SearcharxivSearch

arXiv subjects

Mary R. Matthews

Publications and source records attributed to Mary R. Matthews.

2 recordsLinked to original sources

Pulse-Duration Control of Subcycle Multiband Electron Dynamics Extends the High-Harmonic Cutoff in a Light-Driven Insulator

We demonstrate pathway-selective control of extreme-ultraviolet high-harmonic generation by jointly tuning laser pulse duration ($5$ - $29$ fs) and intensity ($0.8$ - $74$ TW/cm$^2$). Many-cycle pulses at moderate intensities, $\sim 6$ TW/cm$^2$, promote cumulative carrier transfer over successive optical cycles, progressively accessing higher conduction bands. In contrast, few-cycle, high-intensity, $\sim 22$ TW/cm$^2$, pulses drive subcycle multiband dynamics that reach $25$ - $50$ eV photon energies before decoherence can suppress coherent emission. These results reveal pulse duration and intensity as decisive control knobs for high-harmonic emission, opening a route to band-structure-guided pulse design for higher energy extreme-ultraviolet light sources.

physics.optics

The mechanism of high harmonic generation in liquid alcohol

The observation of non-perturbative harmonic emission in solids from ultrashort laser pulses [1] sparked a wave of studies [2,3] as a probe of charge carrier dynamics in solids under strong fields and a route to extreme ultraviolet (XUV) attosecond photonic devices [4]. High harmonic generation (HHG) in liquids [5,6] is far less explored, despite their relevance to biological media, and the mechanism is hotly debated. Using few-cycle pulses below the breakdown threshold, we demonstrate HHG in alcohol with data showing carrier-envelope-phase-dependent XUV spectra extending to 50 eV from isopropanol. We study the mechanism of the harmonic emission through its dependence on the driving field and find it to be consistent with a strong-field recombination mechanism. This maps emitted photon energy to the electron trajectories. We explore the role of the liquid environment in scattering the trajectories and find evidence that information on electron scattering from neighbouring molecules is encoded in the harmonic spectra. Using simulations we exploit this to estimate the scattering cross section and we confirm that the cross-section in liquid isopropanol is significantly reduced compared to vapour. Our findings suggest an \textit{in situ} measurement strategy for retrieving accurate values of scattering cross sections in liquids, and also a pathway to liquid-based attosecond XUV devices.

physics.optics