Réalisation de détecteurs en germanium compensés au lithium

Nous avons étudié par gammagraphie un certain nombre de détecteurs Ge(Li), en particulier un détecteur pseudo-coaxial, dont les performances se sont nettement améliorées après ablation de la zone mauvaise. Pour améliorer le rapport photopic/Compton des détecteurs coaxiaux, nous avons enlevé le coeur de type P par étincelage. Deux diodes de ce type sont présentées

Ptychographic reconstruction of attosecond pulses

We demonstrate a new attosecond pulse reconstruction modality which uses an algorithm that is derived from ptychography. In contrast to other methods, energy and delay sampling are not correlated, and as a result, the number of electron spectra to record is considerably smaller. Together with the robust algorithm, this leads to a more precise and fast convergence of the reconstruction.Comment: 12 pages, 7 figures, the MATLAB code for the method described in this paper is freely available at http://figshare.com/articles/attosecond_Extended_Ptychographyc_Iterative_Engine_ePIE_/160187

Mesures de vies moyennes par effet Doppler

Des vies moyennes de niveaux nucléaires ont été déterminées par la méthode de l'effet Doppler. Les rayonnements gamma de désexcitation ont été détectés dans des compteurs Ge(Li). Des vies moyennes ont été obtenues pour les niveaux 0,953 MeV de 12B et 6,44 MeV de 14N

Attosecond screening dynamics mediated by electron-localization

Transition metals with their densely confined and strongly coupled valence electrons are key constituents of many materials with unconventional properties, such as high-Tc superconductors, Mott insulators and transition-metal dichalcogenides. Strong electron interaction offers a fast and efficient lever to manipulate their properties with light, creating promising potential for next-generation electronics. However, the underlying dynamics is a fast and intricate interplay of polarization and screening effects, which is poorly understood. It is hidden below the femtosecond timescale of electronic thermalization, which follows the light-induced excitation. Here, we investigate the many-body electron dynamics in transition metals before thermalization sets in. We combine the sensitivity of intra-shell transitions to screening effects with attosecond time resolution to uncover the interplay of photo-absorption and screening. First-principles time-dependent calculations allow us to assign our experimental observations to ultrafast electronic localization on d-orbitals. The latter modifies the whole electronic structure as well as the collective dynamic response of the system on a timescale much faster than the light-field cycle. Our results demonstrate a possibility for steering the electronic properties of solids prior to electron thermalization, suggesting that the ultimate speed of electronic phase transitions is limited only by the duration of the controlling laser pulse. Furthermore, external control of the local electronic density serves as a fine tool for testing state-of-the art models of electron-electron interactions. We anticipate our study to facilitate further investigations of electronic phase transitions, laser-metal interactions and photo-absorption in correlated electron systems on its natural timescale

High-energy picosecond Nd:YVO4 slab amplifier for OPCPA pumping

We demonstrate 12-ps pulses with up to 0.6-mJ pulse energy at repetition rates of 50 kHz and 100 kHz from a Nd:YVO4 slab amplifier built in a simple four-pass configuration. Excellent noise performance with pulse energy fluctuations below 0.8% rms has been achieved by using 10-μJ seed pulses from a highly stable industrial laser system and moderate gain (30-46) in the slab amplifie

Vies moyennes de niveaux de 53Mn excités par la réaction 50Cr (α, pγ)53Mn

Les propriétés électromagnétiques du noyau 53Mn sont étudiées à l'aide de la réaction 50Cr(α, pγ)53Mn à Eα = 14,5 MeV. Les rayonnements γ sont détectés en coïncidence avec les groupes de protons observés à l'aide d'un détecteur annulaire placé à 180° dans l'axe du faisceau. Des rapports d'embranchement de transitions γ sont donnés. La méthode d'atténuation de l'effet Doppler a été utilisée pour déduire les vies moyennes : niveau de 3,42 MeV, τ = 1,0 +0,6-0,4 ps ; niveau de 3,44 MeV, τ = 0,13 +0,05-0,04ps ; niveau de 4,15 MeV, τ = 0,07 ± 0,02 ps. Pour les niveaux à Ex < 3 MeV nos valeurs de τ sont en accord avec des résultats obtenus ailleurs. Pour le niveau de 3,44 MeV nous déduisons Jπ = 15/2- sans ambiguïté. Certaines probabilités de transitions B(M1) et B(E2) sont déterminées et comparées aux prédictions des modèles récents

Spectral signature of short attosecond pulse trains

We report experimental measurements of high-order harmonic spectra generated in Ar using a carrier-envelope-offset (CEO) stabilized 12 fs, 800nm laser field and a fraction (less than 10%) of its second harmonic. Additional spectral peaks are observed between the harmonic peaks, which are due to interferences between multiple pulses in the train. The position of these peaks varies with the CEO and their number is directly related to the number of pulses in the train. An analytical model, as well as numerical simulations, support our interpretation

Ultrafast electron localization and screening in a transition metal dichalcogenide

The coupling of light to electrical charge carriers in semiconductors is the foundation of many technological applications. Attosecond transient absorption spectroscopy measures simultaneously how excited electrons and the vacancies they leave behind dynamically react to the applied optical fields. In compound semiconductors, these dynamics can be probed via any of their atomic constituents. Often, the atomic species forming the compound contribute comparably to the relevant electronic properties of the material. One therefore expects to observe similar dynamics, irrespective of the choice of atomic species via which it is probed. Here, we show in the two-dimensional transition metal dichalcogenide semiconductor MoSe2, that through a selenium-based transition we observe charge carriers acting independently from each other, while when probed through molybdenum, the collective, many-body motion of the carriers dominates. Such unexpectedly contrasting behavior can be traced back to a strong localization of electrons around molybdenum atoms following absorption of light, which modifies the local fields acting on the carriers. We show that similar behavior in elemental titanium metal carries over to transition metal-containing compounds and is expected to play an essential role for a wide range of such materials. Knowledge of independent particle and collective response is essential for fully understanding these materials

Attosecond timing of the dynamical Franz–Keldysh effect

To what extent do intra- or inter-band transitions dominate the optical response of dielectrics when pumped by a few-cycle near-infrared transient electric field? In order to find an answer to this question we investigate the dynamical Franz–Keldysh effect in polycrystalline diamond and discuss in detail the attosecond delay of the induced electron dynamics with regard to the driving transient electric field while the peak intensity is varied between 1 × 1012 and 10 × 1012 W cm−2. We found that the main oscillating feature in transient absorption at 43 eV is in phase with the electric field of the pump, to within 49 ± 78 as. However, the phase delay shows a slightly asymmetric V-shaped linear energy dispersion with a rate of about 200 as eV–1. Theoretical calculations within the dipole approximation reproduce the data and allow us to conclude that intra-band motion dominates under our experimental conditions