Orientational relaxation in a dispersive dynamic medium : Generalization of the Kubo-Ivanov-Anderson jump diffusion model to include fractional environmental dynamics

Ivanov-Anderson (IA) model (and an earlier treatment by Kubo) envisages a decay of the orientational correlation by random but large amplitude molecular jumps, as opposed to infinitesimal small jumps assumed in Brownian diffusion. Recent computer simulation studies on water and supercooled liquids have shown that large amplitude motions may indeed be more of a rule than exception. Existing theoretical studies on jump diffusion mostly assume an exponential (Poissonian) waiting time distribution for jumps, thereby again leading to an exponential decay. Here we extend the existing formalism of Ivanov and Anderson to include an algebraic waiting time distribution between two jumps. As a result, the first and second rank orientational time correlation functions show the same long time power law, but their short time decay behavior is quite different. The predicted Cole-Cole plot of dielectric relaxation reproduces various features of non-Debye behaviour observed experimentally. We also developed a theory where both unrestricted small jumps and large angular jumps coexist simultaneously. The small jumps are shown to have a large effect on the long time decay, particularly in mitigating the effects of algebraic waiting time distribution, and in giving rise to an exponential-like decay, with a time constant, surprisingly, less than the time constant that arises from small amplitude decay alone.Comment: 14 figure

Fractional Reaction-Diffusion Equation

A fractional reaction-diffusion equation is derived from a continuous time random walk model when the transport is dispersive. The exit from the encounter distance, which is described by the algebraic waiting time distribution of jump motion, interferes with the reaction at the encounter distance. Therefore, the reaction term has a memory effect. The derived equation is applied to the geminate recombination problem. The recombination is shown to depend on the intrinsic reaction rate, in contrast with the results of Sung et al. [J. Chem. Phys. {\bf 116}, 2338 (2002)], which were obtained from the fractional reaction-diffusion equation where the diffusion term has a memory effect but the reaction term does not. The reactivity dependence of the recombination probability is confirmed by numerical simulations.Comment: to appear in Journal of Chemical Physic

Dispersive photoluminescence decay by geminate recombination in amorphous semiconductors

The photoluminescence decay in amorphous semiconductors is described by power law $t^{-delta}$ at long times. The power-law decay of photoluminescence at long times is commonly observed but recent experiments have revealed that the exponent, $delta sim 1.2-1.3$, is smaller than the value 1.5 predicted from a geminate recombination model assuming normal diffusion. Transient currents observed in the time-of-flight experiments are highly dispersive characterized by the disorder parameter $alpha$ smaller than 1. Geminate recombination rate should be influenced by the dispersive transport of charge carriers. In this paper we derive the simple relation, $delta = 1+ alpha/2$. Not only the exponent but also the amplitude of the decay calculated in this study is consistent with measured photoluminescence in a-Si:H.Comment: 18pages. Submitted for the publication in Phys. Rev.

Dispersive diffusion controlled distance dependent recombination in amorphous semiconductors

The photoluminescence in amorphous semiconductors decays according to power law $t^{-delta}$ at long times. The photoluminescence is controlled by dispersive transport of electrons. The latter is usually characterized by the power $alpha$ of the transient current observed in the time-of-flight experiments. Geminate recombination occurs by radiative tunneling which has a distance dependence. In this paper, we formulate ways to calculate reaction rates and survival probabilities in the case carriers execute dispersive diffusion with long-range reactivity. The method is applied to obtain tunneling recombination rates under dispersive diffusion. The theoretical condition of observing the relation $delta = alpha/2 + 1$ is obtained and theoretical recombination rates are compared to the kinetics of observed photoluminescence decay in the whole time range measured.Comment: To appear in Journal of Chemical Physic

Exact asymptotics for non-radiative migration-accelerated energy transfer in one-dimensional systems

We study direct energy transfer by multipolar or exchange interactions between diffusive excited donor and diffusive unexcited acceptors. Extending over the case of long-range transfer of an excitation energy a non-perturbative approach by Bray and Blythe [Phys. Rev. Lett. 89, 150601 (2002)], originally developed for contact diffusion-controlled reactions, we determine exactly long-time asymptotics of the donor decay function in one-dimensional systems.Comment: 16 page

Corrections to the Law of Mass Action and Properties of the Asymptotic t=∞t = \infty State for Reversible Diffusion-Limited Reactions

On example of diffusion-limited reversible $A+A \rightleftharpoons B$ reactions we re-examine two fundamental concepts of classical chemical kinetics - the notion of "Chemical Equilibrium" and the "Law of Mass Action". We consider a general model with distance-dependent reaction rates, such that any pair of $A$ particles, performing standard random walks on sites of a $d$-dimensional lattice and being at a distance $\mu$ apart of each other at time moment $t$, may associate forming a $B$ particle at the rate $k_+(\mu)$. In turn, any randomly moving $B$ particle may spontaneously dissociate at the rate $k_-(\lambda)$ into a geminate pair of $A$s "born" at a distance $\lambda$ apart of each other. Within a formally exact approach based on Gardiner's Poisson representation method we show that the asymptotic $t = \infty$ state attained by such diffusion-limited reactions is generally \textit{not a true thermodynamic equilibrium}, but rather a non-equilibrium steady-state, and that the Law of Mass Action is invalid. The classical concepts hold \text{only} in case when the ratio $k_+(\mu)/k_-(\mu)$ does not depend on $\mu$ for any $\mu$.Comment: 30 pages, 2 figure

Reversible Diffusion-Limited Reactions: "Chemical Equilibrium" State and the Law of Mass Action Revisited

The validity of two fundamental concepts of classical chemical kinetics - the notion of "Chemical Equilibrium" and the "Law of Mass Action" - are re-examined for reversible \textit{diffusion-limited} reactions (DLR), as exemplified here by association/dissociation $A+A \rightleftharpoons B$ reactions. We consider a general model of long-ranged reactions, such that any pair of $A$ particles, separated by distance $\mu$, may react with probability $\omega_+(\mu)$, and any $B$ may dissociate with probability $\omega_-(\lambda)$ into a geminate pair of $A$s separated by distance $\lambda$. Within an exact analytical approach, we show that the asymptotic state attained by reversible DLR at $t = \infty$ is generally \textit{not a true thermodynamic equilibrium}, but rather a non-equilibrium steady-state, and that the Law of Mass Action is invalid. The classical picture holds \text{only} in physically unrealistic case when $\omega_+(\mu) \equiv \omega_-(\mu)$ for any value of $\mu$.Comment: 4 page