Many-body effects play an important role in enhancing and modifying optical absorption and other excited-state properties of solids in the perturbative regime, but their role in high harmonic generation (HHG) and other nonlinear response beyond the perturbative regime is not well-understood. We develop here an ab initio many-body method to study nonperturbative HHG based on the real-time propagation of the non-equilibrium Green’s function with the GW self energy. We calculate the HHG of monolayer MoS2and obtain good agreement with experiment, including the reproduction of characteristic patterns of monotonic and nonmonotonic harmonic yield in the parallel and perpendicular responses, respectively. Here, we show that many-body effects are especially important to accurately reproduce the spectral features in the perpendicular response, which reflect a complex interplay of electron-hole interactions (or exciton effects) in tandem with the many-body renormalization and Berry curvature of the independent quasiparticle bandstructure.
High harmonic generation (HHG) in solids has been identified as a promising mechanism for light source generation and for spectroscopy of materials. HHG from bulk solids, however, often suffers from nonlinear propagation effects, resulting in a loss of spectral coherence and the skewing of spectroscopic measurements. Here, we study HHG in epitaxial ZnO thin films grown on Al2O3substrates using atomic layer deposition. We find that the HHG emission consists of narrow spectral peaks, in contrast to those seen in bulk, and that the dependence of the harmonic yield on the film thickness differs for above-gap and below-gap harmonics, which can be understood from analytical models based on the linear and nonlinear response of the medium. The measured harmonic spectra depend qualitatively on the preparation of the films, with as-grown films generating even harmonic orders, which are absent in annealed films. The results are interpreted using transmission electron microscopy measurements, which indicate different morphologies for the as-grown and annealed films.
more » « less- Award ID(s):
- 2121953
- PAR ID:
- 10487376
- Publisher / Repository:
- Optical Society of America
- Date Published:
- Journal Name:
- Journal of the Optical Society of America B
- Volume:
- 41
- Issue:
- 6
- ISSN:
- 0740-3224; JOBPDE
- Format(s):
- Medium: X Size: Article No. B1
- Size(s):
- Article No. B1
- Sponsoring Org:
- National Science Foundation
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Abstract High harmonic generation (HHG) opens a window on the fundamental science of strong-field light-mater interaction and serves as a key building block for attosecond optics and metrology. Resonantly enhanced HHG from hot spots in nanostructures is an attractive route to overcoming the well-known limitations of gases and bulk solids. Here, we demonstrate a nanoscale platform for highly efficient HHG driven by intense mid-infrared laser pulses: an ultra-thin resonant gallium phosphide (GaP) metasurface. The wide bandgap and the lack of inversion symmetry of the GaP crystal enable the generation of even and odd harmonics covering a wide range of photon energies between 1.3 and 3 eV with minimal reabsorption. The resonantly enhanced conversion efficiency facilitates single-shot measurements that avoid material damage and pave the way to study the controllable transition between perturbative and non-perturbative regimes of light-matter interactions at the nanoscale.more » « less
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Explicit formula for high-order sideband polarization by extreme tailoring of Feynman path integralsHigh-order sideband generation (HSG), as an analog of the interband processes in high-harmonic generation (HHG) in solids, is a nonperturbative nonlinear optical phenomenon in semiconductors that are simultaneously driven by a relatively weak near-infrared (NIR) laser and a sufficiently strong terahertz (THz) field. We derive an explicit formula for sideband polarization vectors in a prototypical two-band model based on the saddle-point method. Our formula connects the sideband amplitudes with the laser-field parameters, electronic structures, and nonequilibrium dephasing rates in a highly nontrivial manner. Our results indicate the possibility of extracting information on band structures and dephasing rates from high-order sideband generation experiments with simple algebraic calculations. We also expect our approach to be useful on the quantitative understanding of the interband HHG.more » « less
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High harmonic generation (HHG) makes it possible to measure spin and charge dynamics in materials on femtosecond to attosecond timescales. However, the extreme nonlinear nature of the high harmonic process means that intensity fluctuations can limit measurement sensitivity. Here we present a noise-canceled, tabletop high harmonic beamline for time-resolved reflection mode spectroscopy of magnetic materials. We use a reference spectrometer to independently normalize the intensity fluctuations of each harmonic order and eliminate long term drift, allowing us to make spectroscopic measurements near the shot noise limit. These improvements allow us to significantly reduce the integration time required for high signal-to-noise (SNR) measurements of element-specific spin dynamics. Looking forward, improvements in the HHG flux, optical coatings, and grating design can further reduce the acquisition time for high SNR measurements by 1–2 orders of magnitude, enabling dramatically improved sensitivity to spin, charge, and phonon dynamics in magnetic materials.
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Abstract High-order harmonic generation (HHG) has become an indispensable process for generating attosecond pulse trains and single attosecond pulses used in the observation of nuclear and electronic motion. As such, improved control of the HHG process is desirable, and one such possibility for this control is through the use of structured laser pulses. We present numerical results from solving the one-dimensional time-dependent Schrödinger equation for HHG from hydrogen using Airy and Gaussian pulses that differ only in their spectral phase. Airy pulses have identical power spectra to Gaussian pulses, but different spectral phases and temporal envelopes. We show that the use of Airy pulses results in less ground state depletion compared to the Gaussian pulse, while maintaining harmonic yield and cutoff. Our results demonstrate that Airy pulses with higher intensity can produce similar HHG spectra to lower intensity Gaussian pulses without depleting the ground state. The different temporal envelopes of the Gaussian and Airy pulses lead to changes in the dynamics of the HHG process, altering the time-dependence of the ground state population and the emission times of the high harmonics.
Graphical abstract
