Implications of the fractional charge of hydroxide at the electrochemical interface. Issue 13 (18th March 2020)

• Record Type: Journal Article
• Authors: Gauthier, Joseph A.; Chen, Leanne D.; Bajdich, Michal; Chan, Karen
• Is Part Of: Physical chemistry chemical physics. Volume 22:Issue 13(2020)
• Page Start: 6964
• Page End: 6969
• Publication Date: 2020-03-18
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c9cp05952k
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Rational design of materials that efficiently convert electrical energy into chemical bonds will ultimately depend on a thorough understanding of the electrochemical interface at the atomic level. Abstract : Rational design of materials that efficiently convert electrical energy into chemical bonds will ultimately depend on a thorough understanding of the electrochemical interface at the atomic level. Towards this goal, the use of density functional theory (DFT) at the generalized gradient approximation (GGA) level has been applied widely in the past 15 years. In the calculation of electrochemical reaction energetics using GGA-DFT, it is frequently implicitly assumed that ions in the Helmholtz plane have unit charge. However, the ion charge is observed to be fractional near the interface through both a capacitor model and through Bader charge partitioning. In this work, we show that this spurious charge transfer can be effectively mitigated by continuum charging of the electrolyte. We then show that, similar to hydronium, the observed fractional charge of hydroxide is not due to a GGA level self-interaction error, as the partial charge is observed even when using hybrid level exchange–correlation functionals.