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Updated: Aug 24, 2025

Unraveling Entropic Rate Acceleration Induced by Solvent Dynamics in Membrane Enzymes
Published on: January 16, 2016
Free energy landscape within the hysteresis regime for fluids confined in disordered mesoporous solids
A Alzaidi1, E S Kikkinides2, D Schneider3
1Felix Bloch Institute for Solid State Physics, Leipzig University, Leipzig, Germany.
Abstract:
Adsorption/desorption and melting/freezing in structurally disordered nanoporous solids exhibit strongly non-equilibrium behavior as revealed by the formation of a hysteresis region populated by the multitude of different states. Many questions concerning the free energy spectrum of these states, including the existence of the equilibrium transition, if any, their accessibility in the experiments, and internal relaxation dynamics toward the global energy minimum, still remain poorly addressed. By using a serially connected pore model with the statistical disorder as a minimal model of the pore networks, we explore the system free energies along the solid-liquid and liquid-gas transitions in the pore systems. The rigorous results obtained with this model shed light on the occurrence and nature of the equilibrium transition line in porous solids with arbitrary pore topology. We discuss further the free energies along the experimentally measured boundary and scanning transitions and how close the equilibrium states can be approached in these experiments.
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