ABSTRACT
Recent studies in high-order harmonic generation (HHG) in solid targets reveal new scenarios of extraordinary rich electronic dynamics, in comparison to the atomic and molecular cases. For the later, the main aspects of the process can be described semiclassically in terms of electrons that recombine when the trajectories revisit the parent ion. HHG in solids has been described by an analogous mechanism, in this case involving electron-hole pair recombinations. However, it has been recently reported that a substantial part of the HHG emission corresponds to situations where the electron and hole trajectories do not overlap in space. According to the present knowledge, HHG from this imperfect recollisions reflects the quantum nature of the process, arising in systems with large Berry curvatures or for elliptically polarized driving fields. In this work, we demonstrate that imperfect recollisions are also relevant in the more general case. We show the signature of such recollisions in the HHG spectrum from monolayer graphene -a system with null Berry curvature- irradiated by linearly polarized driving fields. Our calculations also reveal that imperfect multiple-order recollisions contribute to the harmonic emission when electron-hole excursion times exceed one cycle of the driving field. We believe that our work adds a substantial contribution to the full understanding of the sub-femtosecond dynamics of HHG in solid systems.
ABSTRACT
The efficiency of high-harmonic generation (HHG) from a macroscopic sample is strongly linked to the proper phase matching of the contributions from the microscopic emitters. We develop a combined micro+macroscopic theoretical model that allows us to distinguish the relevance of high-order harmonic phase matching in single-layer graphene. For a Gaussian driving beam, our simulations show that the relevant HHG emission is spatially constrained to a phase-matched ring around the beam axis. This remarkable finding is a direct consequence of the non-perturbative behavior of HHG in graphene-whose harmonic efficiency scaling is similar to that already observed in gases- and bridges the gap between the microscopic and macroscopic HHG in single-layer graphene.
ABSTRACT
We study high-order harmonic generation (HHG) in armchair-type single-wall carbon nanotubes (SWNTs) driven by ultrashort, mid-infrared laser pulses. For a SWNT with chiral indices (n, n), we demonstrate that HHG is dominated by bands |m| = n - 1 and that the cut-off frequency saturates with intensity, as it occurs in the case of single layer graphene. As a consequence, HHG in SWNTs can be described effectively as a one-dimensional periodic system, whose high-frequency emission can be modified through the proper control of the structural parameters. Additionally, we show that the HHG mechanism in nanotubes has some similarities to that previously reported in single layer graphene. However, as a main difference, the electron-hole pair excitation in SWNTs is connected to the non-adiabatic crossing through the first van Hove singularity of the |m| = n - 1 bands, instead of the crossing through the Dirac point that takes place in graphene.
ABSTRACT
High harmonic generation in atomic or molecular targets stands as a robust mechanism to produce coherent ultrashort pulses with controllable polarization in the extreme-ultraviolet. However, the production of elliptically or circularly-polarized harmonics is not straightforward, demanding complex combinations of elliptically or circularly-polarized drivers, or the use of molecular alignment techniques. Nevertheless, recent studies show the feasibility of high-harmonic generation in solids. In contrast with atoms and molecules, solids are high-density targets and therefore more efficient radiation sources. Among solid targets, 2D materials are of special interest due to their particular electronic structure, which conveys special optical properties. In this paper, we present theoretical calculations that demonstrate an extraordinary complex light-spin conversion in single-layer graphene irradiated at non perturbative intensities. Linearly-polarized drivings result in the emission of elliptically-polarized harmonics, and elliptically-polarized drivings may result in linearly-polarized or ellipticity-reversed harmonics. In addition, we demonstrate the ultrafast temporal modulation of the harmonic ellipticity.
