RESUMEN
We report on small optical reflection increases after illumination of nanometer thick gold and aluminum thin films on different substrates with single, femtosecond 400 nm wavelength pump laser pulses, in a pre-ablation fluence regime. In this fluence regime, small, irreversible and subtle morphological changes of the sample are observed. Dark-field, scanning electron, and atomic force microscopy images reveal subwavelength spallation features in the aluminum, and delamination in the gold layers in this pre-ablation regime. All of these morphological changes coincide with minute optical increases in the reflectivity, at the 0.1-2% level, as observed in-situ with a weak probe beam. From Liu-analysis, transfer-matrix, and two-temperature model calculations, we infer that in this pre-ablation regime, the aluminum layers already reach the melting temperature. Electron Backscatter Diffraction measurements show that the Al grains melt and resolidify into bigger grains. This suggests that for Al, resolidification into bigger grains is responsible for both the increased reflection, and the spallation in the pre-ablation regime. For gold, the optical change is most likely due to the etalon effect caused by delamination.
RESUMEN
Laser irradiation of metals is widely used in research and applications. In this work, we study how the material geometry affects electron-phonon coupling in nano-sized gold samples: an ultrathin layer, nano-rod, and two types of gold nanoparticles (cubic and octahedral). We use the combined tight-binding molecular dynamics Boltzmann collision integral method implemented within XTANT-3 code to evaluate the coupling parameter in irradiation targets at high electronic temperatures (up to Te~20,000 K). Our results show that the electron-phonon coupling in all objects with the same fcc atomic structure (bulk, layer, rod, cubic and octahedral nanoparticles) is nearly identical at electronic temperatures above Te~7000 K, independently of geometry and dimensionality. At low electronic temperatures, reducing dimensionality reduces the coupling parameter. Additionally, nano-objects under ultrafast energy deposition experience nonthermal damage due to expansion caused by electronic pressure, in contrast to bulk metal. Nano-object ultrafast expansion leads to the ablation/emission of atoms and disorders the inside of the remaining parts. These nonthermal atomic expansion and melting are significantly faster than electron-phonon coupling, forming a dominant effect in nano-sized gold.
RESUMEN
Ultrafast laser irradiation of metals can often be described theoretically with the two-temperature model. The energy exchange between the excited electronic system and the atomic one is governed by the electron-phonon coupling parameter. The electron-phonon coupling depends on both, the electronic and the atomic temperature. We analyze the effect of the dependence of the electron-phonon coupling parameter on the atomic temperature in ruthenium, gold, and palladium. It is shown that the dependence on the atomic temperature induces nonlinear behavior, in which a higher initial electronic temperature leads to faster electron-phonon equilibration. Analysis of the experimental measurements of the transient thermoreflectance of the laser-irradiated ruthenium thin film allows us to draw some, albeit indirect, conclusions about the limits of the applicability of the different coupling parametrizations.
RESUMEN
Studying electron- and X-ray-induced electron cascades in solids is essential for various research areas at free-electron laser facilities, such as X-ray imaging, crystallography, pulse diagnostics or X-ray-induced damage. To better understand the fundamental factors that define the duration and spatial size of such cascades, this work investigates the electron propagation in ten solids relevant for the applications of X-ray lasers: Au, B4C, diamond, Ni, polystyrene, Ru, Si, SiC, Si3N4 and W. Using classical Monte Carlo simulation in the atomic approximation, we study the dependence of the cascade size on the incident electron or photon energy and on the target parameters. The results show that an electron-induced cascade is systematically larger than a photon-induced cascade. Moreover, in contrast with the common assumption, the maximal cascade size does not necessarily coincide with the electron range. It was found that the cascade size can be controlled by careful selection of the photon energy for a particular material. Photon energy, just above an ionization potential, can essentially split the absorbed energy between two electrons (photo- and Auger), reducing their initial energy and thus shrinking the cascade size. This analysis suggests a way of tailoring the electron cascades for applications requiring either small cascades with a high density of excited electrons or large-spread cascades with lower electron densities.
RESUMEN
It is well known that sufficiently thick metals irradiated with ultrafast laser pulses exhibit phonon hardening, in contrast to ultrafast nonthermal melting in covalently bonded materials. It is still an open question how finite size metals react to irradiation. We show theoretically that generally metals, under high electronic excitation, undergo nonthermal phase transitions if material expansion is allowed (e.g. in finite samples). The nonthermal phase transitions are induced via an increase of the electronic pressure which leads to metal expansion. This, in turn, destabilizes the lattice triggering a phase transition without a thermal electron-ion coupling mechanism involved. We find that hexagonal close-packed metals exhibit a diffusionless transition into a cubic phase, whereas metals with a cubic lattice melt. In contrast to covalent solids, nonthermal phase transitions in metals are not ultrafast, predicative on the lattice expansion.
RESUMEN
Ruthenium is a perspective material to be used for XUV mirrors at free-electron laser facilities. Yet, it is still poorly studied in the context of ultrafast laser-matter interaction. In this work, we present single-shot damage studies of thin Ru films irradiated by femtosecond XUV free-electron laser pulses at FLASH. Ex-situ analysis of the damaged spots, performed by different types of microscopy, shows that the weakest detected damage is surface roughening. For higher fluences we observe ablation of Ru. Combined simulations using Monte-Carlo code XCASCADE(3D) and the two-temperature model reveal that the damage mechanism is photomechanical spallation, similar to the case of irradiating the target with optical lasers. The analogy with the optical damage studies enables us to explain the observed damage morphologies.
RESUMEN
The durability of grazing- and normal-incidence optical coatings has been experimentally assessed under free-electron laser irradiation at various numbers of pulses up to 16 million shots and various fluence levels below 10% of the single-shot damage threshold. The experiment was performed at FLASH, the Free-electron LASer in Hamburg, using 13.5â nm extreme UV (EUV) radiation with 100â fs pulse duration. Polycrystalline ruthenium and amorphous carbon 50â nm thin films on silicon substrates were tested at total external reflection angles of 20° and 10° grazing incidence, respectively. Mo/Si periodical multilayer structures were tested in the Bragg reflection condition at 16° off-normal angle of incidence. The exposed areas were analysed post-mortem using differential contrast visible light microscopy, EUV reflectivity mapping and scanning X-ray photoelectron spectroscopy. The analysis revealed that Ru and Mo/Si coatings exposed to the highest dose and fluence level show a few per cent drop in their EUV reflectivity, which is explained by EUV-induced oxidation of the surface.
