No Arabic abstract
Various interference effects are known to exist in the process of high harmonic generation (HHG) both at the single atom and macroscopic levels. In particular, the quantum path difference between the long and short trajectories of electron excursion causes the HHG yield to experience interference-based temporal and spectral modulations. In solids, due to additional phenomena such as multi-band superposition and crystal symmetry dependency, the HHG mechanism appears to be more complicated than in gaseous atoms in identifying accompanying interference phenomena. Here, we first report experimental data showing intensity-dependent spectral modulation and broadening of high harmonics observed from bulk sapphire. Then, by adopting theoretical simulation, the extraordinary observation is interpreted as a result of the quantum path interference between the long and short electron/hole trajectories. Specifically, the long trajectory undergoes an intensity-dependent redshift, which coherently combines with the short trajectory to exhibit spectral splitting in an anomalous way of inverse proportion to the driving laser intensity. This quantum interference may be extended to higher harmonics with increasing the laser intensity, underpinning the potential for precise control of the phase matching and modulation even in the extreme ultraviolet and soft X-ray regime. Further, this approach may act as a novel tool for probing arbitrary crystals so as to adjust the electron dynamics of higher harmonics for attosecond spectroscopy.
High-order harmonic generation (HHG) in isolated atoms and molecules has been widely utilized in extreme ultraviolet (XUV) photonics and attosecond pulse metrology. Recently, HHG has also been observed in solids, which could lead to important applications such as all-optical methods to image valance charge density and reconstruction of electronic band structures, as well as compact XUV light sources. Previous HHG studies are confined on crystalline solids; therefore decoupling the respective roles of long-range periodicity and high density has been challenging. Here, we report the first observation of HHG from amorphous fused silica. We decouple the role of long-range periodicity by comparing with crystal quartz, which contains same atomic constituents but exhibits long-range periodicity. Our results advance current understanding of strong-field processes leading to high harmonic generation in solids with implications in robust and compact coherent XUV light sources.
High-harmonic generation by a highly non-linear interaction of infrared laser fields with matter allows for the generation of attosecond pulses in the XUV spectral regime. This process, well established for atoms, has been recently extended to the condensed phase. Remarkably well pronounced harmonics up to order ~30 have been observed for dielectrics. We present the first ab-initio multi-scale simulation of solid-state high-harmonic generation. We find that mesoscopic effects of the extended system, in particular the realistic sampling of the entire Brillouin zone, the pulse propagation in the dense medium, and the inhomogeneous illumination of the crystal have a strong effect on the formation of clean harmonic spectra. Our results provide a novel explanation for the formation of clean harmonics and have implications for a wide range of non-linear optical processes in dense media.
We propose a novel picture of high-harmonic generation (HHG) in solids based on the concept of temporally changing band structures. To demonstrate the utility of this picture, we focus on the high-order sideband generation (HSG) caused by strong terahertz (THz) and weak near-infrared (NIR) light in the context of pump-probe spectroscopy. We find that the NIR frequency dependence of the HSG indicates the existence of new energy levels (sub-bands) around the band-gap energy, which have multiple frequencies of THz light. This sub-band picture explains why the HSG intensity becomes a non-monotonic function of the THz light amplitude. The present analysis not only reveals the origin of the plateau structure in HHG spectra, but also provides a connection to other high-field phenomena.
We consider several aspects of high-order harmonic generation in solids: the effects of elastic and inelastic scattering; varying pulse characteristics; and inclusion of material-specific parameters through a realistic band structure. We reproduce many observed characteristics of high harmonic generation experiments in solids including the formation of only odd harmonics in inversion-symmetric materials, and the nonlinear formation of high harmonics with increasing field. We find that the harmonic spectra are fairly robust against elastic and inelastic scattering. Furthermore, we find that the pulse characteristics play an important role in determining the harmonic spectra.
Since the new millennium coherent extreme ultra-violet and soft x-ray radiation has revolutionized the understanding of dynamical physical, chemical and biological systems at the electrons natural timescale. Unfortunately, coherent laser-based upconversion of infrared photons to vacuum-ultraviolet and soft x-ray high-order harmonics in gaseous, liquid and solid targets is notoriously inefficient. In dense nonlinear media, the limiting factor is strong re-absorption of the generated high-energy photons. Here we overcome this limitation by allowing high-order harmonics generated from a periodic array of thin one-dimensional crystalline silicon ridge waveguides to propagate in the vacuum gaps between the ridges, thereby avoiding the high absorption loss of the bulk nonlinear material and resulting in a ~ 100-fold increase in propagation length. As the grating period is varied, each high-harmonic shows a different and marked modulation, indicating the onset of coherent addition which is otherwise suppressed in absorption-limited emission. By beating the absorption limit, our results pave the way for bright coherent short-wavelength sources and their implementation in nano-photonic devices.