal information from a HOM interferometer quickly and efficiently and will be a very useful tool for many quantum technology applications and fundamental quantum optics research.

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. Finally, we explore the feasibility of transmitting polarization states as well as spatial modes through the underwater channel for applications in quantum cryptography., 5 pages, 4 figures. Comments welcome

We investigate the use of correlated photon pair sources for the improved quantum-level detection of a target in the presence of a noise background. Photon pairs are generated by spontaneous four-wave mixing, one photon from each pair (the herald) is measured locally while the other (the signal) is sent to illuminate the target. Following diffuse reflection from the target, the signal photons are detected by a receiver and non-classical timing correlations between the signal and herald are measured in the presence of a configurable background noise source. Quantum correlations from the photon pair source can be used to provide an enhanced signal-to-noise ratio when compared to a classical light source of the same intensity., Comment: 8 pages, 9 figures

Cylindrical vector (CV) beams are a set of transverse spatial modes that exhibit a cylindrically symmetric intensity profile and a variable polarization about the beam axis. They are composed of a non-separable superposition of orbital and spin angular momenta. Critically, CV beams are also the eigenmodes of optical fiber and, as such, are of widespread practical importance in photonics and have the potential to increase communications bandwidth through spatial multiplexing. Here, we derive the coupled amplitude equations that describe the four-wave mixing (FWM) of CV beams in optical fibers. These equations allow us to determine the selection rules that govern the interconversion of CV modes in FWM processes. With these selection rules, we show that FWM conserves the total angular momentum, the sum of orbital and spin angular momenta, in the conversion of two input photons to two output photons. When applied to spontaneous FWM, the selection rules show that photon pairs can be generated in CV modes directly and can be entangled in those modes. Such quantum states of light in CV modes could benefit technologies such as quantum key distribution with satellites.

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. Two- and four-pulse signal trains are also generated by adding birefringent α-BBO plates in the pump beam. These results highlight an ultrafast light source with intrinsic timing stability and pulse-to-pulse phase coherence, where pulse generation could be adapted to wavelengths ranging from ultraviolet to infrared.

Quantum frequency conversion is a powerful tool for the construction of hybrid quantum photonic technologies. Raman quantum memories are a promising method of conversion due to their broad bandwidths. Here we demonstrate frequency conversion of THz-bandwidth, fs-duration photons at the single-photon level using a Raman quantum memory based on the rotational levels of hydrogen molecules. We shift photons from 765 nm to wavelengths spanning from 673 to 590 nm---an absolute shift of up to 116 THz. We measure total conversion efficiencies of up to 10% and a maximum signal-to-noise ratio of 4.0(1):1, giving an expected conditional fidelity of 0.75, which exceeds the classical threshold of 2/3. Thermal noise could be eliminated by cooling with liquid nitrogen, giving noiseless conversion with wide tunability in the visible and infrared.

The encoding of quantum information in photonic time-bin qubits is apt for long-distance quantum communication schemes. In practice, due to technical constraints such as detector response time, or the speed with which copolarized time-bins can be switched, other encodings, e.g., polarization, are often preferred for operations like state detection. Here, we present the conversion of qubits between polarization and time-bin encodings by using a method that is based on an ultrafast optical Kerr shutter and attain efficiencies of 97% and an average fidelity of $0.827\ifmmode\pm\else\textpm\fi{}0.003$ with shutter speeds near 1 ps. Our demonstration delineates an essential requirement for the development of hybrid and high-rate optical quantum networks.

Bulk diamond phonons have been shown to be a versatile platform for the generation, storage, and manipulation of high-bandwidth quantum states of light. Here we demonstrate a diamond quantum memory that stores, and releases on demand, an arbitrarily polarized $\ensuremath{\sim}250$ fs duration photonic qubit. The single-mode nature of the memory is overcome by mapping the two degrees of polarization of the qubit, via Raman transitions, onto two spatially distinct optical phonon modes located in the same diamond crystal. The two modes are coherently recombined upon retrieval and quantum process tomography confirms that the memory faithfully reproduces the input state with average fidelity $0.784\ifmmode\pm\else\textpm\fi{}0.004$ with a total memory efficiency of $(0.76\ifmmode\pm\else\textpm\fi{}0.03)%$. In an additional demonstration, one photon of a polarization-entangled pair is stored in the memory. We report that entanglement persists in the retrieved state for up to 1.3 ps of storage time. These results demonstrate that the diamond phonon platform can be used in concert with polarization qubits, a key requirement for polarization-encoded photonic processing.

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. Preservation of the single-photon properties 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 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.

The ability to store multiple optical modes in a quantum memory allows for increased efficiency of quantum communication and computation. Here we compute the multimode capacity of a variety of quantum memory protocols based on light storage in ensembles of atoms. We find that adding a controlled inhomogeneous broadening improves this capacity significantly., Published version. Many thanks are due to Christoph Simon for his help and suggestions. (This acknowledgement is missing from the final draft: apologies!)

We propose a scheme for preparation of high-coherence molecular dynamics which are phase stable with respect to ultrashort pulses. We experimentally demonstrate an example of this scheme using a phase-independent, nanosecond-duration, pump pulse to prepare a rotational coherence in molecular hydrogen. This rotational coherence is made phase stable with respect to a separate source of ultrashort pulses by seeding. The coherence is used to generate spectral broadening of femtosecond probe radiation by molecular phase modulation.

Received 12 April 2008; revised manuscript received 1 September 2008; published 9 October 2008A technique to measure the decoherence time of optical phonons in a solid is presented. Phonons are excitedwith a pair of time-delayed 80 fs near infrared pulses via spontaneous transient Raman scattering. The spectralfringe visibility of the resulting Raman pulse pair, as a function of time delay, is used to measure the phonondephasing time. The method avoids the need to use either narrow band or few femtosecond pulses and is usefulfor low phonon excitations. The dephasing time of phonons created in bulk diamond is measured to be =6.8 ps −1 =1.56 cm .DOI: 10.1103/PhysRevB.78.155201 PACS number s : 78.30.Am, 81.70.Fy, 65.40. b, 63.20.Ry

We propose and experimentally demonstrate a scheme to generate optically controlled delays based on off-resonant Raman absorption. Dispersion in a transparency window between two neighboring, optically activated Raman absorption lines is used to reduce the group velocity of broadband 765 nm pulses. We implement this approach in a potassium titanyl phosphate (KTP) waveguide at room temperature, and demonstrate Raman-induced delays of up to 140 fs for a 650-fs duration, 1.8-THz bandwidth, pulse. Our approach should be applicable to single-photon signals, offers wavelength tunability, and is a step toward processing ultrafast photons.

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., Controlling the spectral properties of single photons is important for emerging optical quantum technologies, but doing so in a frequency-multiplexed framework is challenging. Here, the authors demonstrate quantum frequency conversion with a Raman quantum memory in room-temperature diamond.

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 nonlinear optics. We review recent experimental and theoretical developments, and their impacts on more advanced photonic quantum technologies based on quantum memories., Review paper. Comments are welcome!

The dynamic Stark effect is the quasistatic shift in energy levels due to the application of optical fields. The effect is in many ways similar to the static Stark effect. However, the dynamic Stark effect can be applied on rapid time scales and with high energies, comparable to those of atoms and molecules themselves. The dynamic Stark effect due to nonresonant laser fields is used in a myriad of contemporary experiments to hold and align molecules, to shape potential energy surfaces, and to make rapid transient birefringence. Five approaches of increasing sophistication are used to describe the dynamic Stark effect. One application, molecular alignment, is summarized and a comparison is made between the dynamic Stark effect and Stokes light generation in a Raman scattering process. © 2011 American Association of Physics Teachers.

Transient Coherent Ultrafast Phonon Spectroscopy (TCUPS) is utilized to study phonon dephasing lifetimes in various diamond types. Samples of natural, chemical vapour deposited, and high pressure high temperature diamond are compared showing significant differences. Dephasing mechanisms are discussed. © 2010 Elsevier B.V. All rights reserved.

The absorption of broadband photons in atomic ensembles requires either an effective broadening of the atomic transition linewidth, or an off-resonance Raman interaction. Here we propose a scheme for a quantum memory capable of storing and retrieving ultrafast photons in an ensemble of two-level atoms by using a propagation medium with a time-dependent refractive index generated from aligning an ensemble of gas-phase diatomic molecules. The refractive index dynamics generates an effective longitudinal inhomogeneous broadening of the two-level transition. We numerically demonstrate this scheme for storage and retrieval of a weak pulse as short as 50 fs, with a storage time of up to 20 ps. With additional optical control of the molecular alignment dynamics, the storage time can be extended about one nanosecond leading to time-bandwidth products of order $10^4$. This scheme could in principle be achieved using either a hollow-core fiber or a high-pressure gas cell, in a gaseous host medium comprised of diatomic molecules and a two-level atomic vapor at room temperature., Comment: 7 pages, 6 figures. Fixed typos

We report the storage and retrieval of single photons, via a quantum memory, in the optical phonons of room-temperature bulk diamond. The THz-bandwidth heralded photons are generated by spontaneous parametric downconversion 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 $g^{(2)}(0) = 0.65 \pm 0.07$, demonstrating preservation of non-classical 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., 6 pages, 4 figures

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.

A new algorithm was developed to classify populations of binary (black and white) images of cloud particles collected with Particle Measuring Systems (PMS) Optical Array Probes (OAPA). The algorithm classifies images into four habit categories: ‘‘spheres,’’ ‘‘irregulars,’’ ‘‘needles,’’ and ‘‘dendrites.’’ The present algorithm derives the particle habits from an analysis of dimensionless ratios of simple geometrical measures such as the x and y dimensions, perimeter, and image area. For an ensemble of images containing a mixture of different habits, the distribution of a particular ratio will be a linear superposition of basis distributions of ratios of the individual habits. The fraction of each habit in the ensemble is found by solving the inverse problem. One of the advantages of the suggested scheme is that it provides recognition analysis of both ‘‘complete’’ and ‘‘partial’’ images, that is, images that are completely or partially contained within the sample area of the probe. The ability to process ‘‘partial’’ images improves the statistics of the recognition by approximately 50% when compared with retrievals that use ‘‘complete’’ images only. The details of this algorithm are discussed in this study.

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 1ns, enabling 10,000 operational time bins. The results demonstrate the promise of molecules for constructing compact ultrafast quantum photonic technologies., Comment: 5 pages, 3 figures, 1 table

Time-resolved photoelectron imaging was used to investigate the dynamical evolution of the initially prepared S(1) (ππ*) excited state of phenol (hydroxybenzene), catechol (1,2-dihydroxybenzene), resorcinol (1,3-dihydroxybenzene), and hydroquinone (1,4-dihydroxybenzene) following excitation at 267 nm. Our analysis was supported by ab initio calculations at the coupled-cluster and CASSCF levels of theory. In all cases, we observe rapid (

We demonstrate entanglement between the vibrational mode of two macroscopic, spatially-separated diamonds at room temperature with ultrashort pulses and a far-off-resonant Raman interaction. © 2012 OSA., 2012 Conference on Lasers and Electro-Optics, CLEO 2012, May 6-11, 2012, San Jose, CA, USA

The non-resonant dynamic Stark effect is a powerful and general way of manipulating ultrafast processes in atoms, molecules, and solids with exquisite precision. We discuss the physics behind this effect, and demonstrate its efficacy as a method of control in a variety of systems. These applications range from the control of molecular rotational dynamics to the manipulation of chemical reaction dynamics, and from the suppression of vacuum fluctuation effects in coherent preparation of matter, to the dynamic generation of bandwidth for storage of broadband quantum states of light.

We present an overview of developments using the nonresonant dynamic Stark effect within the fields of time-resolved molecular dynamics and quantum control, drawing on examples from our own recent work. Particular emphasis is placed on the notion that “dynamics” and “control” are not distinct disciplines and that a clear synergy exits between these areas which has, up to now, been somewhat underexploited. The dynamic Stark effect is a universal interaction which we expect to have broad applicability.

We demonstrate the coherent storage and retrieval of sub-nanosecond low-intensity light pulses with spectral bandwidths exceeding 1 GHz in cesium vapor, using the novel, far off-resonant two-photon Raman memory protocol. © 2010 Optical Society of America.

Quantum memories, capable of controllably storing and releasing a photon, are a crucial component for quantum computers and quantum communications. So far, quantum memories have operated with bandwidths that limit data rates to MHz. Here we report the coherent storage and retrieval of sub-nanosecond low intensity light pulses with spectral bandwidths exceeding 1 GHz in cesium vapor. The novel memory interaction takes place via a far off-resonant two-photon transition in which the memory bandwidth is dynamically generated by a strong control field. This allows for an increase in data rates by a factor of almost 1000 compared to existing quantum memories. The memory works with a total efficiency of 15% and its coherence is demonstrated by directly interfering the stored and retrieved pulses. Coherence times in hot atomic vapors are on the order of microsecond - the expected storage time limit for this memory., 13 pages, 5 figures

In general, many different diagrams can contribute to the signal measured in broadband four-wave mixing experiments. Care must therefore be taken when designing an experiment to be sensitive to only the desired diagram by taking advantage of phase matching, pulse timing, sequence, and the wavelengths employed. We use sub-25 fs pulses to create and monitor vibrational wavepackets in gaseous iodine, bromine, and iodine bromide through time- and frequency-resolved femtosecond coherent anti-Stokes Raman scattering (CARS) spectroscopy. We experimentally illustrate this using iodine, where the broad bandwidths of our pulses, and Boltzmann population in the lower three vibrational levels conspire to make a single diagram dominant in one spectral region of the signal spectrum. In another spectral region, however, the signal is the sum of two almost equally contributing diagrams, making it difficult to directly extract information about the molecular dynamics. We derive simple analytical expressions for the time- and frequency-resolved CARS signal to study the interplay of different diagrams. Expressions are given for all five diagrams which can contribute to the CARS signal in our case.

The focusing of coherent light, modified by a spatial light modulator (SLM) based 4-f pulse shaper, is discussed in the context of scalar diffraction theory. Diffractive effects (including space-time coupling) in SLMs may alter the size and shape of a subsequent laser focus. A numerical approach is used to investigate the effects of some common phase masks on the properties of the laser focus. The extreme case of an alternating phase mask is considered in some detail, as it clearly illustrates the effects of space-time coupling. The results are compared to a simple analytic model. The potential influence of SLM diffractive effects on multiphoton quantum control studies is discussed and some approaches to minimizing undesirable diffractive effects are suggested.

We propose a method that enables efficient storage and retrieval of a photonic excitation stored in an ensemble quantum memory consisting of Lambda-type absorbers with non-zero Stokes shift. We show that this can be used to implement a multimode quantum memory storing multiple frequency-encoded qubits in a single ensemble, and allowing their selective retrieval. The read-out scheme applies to memory setups based on both electromagnetically-induced transparency and stimulated Raman scattering, and spatially separates the output signal field from the control fields.

Nonperturbative quantum control schemes in the intermediate field strength (nonionizing) regime are investigated. We restrict the matter-field interaction to the nonresonant dynamic Stark effect (NRDSE) as induced by infrared laser fields, which we argue is a new and general tool for quantum control of atomic and molecular dynamics. For the case of Raman coupled matter states, an effective Hamiltionian may be constructed, and quantum control via NRDSE may be thought of as reversibly modifying the effective Hamiltonian during system propagation, thus leading to control over dynamic processes. As an illustration, the creation of field-free “switched” wave packets through the adiabatic turn on and sudden turn off of the NRDSE is considered and experimentally demonstrated. Wave packets generated through the switched NRDSE interaction may be very different in form and content than wave packets generated via resonant transitions with Gaussian optical pulses. In order to provide an example, we discuss the specific case of rotational wave packet dynamics where the NRDSE manifests itself as molecular axis alignment. This technique is applied to the creation of field-free molecular axis alignment using an intense switched 1.064μm laser pulse. This switched laser pulse was generated via a plasma shuttering technique, giving a pulse with a rise time of 150ps and a fall time of 170fs. The temporal evolution of the molecular axis alignment is probed via the optical Kerr effect. Field-free alignment via the switched NRDSE is demonstrated for both linear (CO2, CS2) and symmetric top (1,2-propadiene) polyatomic molecules.

The nonresonant dynamic Stark effect (NRDSE) is investigated as a general tool for quantum control in the intermediate field strength regime (nonperturbative but nonionizing). We illustrate this scheme for the case of nonadiabatic molecular photodissociation at an avoided crossing. Using the NRDSE exclusively, both the electronic branching ratio and predissociation lifetime may be controlled. Infrared control pulses are used to modify the field-free dynamical evolution during traversal of the avoided crossing, thus controlling the nonadiabatic branching ratio. Predissociation lifetimes may be either increased or decreased using properly timed short infrared pulses to modify phase differences between the diabatic wave packets. In contrast with the limiting cases of perturbative control (interference between transitions) and strong field control with ionizing laser fields, control via the NRDSE may be thought of as reversibly modifying the effective Hamiltonian during system propagation.

We investigate strategies for field-free three dimensional molecular axis alignment using strong nonresonant laser fields under experimentally realistic conditions. Using the polarizabilites and rotational constants of an asymmetric top rotor molecule (ethene, C2H4), we consider three different methods for axis alignment of a Boltzmann distribution of rotors at 4 K. Specifically, we compare the use of impulsive kick laser pulses having both linear and elliptical polarization to the use of elliptically polarized switched laser pulses. We show that an enhanced degree of field-free three dimensional alignment of ground vibronic state molecules obtains from the use of two orthogonally polarized, time-separated laser pulses.

The dynamic Stark effect due to a strong nonresonant but nonionizing laser field provides a route to quantum control via the creation of novel superposition states. We consider the creation of a field-free "switched" wave packet through adiabatic turn-on and sudden turn-off of a strong dynamic Stark interaction. There are two limiting cases for such wave packets. The first is a Raman-type coupling, illustrated by the creation of field-free molecular axis alignment. An experimental demonstration is given. The second case is that of dipole-type coupling, illustrated by the creation of charge localization in an array of quantum wells.

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. Since the pulse energy is a continuous variable, multiple bits can be extracted from a single measurement. Our approach can be generalized to a wide range of Raman active materials; here we demonstrate a prototype using the optical phonon line in bulk diamond.

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. © Published under licence by IOP Publishing Ltd.

Underwater quantum communication has recently been explored using polarization and orbital angular momentum (OAM). Here, we show that spatially structured modes, e.g., a coherent superposition of beams carrying both polarization and OAM, can also be used for underwater quantum cryptography. We also use the polarization degree of freedom to investigate the impact of the channel length on key rates for quantum communication applications. The underwater channel proves to be a difficult environment for establishing quantum communication as underwater optical turbulence results in significant beam wandering and distortions. However, the errors associated to the turbulence do not result in error rates above the threshold for establishing a positive key in a quantum communication link with both the polarization and spatially structured photons. The impact of the underwater channel on the spatially structured modes is also investigated at different distances using polarization tomography.