Dynamic scaling of stochastic thermodynamic observables for chemical reactions at and away from equilibrium.

Physical kinetic roughening processes are well-known to exhibit universal scaling of observables that fluctuate in space and time. Are there analogous dynamic scaling laws that are unique to the chemical reaction mechanisms available synthetically and occurring naturally? Here, we formulate an approach to the dynamic scaling of stochastic fluctuations in thermodynamic observables at and away from equilibrium. Both analytical expressions and numerical simulations confirm our dynamic scaling ansatz with associated scaling exponents, function, and law.

Entrance and escape dynamics for the typical set.

According to the asymptotic equipartition property, sufficiently long sequences of random variables converge to a set that is typical. While the size and probability of this set are central to information theory and statistical mechanics, they can often only be estimated accurately in the asymptotic limit due to the exponential growth in possible sequences. Here we derive a time-inhomogeneous dynamics that constructs the properties of the typical set for all finite length sequences of independent and identically distributed random variables.