178 research outputs found

    Microscopic Model of Charge Carrier Transfer in Complex Media

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    We present a microscopic model of a charge carrier transfer under an action of a constant electric field in a complex medium. Generalizing previous theoretical approaches, we model the dynamical environment hindering the carrier motion by dynamic percolation, i.e., as a medium comprising particles which move randomly on a simple cubic lattice, constrained by hard-core exclusion, and may spontaneously annihilate and re-appear at some prescribed rates. We determine analytically the density profiles of the "environment" particles, as seen from the stationary moving charge carrier, and calculate its terminal velocity as the function of the applied field and other system parameters. We realize that for sufficiently small external fields the force exerted on the carrier by the "environment" particles shows a viscous-like behavior and define an analog of the Stokes formula for such dynamic percolative environments. The corresponding friction coefficient is also derived.Comment: appearing in Chem. Phys. Special Issue on Molecular Charge Transfer in Condensed Media - from Physics and Chemistry to Biology and Nano-Engineering, edited by A.Kornyshev (Imperial College London), M.Newton (Brookhaven Natl Lab) and J.Ulstrup (Technical University of Denmark

    Random Walks on a Fluctuating Lattice: A Renormalization Group Approach Applied in One Dimension

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    We study the problem of a random walk on a lattice in which bonds connecting nearest neighbor sites open and close randomly in time, a situation often encountered in fluctuating media. We present a simple renormalization group technique to solve for the effective diffusive behavior at long times. For one-dimensional lattices we obtain better quantitative agreement with simulation data than earlier effective medium results. Our technique works in principle in any dimension, although the amount of computation required rises with dimensionality of the lattice.Comment: PostScript file including 2 figures, total 15 pages, 8 other figures obtainable by mail from D.L. Stei

    Crossover from percolation to diffusion

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    A problem of the crossover from percolation to diffusion transport is considered. A general scaling theory is proposed. It introduces phenomenologically four critical exponents which are connected by two equations. One exponent is completely new. It describes the increase of the diffusion below percolation threshold. As an example, an exact solution of one dimensional lattice problem is given. In this case the new exponent q=2q=2.Comment: 10 pages, 1 figur

    Generalized model for dynamic percolation

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    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, ρs\rho_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 ρs\rho_s and the relaxation towards ρs\rho_s may proceed differently depending on whether the particles number is or is not explicitly conserved.Comment: Latex, 32 pages, 4 ps-figures, submitted to PR

    Diffusion with rearranging traps

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    A model for diffusion on a cubic lattice with a random distribution of traps is developed. The traps are redistributed at certain time intervals. Such models are useful for describing systems showing dynamic disorder, such as ion-conducting polymers. In the present model the traps are infinite, unlike an earlier version with finite traps, this model has a percolation threshold. For the infinite trap version a simple analytical calculation is possible and the results agree qualitatively with simulation.Comment: Latex, five figure

    University Physics Volume 2

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    University Physics is a three-volume collection that meets the scope and sequence requirements for two- and three-semester calculus-based physics courses. Volume 1 covers mechanics, sound, oscillations, and waves. Volume 2 covers thermodynamics, electricity and magnetism, and Volume 3 covers optics and modern physics. This textbook emphasizes connections between theory and application, making physics concepts interesting and accessible to students while maintaining the mathematical rigor inherent in the subject. Frequent, strong examples focus on how to approach a problem, how to work with the equations, and how to check and generalize the result.https://commons.erau.edu/oer-textbook/1002/thumbnail.jp

    Conformational disorder and energy migration in MEH-PPV with partially broken conjugation

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    In order to obtain a better understanding of the role of conformational disorder in the photophysics of conjugated polymers the ultrafast transient absorption anisotropy of partially deconjugated MEH-PPV has been measured. These data have been compared to the corresponding kinetics of Monte Carlo-simulated polymer chains, and estimates of the energy hopping time and energy migration distances for the polymers have been obtained. We find that the energy migration in the investigated MEH-PPV is approximately 3 times faster than in previously studied polythiophenes. We attribute this to a more disordered chain conformation in MEH-PPV. (C) 2003 American Institute of Physics
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