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Christian Cornaggia

Publications and source records attributed to Christian Cornaggia.

3 recordsLinked to original sources

Ultrafast Molecular Imaging by Laser Induced Electron Diffraction

We address the feasibility of imaging geometric and orbital structure of a polyatomic molecule on an attosecond time-scale using the laser induced electron diffraction (LIED) technique. We present numerical results for the highest molecular orbitals of the CO2 molecule excited by a near infrared few-cycle laser pulse. The molecular geometry (bond-lengths) is determined within 3% of accuracy from a diffraction pattern which also reflects the nodal properties of the initial molecular orbital. Robustness of the structure determination is discussed with respect to vibrational and rotational motions with a complete interpretation of the laser-induced mechanisms.

quant-ph

H2 Double Ionization with Few-Cycle Laser Pulses

The temporal dynamics of double ionization of H2 has been investigated both experimentally and theoretically with few-cycle laser pulses. The main observables are the proton spectra associated to the H^+ + H^+ fragmentation channel. The model is based on the time-dependent Schrödinger equation and treats on the same level the electronic and nuclear coordinates. Therefore it allows to follow the ultrafast nuclear dynamics as a function of the laser pulse duration, carrier-envelope phase offset and peak intensity. We mainly report results in the sequential double ionization regime above 2 10^{14} W/cm^2. The proton spectra are shifted to higher energies as the pulse duration is reduced from 40fs down to 10fs. The good agreement between the model predictions and the experimental data at 10fs permits a theoretical study with pulse durations down to a few femtoseconds. We demonstrate the very fast nuclear dynamics of the H2^+ ion for a pulse duration as short as 1fs between the two ionization events giving respectively H2^+ from H2 and H^+ + H^+ from H2^+. Carrier-envelope phase offset only plays a significant role for pulse durations shorter than 4fs. At 10fs, the laser intensity dependence of the proton spectra is fairly well reproduced by the model.

quant-ph

Ultrafast electro-nuclear dynamics of H2 double ionization

The ultrafast electronic and nuclear dynamics of H2 laser-induced double ionization is studied using a time-dependent wave packet approach that goes beyond the fixed nuclei approximation. The double ionization pathways are analyzed by following the evolution of the total wave function during and after the pulse. The rescattering of the first ionized electron produces a coherent superposition of excited molecular states which presents a pronounced transient H+H- character. This attosecond excitation is followed by field-induced double ionization and by the formation of short-lived autoionizing states which decay via double ionization. These two double ionization mechanisms may be identified by their signature imprinted in the kinetic-energy distribution of the ejected protons.

quant-ph