Nonlinear and thermo-optical characterisation of bare imidazolium ionic liquids.

Nonlinear optical (NLO) and thermo-optical properties of two pure ionic liquids, BMIOMe.NTf2 and BMIOMe.N(CN)2, were examined in this study. This was the first nonlinear refractive index determination of a pristine ionic liquid by a standard self-refraction experiment. The NLO characterisations were performed using Z-scan and EZ-scan techniques in the thermally managed approach, with a mode-locked femtosecond laser source. Thermal properties were analysed concomitantly, and the thermo-optical coefficient, thermal characteristic time, and lens strength were characterised. These results define the parameters to be adopted in the method of nanoparticles formation by laser ablation in an ionic liquid solution and indicate that BMIOMe.NTf2 is a prominent material to be engineered for photonics applications.

Super rogue wave generation in the linear regime.

Extreme or rogue waves are large and unexpected waves appearing with higher probability than predicted by Gaussian statistics. Although their formation is explained by both linear and nonlinear wave propagation, nonlinearity has been considered a necessary ingredient to generate super rogue waves, i.e., an enhanced wave amplification, where the wave amplitudes exceed by far those of ordinary rogue waves. Here we show, experimentally and theoretically, that optical super rogue waves emerge in the simple case of linear light diffraction in one transverse dimension. The underlying physics is a long-range correlation on the random initial phases of the light waves. When subgroups of random phases appear recurrently along the spatial phase distribution, a more ordered phase structure greatly increases the probability of constructive interference to generate super rogue events (non-Gaussian statistics with superlong tails). Our results consist in a significant advance in the understanding of extreme waves formation by linear superposition of random waves, with applications in a large variety of wave systems.

Light with Tunable Non-Markovian Phase Imprint.

We introduce a simple and flexible method to generate spatially non-Markovian light with tunable coherence properties in one and two dimensions. The unusual behavior of this light is demonstrated experimentally by probing the far field and by recording its diffraction pattern after a double slit: In both cases we observe, instead of a central intensity maximum, a line- or cross-shaped dark region, whose width and profile depend on the non-Markovian coherence properties. Because these properties can be controlled and easily reproduced in experiment, the presented approach lends itself to serving as a test bed to study and gain a deeper understanding of non-Markovian processes.

Simple modeling of plasmon resonances in Ag/SiO2 nanocomposite monolayers.

Normal incidence transmittance and reflectance spectra of sputtered nanocomposite monolayer films of Ag in SiO2, buried and unburied, showed significant redshifted plasmon resonances from 410 to 455 nm, which could be well interpreted with a simple model that starts from the Maxwell Garnett theory and the Kreibig extension of the Drude-Lorentz equation, but with a further extension related to the dipolar interaction between the metal particles distributed on a surface.

Structural control of gold nanoparticles self-assemblies by layer-by-layer process.

This work presents a novel way to introduce gold nanoparticles (Au NPs) in a multilayer polymer produced by the layer-by-layer (LbL) assembling technique. The technique chosen shows that, depending on the pH used, different morphological structures can be obtained from monolayer or bilayer Au NPs. The MEIS and RBS techniques allowed for the modelling of the interface polymer-NPs, as well as the understanding of the interaction of LbL system, when adjusting the pH in weak polyelectrolytes. The process reveals that the optical properties of multilayer systems could be fine-tuned by controlling the addition of metallic nanoparticles, which could also modify specific polarization responses.

Molecular dynamics investigation with the time resolved optical Kerr effect on the CS2-C6H6 mixtures.

An investigation of the molecular dynamics in pure liquids and in mixtures through the technique of time resolved optical Kerr effect is performed. The samples studied were the mixtures of carbon disulfide (CS(2)) with benzene (C(6)H(6)). The molecular dynamics of the pure liquids is briefly discussed while the main results are obtained for the mixtures. A slow dynamics component is observed for the optical heterodyne detected optical Kerr effect transient decaying exponentially with time constants on picosecond time scale. The fast subpicosend time relaxations are analyzed in terms of the nondiffusive component of the spectral response that is associated with the molecular dynamics. The modifications of the spectrum are quantified, and the explanation of the observed changes is given in terms of the structural interaction configurations that produced changes in the intermolecular potential within which the molecules execute librational motions.

Time-resolved optical Kerr-effect investigation on CS2/polystyrene mixtures.

The relaxation dynamics of carbon disulfide are investigated in mixtures with polystyrene (PS) using the time-resolved optical heterodyne-detected optical Kerr effect (OHD-OKE). The data are analyzed using both the model-dependent approach, which assumes four distinct temporal responses, and the model-independent Fourier transform approach, which generates a spectral response that can be compared with results obtained by depolarized Rayleigh scattering. A slow dynamics is observed for the OHD-OKE transient decaying exponentially with a time constant that varies from 1.68 ps for neat CS2 to 3.76 ps for the most concentrated CS2PS mixture. The increase of this time constant accompanies an increase in the viscosity of the mixture, so we can associate this component with the diffusive reorientation process of the induced polarizability anisotropy of the carbon disulfide in the mixture. The short-time nuclear response is characterized in the frequency domain by a broad band that peaks around 30 cm(-1) for neat carbon disulfide, and is associated with a complex relaxation pattern. The vibrational distribution shifts to higher frequencies when the PS concentration is increased in the mixture. This result is discussed in terms of an increase in the interaction strength between the PS phenyl rings and the carbon disulfide molecules.

Characterization of ultrashort pulses by a modified grating-eliminated no-nonsense observation of ultrafast incident laser light E fields (GRENOUILLE) method.

The measurement and characterization of ultrashort laser pulses remains an arduous task. The most commonly used pulse-measurement method is known as frequency-resolved optical gating (FROG), and another version with great experimental simplification and low-priced setup is known as grating-eliminated no-nonsense observation of ultrafast incident laser light E fields (GRENOUILLE). Nevertheless, there is interest in elaborating other, more accessible or simpler and cheaper, setups with equal or better assets. We explored modification of the GRENOUILLE method in which we replaced the original Fresnel biprism with a beam splitter and two mirrors and used a cheap webcam to measure the pulse traces. We have evaluated our system, and we propose a method to correct border effects caused by the beam intensity's profile based on the characterization of three pulse classes: Fourier-transform limited, double, and chirped. We compare the recovered electric field with further spectral and second-order correlation data of the corresponding pulses.