Ultrafast Large Area Micropattern Generation in Non-absorbing Polymer Thin-Films by Pulsed Laser Diffraction

We report an ultrafast, parallel and beyond-the-master micro-patterning technique for ultrathin (30 nm-400 nm) non-absorbing polymer films by diffraction of a laser light through a two dimensional periodic aperture. The redistribution of laser energy absorbed by the substrate causes self-organization of polymer thin-film in the form of wrinkle like surface relief structures caused by localized melting and freezing of the thin-film. Unlike the conventional laser ablation and laser writing processes, low laser fluence is employed to only passively swell the polymer as a pre-ablative process without the loss of material, and without absorption/reaction with the incident radiation. Self-organization in the thin polymer film aided by the diffraction pattern produces micro-structures made up of thin raised lines. These regular microstructures have far more complex morphologies than the mask geometry and very narrow line widths that can be an order of magnitude smaller than the openings in the mask. The microstructure morphology is easily modulated by changing the film thickness, aperture size and geometry and by changing the diffraction pattern, e.g., by changing the aperture-substrate distance.Comment: 23 page

A charge density study of an intramolecular charge-transfer quinoid compound with strong NLO properties

An experimental charge density investigation of 7,7-di[(S)-(+)-2-(methoxymethyl)pyrrolidino]-8,8-dicyanoquinodimethane establishes the presence of a large charge separation as well as a high in-crystal dipole moment compared to the free molecule in frozen geometry, consistent with the high SHG activity of the compound

Metal hierarchical patterning by direct nanoimprint lithography

Three-dimensional hierarchical patterning of metals is of paramount importance in diverse fields involving photonics, controlling surface wettability and wearable electronics. Conventionally, this type of structuring is tedious and usually involves layer-by-layer lithographic patterning. Here, we describe a simple process of direct nanoimprint lithography using palladium benzylthiolate, a versatile metal-organic ink, which not only leads to the formation of hierarchical patterns but also is amenable to layer-by-layer stacking of the metal over large areas. The key to achieving such multi-faceted patterning is hysteretic melting of ink, enabling its shaping. It undergoes transformation to metallic palladium under gentle thermal conditions without affecting the integrity of the hierarchical patterns on micro- as well as nanoscale. A metallic rice leaf structure showing anisotropic wetting behavior and woodpile-like structures were thus fabricated. Furthermore, this method is extendable for transferring imprinted structures to a flexible substrate to make them robust enough to sustain numerous bending cycles

Metal nanoparticles and their assemblies

Metal nanoparticles of varying sizes can be prepared by physical as well as chemical methods. They exhibit many fascinating properties, the size-dependent metal to nonmetal transition being an important one. Metal nanoparticles capped by thiols can be organized into ordered one-, two- and three-dimensional structures and these structures have potential applications in nanodevices. In this context, organization of arrays of metal nanoparticles with a fixed number of atoms assumes significance

Solution processed large area fabrication of Ag patterns as electrodes for flexible heaters, electrochromics and organic solar cells

A simple method for producing patterned Ag electrodes on transparent and flexible substrates is reported. The process makes use of a laser printed toner as a sacrificial template for an organic precursor, which upon thermolysis and toner lift off produced highly conducting Ag electrodes. Thus, the process takes only a few minutes without any expensive instrumentation. The electrodes exhibited excellent adhesion and mechanical properties, important for flexible device applications. Using Ag patterned electrodes, heaters operating at low voltages, pixelated electrochromic displays as well as organic solar cells have been demonstrated. The method is extendable to produce defect-free patterns over large areas as demonstrated by roll coating

An experimental charge density study of the effect of the noncentric crystal field on the molecular properties of organic NLO materials

The structure, packing, and charge distribution in molecules of nonlinear optical materials have been analysed with reference to their counterparts in centrosymmetric structures based on low temperature X-ray measurements. The systems studied are the centric and noncentric polymorphs of 5-nitrouracil as well as the diamino, dithio, and thioamino derivatives of 1,1-ethylenedicarbonitrile; the latter possesses a noncentric structure. The molecular structure of 5-nitrouracil is invariant between the two forms, while the crystal packing is considerably different, leading to dimeric N-H···O rings in the centric polymorph and linear chains in noncentric one. There is an additional C-H···O contact in the centric form with a significant overlap of the electrostatic potentials between the alkenyl hydrogen atom and an oxygen atom of the nitro group. The dipole moment of 5-nitrouracil in the noncentric form is much higher (μ=9 D) than in the centric form (≈6 D). Among the 1,1-ethylenedicarbonitriles, there is an increased charge separation in the noncentric thioamino derivative, leading to an enhanced dipole of 15 D compared to the centric diamino (5 D) and dithio (6 D) derivatives. The effect of the crystal field is borne out by semiempirical AM1 calculations on the two systems. Dipole moments calculated for the molecules in the frozen geometries match closely with those obtained for centric crystals from the experimental charge densities. The calculated values of the dipole moment in the frozen or optimized geometries in the noncentric structures are, however, considerably lower than the observed value. Furthermore, the conformation of the S-CH3 group in the noncentric crystal is anti with respect to the central C=C bond while the syn conformation is predicted for the free molecule in the optimized geometry

Asymptotic analysis of the form-factors of the quantum spin chains

Les systèmes intégrables quantiques restaient longtemps un domaine où des méthodes mathématiques modernes permettaient d’accéder aux résultats intéressants pour l‘étude de systèmes physiques. Le calcul exacte, numérique et asymptotique de fonction de corrélation reste un de sujets les plus importants de la théorie de modèles intégrables quantiques. Dans ce cadre l’approche basée sur le calcul des facteurs de forme s’est révélée la plus efficace. Dans ce thèse, une méthode alternative fondée sur l'ansatz de Bethe algébrique est développée pour calculer des facteurs de formes dans la limite thermodynamique. Elle est appliqué et décrit dans le contexte de chaîne de spin isotrope XXX, qui est un des cas plus intéressant des modèles critiques où la zone de fermi est non-compacte.Since a long-time, the quantum integrable systems have remained an area where modern mathematical methods have given an access to interesting results in the study of physical systems. The exact computations, both numerical and asymptotic, of the correlation function is one of the most important subject of the theory of the quantum integrable models. In this context an approach based on the calculation of form factors has been proved to be a more effective one. In this thesis, we develop a new method based on the algebraic Bethe ansatz is proposed for the computation of the form-factors in thermodynamic limit. It is applied to and described in the context of isotropic XXX Heisenberg chain, which is one of the example of an interesting case of critical models where the Fermi-zone is non-compact