Laser beam shaping using a photoinduced azopolymer droplet-based mask.

The dewetting of an azopolymer droplet, followed by the photostructuration of the evaporated droplet, is employed to create an amplitude mask. This straightforward process yields a large area featuring periodic micro- and nanostructures. The resulting pattern is utilized to generate a nondiffracting beam. Starting with a Gaussian beam illuminating the amplitude mask, the critical aspect is the production of a bright, ring-shaped beam with a high radius-to-width ratio and symmetric central laser spots, each with the same intensity. This alternative approach to shaping a laser beam is demonstrated as a rapid and cost-effective fabrication technique.

Topological reconstruction of a stretched transparent surface relief grating via an optical diffraction pattern.

The optical characterization of transparent and stretchable patterned surfaces replicated from the fabrication of quasicrystal structures on azopolymer thin films is presented. The complexity of the quasicrystal surface fabrication is obtained by superimposed multiple light exposures. Azopolymer surface patterns are used as a replica molding master. The microscopic elongation of nanocavities induced by macroscopic stretchings of the elastomeric quasicrystal replication is characterized via optical diffraction. An original numerical method is presented to reconstruct the structured surface deduced from the optical diffraction measurements. The measurements show that drastic topologic changes, e.g., going from cavities to a canal, happens on the surface. This could be ingeniously used for creating actionable structured surfaces or nanoparticles trapping surfaces.

Characterizations and morphology of sodium tungstate particles.

A solid-state reaction technique was used to synthesize polycrystalline Na2WO4. Preliminary X-ray studies revealed that the compound has a cubic structure at room temperature. The formation of the compound has been confirmed by X-ray powder diffraction studies and Raman spectroscopy. Electrical and dielectric properties of the compound have been studied using complex impedance spectroscopy in the frequency range 209 Hz-1 MHz and temperature range 586-679 K. The impedance data were modellized by an equivalent circuit consisting of series of a combination of grains and grains boundary. We use complex electrical modulus M* at various temperatures to analyse dielectric data. The modulus plots are characterized by the presence of two relaxation peaks thermally activated. The morphologies and the average particle size of the resultant sodium tungstate sample were demonstrated by atomic force microscopy, scanning electron microscopy and transmission electron microscopy. The thicknesses and optical constants of the sample have been calculated using ellipsometric measurements in the range of 200-22 000 nm by means of new amorphous dispersion formula which is the objective of the present work. The results were obtained for Na2WO4 particles from experimental (EXP) and measured (FIT) data showed an excellent agreement. In addition, the energy gap of the Na2WO4 sample has been determined using ellipsometry and confirmed by spectrophotometry measurements.

Light mediated emergence of surface patterns in azopolymers at low temperatures.

Polymer thin films doped with azobenzene molecules do have the ability to organize themselves in spontaneous surface relief gratings (SRG) under irradiation using a single polarized beam. To shed some light on this still unexplained phenomenon, we use a new method that permits us to access experimentally the very first steps of the pattern formation process. By decreasing the temperature, we slow down the formation and organization of patterns, due to the large increase in the viscosity and relaxation time of the azopolymer. As a result, decreasing the temperature allows us to access and study much shorter time scales, in the physical mechanisms underlying the pattern formation, than those previously reported. We find that the patterns organize themselves in sub-structures which size increases with the temperature, following the diffusion coefficient evolution of the material. This result suggests that the pattern formation and organization are mainly governed by diffusive processes, in agreement with some theories of SRG formation. Upon decreasing the temperature further, we observe the emergence of small voids located at the junction of the sub-structures.

Photo-responsive polymer with erasable and reconfigurable micro- and nano-patterns: an in vitro study for neuron guidance.

The interaction of cells with nanoscale topography has proven to be an important modality in controlling cell responses. Topographic parameters on material surfaces play a role in cell growth. We have synthesized a new bio compatible polymer containing photoswitching molecules. Stripepatterned (groove/ridge pattern) were patterned and erased with ease on this bio azopolymer with two different set-ups: one with the projection of an optical interference pattern and the other one by molecular self-organization with one single laser beam. These two set-ups allow the re-writing of pattern after erasing and its inscription in vitro. PC12 cells were cultured on the bio-photoswitching patterned polymer and compared with PC12 cells growing on a well know substrate: poly-L-lysine. This result is of interest for facilitating contact guidance and designing reconfigurable scaffold for neural network formation in vitro.

Incoherent light-induced self-organization of molecules.

Although coherent light is usually required for the self-organization of regular spatial patterns from optical beams, we show that peculiar light-matter interaction can break this evidence. In the traditional method of recording laser-induced periodic surface structures, a light intensity distribution is produced at the surface of a polymer film by an interference between two coherent optical beams. We report on the self-organization followed by propagation of a surface relief pattern. It is induced in a polymer film by using a low-power and small-size coherent beam assisted by a high-power and large-size incoherent and unpolarized beam. We demonstrate that we can obtain large size and well-organized patterns starting from a dissipative interaction. Our experiments open new directions to improving optical processing systems.

Multistate polarization addressing using a single beam in an azo polymer film.

Peculiar light-matter interactions can break the rule that a single beam polarization can address only two states in an optical memory device. Multistate storage of a single beam polarization is achieved using self-induced surface diffraction gratings in a photoactive polymer material. The grating orientation follows the incident light beam's polarization direction. The permanent self-induced surface relief grating can be read out in real time using the same laser beam.

Nondestructive analysis of the transverse structure of novel optical fibers by third-harmonic-generation microscopy.

We demonstrate the suitability of the third-harmonic-generation technique as a new nonlinear microprobe for nondestructive determination of the index profile of optical fibers. Photonic bandgap (Bragg-type) and air-silica microstructure (ASM) fibers were tested. The complete spatial characteristics, such as hole diameter and spacing into ASM fibers or sandwiched layer thickness into Bragg fibers, were demonstrated to be attainable anywhere along a bare fiber.

Nonlinearity measurements of thin films by third-harmonic-generation microscopy.

We show that the electronic part of the nonlinear susceptibility chi(3) of thin films can be easily measured by third harmonic microscopy. The phenomenon of third harmonic generation (THG) is excited by a femtosecond laser beam focused at the interface between the thin film and a reference layer. The value of chi(3) is deduced from the THG intensity measurements with the help of a classical model. The validity of this simple and alternative method is established by testing reference liquid films.

Imaging of Ca(2)+ intracellular dynamics with a third-harmonic generation microscope.

We describe the promising development of third-harmonic generation (THG) in laser scanning microscopy for study of the functional imaging of live biological cells. The dynamics of Ca(2+) in biological cells is shown. The Ca(2+) signal consists of a transient increase in the intracellular concentration. THG microscopy allows one to temporally visualize the release of Ca(2+) from internal stores and (or) calcium influx.