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A compact, high-repetition rate OPCPA system with CEP-stable 6.3 fs pulses duration and 10 μJ of pulse energy is presented together with results from numerical simulations. First results of high harmonic generation will be shown.
We demonstrate a dispersion-free split mirror interferometric autocorrelator suitable for measuring pulses with durations from hundreds of attoseconds to tens of femtoseconds and spectral content from the near-UV to near-IR.
We present experimental measurements and theoretical calculations of single and double ionization time delays in various noble gases using an interferometric method. The measured delays allow us to extract information on the electron correlation.
We study the temporal and spectral behaviour of high order harmonics generated by pulses with temporally modulated polarization. We observe a harmonic temporal confinement and a harmonic spectral broadening, compatible with 1 -or-2 attosecond pulse emission.
We employ a pump-probe approach to molecular photoionization to study fast dissociation of Rydberg states in acetylene. By using time-resolved photoelectron spectroscopy to study the electronic state of the resulting ions we are able to monitor the system continuously during dissociation or rearrangement. We find that the predissociative lifetime for the 3R‴ (v′2 = 1) Rydberg state is about 150 fs
We perform interferometric attosecond timing measurements to study XUV photoionization in noble gases, to diagnose macroscopic phase-matching conditions in high-order harmonic generation, and to investigate single-photon double-ionization by detecting electron pairs in coincidence.
We present two interferometry schemes in the extreme ultraviolet, based on either the wave-front division of a unique harmonic beam (1st scheme) or two spatially separated, phase-locked harmonic sources (2nd scheme). In the first scheme using a Fresnel bimirror interferometer, we measure the degree of spatial coherence of the 13 th harmonic generated in xenon, as a function of different parameters
Along with the review of the technological frame that will be available at the Extreme Light Infrastructure Attosecond Light Pulse Source (ELI-ALPS) we present considerations applicable to large-scale attosecond sources driven by high-power laser pulses.
Scaling attosecond sources to higher pulse energy and/or repetition rate can benefit many applications. We present a scaling framework for nonlinear light-matter interactions, applicable to attosecond pulse generation and other nonlinear phenomena as e.g. filamentation.
We investigate the influence of a Fano resonance on the delays for electron emission in two-photon, near-resonant ionization of argon. The delays were measured using an interferometric method that employed an attosecond pulse train.
A compact, high-repetition rate optical parametric chirped pulse amplifier system emitting CEP-stable, few-cycle pulses with 10 μJ of pulse energy is reported for the purpose of high-order harmonic generation. The system is seeded from a commercially available, CEP-stabilized Ti:sapphire oscillator, delivering an octave-spanning spectrum from 600-1200 nm. The oscillator output serves on the one ha
The recently demonstrated momentum shearing interferometry technique, aimed at recovering phase information about electronic wave packets (EWP) will be presented. Possibilities to improve this technique will be discussed.
Ultrashort light pulses, as short as 100 as, can be produced from high harmonic generation (HHG) in an atomic gas medium. This major achievement of the last 6 years in high field physics has now been demonstrated in different conditions of medium-field interaction [1].
We measured the frequency chirp rate of harmonics 13 to 23 in argon by cross-correlation with a short femtosecond probe pulse. We directly measured the negative chirp due to the atomic dipole phase and demonstrated that an additional chirp on the pump pulse was transferred to the qth harmonic as q times the fundamental chirp.
We present one-color (IR) and two-color (single attosecond XUV pulse + IR) experiments where the sub-cycle evolution of the electric field of light is used to control the dissociative ionization of hydrogen and deuterium molecules.
We modulate temporally the polarization of a ∼ 30 fs, 800 nm IR pulse and use it to generate high order harmonics. The harmonic emission can clearly be confined and the XUV pulse duration can be continuously tuned from - 5 - 7 fs to 50 fs.
We present experiments, supported by time-dependent Schrödinger simulations, on the dynamics of Helium bound states after an attosecond excitation in the presence of a strong infrared laser field.
