Dynamical Model for Chemically Driven Running Droplets

We propose coupled evolution equations for the thickness of a liquid film and the density of an adsorbate layer on a partially wetting solid substrate. Therein, running droplets are studied assuming a chemical reaction underneath the droplets that induces a wettability gradient on the substrate and provides the driving force for droplet motion. Two different regimes for moving droplets -- reaction-limited and saturated regime -- are described. They correspond to increasing and decreasing velocities with increasing reaction rates and droplet sizes, respectively. The existence of the two regimes offers a natural explanation of prior experimental observations.Comment: 4 pages, 5 figure

Interfacial layering in a three-component polymer system

We study theoretically the temporal evolution and the spatial structure of the interface between two polymer melts involving three different species (A, A* and B). The first melt is composed of two different polymer species A and A* which are fairly indifferent to one another (Flory parameter chi_AA* ~ 0). The second melt is made of a pure polymer B which is strongly attracted to species A (chi_AB 0). We then show that, due to these contradictory tendencies, interesting properties arise during the evolution of the interface after the melts are put into contact: as diffusion proceeds, the interface structures into several adjacent "compartments", or layers, of differing chemical compositions, and in addition, the central mixing layer grows in a very asymmetric fashion. Such unusual behaviour might lead to interesting mechanical properties, and demonstrates on a specific case the potential richness of multi-component polymer interfaces (as compared to conventional two-component interfaces) for various applications.Comment: Revised version, to appear in Macromolecule

Dynamics of Strongly Deformed Polymers in Solution

Bead spring models for polymers in solution are nonlinear if either the finite extensibility of the polymer, excluded volume effects or hydrodynamic interactions between polymer segments are taken into account. For such models we use a powerful method for the determination of the complete relaxation spectrum of fluctuations at {\it steady state}. In general, the spectrum and modes differ significantly from those of the linear Rouse model. For a tethered polymer in uniform flow the differences are mainly caused by an inhomogeneous distribution of tension along the chain and are most pronounced due to the finite chain extensibility. Beyond the dynamics of steady state fluctuations we also investigate the nonlinear response of the polymer to a {\em large sudden change} in the flow. This response exhibits several distinct regimes with characteristic decay laws and shows features which are beyond the scope of single mode theories such as the dumbbell model.Comment: 7 pages, 3 figure

Two-loop Functional Renormalization Group of the Random Field and Random Anisotropy O(N) Models

We study by the perturbative Functional Renormalization Group (FRG) the Random Field and Random Anisotropy O(N) models near $d=4$, the lower critical dimension of ferromagnetism. The long-distance physics is controlled by zero-temperature fixed points at which the renormalized effective action is nonanalytic. We obtain the beta functions at 2-loop order, showing that despite the nonanalytic character of the renormalized effective action, the theory is perturbatively renormalizable at this order. The physical results obtained at 2-loop level, most notably concerning the breakdown of dimensional reduction at the critical point and the stability of quasi-long range order in $d<4$, are shown to fit into the picture predicted by our recent non-perturbative FRG approach.Comment: 19 pages, 20 figures. Minor correction

Viscoelastic Effect on Hydrodynamic Relaxation in Polymer Solutions

The viscoelastic effect on the hydrodynamic relaxation in semidilute polymer solutions is investigated. From the linearized two-fluid model equations, we predict that the dynamical asymmetry coupling between the velocity fluctuations and the viscoelastic stress influences on the hydrodynamic relaxation process, resulting in a wave-number-dependent shear viscosity.Comment: 7pages; To be published in Journal of the Physical Society of Japan,Vol 72,No2,(2003

Simple experimental methods for trapped ion quantum processors

Two techniques are described that simplify the experimental requirements for measuring and manipulating quantum information stored in trapped ions. The first is a new technique using electron shelving to measure the populations of the Zeeman sublevels of the ground state, in an ion for which no cycling transition exists from any of these sublevels. The second technique is laser cooling to the vibrational ground state, without the need for a trap operating in the Lamb-Dicke limit. This requires sideband cooling in a sub-recoil regime. We present a thorough analysis of sideband cooling on one or a pair of sidebands simultaneously

Monomer dynamics of a wormlike chain

We derive the stochastic equations of motion for a tracer that is tightly attached to a semiflexible polymer and confined or agitated by an externally controlled potential. The generalised Langevin equation, the power spectrum, and the mean-square displacement for the tracer dynamics are explicitly constructed from the microscopic equations of motion for a weakly bending wormlike chain by a systematic coarse-graining procedure. Our accurate analytical expressions should provide a convenient starting point for further theoretical developments and for the analysis of various single-molecule experiments and of protein shape fluctuations.Comment: 6 pages, 4 figure

Viscoelasticity of two-layer-vesicles in solution

The dynamic shape relaxation of the two-layer-vesicle is calculated. In additional to the undulation relaxation where the two bilayers move in the same direction, the squeezing mode appears when the gap between the two bilayers is small. At large gap, the inner vesicle relaxes much faster, whereas the slow mode is mainly due to the outer layer relaxation. We have calculated the viscoelasticity of the dilute two-layer-vesicle suspension. It is found that for small gap, the applied shear drives the undulation mode strongly while the slow squeezing mode is not much excited. In this limit the complex viscosity is dominated by the fast mode contribution. On the other hand, the slow mode is strongly driven by shear for larger gap. We have determined the crossover gap which depends on the interaction between the two bilayers. For a series of samples where the gap is changed systematically, it is possible to observe the two amplitude switchings

Straightening of Thermal Fluctuations in Semi-Flexible Polymers by Applied Tension

We investigate the propagation of a suddenly applied tension along a thermally excited semi-flexible polymer using analytical approximations, scaling arguments and numerical simulation. This problem is inherently non-linear. We find sub-diffusive propagation with a dynamical exponent of 1/4. By generalizing the internal elasticity, we show that tense strings exhibit qualitatively different tension profiles and propagation with an exponent of 1/2.Comment: Latex file; with three postscript figures; .ps available at http://dept.physics.upenn.edu/~nelson/pull.p

Theoretical study of dislocation nucleation from simple surface defects in semiconductors

Large-scale atomistic calculations, using empirical potentials for modeling semiconductors, have been performed on a stressed system with linear surface defects like steps. Although the elastic limits of systems with surface defects remain close to the theoretical strength, the results show that these defects weaken the atomic structure, initializing plastic deformations, in particular dislocations. The character of the dislocation nucleated can be predicted considering both the resolved shear stress related to the applied stress orientation and the Peierls stress. At low temperature, only glide events in the shuffle set planes are observed. Then they progressively disappear and are replaced by amorphization/melting zones at a temperature higher than 900 K