Diblock copolymer ordering induced by patterned surfaces

We use a Ginzburg-Landau free energy functional to investigate diblock copolymer morphologies when the copolymer melt interacts with one surface or is confined between two chemically patterned surfaces. For temperatures above the order-disorder transition a complete linear response description of the copolymer melt is given, in terms of an arbitrary two-dimensional surface pattern. The appearance of order in the direction parallel to the surface is found as a result of the order in the perpendicular direction. Below the order-disorder point and in a thin-film geometry, our procedure enables the analytic calculation of distorted perpendicular and tilted lamellar phases in the presence of uniform or modulated surface fields.Comment: 8 pages, 3 figures, to be published in Europhys. Let

Orienting Ion-Containing Block Copolymers Using AC Electric Field

We consider orientation mechanisms for block copolymers in an electric field. Theoretical and experimental studies have shown that nonuniformity of the dielectric constant gives rise to a preferred orientation of the melt with respect to the applied field. We show that the presence of ions, as found in anionically prepared copolymers, may increase the alignment effect markedly. Time-varying (ac) and static (dc) fields are considered within a unified framework. We find that orientation of block copolymers can in principle be achieved without a dielectric contrast if there is a mobility contrast. The presence of ions is especially important at small field frequencies, as is in most experiments. Unlike the no-ions case, it is found that orienting forces depend on the polymer chain lengths. The mobile-ions mechanism suggested here can be used to reduce the magnitude of orienting fields as well as to discriminate between block copolymers of different lengths.Comment: 8 pages, 2 figure

Surface induced ordering in thin film diblock copolymers: tilted lamellar phases

We investigate the effect of chemically patterned surfaces on the morphology of diblock copolymers below the order-disorder transition. Profiles for lamellar phases in contact with one surface, or confined between two surfaces are obtained in the weak segregation limit using a Ginzburg-Landau expansion of the free energy, and treating it with mean-field theory. The periodically patterned surface induces a tilt of the lamellae in order to match the surface periodicity. The lamellae relax from the constrained periodicity close to the surface to the bulk periodicity far from it. The phases we investigate are a generalization to the mixed (perpendicular and parallel to the surface) lamellar phases occurring when the two surfaces are homogeneous. A special case when the surface pattern has a period equal to the bulk lamellar period showing ``T-junction'' morphology is examined. Our analytic calculation agrees with previous computer simulations and self consistent field theories.Comment: 7 figures, replaced with minor modification

Frustrated Rotations in Nematic Monolayers

Tabe and Yokoyama found recently that the optical axis in a chiral monolayer of a ferronematic rotates when water evaporates from the bath: the chiral molecules act as propellers. When the axis is blocked at the lateral walls of the trough, the accumulated rotation inside creates huge splays and bends. We discuss the relaxation of these tensions, assuming that a single dust particle nucleates disclination pairs. For the simplest geometry, we then predict a long delay time followed by a non-periodic sequence of ``bursts''. These ideas are checked by numerical simulations.Comment: 5 pages, 4 figures, submitted to Eur. Phys. J.

Block Copolymer at Nano-Patterned Surfaces

We present numerical calculations of lamellar phases of block copolymers at patterned surfaces. We model symmetric di-block copolymer films forming lamellar phases and the effect of geometrical and chemical surface patterning on the alignment and orientation of lamellar phases. The calculations are done within self-consistent field theory (SCFT), where the semi-implicit relaxation scheme is used to solve the diffusion equation. Two specific set-ups, motivated by recent experiments, are investigated. In the first, the film is placed on top of a surface imprinted with long chemical stripes. The stripes interact more favorably with one of the two blocks and induce a perpendicular orientation in a large range of system parameters. However, the system is found to be sensitive to its initial conditions, and sometimes gets trapped into a metastable mixed state composed of domains in parallel and perpendicular orientations. In a second set-up, we study the film structure and orientation when it is pressed against a hard grooved mold. The mold surface prefers one of the two components and this set-up is found to be superior for inducing a perfect perpendicular lamellar orientation for a wide range of system parameters

Self Trapping of a Single Bacterium in its Own Chemoattractant

Bacteria (e.g. E. Coli) are very sensitive to certain chemoattractants (e.g. asparate) which they themselves produce. This leads to chemical instabilities in a uniform population. We discuss here the different case of a single bacterium, following the general scheme of Brenner, Levitov and Budrene. We show that in one and two dimensions (in a capillary or in a thin film) the bacterium can become self-trapped in its cloud of attractant. This should occur if a certain coupling constant $g$ is larger than unity. We then estimate the reduced diffusion D_eff of the bacterium in the strong coupling limit, and find D_eff ~ 1/g.Comment: 4 pages, absolutely no figure

Localized Joule heating produced by ion current focusing through micron-size holes

We provide an experimental demonstration that the focusing of ionic currents in a micron size hole connecting two chambers can produce local temperature increases of up to $100^\circ$ C with gradients as large as $1^\circ$ K$\mu m^{-1}$. We find a good agreement between the measured temperature profiles and a finite elements-based numerical calculation. We show how the thermal gradients can be used to measure the full melting profile of DNA duplexes within a region of 40 $\mu$m. The possibility to produce even larger gradients using sub-micron pores is discussed.Comment: 3 pages, accepted to Appl. Phys. Lett

Phase separation transition in liquids and polymers induced by electric field gradients

Spatially uniform electric fields have been used to induce instabilities in liquids and polymers, and to orient and deform ordered phases of block-copolymers. Here we discuss the demixing phase transition occurring in liquid mixtures when they are subject to spatially nonuniform fields. Above the critical value of potential, a phase-separation transition occurs, and two coexisting phases appear separated by a sharp interface. Analytical and numerical composition profiles are given, and the interface location as a function of charge or voltage is found. The possible influence of demixing on the stability of suspensions and on inter-colloid interaction is discussed.Comment: 7 pages, 3 figures. Special issue of the J. Phys. Soc. Ja

The interaction between colloids in polar mixtures above Tc

We calculate the interaction potential between two colloids immersed in an aqueous mixture containing salt near or above the critical temperature. We find an attractive interaction far from the coexistence curve due to the combination of preferential solvent adsorption at the colloids' surface and preferential ion solvation. We show that the ion-specific interaction strongly depends on the amount of salt added as well as on the mixture composition. Our results are in accord with recent experiments. For a highly antagonistic salt of hydrophilic anions and hydrophobic cations, a repulsive interaction at an intermediate inter-colloid distance is predicted even though both the electrostatic and adsorption forces alone are attractive.Comment: 9 pages, 6 figure

Organization of Block Copolymers using NanoImprint Lithography: Comparison of Theory and Experiments

We present NanoImprint lithography experiments and modeling of thin films of block copolymers (BCP). The NanoImprint lithography is used to align perpendicularly lamellar phases, over distances much larger than the natural lamellar periodicity. The modeling relies on self-consistent field calculations done in two- and three-dimensions. We get a good agreement with the NanoImprint lithography setups. We find that, at thermodynamical equilibrium, the ordered BCP lamellae are much better aligned than when the films are deposited on uniform planar surfaces