SPECIAL TOPIC — Strong-field atomic and molecular physics null
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.
We ab initio investigate the interaction between the hydrogen atom and the inhomogeneous field which is induced by resonant plasmons within a metal nanostructure. Same as normal laser pulse (homogeneous field), only odd-harmonic generation occurs when the bow-tie nanostructure is utilized. For the single nanotip case, the even-harmonic generation can be distinctly found in the harmonic emission spectrum. By investigating the symmetry and trajectories of different inhomogeneous fields, we demonstrate that the breaking symmetry of system can enable even high harmonic generations.
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.