No Arabic abstract
High-order harmonics generated by bicircular laser field have helicities which alternate between $+1$ and $-1$. In order to generate circularly polarized high-harmonic pulses, which are important for applications, it is necessary to achieve asymmetry in emission of harmonics having opposite helicities. We theoretically investigated a wide range of bicircular field component intensities and found areas where both the harmonic intensity is high and the helicity asymmetry is large. We investigated the cases of $omega$--$2omega$ and $omega$--$3omega$ bicircular fields and atoms having the $s$ and $p$ ground states, exemplified by He and Ne atoms, respectively. We have shown that for He atoms strong high harmonics having positive helicity can be generated using $omega$--$3omega$ bicircular field with a much stronger second field component. For Ne atoms the helicity asymmetry can be large in a wider range of the driving field component intensities and for higher harmonic orders. For the stronger second field component the harmonic intensity is higher and the helicity asymmetry parameter is larger for higher harmonic orders. The results for Ne atoms are illustrated with the parametric plots of elliptically polarized attosecond high-harmonic field.
High-order harmonic generation by a bicircular field, which consists of two coplanar counter-rotating circularly polarized fields of frequency $romega$ and $somega$ ($r$ and $s$ are integers), is investigated for a polyatomic molecule. This field possesses dynamical symmetry, which can be adjusted to the symmetry of the molecular Hamiltonian and used to investigate the molecular symmetry. For polyatomic molecules having the $C_{r+s}$ symmetry only the harmonics $n=q(r+s)pm r$, $q=1,2,ldots$, are emitted having the ellipticity $varepsilon_n=pm 1$. We illustrate this using the example of the planar molecules BH$_3$ and BF$_3$, which obey the $C_3$ symmetry. We show that for the BF$_3$ molecule, similarly to atoms with a $p$ ground state, there is a strong asymmetry in the emission of high harmonics with opposite helicities. This asymmetry depends on the molecular orientation.
It is demonstrated by single-atom simulations that X-ray signals in the 3.4 to 4 keV region from an 8 micron laser driven high harmonic generation can be increased by more than two orders of magnitude when a single-cycle pulse centered at 800 nm is added. The ionization probability of a helium atom by the two-pulse field is set to 4.56x10^-5, which is needed for balancing the index of refraction of free electrons with that of neutral helium atoms to achieve phase matching.
The present work reports on the generation of short-pulse coherent extreme ultraviolet radiation of controlled polarization. The proposed strategy is based on high-order harmonics generated in pre-aligned molecules. Field-free molecular alignment produced by a short linearly-polarized infrared laser pulse is used to break the isotropy of a gas medium. Driving the aligned molecules by a circularly-polarized infrared pulse allows to transfer the anisotropy of the medium to the polarization of the generated harmonic light. The ellipticity of the latter is controlled by adjusting the angular distribution of the molecules at the time they interact with the driving pulse. Extreme ultraviolet radiation produced with high degree of ellipticity (close to circular) is demonstrated.
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 a method to distinguish the high harmonics generated in individual half-cycle of the driving laser pulse by mixing a weak ultraviolet pulse, enabling one to observe the cutoff of each half-cycle harmonic. We show that the detail information of the driving laser pulse, including the laser intensity, pulse duration and carrier-envelope phase, can be {it in situ} retrieved from the harmonic spectrogram. In addition, our results show that this method also distinguishes the half-cycle high harmonics for a pulse longer than 10 fs, suggesting a potential to extend the CEP measurement to the multi-cycle regime.