We demonstrate control of short and long quantum trajectories in high harmonic emission through the use of an orthogonally polarized two color field. By controlling the relative phase φ between the two fields we show via classical and quantum calculations that we can steer the 2-dimensional trajectories to return, or not, to the core and so control the relative strength of the short or long quantum trajectory contribution. In experiments we demonstrate that this leads to robust control over the trajectory contributions using a drive field from a femtosecond laser composed of the fundamental ω at 800 nm (intensity ∼ 1.2 × 10 14 W cm −2 ) and its weaker orthogonally polarized second harmonic 2ω (intensity ∼ 0.3 × 10 14 W cm −2 ) with the relative phase between the ω and 2ω fields varied simply by tilting a fused silica plate. This is the first demonstration of short and long quantum trajectory control at the single-atom level.High harmonic generation (HHG) has been extensively studied in the last decade as, for instance, a tool to generate attosecond pulses [1] and to measure both fast nuclear dynamics [2] and hole migration in molecular cations [3,4]. Measuring nuclear and electron dynamics from the emitted harmonics is termed HHG spectroscopy and has hitherto concentrated upon isolating the contribution of the electron trajectories that return most quickly to the core [5] (the short trajectories) to provide a well defined temporal mapping for the emission of different frequency harmonics in the spectrum [2]. To extend these measurement concepts we would like to harness the second set of quantum trajectories, the long trajectories, which return after a longer time in the continuum and so increase the temporal range available in the measurement. Ideally this should be done without changing any other aspect of the experimental conditions e.g. the intensity. Hitherto long trajectories could only be optimised by adjusting the macroscopic phase-matching, a procedure that inevitably alters the experimental intensity. We demonstrate a simple experimental technique that provides a powerful tool to achieve the direct selection of the quantum trajectories for a single atom without changing the field intensity. We find that the phase between two orthogonally polarized fields at ω and 2ω determines whether the momentum transfer from the 2ω field permits or frustrates the recollision. We observed that the phases of the second harmonic field that optimise the recollision differ by π/2 for the short and long trajectory. This provides robust control over the single atom quantum trajectories and allows to efficiently switch between trajectories, shifting the emission time for some harmonics by more than 0.3 of an optical period.In the simplified picture, commonly applied to describe HHG, an electron is ionised near the peak of the laser electric field and is driven away from its parent ion. When the field changes direction, the electron is driven back and may recombine [5], emitting a photon with fre- quency that is an odd multip...

We describe a complete technological system at Imperial College London for Attosecond Science studies. The system comprises a few-cycle, carrier envelope phase stabilized laser source which delivers sub 4 fs pulses to a vibration-isolated attosecond vacuum beamline. The beamline is used for the generation of isolated attosecond pulses in the extreme ultraviolet (XUV) at kilohertz repetition rates through laser-driven high harmonic generation in gas targets. The beamline incorporates: interferometers for producing pulse sequences for pump-probe studies; the facility to spectrally and spatially filter the harmonic radiation; an in-line spatially resolving XUV spectrometer; and a photoelectron spectroscopy chamber in which attosecond streaking is used to characterize the attosecond pulses. We discuss the technology and techniques behind the development of our complete system and summarize its performance. This versatile apparatus has enabled a number of new experimental investigations which we briefly describe.

We report on the observation of enhanced high harmonics from a carbon plasma using sub-5-fs laser pulses. The efficiency of harmonic generation in the range of 14-25 eV was up to five times higher in the case of a plasma medium (graphite ablation) compared with gas (argon) under similar experimental conditions. The harmonic enhancement can be attributed to the presence of carbon nanoparticles in the ablation plumes.

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We report studies of high-order harmonic generation in laser-produced manganese plasmas using sub-4-fs drive laser pulses. The measured spectra exhibit resonant enhancement of a small spectral region of about 2.5 eV width around the 31st harmonic (~50eV). The intensity contrast relative to the directly adjacent harmonics exceeds one order of magnitude. This finding is in sharp contrast to the results reported previously for multi-cycle laser pulses [Physical Review A 76, 023831 (2007)]. Theoretical modelling suggests that the enhanced harmonic emission forms an isolated sub-femtosecond pulse.