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Attosecond pulses created by high-order harmonic generation in gases often exhibit strong chromatic aberrations, arising from the broad bandwidth and wavelength-dependent nonlinear light-matter interaction. When the driving laser intensity varies spatially, as for Gaussian driving beams, the apparent source position of the harmonics differs significantly from one order to the next, thus affecting the achievable intensity and duration of the attosecond pulses when they are focused on a target. We show that these chromatic aberrations can be reduced by spatially shaping the fundamental beam to generate high-order harmonics with a driver having a flat-top profile inside the gas medium. By measuring both the intensity profile and wavefront for each harmonic in a plane, we access the extreme ultra-violet (XUV) beam properties and investigate these properties near focus. We observe that controlling chromatic aberrations by flat-top spatial shaping strongly reduces the variation of the XUV spectrum on the beam axis during propagation and, in return, the longitudinal sensitivity of both the temporal profiles and the temporal shifts of the focused attosecond pulses., Comment: 12 pages, 8 figures + supplementary material: 10 pages, 13 figures

High-order harmonic generation (HHG) in gases leads to short-pulse extreme ultraviolet (XUV) radiation useful in a number of applications, for example, attosecond science and nanoscale imaging. However, this process depends on many parameters and there is still no consensus on how to choose the target geometry to optimize the source efficiency. Here, we review the physics of HHG with emphasis on the macroscopic aspects of the nonlinear interaction. We analyze the influence of medium length, pressure, position of the medium and intensity of the driving laser on the HHG conversion efficiency (CE), using both numerical modelling and analytical expressions. We find that efficient high-order harmonic generation can be realized over a large range of pressures and medium lengths, if these follow a certain hyperbolic equation. The spatial and temporal properties of the generated radiation are, however, strongly dependent on the choice of pressure and medium length. Our results explain the large versatility in gas target design for efficient HHG and provide design guidance for future high-flux XUV sources., Comment: 15 pages, 10 figures

We present a recently developed terahertz platform. An air plasma produced by an ultrashort two-color laser pulse serves as a broadband terahertz source, with electric field that has peak amplitude in the MV/cm range. Air biased coherent detection of the terahertz field is employed where a peak detector associated with a micro-controller board acquires the signal coming from an avalanche photodiode. The temporal and spectral profiles of the produced terahertz electric field are presented, in excellent agreement with numerical simulations of the whole setup. We illustrate the capabilities of this platform by performing spectroscopy on water vapor and of a polystyrene reference sample., Comment: 8 pages, 8 figures

We observe a new regime of coherent XUV radiation generation in noble gases induced by femtosecond pulses at very high intensities. This XUV emission has both a reduced divergence and spectral width as compared to high-order harmonic generation (HHG). It is not emitted at a moderate intensity of the driving pulses where only high-order harmonics are generated. At high driving intensities, the additional XUV comb appears near all harmonic orders and even exceeds the HHG signal on the axis. The peaks are observed in several gases and their frequencies do not depend on the driving intensity or gas pressure. We analyze the divergence, spectral width and spectral shift of this XUV emission. We show that these specific features are well explained by high-order parametric generation (HPG) involving multiphoton absorption and combined emission of an idler THz radiation and an XUV beam with remarkably smooth spatial and spectral characteristics., Comment: 18 pages, 12 figures. To be published in a peer-reviewed scientific journal

Controlling the wavefront of an extreme ultraviolet (XUV) high-order harmonic beam during the generation process offers to focus the beam without resorting to any XUV optics. By characterizing the XUV intensity profile and wavefront, we quantitatively retrieve both the size and the position of the waist of each generated harmonics and show that optics-free focusing leads to focused XUV spot with micrometer size. We use this remarkable coherent effect to demonstrate efficient and adjustable spectral filtering of the XUV light, along with a strong rejection of the fundamental beam, without using any XUV optics.

By experimentally studying high-order harmonic beams generated in gases, we show how the spatial characteristics of these ultrashort XUV beams can be finely controlled under standard generation conditions. For the first time, we demonstrate that these XUV beams can be emitted as converging beams and get thereby focused after generation. We study this mirrorless focusing using a spatially chirped beam that acts as a spatially localized probe located inside the harmonic generation medium. We analyze the XUV beam evolution with an analytical model providing the beam characteristics and obtain very good agreement with experimental measurements. The XUV foci sizes and positions vary strongly with the harmonic order and the XUV waist can be located at arbitrarily large distances from the generating medium. We discuss how intense XUV fields can be obtained with mirrorless focusing and how such order-dependent XUV beam characteristics are compatible with broadband XUV irradiation and attosecond science., Comment: Main paper with 16 pages and 5 figures and supplementary informations with 10 pages and 10 figures

We study theoretically and experimentally the electronic relaxation of NO2 molecules excited by absorption of one ~400 nm pump photon. Semi-classical simulations based on trajectory surface hopping calculations are performed. They predict fast oscillations of the electronic character around the intersection of the ground and first excited diabatic states. An experiment based on high-order harmonic transient grating spectroscopy reveals dynamics occuring on the same timescale. A systematic study of the detected transient is conducted to investigate the possible influence of the pump intensity, pump wavelength, and rotational temperature of the molecules. The quantitative agreement between measured and predicted dynamics shows that, in NO2, high harmonic transient grating spectroscopy encodes vibrational dynamics underlying the electronic relaxation., Comment: The following article has been accepted by Journal of Chemical Physics. After it is published, it will be found at http://jcp.aip.org/

We study the Cooper minimum in high harmonic generation from argon atoms using long wavelength laser pulses. We find that the minimum in high harmonic spectra is systematically shifted with respect to total photoionization cross section measurements. We use a semi-classical theoretical approach based on Classical Trajectory Monte Carlo and Quantum Electron Scattering methods (CTMC-QUEST) to model the experiment. Our study reveals that the shift between photoionization and high harmonic emission is due to several effects: the directivity of the recombining electrons and emitted polarization, and the shape of the recolliding electron wavepacket., Comment: 13 pages