In the present work, we report the third order nonlinear optical properties of ZnO thin films deposited using self assembly, sol gel process as well as pulsed laser ablation by z scan technique. ZnO thin films clearly exhibit a negative nonlinear index of refraction at 532nm and the observed nonlinear refraction is attributed to two photon absorption followed by free carrier absorption. Although the absolute nonlinear values for these films are comparable, there is a change in the sign of the absorptive nonlinearity of the films. The films developed by dip coating and pulsed laser ablation exhibit reverse saturable absorption whereas the self assembled film exhibits saturable absorption. These different nonlinear characteristics in the self assembled films can be mainly attributed to the saturation of linear absorption of the ZnO defect states.

In the present work, we have investigated the nonlinear optical properties of self-assembled films formed from ZnO colloidal spheres by z-scan technique. The sign of the nonlinear component of refractive index of the material remains the same; however, a switching from reverse saturable absorption to saturable absorption has been observed as the material changes from colloid to self-assembled film. These different nonlinear characteristics can be mainly attributed to ZnO defect states and electronic effects when the colloidal solution is transformed into self-assembled monolayers. We investigated the intensity, wavelength and size dependence of saturable and reverse saturable absorption of ZnO self-assembled films and colloids. Values of the imaginary part of third-order susceptibility are calculated for particles of size in the range 20–300 nm at different intensity levels ranging from 40 to 325 MW/cm2 within the wavelength range of 450–650 nm.

Light-scattering experiments gained prominence as potential applications of quantum optics, non-linear optics, and photon localization. The possibility of the realization of lasing action in random media has created much interest in the study of the coherent structure of the backscattered light from disordered media. Backscattering (BS) studies are carried out to analyze the possibilities of photon localization in colloidal silica. The scattering enhancement is best associated with the density of the scatterers. The width of the BS cone and, hence, the mean-free path is related to the concentration of the medium. The dependence of the photon wavelength on the possible characteristics of the scattering is presented.

We have investigated the third-order nonlinearity in ZnO nanocolloids with particle sizes in the range 6–18 nm by the z-scan technique. The third-order optical susceptibility χ(3) increases with increasing particle size (R) within the range of our investigations. In the weak confinement regime, an R2 dependence of χ(3) is obtained for ZnO nanocolloids. The optical limiting response is also studied against particle size.

In this article we present size dependent spectroscopic observations of nanocolloids of ZnO. ZnO is reported to show two emission bands, an ultraviolet (UV) emission band and another in the green region. Apart from the known band gap 380 nm and impurity 530 nm emissions, we have found some peculiar features in the fluorescence spectra that are consistent with the nanoparticle size distribution. Results show that additional emissions at 420 and 490 nm are developed with particle size. The origin of the visible band emission is discussed. The mechanism of the luminescence suggests that UV luminescence of ZnO colloid is related to the transition from conduction band edge to valence band, and visible luminescence is caused by the transition from deep donor level to valence band due to oxygen vacancies and by the transition from conduction band to deep acceptor level due to impurities and defect states. A correlation analysis between the particle size and spectroscopic observations is also discussed.

Laser-induced photoacoustic technique in the closed cell configuration has been employed to study the anisotropy in thermal parameters of urea l-malic acid, a nonlinear optical crystal. Thermal diffusivity values of the specimen along different crystallographic axes are evaluated from the measured amplitude and phase spectra of photoacoustic signal using one-dimensional model of Rosencwaig and Gersho. Thermal conductivity of the crystal along different axes is calculated using the measured thermal diffusivity and specific heat values. The measured thermal parameters are correlated with mechanical hardness as well as the bonding scheme of the crystal. Analyses of the results show that there is considerable anisotropy in heat diffusion parameters along different crystal orientations. Results are explained on the basis of crystallographic structure and the phonon-assisted heat diffusion mechanism in crystals.

In this paper, the fluorescence behaviour of nano colloids of ZnO has been studied as a function of the excitation wavelength. We have found that excitation at the tail of the absorption band gives rise to an emission that shifts with the change of the excitation wavelength. The excitation wavelength dependent shift of the fluorescence maximum is measured to be between 60 and 100 nm. This kind of excitation wavelength dependent fluorescence behaviour, which may appear to be in violation of Kasha's rule of excitation wavelength independence of the emission spectrum, has been observed for nano ZnO colloids prepared by two different chemical routes and different capping agents. It is shown that the existence of a distribution of energetically different molecules in the ground state coupled with a low rate of the excited state relaxation processes, namely, solvation and energy transfer, are responsible for the excitation wavelength dependent fluorescence behaviour of the systems.

We report enhanced back scattering in nanometer-sized ZnO colloids prepared in two different media, by different methods. The FWHM of the back scattered cone and hence the mean free path varied with concentration of ZnO as well as particle size. The Lorentzian profile of backscattered cone indicates the presence of coherence.

A detailed study of surface laser damage performed on a nonlinear optical crystal, urea L-malic acid, using 7ns laser pulses at 10Hz repetition rate from a Q-switched Nd:YAG laser at wavelengths of 532 and 1064nm is reported. The single shot and multiple shot surface laser damage threshold values are determined to be 26.64±0.19 and 20.60±0.36GWcm−2 at 1064nm and 18.44±0.31 and 7.52±0.22GWcm−2 at 532nm laser radiation, respectively. The laser damage anisotropy is consistent with the Vickers mechanical hardness measurement performed along three crystallographic directions. The Knoop polar plot also reflects the damage morphology. Our investigation reveals a direct correlation between the laser damage profile and hardness anisotropy. Thermal breakdown of the crystal is identified as the possible mechanism of laser induced surface damage.

We report all-optical switching due to state-filling in quantum dots (QDs). The switching energy is as low as 6 fJ since state-filling requires only 2 electron-hole pairs per QD. The single layer of InAs/InP QDs is inserted within a InGaAsP/InP waveguide, which is processed into a Mach-Zehnder Interferometric space switch (MZI). A 1530-1570 nm probe beam is switched by optical excitation of one MZI-arm from above. By exciting below the InGaAsP bandgap, we prove that the refractive index nonlinearity is entirely due to state-filling in the QDs.

We report all-optical switching due to state filling in quantum dots (QDs) within a Mach–Zehnder interferometric switch (MZI). The MZI was fabricated using InGaAsP/InP waveguides containing a single layer of InAs/InP QDs. A 1530–1570 nm probe beam is switched by optical excitation of one MZI arm. By exciting below the InGaAsP band gap, we prove that the refractive index nonlinearity is entirely due to the QDs. The switching efficiency is 5 rad/(μW absorbed power), corresponding to a 6 fJ switching energy. Probe wavelength insensitivity was obtained using a broad size distribution of QDs.

Glycine Phosphite [NH3CH2COOH3PO3], abbreviated as GPI, undergoes a para-ferroelectric phase transition from the monoclinic symmetry P2(1)/a to P2(1) at 224.7 K. We report here a systematic study of the polarization switching process in this crystal. Growth of these crystals from aqueous solution has been undertaken employing both solvent evaporation and slow cooling methods. Hysteresis loop measurements along the polar b-axis yielded a spontaneous polarization value of 0.5 muC/cm(2) and a coercive field of 2.5 kV/cm. Conventional Merz technique was employed for polarization switching studies, wherein bipolar square pulses were applied to the sample to induce domain reversal. The transient switching pulse that flows through the sample on application of the field was recorded. The maximum switching time required for domain switching was measured both as a function of electric field and temperature. The experimentally observed switching curves were fitted with the model based on the Pulvari-Kuebler theory of nucleation and growth of domains. From the experimental data, the values of mobility and activation field were obtained. It was observed that switching process in this crystal is predominantly governed by the forward growth of domain walls in the high field region. However, switching process in GPI crystal was found to be slower than that found in other glycine based ferroelectric crystals.

Potassium titanyl phosphate single crystals were irradiated with 48 MeV lithium ions at fluences varying from 5×1012 to 1016 ions/cm2. The defects created in the crystal have been characterized using x-ray rocking curve measurements, optical transmittance, and photoluminescence spectroscopy. From x-ray rocking curve studies, the full width at half maximum for the irradiated samples was observed to increase, indicating lattice strain caused by the energetic ions. Optical transparency of these samples was found to decrease upon irradiation. The irradiated samples exhibited a broadband luminescence in the 700–900 nm region, for fluences above 5×1013 ions/cm2. The results indicate that ion-beam-induced optical effects in KTiOPO4 single crystals are very similar to the ones obtained for crystals with “gray tracks,” which are attributed to the electronic transitions in the Ti3+ levels.

A photopyroelectric measurement of the thermal parameters of glycine phosphite (GPI) single crystals across the ferroelectric phase transition temperature has been carried out. The thermal parameters—thermal diffusivity (α), thermal effusivity (e), thermal conductivity (K), and heat capacity (cp)—of GPI single crystals are reported. The para-ferroelectric phase transition is reflected in these thermal parameters as anomalies at the transition point. The anisotropy in thermal wave propagation is established by measuring thermal conductivity along the a, b, and c crystal axes. The anomalous variations in the thermal parameters across the phase transition temperature reveal an order-disorder type transition at 224 K in this crystal.

Single crystals of a recent ferroelectric material, glycine phosphite were grown from aqueous solution employing the techniques of slow cooling and controlled evaporation. Powder X-ray diffraction studies as well as thermal analysis were carried out on the grown crystals. The morphology of the crystal has been determined using contact and optical goniometry. The mechanical hardness of the crystal was evaluated by Vickers indentation method. Thickness dependence of the dielectric properties has been investigated and the results can be interpreted in terms of a surface layer of lower dielectric constant.

A detailed ultrasonic study of the elastic properties of glycine phosphite single crystals has been carried out at room temperature as well as across the ferroelectric phase-transition temperature. All 13 elastic stiffness moduli of this monoclinic crystal at room temperature have been determined by measuring the velocities of ultrasonic waves of different polarizations, propagating along different symmetry directions using the pulse echo overlap technique. The anisotropy in elastic wave propagation is established employing polar plots of the phase velocity surfaces in the ab, ac, and bc planes. Variation of selected mode velocities with temperature establishes the reported ferroelectric phase transition in this crystal at 224 K.