Tunable sub-luminal propagation of narrowband x-ray pulses

Group velocity control is demonstrated for x-ray photons of 14.4 keV energy via a direct measurement of the temporal delay imposed on spectrally narrow x-ray pulses. Sub-luminal light propagation is achieved by inducing a steep positive linear dispersion in the optical response of ${}^{57}$Fe M\"ossbauer nuclei embedded in a thin film planar x-ray cavity. The direct detection of the temporal pulse delay is enabled by generating frequency-tunable spectrally narrow x-ray pulses from broadband pulsed synchrotron radiation. Our theoretical model is in good agreement with the experimental data.Comment: 8 pages, 4 figure

Attosecond double-slit experiment

A new scheme for a double-slit experiment in the time domain is presented. Phase-stabilized few-cycle laser pulses open one to two windows (``slits'') of attosecond duration for photoionization. Fringes in the angle-resolved energy spectrum of varying visibility depending on the degree of which-way information are observed. A situation in which one and the same electron encounters a single and a double slit at the same time is discussed. The investigation of the fringes makes possible interferometry on the attosecond time scale. The number of visible fringes, for example, indicates that the slits are extended over about 500as.Comment: 4 figure

Robustesse des approches chimiométriques pour la reconstruction de profils moléculaires

Ce papier traite des approches chimiométriques pour la reconstruction de profils moléculaires. La quantification de protéines du sang est réalisée à partir du traitement par analyse factorielle de spectrogrammes issus d'une chaîne d'analyse contenant une colonne de nano-chromatographie et un spectromètre de masse. Nous nous intéressons plus particulièrement à la comparaison de la robustesse des méthodes de régression de type Unfold-PLS, N-PLS et PARAFAC vis-à-vis du problème de décalage temporel des pics contenus dans les spectrogrammes. Les méthodes multidimensionnelles type N-PLS et PARAFAC fournissent de meilleurs résultats ce qui permet d'envisager une quantification des protéines avec une plus grande tolérance sur le recalage des pics en temps de rétention

Resonant enhancements of high-order harmonic generation

Solving the one-dimensional time-dependent Schr\"odinger equation for simple model potentials, we investigate resonance-enhanced high-order harmonic generation, with emphasis on the physical mechanism of the enhancement. By truncating a long-range potential, we investigate the significance of the long-range tail, the Rydberg series, and the existence of highly excited states for the enhancements in question. We conclude that the channel closings typical of a short-range or zero-range potential are capable of generating essentially the same effects.Comment: 7 pages revtex, 4 figures (ps files

Adiabatic Theory of Electron Detachment from Negative Ions in Two-Color Laser Field

Negative ion detachment in bichromatic laser field is considered within the adiabatic theory. The latter represents a recent modification of the famous Keldysh model for multiphoton ionization which makes it quantitatively reliable. We calculate angular differential detachment rates, partial rates for particular ATD (Above Threshold Detachment) channels and total detachment rates for the Hydrogen ion in a bichromatic field with 1:3 frequency ratio and various phase differences. Reliability of the present, extremely simple approach is testified by comparison with much more elaborate earlier calculations.Comment: 22 pages, 6 Postscript figure

Reconstruction bayésienne de profils moléculaires

L'étude des protéines laisse entrevoir de grands espoirs pour la médecine de demain. Cependant pour répondre à ces promesses, les méthodes actuelles doivent gagner en sensibilité, en spécificité et en robustesse. Dans cette optique, le CEA développe un laboratoire sur puce et des méthodes de traitement numérique dédiées aux analyses protéomiques par LC-MS. Nous présentons dans cet article une approche bayésienne pour la reconstruction des profils de concentrations de protéines. Dans un premier temps nous proposons un modèle pour le dispositif de mesure complet. Puis nous décrivons une méthode d'estimation des concentrations de protéines présentes, les paramètres instrumentaux étant fixés. Enfin nous estimons conjointement les concentrations et les paramètres instrumentaux

Complete characterization of single-cycle double ionization of argon from the nonsequential to the sequential ionization regime

Citation: Kubel, M., Burger, C., Kling, N. G., Pischke, T., Beaufore, L., Ben-Itzhak, I., . . . Bergues, B. (2016). Complete characterization of single-cycle double ionization of argon from the nonsequential to the sequential ionization regime. Physical Review A, 93(5), 9. doi:10.1103/PhysRevA.93.053422Selected features of nonsequential double ionization have been qualitatively reproduced by a multitude of different (quantum and classical) approaches. In general, however, the typical uncertainty of laser pulse parameters and the restricted number of observables measured in individual experiments leave room for adjusting theoretical results to match the experimental data. While this has been hampering the assessment of different theoretical approaches leading to conflicting interpretations, comprehensive experimental data that would allow such an ultimate and quantitative assessment have been missing so far. To remedy this situation we have performed a kinematically complete measurement of single-cycle multiple ionization of argon over a one order of magnitude range of intensity. The momenta of electrons and ions resulting from the ionization of the target gas are measured in coincidence, while each ionization event is tagged with the carrier-envelope phase and intensity of the 4-fs laser pulse driving the process. The acquired highly differential experimental data provide a benchmark for a rigorous test of the many competing theoretical models used to describe nonsequential double ionization

Attosecond electronic recollision as field detector

We demonstrate the complete reconstruction of the electric field of visible-infrared pulses with energy as low as a few tens of nanojoules. The technique allows for the reconstruction of the instantaneous electric field vector direction and magnitude, thus giving access to the characterisation of pulses with an arbitrary time-dependent polarisation state. The technique combines extreme ultraviolet interferometry with the generation of isolated attosecond pulses.Comment: 5 figure