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P E Parris

Publications and source records attributed to P E Parris.

3 recordsLinked to original sources

Variational formula for the relaxation time in the Boltzmann equation.

The relaxation time approximation (RTA) is commonly employed in nonequilibrium statistical mechanics to approximate solutions to the Boltzmann equation in terms of an exponential relaxation to equilibrium. Despite its common use, the RTA suffers from the drawback that relaxation times commonly employed are independent of initial conditions. We derive a variational principle for solutions to the Boltzmann equation, which allows us to extend the standard RTA using relaxation times that depend on the initial distribution. Tests of the approach on a calculation of the mobility for a one-dimensional (1D) tight-binding band indicate that our analysis typically provides a better approximation than the standard RTA.

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Static pairwise annihilation in complex networks.

We study static annihilation on complex networks, in which pairs of connected particles annihilate at a constant rate during time. Through a mean-field formalism, we compute the temporal evolution of the distribution of surviving sites with an arbitrary number of connections. This general formalism, which is exact for disordered networks, is applied to Kronecker, Erdös-Rényi (i.e., Poisson), and scale-free networks. We compare our theoretical results with extensive numerical simulations obtaining excellent agreement. Although the mean-field approach applies in an exact way neither to ordered lattices nor to small-world networks, it qualitatively describes the annihilation dynamics in such structures. Our results indicate that the higher the connectivity of a given network element, the faster it annihilates. This fact has dramatic consequences in scale-free networks, for which, once the "hubs" have been annihilated, the network disintegrates and only isolated sites are left.

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Nature of charge carriers in disordered molecular solids: are polarons compatible with observations?

Polaronic theories for charge transport in disordered organic solids, particularly molecularly doped polymers, have been plagued by issues of internal consistency related to the magnitude of physical parameters. We present a natural resolution of the problem by showing that, in the presence of correlated disorder, polaronic carriers with binding energies Delta approximately 50-500 meV and transfer integrals J approximately 1-20 meV are completely consistent with the magnitudes of field and temperature dependent mobilities observed.

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