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G. Oshanin

Publications and source records attributed to G. Oshanin.

At least 91 records · Page 5Linked to original sources

Ultra-Slow Vacancy-Mediated Tracer Diffusion in Two Dimensions: The Einstein Relation Verified

We study the dynamics of a charged tracer particle (TP) on a two-dimensional lattice all sites of which except one (a vacancy) are filled with identical neutral, hard-core particles. The particles move randomly by exchanging their positions with the vacancy, subject to the hard-core exclusion. In case when the charged TP experiences a bias due to external electric field ${\bf E}$, (which favors its jumps in the preferential direction), we determine exactly the limiting probability distribution of the TP position in terms of appropriate scaling variables and the leading large-N ($n$ being the discrete time) behavior of the TP mean displacement $\bar{\bf X}_n$; the latter is shown to obey an anomalous, logarithmic law $|\bar{\bf X}_n| = α_0(|{\bf E}|) \ln(n)$. On comparing our results with earlier predictions by Brummelhuis and Hilhorst (J. Stat. Phys. {\bf 53}, 249 (1988)) for the TP diffusivity $D_n$ in the unbiased case, we infer that the Einstein relation $μ_n = βD_n$ between the TP diffusivity and the mobility $μ_n = \lim_{|{\bf E}| \to 0}(|\bar{\bf X}_n|/| {\bf E} |n)$ holds in the leading in $n$ order, despite the fact that both $D_n$ and $μ_n$ are not constant but vanish as $n \to \infty$. We also generalize our approach to the situation with very small but finite vacancy concentration $ρ$, in which case we find a ballistic-type law $|\bar{\bf X}_n| = πα_0(|{\bf E}|) ρn$. We demonstrate that here, again, both $D_n$ and $μ_n$, calculated in the linear in $ρ$ approximation, do obey the Einstein relation.

cond-mat.stat-mech↗

Force-velocity relation and density profiles for biased diffusion in an adsorbed monolayer

In this paper, which completes our earlier short publication [Phys. Rev. Lett. 84, 511 (2000)], we study dynamics of a hard-core tracer particle (TP) performing a biased random walk in an adsorbed monolayer, composed of mobile hard-core particles undergoing continuous exchanges with a vapor phase. In terms of an approximate approach, based on the decoupling of the third-order correlation functions, we obtain the density profiles of the monolayer particles around the TP and derive the force-velocity relation, determining the TP terminal velocity, V_{tr}, as the function of the magnitude of external bias and other system's parameters. Asymptotic forms of the monolayer particles density profiles at large separations from the TP, and behavior of V_{tr} in the limit of small external bias are found explicitly.

cond-mat.soft↗

Generalized model for dynamic percolation

We study the dynamics of a carrier, which performs a biased motion under the influence of an external field E, in an environment which is modeled by dynamic percolation and created by hard-core particles. The particles move randomly on a simple cubic lattice, constrained by hard-core exclusion, and they spontaneously annihilate and re-appear at some prescribed rates. Using decoupling of the third-order correlation functions into the product of the pairwise carrier-particle correlations we determine the density profiles of the "environment" particles, as seen from the stationary moving carrier, and calculate its terminal velocity, V_c, as the function of the applied field and other system parameters. We find that for sufficiently small driving forces the force exerted on the carrier by the "environment" particles shows a viscous-like behavior. An analog Stokes formula for such dynamic percolative environments and the corresponding friction coefficient are derived. We show that the density profile of the environment particles is strongly inhomogeneous: In front of the stationary moving carrier the density is higher than the average density, $ρ_s$, and approaches the average value as an exponential function of the distance from the carrier. Past the carrier the local density is lower than $ρ_s$ and the relaxation towards $ρ_s$ may proceed differently depending on whether the particles number is or is not explicitly conserved.

cond-mat.stat-mech↗

Influence of auto-organization and fluctuation effects on the kinetics of a monomer-monomer catalytic scheme

We study analytically kinetics of an elementary bimolecular reaction scheme of the Langmuir-Hinshelwood type taking place on a d-dimensional catalytic substrate. We propose a general approach which takes into account explicitly the influence of spatial correlations on the time evolution of particles mean densities and allows for the analytical analysis. In terms of this approach we recover some of known results concerning the time evolution of particles mean densities and establish several new ones.

cond-mat.stat-mech↗

Kinetics of stochastically-gated diffusion-limited reactions and geometry of random walk trajectories

In this paper we study the kinetics of diffusion-limited, pseudo-first-order A + B -> B reactions in situations in which the particles' intrinsic reactivities vary randomly in time. That is, we suppose that the particles are bearing "gates" which interchange randomly and independently of each other between two states - an active state, when the reaction may take place, and a blocked state, when the reaction is completly inhibited. We consider four different models, such that the A particle can be either mobile or immobile, gated or ungated, as well as ungated or gated B particles can be fixed at random positions or move randomly. All models are formulated on a $d$-dimensional regular lattice and we suppose that the mobile species perform independent, homogeneous, discrete-time lattice random walks. The model involving a single, immobile, ungated target A and a concentration of mobile, gated B particles is solved exactly. For the remaining three models we determine exactly, in form of rigorous lower and upper bounds, the large-N asymptotical behavior of the A particle survival probability. We also realize that for all four models studied here such a probalibity can be interpreted as the moment generating function of some functionals of random walk trajectories, such as, e.g., the number of self-intersections, the number of sites visited exactly a given number of times, "residence time" on a random array of lattice sites and etc. Our results thus apply to the asymptotical behavior of the corresponding generating functions which has not been known as yet.

cond-mat.stat-mech↗

Stokes formula and density perturbances for driven tracer diffusion in an adsorbed monolayer

We study the intrinsic friction of monolayers adsorbed on solid surfaces from a gas phase or vapor. Within the framework of the Langmuir model of delocalized adsorption, we calculate the resistance offered by the mobile adsorbate's particles to some impure tracer molecule, whose diffusive random motion is biased by a constant external force. We find that for sufficiently small driving forces the force exerted on the tracer shows viscous-like behavior. We derive then the analog of the Stokes formula for two-dimensional adsorbates, calculate the corresponding friction coefficient and determine the stationary particle distribution in the monolayer as seen from the driven impurity.

cond-mat.stat-mech↗

Phase boundary dynamics in a one-dimensional non-equilibrium lattice gas

We study dynamics of a phase boundary in a one-dimensional lattice gas, which is initially put into a non-equilibrium configuration and then is let to evolve in time by particles performing nearest-neighbor random walks constrained by hard-core interactions. Initial non-equilibrium configuration is characterized by an $S$-shape density profile, such that particles density from one side of the origin (sites $X \leq 0$) is larger (high density phase, HDP) than that from the other side (low-density phase, LDP). We suppose that all the lattice gas particles, except for the rightmost particle of the HDP, have symmetric hopping probabilities. The rightmost particle of the HDP, which determines the position of the phase separating boundary, is subject to a constant force $F$, oriented towards the HDP; in our model this force mimics an effective tension of the phase separating boundary. We find that, in the general case, the mean displacement $\bar{X(t)}$ of the phase boundary grows with time as $\bar{X(t)} = α(F) t^{1/2}$, where the prefactor $α(F)$ depends on $F$ and on the initial densities in the HDP and LDP. We show that $α(F)$ can be positive or negative, which means that depending on the physical conditions the HDP may expand or get compressed. In the particular case when $α(F) = 0$, i.e. when the HDP and LDP coexist with each other, the second moment of the phase boundary displacement is shown to grow with time sublinearly, $\bar{X^2(t)} = γt^{1/2}$, where the prefactor $γ$ is also calculated explicitly. Our analytical predictions are shown to be in a very good agreement with the results of Monte Carlo simulations.

cond-mat.stat-mech↗

Directed random walk in adsorbed monolayer

We study the dynamics of a tracer particle, which performs a totally directed random walk in an adsorbed monolayer composed of mobile hard-core particles undergoing continuous exchanges with a vapour phase. In terms of a mean-field-type approach, based on the decoupling of the tracer-particle-particle correlation functions into the product of pairwise, tracer-particle correlations, we determine the density profiles of the monolayer particles, as seen from the stationary moving tracer, and calculate its terminal velocity, V_{tr}. In the general case the latter is determined implicitly, as the solution of a certain transcendental equation. In two extreme limits of slow and fast monolayer particles diffusion, we obtain explicit asymptotic forms of V_{tr}. We show next that the density profile in the monolayer is strongly inhomogeneous: In front of the stationary moving tracer the local density is higher than the average value, ρ_L, and approaches ρ_L as an exponential function of the distance from the tracer. Past the tracer the local density is lower than ρ_L and the approach to ρ_L may proceed differently depending whether the particles number in the monolayer is not or is explicitly conserved. In the former case the approach is described by an exponential dependence with a different characteristic length, compared to the behavior in front of the tracer; in the latter case, the density tends to ρ_L algebraically. The characteristic lengths and the amplitudes of the density relaxation functions are also determined explicitly

cond-mat.stat-mech↗

Anchoring of polymers by traps randomly placed on a line

We study dynamics of a Rouse polymer chain, which diffuses in a three-dimensional space under the constraint that one of its ends, referred to as the slip-link, may move only along a one-dimensional line containing randomly placed, immobile, perfect traps. For such a model we compute exactly the time evolution of the probability $P_{sl}(t)$ that the chain slip-link will not encounter any of the traps until time $t$ and consequently, that until this time the chain will remain mobile.

cond-mat.stat-mech↗

Biased diffusion in a one-dimensional adsorbed monolayer

We study dynamics of a probe particle, which performs biased diffusive motion in a one-dimensional adsorbed monolayer of mobile hard-core particles undergoing continuous exchanges with a vapor phase. In terms of a mean-field-type approach, based on the decoupling of the third-order correlation functions into a product of the pairwise correlations, we determine analytically the density profiles of the monolayer particles, as seen from the stationary moving probe, and calculate the terminal velocity, mobility and the self-diffusion coefficient of the probe. Our analytical results are confirmed by Monte Carlo simulations.

cond-mat.stat-mech↗

Droplet Spreading: Partial Wetting Regime Revisited

We study the time evolution of a sessile liquid droplet, which is initially put onto a solid surface in a non-equilibrium configuration and then evolves towards its equilibrium shape. We adapt here the standard approach to the dynamics of mechanical dissipative systems, in which the driving force, i.e. the gradient of the system's Lagrangian function, is balanced against the rate of the dissipation function. In our case the driving force is the loss of the droplet's free energy due to the increase of its base radius, while the dissipation occurs due to viscous flows in the core of the droplet and due to frictional processes in the vicinity of the advancing contact line, associated with attachment of fluid particles to solid. Within this approach we derive closed-form equations for the evolution of the droplet's base radius, and specify several regimes at which different dissipation channels dominate. Our analytical predictions compare very well with experimental data.

cond-mat.mtrl-sci↗

Kinetics of Anchoring of Polymer Chains on Substrates with Chemically Active Sites

We consider dynamics of an isolated polymer chain with a chemically active end-bead on a 2D solid substrate containing immobile, randomly placed chemically active sites (traps). For a particular situation when the end-bead can be irreversibly trapped by any of these sites, which results in a complete anchoring of the whole chain, we calculate the time evolution of the probability $P_{ch}(t)$ that the initially non-anchored chain remains mobile until time $t$. We find that for relatively short chains $P_{ch}(t)$ follows at intermediate times a standard-form 2D Smoluchowski-type decay law $ln P_{ch}(t) \sim - t/ln(t)$, which crosses over at very large times to the fluctuation-induced dependence $ln P_{ch}(t) \sim - t^{1/2}$, associated with fluctuations in the spatial distribution of traps. We show next that for long chains the kinetic behavior is quite different; here the intermediate-time decay is of the form $ln P_{ch}(t) \sim - t^{1/2}$, which is the Smoluchowski-type law associated with subdiffusive motion of the end-bead, while the long-time fluctuation-induced decay is described by the dependence $ln P_{ch}(t) \sim - t^{1/4}$, stemming out of the interplay between fluctuations in traps distribution and internal relaxations of the chain.

cond-mat.soft↗

Dewetting, partial wetting and spreading of a two-dimensional monolayer on solid surface

We study the behavior of a semi-infinite monolayer, which is placed initially on a half of an infinite in both directions, ideal crystalline surface, and then evolves in time due to random motion of the monolayer particles. Particles dynamics is modeled as the Kawasaki particle-vacancy exchange process in the presence of long-range attractive particle-particle interactions. In terms of an analytically solvable mean-field-type approximation we calculate the mean displacement X(t) of the monolayer edge and discuss the conditions under which such a monolayer spreads (X(t) > 0), partially wets (X(t) = 0) or dewets from the solid surface (X(t) < 0).

cond-mat.soft↗

Microscopic model for spreading of a two-dimensional monolayer

We study the behavior of a monolayer, which occupies initially a bounded region on an ideal crystalline surface and then evolves in time due to random hopping motion of the monolayer particles. In the case when the initially occupied region is the half-plane $X \leq 0$, we determine explicitly, in terms of an analytically solvable mean-field-type approximation, the mean displacement $X(t)$ of the monolayer edge. We find that $X(t) \approx A \sqrt{D_{0} t}$, in which law $D_{0}$ denotes the bare diffusion coefficient and the prefactor $A$ is a function of the temperature and of the particle-particle interactions parameters. We show that $A$ can be greater, equal or less than zero, and specify the critical parameter which distinguishes between the regimes of spreading ($A > 0)$, partial wetting ($A = 0$) and dewetting ($A < 0$).

cond-mat.soft↗

Molecular Weight Dependence of Spreading Rates of Ultrathin Polymeric Films

We study experimentally the molecular weight $M$ dependence of spreading rates of molecularly thin precursor films, growing at the bottom of droplets of polymer liquids. In accord with previous observations, we find that the radial extension R(t) of the film grows with time as R(t) = (D_{exp} t)^{1/2}. Our data substantiate the M-dependence of D_{exp}; we show that it follows D_{exp} \sim M^{-γ}, where the exponent γis dependent on the chemical composition of the solid surface, determining its frictional properties with respect to the molecular transport. In the specific case of hydrophilic substrates, the frictional properties can be modified by the change of the relative humidity (RH). We find that γ\approx 1 at low RH and tends to zero when RH gets progressively increased. We propose simple theoretical arguments which explain the observed behavior in the limits of low and high RH.

cond-mat.soft↗

Dynamics of a driven probe molecule in a liquid monolayer

We study dynamics of a probe molecule, driven by an external constant force in a liquid monolayer on top of solid surface. In terms of a microscopic, mean-field-type approach, we calculate the terminal velocity of the probe molecule. This allows us to establish the analog of the Stokes formula, in which the friction coefficient is interpreted in terms of the microscopic parameters characterizing the system. We also determine the distribution of the monolayer particles as seen from the stationary moving probe molecule and estimate the self-diffusion coefficient for diffusion in a liquid monolayer.

cond-mat.soft↗

Kinetic description of diffusion-limited reactions in random catalytic media

We study the kinetics of bimolecular, catalytically-activated reactions (CARs) in d-dimensions. The elementary reaction act between reactants takes place only when these meet in the vicinity of a catalytic site; such sites are assumed to be immobile and randomly distributed in space. For CARs we develop a kinetic formalism, based on Collins-Kimball-type ideas; within this formalism we obtain explicit expressions for the effective reaction rates and for the decay of the reactants' concentrations.

cond-mat↗