Search arXivSearch

arXiv · cond-mat/0307522

Production of kinks in an inhomogenous medium

Abstract

The purpose of this report is presentation of the main modifications of the standard Kibble-Zurek formalism caused by the existence of the unperfections in the system. We know that the distribution of kinks created during a second order phase transition in pure systems is determined solely by the correlation length at freeze-out time. The correlation length at that instant of time intuitively describes the size of the defect and therefore the number density of defects is limited by the possibility of holding kinks in a unit volume. On the other hand if the system is populated by the impurities then kinks emerge mainly in knots of the force distribution which correspond to extremes of the impurity potential i.e. positions of imperfections. The purpose of this report is to show that, due to existence of the strong gradients of the impurity potential, kinks can be created mainly in the close vicinity of the impurities. It seems that this simple mechanism can be responsible for occurrence, in the number density formula, the additional length scale describing the impurity distribution. We know that in pure systems, as a consequence of kink-antikink annihilation, the number density of kinks decrease in time. In contradiction to pure systems, kinks produced in the systems populated by impurities could be confined by the impurity centers and therefore they may not disappear from the system and may remain above the level established by thermal nucleation of pairs.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Tomasz Dobrowolski. 2003-07-22. Production of kinks in an inhomogenous medium. https://arxiv.org/abs/cond-mat/0307522

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Transient Elasticity -- A Unifying Framework for Thixotropy, Polymers, and Granular Media

Thixotropic yield stress fluids, such as paint or ketchup, are traditionally viewed as elastic structures that, under shear rates, break into viscous liquids with lumps, and reconnect at rest. An alternative framework is presented here: Upon shear, structural destruction is incomplete, leaving sufficient connections. As a result, elasticity fundamentally underlies their non-Newtonian behavior, though they do appear purely viscous under a steady shear, displaying little direct evidence of elastic rebound---same as granular media and polymers. Consequently, all three are described by the same set of evolution equations, differing only in their parameters. These equations are set up by starting from solid dynamics and allowing the elastic strain $\varepsilon^e$ to relax, which in effect interpolates between solid and fluid behavior, appropriate for systems that display both types of behavior. Incorporating in addition a two-temperature framework, tracking how energy is dissipated in two consecutive stages, yields the nonlinear model of Transient Elasticity (TE). It describes an elasticity that is transient in time yet persistent under shear. Previously validated for polymers and granular media, TE is here applied to thixotropic yield-stress fluids. As shown, it successfully accounts for a wide range of characteristic phenomena, including over- and undershoot, viscosity bifurcation, shear banding, and oscillatory rheography. Given its appropriateness across structurally diverse systems, TE offers a unified, surprisingly general account of non-Newtonian phenomena.

cond-mat.soft

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft