Searcharxiv⌕ Search

arXiv subjects

Aljaz Godec

Publications and source records attributed to Aljaz Godec.

22 records · Page 2Linked to original sources

First passage statistics for aging diffusion in annealed and quenched disorder

Aging, the dependence of the dynamics of a physical process on the time $t_a$ since its original preparation, is observed in systems ranging from the motion of charge carriers in amorphous semiconductors over the blinking dynamics of quantum dots to the tracer dispersion in living biological cells. Here we study the effects of aging on one of the most fundamental properties of a stochastic process, the first passage dynamics. We find that for an aging continuous time random walk process the scaling exponent of the density of first passage times changes twice as the aging progresses and reveals an intermediate scaling regime. The first passage dynamics depends on $t_a$ differently for intermediate and strong aging. Similar crossovers are obtained for the first passage dynamics for a confined and driven particle. Comparison to the motion of an aged particle in the quenched trap model with a bias shows excellent agreement with our analytical findings. Our results demonstrate how first passage measurements can be used to unravel the age $t_a$ of a physical system.

cond-mat.stat-mech↗

Diffusion of finite-size particles in channels with random walls

Diffusion of chemicals or tracer molecules through complex systems containing irregularly shaped channels is important in many applications. Most theoretical studies based on the famed Fick-Jacobs equation focus on the idealised case of infinitely small particles and reflecting boundaries. In this study we use numerical simulations to consider the transport of finite-sized particles through asymmetrical two-dimensional channels. Additionally, we examine transient binding of the molecules to the channel walls by applying sticky boundary conditions. With the application of diffusing pathogens in hydrogels in mind, we consider an ensemble of particles diffusing in independent channels, which are characterised by common structural parameters. We compare our results for the long-time effective diffusion coefficient with a recent theoretical formula obtained by Dagdug and Pineda [J. Chem. Phys., 2012, 137, 024107].

cond-mat.stat-mech↗

Finite-time effects and ultraweak ergodicity breaking in superdiffusive dynamics

We study the ergodic properties of superdiffusive, spatiotemporally coupled Levy walk processes. For trajectories of finite duration, we reveal a distinct scatter of the scaling exponents of the time averaged mean squared displacement delta**2 around the ensemble value 3-alpha (1<alpha<2) ranging from ballistic motion to subdiffusion, in strong contrast to the behavior of subdiffusive processes. In addition we find a significant dependence of the trajectory-to-trajectory average of delta**2 as function of the finite measurement time. This so-called finite-time amplitude depression and the scatter of the scaling exponent is vital in the quantitative evaluation of superdiffusive processes. Comparing the long time average of the second moment with the ensemble mean squared displacement, these only differ by a constant factor, an ultraweak ergodicity breaking.

cond-mat.stat-mech↗

Physical origin underlying the entropy loss upon hydrophobic hydration

The hydrophobic effect (HE) is commonly associated with the demixing of oil and water at ambient conditions and plays the leading role in determining the structure and stability of biomolecular assembly in aqueous solutions. On the molecular scale HE has an entropic origin. It is believed that hydrophobic particles induce order in the surrounding water by reducing the volume of con- figuration space available for hydrogen bonding. Here we show with computer simulation results that this traditional picture is not correct. Analyzing collective fluctuations in water clusters we are able to provide a fundamentally new picture of HE based on pronounced many-body correlations affecting the switching of hydrogen bonds between molecules. These correlations emerge as a non-local compensation of reduced fluctuations of local electrostatic fields in the presence of an apolar solute.

cond-mat.stat-mech↗