Advances of quantum control technology have led to nearly perfect single-qubit control of nuclear spins and atomic hyperfine ground states. In contrast, quantum control of strong optical transitions, even for free atoms, are far from being perfect. Developments of such quantum control appears to be limited by available laser technology for generating isolated, sub-nanosecond optical waveforms with 10's of GHz programming bandwidth. Here we propose a simple and robust method for the desired pulse shaping, based on precisely stacking multiple delayed picosecond pulses. Our proof-of-principal demonstration leads to arbitrarily shapeable optical waveforms with 30 GHz bandwidth and 100 ps duration. We confirm the stability of the waveforms by interfacing the pulses with laser-cooled atoms, resulting in "super-resolved" spectroscopic signals. This pulse shaping method may open exciting perspectives in quantum optics, and for fast laser cooling and atom interferometry with mode-locked lasers.
Advances of quantum control technology have led to nearly perfect single-qubit control of nuclear spins and atomic hyperfine ground states. In contrast, quantum control of strong optical transitions, even for free atoms, are far from being perfect. Developments of such quantum control appears to be limited by available laser technology for generating isolated, sub-nanosecond optical waveforms with 10's of GHz programming bandwidth. Here we propose a simple and robust method for the desired pulse shaping, based on precisely stacking multiple delayed picosecond pulses. Our proof-of-principal demonstration leads to arbitrarily shapeable optical waveforms with 30 GHz bandwidth and 100 ps duration. We confirm the stability of the waveforms by interfacing the pulses with laser-cooled atoms, resulting in "super-resolved" spectroscopic signals. This pulse shaping method may open exciting perspectives in quantum optics, and for fast laser cooling and atom interferometry with mode-locked lasers.
Creating and controlling well-defined single-photon states is important for many quantum enhanced technologies. Information can be encoded in any degree of freedom associated with a single-photon field excitation, for example in the polarization or transverse spatial mode structure. The ability to encode multiple qubits in these states is desirable for high data transmission rates and increased information processing capacity. The spectral-temporal domain offers a large Hilbert space for encoding information, well suited to integrated optical architectures owing to the low cross-talk between channels. Indeed, time-frequency encoding is an integral component of existing information technologies infrastructure. Thus, complete, coherent control of the spectral-temporal mode structure of light is essential to advancing optical quantum technologies. Arbitrary control of single-photon states has been demonstrated in the polarization and spatial-momentum degrees of freedom however, is yet to be established in the spectral-temporal domain. Recently it was shown that spectral-temporal pulse shaping is experimentally feasible using nonlinear optical methods. However, such techniques can introduce noise photons, are challenging to implement deterministically and require specially prepared auxiliary pump pulses. Furthermore, they are typically only possible at relatively low repetition rates to avoid damage of nonlinear optical materials. Here, we demonstrate deterministic pulse shaping of single-photon wave packets by introducing a time-varying phase. Applying linear or quadratic phase to the wave packet introduces a spectral shift or spectral broadening, respectively. Achieving significant spectral manipulation requires temporal-phase modulation on the order of π. The phase must also vary on the same time scale as the optical pulses, approximately 1 ps in duration here. This relatively rapid phase variation is achieved using a fast electro-optic phase modulator. The modulator is driven by a time-varying voltage that is synchronized with a pulse train of single-photon wave packets for accurate temporal phase control. In this thesis, we experimentally demonstrate control of the spectral-temporal state of single-photon wave packets using this method. Heralded single-photon wave packets are generated by spontaneous parametric down conversion pumped by a frequency-doubled Titanium-Sapphire laser oscillator with 80 MHz repetition rate. To achieve significant modulation of single-photon pulses a 10 V peak-to-peak radio-frequency signal of 40 GHz drives the phase modulator, which requires approximately 3.6 V to achieve a π phase shift. The signal is synchronized with the oscillator pulse train using custom designed electronics. Details of these electronics are presented, resulting in a robust phase and amplitude controllable 40 GHz voltage source, phase locked to the single-photon pulse train. To demonstrate the utility of this pulse-shaping method we experimentally show spectral shearing of almost 1 nm for single-photon wave packets with 830 nm central wavelength and 1 nm bandwidth. Measurement of the second-order intensity correlation before and after the wave-packet manipulation remains constant within uncertainty of the measurement, showing that the quantum nature of the single-photon source is not deteriorated by the modulator. Preservation of the wave-packet coherence is verified by two-photon interference between spectrally sheared and non-modulated single-photons.
The absorption of traveling photons resonant with electric dipole transitions of an atomic gas naturally leads to electric dipole spin-wave excitations.For a number of applications, it would be highly desirable to shape and coherently control the spatial waveform of the spin waves before spontaneous emission can occur.This paper details a recently developed optical control technique to achieve this goal, where counterpropagating, shaped subnanosecond pulses impart subwavelength geometric phases to the spin waves by cyclically driving an auxiliary transition.In particular, we apply this technique to reversibly shift the wave vector of a spin wave on the D2 line of laser-cooled 87 Rb atoms by driving an auxiliary D1 transition with shape-optimized pulses, so as to shut off and recall superradiance on demand.We investigate a spin-dependent momentum transfer during the spin-wave control process, which leads to a transient optical force as large as ∼1hk/ns, and study the limitations to the achieved 70 ∼ 75% spin-wave control efficiency by jointly characterizing the spin-wave control and matter-wave acceleration.Aided by numerical modeling, we project potential future improvements of the control fidelity to the 99% level when the atomic states are better prepared and by equipping a faster and more powerful pulse shaper.Our technique also enables a background-free measurement of the superradiant emission to unveil the precise scaling of the emission intensity and decay rate with optical depth.
Mixing light waves of different frequencies is a routine technique for synthesizing waveforms of arbitrary shape and spectral composition. For applications in coherent quantum control, ultrafast optical pulses over a range of wavelengths may be required. Shelton et al. (p. 1286; see the Perspective by Brown et al. ), building on recent advances involving phase-locking of femtosecond optical pulses, generation of a comb of optical frequencies, and precision measurement of optical frequencies, now show that two waveforms can be coherently stitched together from separate femtosecond lasers to form a coherent pulse train.
The laser cooling of atoms to ultracold temperatures has propelled many groundbreaking advances in fundamental research and precision measurement, through such applications as quantum simulators and interferometric sensors. Laser cooling remains, however, highly species-selective, and techniques for its application to molecules are still in their infancy. This thesis broadly concerns the development of laser cooling schemes, based on sequences of coherent optical pulses, which can in principle be applied to a wide range of species. We describe a cooling scheme, in which a velocity-selective impulse analogous to that in Doppler cooling is generated by a light-pulse Ramsey interferometer, and present a proof-of-concept demonstration of the scheme using ultracold rubidium-85 atoms as a test-bed. We realise an interferometer for the atoms, as they are in free-fall after release from a magneto-optical trap, by inducing stimulated Raman transitions between their ground hyperfine states. We provide a comprehensive characterisation of these Raman light-pulse interferometer optics, where particular attention is paid to light shift effects. Raman pulses, and indeed coherent operations in any quantum control system, unavoidably suffer from systematic errors in the control field intensity and frequency, and these lead to reductions in pulse fidelity and readout contrast. In parallel to the work on interferometric cooling in this thesis, we report our preliminary investigations into composite pulses, whereby 'naive' single pulses are replaced by sequences of rotations with tailored durations and phases, for improving pulse fidelity in the presence of inhomogeneities. We find that composite pulses can indeed be highly effective in our cold atom system, and propose that their application in such devices as interferometric sensors is a promising prospect.
We demonstrate a system for fast and agile digital control of laser phase, amplitude and frequency for applications in coherent atomic systems. The full versatility of a direct digital synthesis radiofrequency source is faithfully transferred to laser radiation via acousto-optic modulation. Optical beatnotes are used to measure phase steps up to 2π, which are accurately implemented with a resolution of ≤ 10 mrad. By linearizing the optical modulation process, amplitude-shaped pulses of durations ranging from 500 ns to 500 ms, in excellent agreement with the programmed functional form, are demonstrated. Pulse durations are limited only by the 30 ns rise time of the modulation process, and a measured extinction ratio of > 5 × 10(11) is achieved. The system presented here was developed specifically for controlling the quantum state of trapped ions with sequences of multiple laser pulses, including composite and bichromatic pulses. The demonstrated techniques are widely applicable to other atomic systems ranging across quantum information processing, frequency metrology, atom interferometry, and single-photon generation.
A demonstration of coherent quantum control for ultrafast precise selection of closely-lying states is reported. A phase-locked pair of femtosecond laser pulses is generated through a pulse shaper to excite the ground-state cesium atom to the Cs(7D3∕2) and Cs(7D5∕2) states by two-photon absorption. The excited state population is measured by detecting fluorescence from each spin-orbit state. By controlling the phase-difference of the pulse pair, an ultrafast precise selection is accomplished. The contrast ratio of the maximal to minimal selection ratio exceeds 103 with the delay less than 400fs.