Publications by authors named "J Seres"

We report the realization of an intra-oscillator high harmonic source based on a Kerr lens mode locked Ti:sapphire laser running at 80 MHz repetition rate. A nonlinear medium consisting of an AlN nanofilm on a thin sapphire substrate is placed inside the oscillator cavity. The harmonics are generated, in reflection geometry, on the AlN nanofilm, directing the harmonic beam out of the cavity.

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Parametric amplification of attosecond coherent pulses around 100 eV at the single-atom level is demonstrated for the first time by using the 3D time-dependent Schrödinger equation in high-harmonic generation processes from excited states of He. We present the attosecond dynamics of the amplification process far from the ionization threshold and resolve the physics behind it. The amplification of a particular central photon energy requires the seed XUV pulses to be perfectly synchronized in time with the driving laser field for stimulated recombination to the He ground state and is only produced in a few specific laser cycles in agreement with the experimental measurements.

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We realized a solid-state-based vacuum ultraviolet frequency comb by harmonics generation in an external enhancement cavity. Optical conversions were so far reported by only using gaseous media. We present a theory that allows the most suited solid generation medium to be selected for specific target harmonics by adapting the material's bandgap.

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We demonstrate non-perturbative 3rd (267 nm) and 5th (160 nm) harmonic generation in solids from a Ti:sapphire frequency comb (800 nm) at 108 MHz repetition rate. The experiments show that non-perturbative low harmonics are dominantly generated on the surface and on the interface between solids, and that they are not produced by bulk processes from the near-surface layer of the material. Measurements reveal that due to the lack of phase matching, the generated harmonics in bulk are suppressed by orders of magnitude compared to the signal generated on the surface.

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Applying extreme ultraviolet (XUV) transient absorption spectroscopy, the dynamics of the two laser dressed transitions 3d-to-5p and 3p-to-5s at photon energies of 91.3 eV and 210.4 eV were examined with attosecond temporal resolution.

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