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1.
Science ; 354(6313): 734-738, 2016 11 11.
Artículo en Inglés | MEDLINE | ID: mdl-27846602

RESUMEN

The dynamics of quantum systems are encoded in the amplitude and phase of wave packets. However, the rapidity of electron dynamics on the attosecond scale has precluded the complete characterization of electron wave packets in the time domain. Using spectrally resolved electron interferometry, we were able to measure the amplitude and phase of a photoelectron wave packet created through a Fano autoionizing resonance in helium. In our setup, replicas obtained by two-photon transitions interfere with reference wave packets that are formed through smooth continua, allowing the full temporal reconstruction, purely from experimental data, of the resonant wave packet released in the continuum. In turn, this resolves the buildup of the autoionizing resonance on an attosecond time scale. Our results, in excellent agreement with ab initio time-dependent calculations, raise prospects for detailed investigations of ultrafast photoemission dynamics governed by electron correlation, as well as coherent control over structured electron wave packets.

2.
Opt Express ; 19(21): 19935-41, 2011 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-21997002

RESUMEN

Using an original CEP stabilization technique based on the linear electro-optical effect in a specific crystal, we achieved long term CEP stabilization of a 20 W, 1 kHz laser with residual noise as low as 440 mrad (rms). At 3 W, the CEP shot to shot noise is kept as low as 320 mrad (rms) over half an hour.

3.
Opt Express ; 19(4): 3677-85, 2011 Feb 14.
Artículo en Inglés | MEDLINE | ID: mdl-21369193

RESUMEN

We present the first measurement of the attosecond emission generated from underdense plasma produced on a solid target. We generate high-order harmonics of a femtosecond Ti:sapphire laser focused in a weakly ionized underdense chromium plasma. Using the "Reconstruction of Attosecond Beating by Interference of Two-photon Transitions" (RABITT) technique, we show that the 11th to the 19th harmonic orders form in the time domain an attosecond pulse train with each pulse having 300 as duration, which is only 1.05 times the theoretical Fourier transform limit. Measurements reveal a very low positive group delay dispersion of 4200 as2. Beside its fundamental interest, high-order harmonic generation in plasma plumes could thus provide an intense source of attosecond pulses for applications.

4.
Opt Express ; 19(6): 5410-8, 2011 Mar 14.
Artículo en Inglés | MEDLINE | ID: mdl-21445180

RESUMEN

We present a new method to control the Carrier-Envelope Phase of ultra-short laser pulses by using the linear Electro-Optic Effect. Experimental demonstration is carried out on a Chirped Pulse Amplification based laser. Phase shifts greater than π radian can be obtained by applying moderate voltage on a LiNbO3 crystal with practically no changes to all other parameters of the pulse with the exception of its group delay. Time response of the Electro-Optic effect makes possible shaping at a high repetition rate or stabilization of the CEP of ultra short CPA laser systems.

5.
J Phys Chem A ; 110(23): 7355-63, 2006 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-16759123

RESUMEN

The Ca* + CH3F --> CaF + CH3 reaction was photoinduced in 1:1 Ca...CH3F complexes formed in a supersonic expansion. The transition state of the reaction was explored by monitoring the electronically excited product, CaF, while scanning the laser that turns on the reaction. Moreover, the electronic structure of the Ca...FCH3 system was studied using ab initio methods by associating a pseudopotential description of the [Ca2+] and [F7+] cores, a core polarization operator on calcium, an extensive Gaussian basis and a treatment of the electronic problem at the CCSD(T) (ground state) and RSPT2 (excited states) level. In this contribution we present experimental results for the free complex and a comparison with the results of a previous experiment where the Ca...CH3F complexes are deposited at the surface of large argon clusters. The ab initio calculations allowed an interpretation of the experimental data in terms of two reaction mechanisms, one involving a partial charge transfer state, the other involving the excitation of the C-F stretch in the CH3F moiety prior to charge transfer.

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