Professor Ian Walmsley CBE FRS FCGI

Abstract:

We demonstrate that multiple spectral-shearing interferometry increases the precision and accuracy of measurements of the spectral phase of a complex pulse (time-bandwidth product $=$ 125) arising from self-phase modulation in a gas filled capillary. We verify that the measured interferometric phase is accurate to 0.1 rad across the full bandwidth by checking the consistency between the spectral phases of each individual shear measurement. The accuracy of extracting pulse parameters (group delay dispersion, pulse duration and peak intensity) for single shear measurements were verified to better than 10% by comparison with the multishear reconstruction. High order space-time coupling is quantified across a single transverse dimension, verifying the suitability of such pulses for use in strong field experiments.

Abstract:

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. © 2011 The Royal Society of Chemistry.

Abstract:

The waveforms of attosecond pulses produced by high-harmonic generation carry information on the electronic structure and dynamics in atomic and molecular systems. Current methods for the temporal characterization of such pulses have limited sensitivity and impose significant experimental complexity. We propose a new linear and all-optical method inspired by widely used multidimensional phase retrieval algorithms. Our new scheme is based on the spectral measurement of two attosecond sources and their interference. As an example, we focus on the case of spectral polarization measurements of attosecond pulses, relying on their most fundamental property-being well confined in time. We demonstrate this method numerically by reconstructing the temporal profiles of attosecond pulses generated from aligned CO2 molecules. © 2011 American Physical Society.

Abstract:

Room-temperature, easy-to-operate quantum memories are essential building blocks for future long distance quantum information networks operating on an intercontinental scale, because devices like quantum repeaters, based on quantum memories, will have to be deployed in potentially remote, inaccessible locations. Here we demonstrate controllable, broadband and efficient storage and retrieval of weak coherent light pulses at the single-photon level in warm atomic cesium vapor using the robust far off-resonant Raman memory scheme. We show that the unconditional noise floor of this technically simple quantum memory is low enough to operate in the quantum regime, even in a room-temperature environment.