Literature DB >> 19518427

Ensemble inequivalence in single-molecule experiments.

M Süzen1, M Sega, C Holm.   

Abstract

In bulk systems the calculation of the main thermodynamic quantities leads to the same expectation values in the thermodynamic limit, regardless of the choice of the statistical ensemble. Single linear molecules can be still regarded as statistical systems, where the thermodynamic limit is represented by infinitely long chains. The question of equivalence between different ensembles is not at all obvious and has been addressed in the literature, with sometimes contradicting conclusions. We address this problem by studying the scaling properties of the ensemble difference for two different chain models as a function of the degree of polymerization. By characterizing the scaling behavior of the difference between the isotensional (Gibbs) and isometric (Helmholtz) ensembles in the transition from the low-stretching to the high-stretching regime, we show that ensemble equivalence cannot be reached for macroscopic chains in the low force regime, and we characterize the transition from the inequivalence to the equivalence regime.

Year:  2009        PMID: 19518427     DOI: 10.1103/PhysRevE.79.051118

Source DB:  PubMed          Journal:  Phys Rev E Stat Nonlin Soft Matter Phys        ISSN: 1539-3755


  2 in total

1.  Torque spectroscopy of DNA: base-pair stability, boundary effects, backbending, and breathing dynamics.

Authors:  Florian C Oberstrass; Louis E Fernandes; Paul Lebel; Zev Bryant
Journal:  Phys Rev Lett       Date:  2013-04-25       Impact factor: 9.161

2.  Entropy Production beyond the Thermodynamic Limit from Single-Molecule Stretching Simulations.

Authors:  Eivind Bering; Signe Kjelstrup; Dick Bedeaux; J Miguel Rubi; Astrid S de Wijn
Journal:  J Phys Chem B       Date:  2020-09-25       Impact factor: 2.991

  2 in total

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