4.7 Article

Constant Potential and Constrained Charge Ensembles for Simulations of Conductive Electrodes

Journal

JOURNAL OF CHEMICAL THEORY AND COMPUTATION
Volume 19, Issue 10, Pages 2758-2768

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jctc.3c00153

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Constant potential method molecular dynamics simulation (CPM MD) accurately models atomistic electrode charges at the nanoscale. A theoretical extension of this approach is presented, where the total charge of each conductive electrode is controlled instead of their potential difference. The resulting thermodynamic ensemble is distinct but conjugate to the fixed potential difference ensemble. The success of recent studies using fixed total charges on electrodes is underpinned by this theoretical correspondence, with potential applications for speeding up equilibration and future simulations.
Constant potential method molecular dynamics simulation (CPM MD) enables the accurate modeling of atomistic electrode charges when studying the electrode-electrolyte interface at the nanoscale. Here, we extend the theoretical framework of CPM MD to the case in which the total charge of each conductive electrode is controlled, instead of their potential difference. We show that the resulting thermodynamic ensemble is distinct from that sampled with a fixed potential difference but they are rigorously related as conjugate ensembles. This theoretical correspondence, which we demonstrate using simulations of an ionic liquid supercapacitor, underpins the success of recent studies with fixed total charges on the electrodes. We show that equilibration is usefully sped up in this ensemble and outline some potential applications of these simulations in the future.

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