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Micha Polak

Publications and source records attributed to Micha Polak.

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Intrinsic Matching Frustration in Fluctuating Finite Systems

We show that matching between interacting constituents is intrinsically incomplete in finite systems due to equilibrium fluctuations. While fluctuations in finite populations are a well-established feature of statistical mechanics, their direct impact on processes requiring simultaneous matching has not been explicitly formulated. Because matching is determined by the smaller of fluctuating populations rather than by their average values, equilibrium fluctuations systematically reduce the number of realizable matching events. We formalize this effect as intrinsic matching frustration (IMF), a universal statistical constraint that arises whenever discrete fluctuating populations must be paired. IMF generates a finite population of intact ("spectator") particles even at equilibrium and suppresses matching-dependent processes relative to expectations based on mean populations. For independent Poisson populations, IMF admits an exact solution based on the Skellam distribution, valid for all particle numbers. More generally, interactions and correlations may modify the detailed fluctuation statistics, but for sufficiently large populations the mismatch is determined solely by the variance of the population imbalance and exhibits universal scaling behavior. IMF therefore represents a generic equilibrium property of finite systems, independent of microscopic rates and interaction mechanisms. The effect provides a universal fluctuation-induced limitation on pairwise association, binding, and matching processes, with implications for chemical reactions, molecular binding, nanoscale quantum systems, and biological environments. By identifying a fundamental fluctuation-induced constraint on matching, IMF complements established descriptions of finite-size and equilibrium fluctuation effects in statistical mechanics.

physics.chem-ph

Modeling nanoconfined reaction kinetics: Alternative methodology incorporating equilibrium extent fluctuations

This study reveals that Equilibrium Constant Differential Equations (ECDE) for nanoconfined reactions derived recently in the frameworks of statistical mechanics are useful in modeling stochastic chemical kinetics. It is assumed and verified that if the transient value of the nano-reaction quotient is treated as being an equilibrium constant, the corresponding equilibrium reaction extent and its fluctuations (the variance function) coincide with the respective transient values. The ECDE-computed variance function facilitates the solution of the stochastic kinetics equations (SKE), as is demonstrated for a stoichiometric exchange reaction. The results obtained by this original methodology are in full agreement with those provided by the chemical master equations. Contrary to the commonly used approaches based on the latter and the Gillespie algorithm, which need a lot of computer memory and are time-consuming, the proposed SKE-ECDE method requires to solve only the ECDE and a single stochastic kinetics differential equation.

physics.chem-ph

Chemical Reactions under Nanoconfinement: Unravelling Equilibrium Constant Equations

Equilibrium Constant Differential Equations (ECDE) are derived for several nanoconfined elemental bimolecular reactions in the frameworks of statistical mechanics and the ideal gas model. The ECDEs complement the well-known equilibrium-constant ordinary equations that are used for macroscopic systems. Solving the ECDE numerically or analytically furnishes the average reaction extent, as well as its variance and skewness. This original theoretical-computational methodology fills the gap in studies of nanochemical equilibrium providing a consistent and convenient alternative to derivations based on direct employment of the canonical partition-functions. Whereas the latter become more complex and time-consuming with increased number of molecules, the ECDE-based computations are equally efficient for small as well as large numbers of nanoconfined reacting molecules. The ECDE methodology introduced here is confirmed by a complete agreement with partition-function computations. In addition, the new approach is applied to nanoconfined adsorption.

physics.chem-ph