RESUMO
Growing ultrathin nanogranular (NG) metallic films with continuously varying thickness is of great interest for studying regions of criticality and scaling behaviors in the vicinity of quantum phase transitions. In the present work, an ultrathin gold plasmonic NG film was grown on a sapphire substrate by RF magnetron sputtering with an intentional deposition gradient to create a linearly variable thickness ranging from 5 to 13 nm. The aim is to accurately study the electronic phase transition from the quantum tunneling regime to the metallic conduction one. The film structural characterization was performed by means of high-resolution transmission electron microscopy, atomic force microscopy, as well as x-ray diffraction and reflectivity techniques, which indicate the Volmer-Weber film growth mode. The optical and electrical measurements show a transition from dielectric-isolated gold NPs towards a continuous metallic network when t becomes larger than a critical value of tM = 7.8 nm. Our results show that the onset of the percolation region occurs when a localized surface plasma resonance transforms to display a Drude component, indicative of free charge carriers. We demonstrate that, by using a continuously varying thickness, criteria for metallicity can be unambiguously identified. The onset of metallicity is clearly distinguished by the Drude damping factor and by discontinuities in the plasma frequencies as functions of thickness.
RESUMO
The interaction between two ns-laser-induced plasmas in air at the early-stage of expansion has been analyzed by using a method based on the direct measurement of the perturbation of an externally applied electric field. In this experimental method, the plasmas were produced by focusing two laser beams between the plates of a parallel-plane-charged capacitor. These plasmas produce a perturbation in the electric field of the capacitor which can be measured as a voltage change across a resistor connected to the ground plate. It was found that for delays shorter than 5 ns, the interaction between plasmas is mainly due to the interaction of the dipole-charge distribution of each plasma. For longer time delays, the shielding effect was dominant.
RESUMO
The influence on luminescence from conical bubble collapse (CBL) with varying Ar gas content while perturbing the liquid 1,2-Propanediol (PD) has been investigated. The temporal, spatial, and spectral features were analysed with regards to the dynamics of collapse and liquid degradation. Sulphuric acid and sodium chloride were added to disturb the liquid. The following three cases were studied: PD/Ar, (I), (PD + H(2)SO(4))/Ar, (II), and (PD + H(2)SO(4) + NaCl)/Ar, (III). The intensities of those cases decrease as III > II > I. Temporally, single and multiple light emissions were found to occur. The pulse shape exhibited a large variety of profiles with a main maximum and up to two local maxima around the main maximum. These local maxima resembled those generated by laser cavitation. Spatially, no radial symmetry was detected in the light emissions. Spectrally, the Swan, CH and CN lines were observed at low volumes of gas and driving pressure. The ·OH radical and OH-Ar bands, as well as the Na and K lines, consistently appeared superimposed on an underlying continuum that almost disappeared in (III). The Na line was observed with two satellite diffuse bands representing Na-Ar complexes in (I) and (II), whereas in (III), only the line of sodium could be seen. Weak and diffuse emission lines from the Ar atom in the near-IR region were observed in (I) and (II). The proposed mechanism of bright CBL was based on the energy transfer from electron-excited homolytic cleavage products to the chromophore molecules generated during the collapse-rebound time line (~8200 K and ~1 ms of collapse time from model), which had accumulated inside the liquid and remained on the walls of cavity during the repetition of the collapse. A general mechanism for the bright CBL is broached.
