Iaroslav Gnilitskyi | Searcharxiv

arXiv2020

Ultrafast energy absorption and photoexcitation of bulk plasmon in crystalline silicon subjected to intense near-infrared ultrashort laser pulses

We investigate the non-linear response and energy absorption in bulk silicon irradiated by intense 12-fs near-infrared laser pulses. Depending on the laser intensity, we distinguish two regimes of non-linear absorption of the laser energy: for low intensities, energy deposition and photoionization involve perturbative three-photon transition through the direct bandgap of silicon. For laser intensities near and above 10$^{14}$ W/cm$^2$, corresponding to photocarrier density of order 10$^{22}$ cm$^{-3}$, we find that absorption at near-infrared wavelengths is greatly enhanced due to excitation of bulk plasmon resonance. In this regime, the energy transfer to electrons exceeds a few times the thermal melting threshold of Si. The optical reflectivity of the photoexcited solid is found in good qualitative agreement with existing experimental data. In particular, the model predicts that the main features of the reflectivity curve of photoexcited Si as a function of the laser fluence are determined by the competition between state and band filling associated with Pauli exclusion principle and Drude free-carrier response. The non-linear response of the photoexcited solid is also investigated for irradiation of silicon with a sequence of two strong and temporary non-overlapping pulses. The cumulative effect of the two pulses is non-additive in terms of deposited energy. Photoionization and energy absorption on the leading edge of the second pulse is greatly enhanced due to free carrier absorption.

physics.optics↗

arXiv2017

Mechanism of the single-pulse ablative generation of laser induced periodic surface structures

One of the remarkable capabilities of ultrashort polarized laser pulses is the generation of laser-induced periodic surface structures (LIPSS). The origin of this phenomenon is largely attributed to the interference of the incident laser wave and surface electromagnetic wave that creates a periodic absorption pattern. Although, commonly, LIPSS are produced by repetitive irradiation of the same area by multiple laser pulses in the regime of surface melting and resolidification, recent reports demonstrate the formation of LIPSS in the single pulse irradiation regime at laser fluences well above the ablation threshold. In this paper, we report results of a large-scale molecular dynamics simulation aimed at providing insights into the mechanisms of single pulse ablative LIPSS formation. The simulation performed for a Cr target reveals an interplay of material removal and redistribution in the course of spatially modulated ablation, leading to the transient formation of an elongated liquid wall extending up to ~600 nm above the surface of the target at the locations of the minima of the laser energy deposition. The upper part of the liquid wall disintegrates into droplets while the base of the wall solidifies on the timescale of ~2 ns, producing a ~100 nm-long frozen surface feature extending above the level of the initial surface of the target. The properties of the surface region of the target are modified by the presence of high densities of dislocations and vacancies generated due to the rapid and highly nonequilibrium nature of the melting and resolidification processes. The insights into the LIPSS formation mechanisms may help in designing approaches for increasing the processing speed and improving the quality of the laser-patterned periodic surface structures.

cond-mat.mtrl-sci↗