We macroscopically investigate the effect of the laser intensity and gas density on quantum trajectories in the high-order harmonic generation of Ne atoms irradiated by few-cycle, 800-nm laser pulses. The time-frequency profile of the harmonics shows that the long quantum trajectory is dominant at both lower and higher gas densities for a low laser intensity. At high laser intensities, the long quantum trajectory plays an important role for lower gas densities, while the short quantum trajectory is dominant at higher gas densities. An analysis of the phase mismatch for high-order harmonic generation shows that the primary emission of the quantum trajectories is determined by dynamic changes in the laser electric field during the propagation process.

The high-order harmonic generation from a model solid structure driven by an intense laser pulse is investigated using the semiconductor Bloch equations (SBEs). The main features of harmonic spectrum from SBEs agree well with the result of the time-dependent Schrödinger equation (TDSE), and the cut-off energy can be precisely estimated by the recollision model. With increasing the field strength, the harmonic spectrum shows an extra plateau. Based on the temporal population of electron and the time-frequency analysis, the harmonics in the extra plateau are generated by the Bloch oscillation. Due to the ultrafast time response of the Bloch electron, the generated harmonics provide a potential source of shorter isolated attosecond pulse.

We propose a simple pump-coupling-seed scheme to examine the optical X²Σ_g⁺-A²Π_u coupling in N₂⁺ lasing. We produce the N₂⁺ lasing at 391 nm, corresponding to the B²Σ_u⁺(v'=0)-X²Σ_g⁺(v=0) transition, by externally seeding the N₂⁺ gain medium prepared by irradiation of N₂ with an intense pump pulse. We then adopt a weak coupling pulse in between the pump and seed pulses, and show that the intensity of the 391-nm lasing can be efficiently modulated by varying the polarization direction of the coupling pulse with respect to that of the pump pulse. It is found that when the polarization directions of the pump and coupling pulses are perpendicular, the 391-nm lasing intensity is more sensitive to the coupling laser energy, which reflects the inherent nature of the perpendicular X²Σ_g⁺-A²Π_u transition.

We investigate experimentally multi-orbital effects in high-order harmonic generation (HHG) from aligned CO₂ and N₂O molecules by intense femtosecond laser fields with linear and elliptical polarizations. For either of the aligned molecules, a minimum in the harmonic spectrum is observed, the position of which shifts to lower-order harmonics when decreasing the intensity or increasing the ellipticity of the driving laser. This indicates that the minimum originates from the dynamic interference of different channels, of which the tunneling ionization and recombination are contributed via different molecular orbitals. The results show that both the highest occupied molecular orbital (HOMO) and low-lying HOMO-2 in CO₂ (or HOMO-1 in N₂O) contribute to the molecular HHG in both linearly and elliptically polarized strong laser fields. Our study would pave a way for understanding multi-electron dynamics from polyatomic molecules irradiated by strong laser fields.

Bichromatic circularly polarized fields provide a useful tool to probe the ionization dynamics. In this work, we compare the photoelectron momentum distribution in few-cycle bichromatic field of different helicities. The spectral features are analyzed with semiclassical trajectories derived from the strong field approximation. In particular, the interference fringes in momentum distribution are investigated by tracking the ionization time and tunneling exits of released photoelectrons. Different types of trajectories that contribute to the interference fringes are elucidated.

We experimentally investigate Coulomb exploded directional double ionization of N₂O molecules in elliptically polarized femtosecond laser pulses. The denitrogenation and deoxygenation channels are accessed via various pathways. It leads to distinct asymmetries in directional breaking of the doubly ionized N₂O molecules versus the instantaneous laser field vector, which is revealed by tracing the sum-momentum spectra of the ionic fragments as a recoil of the ejected electrons. Our results demonstrate that the accessibility of the Coulomb exploded double ionization channels of N₂O molecules are ruled by the detailed potential energy curves, and the directional emission of the fragments are governed by the joint effects of the electron localization-assisted enhanced ionization of the stretched molecules and the profiles of the molecular orbitals.