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Register a new userMeasuring Coulomb-Induced Ionization Time Lag with a Calibrated Attoclock
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Electrons in atoms and molecules can not react immediately to the action of intense laser field. A time lag (about 100 attoseconds) between instants of the field maximum and the ionization-rate maximum emerges. This lag characterizes the response time of the electronic wave function to the strong-field ionization event and has important effects on subsequent ultrafast dynamics of the ionized electron. The absolute time lag is not accessible in experiments. Here, a calibrated attoclock procedure, which is related to a simple Coulomb-induced temporal correction to electron trajectories, is proposed to measure the relative lag of two different ionization events. Using this procedure,the difference (i.e., the relative lag) between the ionization time lags of polar molecules in two consecutive half laser cycles can be probed with a high accuracy.
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The role of Coulomb focusing in above-threshold ionization in an elliptically polarized mid-infrared strong laser field is investigated within a semiclassical model incorporating tunneling and Coulomb field effects. It is shown that Coulomb focusing up to moderate ellipticity values is dominated by multiple forward scattering of the ionized electron by the atomic core that creates a characteristic low-energy structure in the photoelectron spectrum and is responsible for the peculiar energy scaling of the ionization normalized yield along the major polarization axis. At higher ellipticities, the electron continuum dynamics is disturbed by the Coulomb field effect mostly at the exit of the ionization tunnel. Due to the latter, the normalized yield is found to be enhanced, with the enhancement factor being sharply pronounced at intermediate ellipticities.
We study photoionization of argon atoms excited by attosecond pulses using an interferometric measurement technique. We measure the difference in time delays between electrons emitted from the $3s^2$ and from the $3p^6$ shell, at different excitation energies ranging from 32 to 42 eV. The determination of single photoemission time delays requires to take into account the measurement process, involving the interaction with a probing infrared field. This contribution can be estimated using an universal formula and is found to account for a substantial fraction of the measured delay.
We apply a fundamental definition of time delay, as the difference between the time a particle spends within a finite region of a potential and the time a free particle spends in the same region, to determine results for photoionization of an electron by an extreme ultraviolet (XUV) laser field using numerical simulations on a grid. Our numerical results are in good agreement with those of the Wigner-Smith time delay, obtained as the derivative of the phase shift of the scattering wave packet with respect to its energy, for the short-range Yukawa potential. In case of the Coulomb potential we obtain time delays for any finite region, while - as expected - the results do not converge as the size of the region increases towards infinity. The impact of an ultrashort near-infrared probe pulse on the time delay is analyzed for both the Yukawa as well as the Coulomb potential and is found to be small for intensities below $10^{13}$ W/cm$^2$.
High-harmonics generation spectroscopy is a promising tool for resolving electron dynamics and structure in atomic and molecular systems. This scheme, commonly described by the strong field approximation, requires a deep insight into the basic mechanism that leads to the harmonics generation. Recently, we have demonstrated the ability to resolve the first stage of the process -- field induced tunnel ionization -- by adding a weak perturbation to the strong fundamental field. Here we generalize this approach and show that the assumptions behind the strong field approximation are valid over a wide range of tunnel ionization conditions. Performing a systematic study -- modifying the fundamental wavelength, intensity and atomic system -- we observed a good agreement with quantum path analysis over a range of Keldysh parameters. The generality of this scheme opens new perspectives in high harmonics spectroscopy, holding the potential of probing large, complex molecular systems.
We present the first experimental data on strong-field ionization of atomic hydrogen by few-cycle laser pulses. We obtain quantitative agreement at the 10% level between the data and an {it ab initio} simulation over a wide range of laser intensities and electron energies.
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