Epsilon-near-zero (ENZ) materials have emerged as viable platforms for strong nonlinear optical (NLO) interactions. The NLO phase shift in materials exhibiting an ENZ condition is extremely large; however, direct experimental measurements of the magnitude and time dynamics of this phenomenon, particularly nondegenerate NLO phase shifts, have so far been lacking. Here, we directly measure the NLO phase shift of an Indium-Tin-Oxide (ITO) thin film using three different techniques. By characterizing the excitation-induced, time-resolved beam deflection (BD) of a probe beam, we measure the nondegenerate NLO effects, allowing a separate determination of the effects of excitation and probe wavelengths on the NLO phase shift as they are varied across the ENZ region. These experiments reveal that having the probe pulse centered at ENZ greatly contributes to this enhancement; however, the NLO phase shift is less sensitive to the excitation wavelength, which only slightly enhances the nonlinearity for obliquely incident TM-polarized light. We also find that the spectral shift of the probe pulse induced by the excitation follows both the magnitude and time dynamics of the NLO phase shift measured via the BD experiments. We observe large, ultrafast cross-phase modulation in agreement with a redistribution of carriers in the conduction band. Finally, using the Z-scan method, we measure the degenerate nonlinear refraction at ENZ near normal incidence. The results of all three measurements agree, revealing a gigantic sub-picosecond NLO phase shift in ITO. At its largest, we consistently measure an effective induced index change greater than the linear index.

In this paper properties of Biaxial-Oriented Polypropylene, Poly Vinyl Chloride and Poly Methyl Methacrylate samples treated by DC glow discharge of N 2 plasma have been investigated by UV-Vis_NIR spectrophotometer. It was found that plasma treatment change chemical structure of polymer surfaces. In addition, absorption coefficient, refractive index and extinction coefficient of all treated samples have been slightly changed.

Space–time (ST) wave packets are a class of pulsed optical beams whose spatiotemporal spectral structure results in propagation invariance, tunable group velocity, and anomalous refractive phenomena. Here, we investigate the refraction of ST wave packets normally incident onto a planar interface between two dispersive, homogeneous, isotropic media. We formulate a new, to the best of our knowledge, refractive invariant for ST wave packets in this configuration, from which we obtain a law of refraction that determines the change in their group velocity across the interface. We verify this new refraction law in ZnSe and CdSe, both of which manifest large chromatic dispersion at near-infrared frequencies in the vicinity of their band edges. ST wave packets can thus be utilized in nonlinear optics for bridging large group-velocity mismatches in highly dispersive scenarios.

The nature of linear photophysical and nonlinear optical properties of a new squaraine derivative 2,4-bis[4-(azetidyl)-2-hydroxyphenyl]squaraine (1) with efficient near-infrared (NIR) emission was comprehensively analyzed based on spectroscopic, photochemical, and two-photon absorption (2PA) measurements, along with quantum chemical analysis. The steady-state absorption, fluorescence, and excitation anisotropy spectra of 1 and its fluorescence emission lifetimes revealed the multiple aspects of the electronic structure of 1, including the relative orientations of the main transition dipoles, effective rotational volumes in solvents of different polarities, and a maximum molar extinction of 1.35 × 10 −5 M −1 •cm −1 , which is unusually small for similar symmetric squaraines. The degenerate 2PA spectrum of 1 was obtained over a broad spectral range under femtosecond excitation, using standard open-aperture Z-scan and two-photon induced fluorescence methods, revealing maximum 2PA cross sections of ∼400 GM. Squaraine 1 exhibited efficient superluminescence emission in the polar solvent (dichloromethane) at room temperature under femtosecond pumping conditions. Quantum chemical analysis of the electronic structure of 1 was performed using the DFT/ TD-DFT level of theory and found to be in good agreement with experimental data. The new squaraine derivative 1 displayed high fluorescence quantum yield, efficient NIR superluminescence, large 2PA cross sections, and high photostability with a photodecomposition quantum yield ∼4 × 10 −6 , suggesting its potential for applications in two-photon fluorescent bioimaging and lasing.

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