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Register a new userAttosecond synchronization of extreme ultraviolet high harmonics from crystals
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The interaction of strong near-infrared (NIR) laser pulses with wide-bandgap dielectrics produces high harmonics in the extreme ultraviolet (XUV) wavelength range. These observations have opened up the possibility of attosecond metrology in solids, which would benefit from a precise measurement of the emission times of individual harmonics with respect to the NIR laser field. Here we show that, when high-harmonics are detected from the input surface of a magnesium oxide crystal, a bichromatic probing of the XUV emission shows a clear synchronization largely consistent with a semiclassical model of electron-hole recollisions in bulk solids. On the other hand, the bichromatic spectrogram of harmonics originating from the exit surface of the 200 $mu$m-thick crystal is strongly modified, indicating the influence of laser field distortions during propagation. Our tracking of sub-cycle electron and hole re-collisions at XUV energies is relevant to the development of solid-state sources of attosecond pulses.
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On the basis of real-time ab initio calculations, we study the non-perturbative interaction of two-color laser pulses with MgO crystal in the strong field regime to generate isolated attosecond pulse from high-harmonic emissions from MgO crystal. In this regard, we examine the impact of incident pulse characteristics such as its shape, intensity, and ellipticity as well as the consequence of the crystal anisotropy on the emitted harmonics and their corresponding isolated attosecond pulses. Our calculations predict the creation of isolated attosecond pulses with a duration of ~ 300 attoseconds; in addition, using elliptical driving pulses, the generation of elliptical isolated attosecond pulses is shown. Our work prepares the path for all solid-state compact optical devices offering perspectives beyond traditional isolated attosecond pulse emitted from atoms.
A compact high repetition rate attosecond light source based on a standard laser oscillator combined with plasmonic enhancement is presented. At repetition rates of tens of MHz, we predict focusable pulses with durations of ~< 300 attoseconds, and collimation angles ~< 5 degrees. Attosecond pulse parameters are robust with respect variations of driver pulse focus and duration.
Circularly-polarized extreme UV and X-ray radiation provides valuable access to the structural, electronic and magnetic properties of materials. To date, this capability was available only at large-scale X-ray facilities such as synchrotrons. Here we demonstrate the first bright, phase-matched, extreme UV circularly-polarized high harmonics and use this new light source for magnetic circular dichroism measurements at the M-shell absorption edges of Co. We show that phase matching of circularly-polarized harmonics is unique and robust, producing a photon flux comparable to the linearly polarized high harmonic sources that have been used very successfully for ultrafast element-selective magneto-optic experiments. This work thus represents a critical advance that makes possible element-specific imaging and spectroscopy of multiple elements simultaneously in magnetic and other chiral media with very high spatial and temporal resolution, using tabletop-scale setups.
We generate high-order harmonics of a mid-infrared laser from a silicon single crystal and find their origin in the recollision of coherently accelerated electrons with their holes, analogously to the atomic and molecular case, and to ZnO [Vampa et al., Nature 522, 462-464 (2015)], a direct bandgap material. Therefore indirect bandgap materials are shown to sustain the recollision process as well as direct bandgap materials. Furthermore, we find that the generation is perturbed with electric fields as low as 30 V/$mu$m, equal to the DC damage threshold. Our results extend high-harmonic spectroscopy to the most technologically relevant material, and open the possibility to integrate high harmonics with conventional electronics.
We theoretically investigate the spectral caustics of high-order harmonics in solids. We analyze the 1-dimension model of solids HHG and find that, apart from the caustics originated from the van Hove singularities in the energy-band structure, another kind of catastrophe singularities also emerge when the different branches of electron-hole trajectories generating high-order harmonics coalesce into a single branch. We solve time-dependent Schrodinger equation in periodic potential and demonstrate the control of this kind of singularities in HHG with the aids of two-color laser fields. The diffraction patterns of the harmonic spectrum near the caustics agree well with the inter-band electron-hole recombination trajectories predicted by the semiconductor semi-classical equation. This work is expected to help to understand the HHG dynamics in solids and manipulate the harmonic spectrum by adjusting driving field parameters.
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