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Register a new userHigh-order phase-dependent asymmetry in the above-threshold ionization plateau
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Above-threshold ionization spectra from cesium are measured as a function of the carrier-envelope phase (CEP) using laser pulses centered at 3.1 $mu$m wavelength. The directional asymmetry in the energy spectra of backscattered electrons oscillates three times, rather than once, as the CEP is changed from $0$ to $2pi$. Using the improved strong-field approximation, we show that the unusual behavior arises from the interference of few quantum orbits. We discuss the conditions for observing the high-order CEP dependence, and draw an analogy with time-domain holography with electron wave packets.
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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.
Multiphoton ionization provides a clear window into the nature of electron correlations in the helium atom. In the present study, the final state energy range extends up to the region near the $N=2$ and $N=3$ ionization thresholds, where two-photon ionization proceeds via continuum intermediate states above the lowest threshold. Our calculations are performed using multichannel quantum defect theory (MQDT) and the streamlined R-matrix method. The sum and integration over all intermediate states in the two-photon ionization amplitude is evaluated using the inhomogeneous R-matrix method developed by Robicheaux and Gao. The seamless connection of that method with MQDT allows us to present high resolution spectra of the final state Rydberg resonances. Our analysis classifies the resonances above the $N=2$ threshold in terms of their group theory quantum numbers. Their dominant decay channels are found to obey the previously conjectured propensity rule far more weakly for these even parity states than was observed for the odd-parity states relevant to single photon ionization.
We investigate the carrier-envelope phase and intensity dependence of the longitudinal momentum distribution of photoelectrons resulting from above-threshold ionization of argon by few-cycle laser pulses. The intensity of the pulses with a center wavelength of 750,nm is varied in a range between $0.7 times 10^{14}$ and $unit[5.5 times 10^{14}]{W/cm^2}$. Our measurements reveal a prominent maximum in the carrier-envelope phase-dependent asymmetry at photoelectron energies of 2,$U_mathrm{P}$ ($U_mathrm{P}$ being the ponderomotive potential), that is persistent over the entire intensity range. Further local maxima are observed at 0.3 and 0.8,$U_mathrm{P}$. The experimental results are in good agreement with theoretical results obtained by solving the three-dimensional time-dependent Schr{o}dinger equation (3D TDSE). We show that for few-cycle pulses, the carrier-envelope phase-dependent asymmetry amplitude provides a reliable measure for the peak intensity on target. Moreover, the measured asymmetry amplitude exhibits an intensity-dependent interference structure at low photoelectron energy, which could be used to benchmark model potentials for complex atoms.
We derive here a new highly selective photoelectron-based chirality-sensing technique that utilizes locally-chiral laser pulses. We show that this approach results in strong chiral discrimination, where the standard forwards/backwards asymmetry of photoelectron circular dichroism (PECD) is lifted. The resulting dichroism is much larger and more robust than conventional PECD, is found in all hemispheres, and is not symmetric or antisymmetric with respect to any symmetry operator. Remarkably, a CD of up to 10% survives in the angularly-integrated above-threshold ionization (ATI) spectra, and of up to 5% in the total ionization rates. We demonstrate these results through ab-initio calculations in the chiral molecules Bromochlorofluoromethane, Limonene, Fenchone, and Camphor. We also explore the parameter-space of the locally-chiral field and show that the observed CD is strongly correlated to the degree of chirality of the light, validating it as a measure for chiral-interaction strengths. Our results pave the way for highly selective probing of ultrafast chirality in ATI, can potentially lead to all-optical enantio-separation, and motivate the use of locally-chiral light for enhancing ultrafast spectroscopies.
We study high-order harmonic generation in aligned molecules close to the ionization threshold. Two distinct contributions to the harmonic signal are observed, which show very different responses to molecular alignment and ellipticity of the driving field. We perform a classical electron trajectory analysis, taking into account the significant influence of the Coulomb potential on the strong-field-driven electron dynamics. The two contributions are related to primary ionization and excitation processes, offering a deeper understanding of the origin of high harmonics near the ionization threshold. This work shows that high harmonic spectroscopy can be extended to the near-threshold spectral range, which is in general spectroscopically rich.
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