720 research outputs found
Van der Waals interactions across stratified media
Working at the Lifshitz level, we investigate the van der Waals interactions
across a series of layers with a periodic motif. We derive the complete form of
the van der Waals interaction as an explicit function of the number of periodic
layers. We then compare our result with an approximation based on an
anisotropic-continuum representation of the stratified medium. Satisfactory
agreement between discrete-layer and continuum models is reached only for
thicknesses of ten or more layers.Comment: 9 pages and 4 figure
Elastic moduli renormalization in self interacting stretchable polyelectrolytes
We study the effect of intersegment interactions on the effective bending and
stretching moduli of a semiflexible polymer chain with a finite stretching
modulus. For an interaction potential of a screened Debye-H\" uckel type
renormalization of the stretching modulus is derived on the same level of
approximation as the celebrated Odijk-Skolnick-Fixman result for the bending
modulus. The presence of mesoscopic intersegment interaction potentials couples
the bending and stretching moduli in a manner different from that predicted by
the macroscopic elasticity theory. We advocate a fundamental change in the
perspective regarding the dependence of elastic moduli of a flexible
polyelectrolyte on the ionic conditions: stretchability. Not only are the
persistence length as well as the stretching modulus dependent on the salt
conditions in the solution, they are fundamentally coupled via the mesoscopic
intersegment interaction potential. The theory presented here compares
favorably with recent experiments on DNA bending and stretching.Comment: 12 pages, 3 figure
Three-body Casimir effects and non-monotonic forces
Casimir interactions are not pair-wise additive. This property leads to
collective effects that we study for a pair of objects near a conducting wall.
We employ a scattering approach to compute the interaction in terms of
fluctuating multipoles. The wall can lead to a non-monotonic force between the
objects. For two atoms with anisotropic electric and magnetic dipole
polarizabilities we demonstrate that this non-monotonic effect results from a
competition between two- and three body interactions. By including higher order
multipoles we obtain the force between two macroscopic metallic spheres for a
wide range of sphere separations and distances to the wall.Comment: 4 pages, 4 figure
Charge Fluctuation Forces Between Stiff Polyelectrolytes in Salt Solution: Pairwise Summability Re-examined
We formulate low-frequency charge-fluctuation forces between charged
cylinders - parallel or skewed - in salt solution: forces from dipolar van der
Waals fluctuations and those from the correlated monopolar fluctuations of
mobile ions. At high salt concentrations forces are exponentially screened. In
low-salt solutions dipolar energies go as or ; monopolar
energies vary as or , where is the minimal separation
between cylinders. However, pairwise summability of rod-rod forces is easily
violated in low-salt conditions. Perhaps the most important result is not the
derivation of pair potentials but rather the demonstration that some of these
expressions may not be used for the very problems that originally motivated
their derivation.Comment: 8 pages and 1 fig in ps forma
Ion Induced Lamellar-Lamellar Phase Transition in Charged Surfactant Systems
We propose a model for the liquid-liquid phase transition observed in osmotic
pressure measurements of certain charged lamellae-forming amphiphiles. The
model free energy combines mean-field electrostatic and phenomenological
non-electrostatic interactions, while the number of dissociated counterions is
treated as a variable degree of freedom that is determined self-consistently.
The model, therefore, joins two well-known theories: the Poisson-Boltzmann
theory for ionic solutions between charged lamellae, and
Langmuir-Frumkin-Davies adsorption isotherm modified to account for charged
adsorbing species. Minimizing the appropriate free energy for each
interlamellar spacing, we find the ionic density profiles and the resulting
osmotic pressure. While in the simple Poisson-Boltzmann theory the osmotic
pressure isotherms are always smooth, we observe a discontinuous liquid-liquid
phase transition when Poisson-Boltzmann theory is self-consistently augmented
by Langmuir-Frumkin-Davies adsorption. This phase transition depends on the
area per amphiphilic headgroup, as well as on non-electrostatic interactions of
the counterions with the lamellae, and interactions between counterion-bound
and counterion-dissociated surfactants. Coupling lateral phase transition in
the bilayer plane with electrostatic interactions in the bulk, our results
offer a qualitative explanation for the existence of the phase-transition of
DDABr (didodecyldimethylammonium bromide), but its apparent absence for the
chloride and the iodide homologues. More quantitative comparisons with
experiment require better understanding of the microscopic basis of the
phenomenological model parameters.Comment: 14 pages, 9 figure
Recursion relations for generalized Fresnel coefficients: Casimir force in a planar cavity
We emphasize and demonstrate that, besides using the usual recursion
relations involving successive layers, generalized Fresnel coefficients of a
multilayer can equivalently be calculated using the recursion relations
involving stacks of layers, as introduced some time ago [M. S. Tomas, Phys.
Rev. A 51, 2545 (1995)]. Moreover, since the definition of the generalized
Fresnel coefficients employed does not imply properties of the stacks, these
nonstandard recursion relations can be used to calculate Fresnel coefficients
not only for local systems but also for a general multilayer consisting of
various types (local, nonlocal, inhomogeneous etc.) of layers. Their utility is
illustrated by deriving a few simple algorithms for calculating the
reflectivity of a Bragg mirror and extending the formula for the Casimir force
in a planar cavity to arbitrary media.Comment: 5 pages, 2 figures, slightly expande
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