The chemical hardness of molecules and the band gap of solids within charge equilibration formalisms

Toward force field-based simulations of redox reactions
Regular Article

DOI: 10.1140/epjb/e2012-21081-8

Cite this article as:
Müser, M.H. Eur. Phys. J. B (2012) 85: 135. doi:10.1140/epjb/e2012-21081-8

Abstract

This work finds that different charge equilibration methods lead to qualitatively different responses of molecules and solids to an excess charge. The investigated approaches are the regular charge equilibration (QE), the atom-atom-charge transfer (AACT), and the split-charge equilibration (SQE) method. In QE, the hardness of molecules and the band gap of solids approaches zero at large particle numbers, affirming the claim that QE induces metallic behavior. AACT suffers from producing negative values of the hardness; moreover valence and conduction bands of solids cross. In contrast to these methods, SQE can reproduce the generic behavior of dielectric molecules or solids. Moreover, first quantitative results for the NaCl molecule are promising. The results derived in this work may have beneficial implications for the modeling of redox reactions. They reveal that by introducing formal oxidation states into force field-based simulations it will become possible to simulate redox reactions including non-equilibrium contact electrification, voltage-driven charging of galvanic cells, and the formation of zwitterionic molecules.

Keywords

Computational Methods

Copyright information

© EDP Sciences, SIF, Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  1. 1.Jülich Supercomputer CentreInstitute for Advanced SimulationJülichGermany