posted on 2022-06-17, 14:09authored bySudarshan Vijay, Georg Kastlunger, Joseph A. Gauthier, Anjli Patel, Karen Chan
Determining ab initio potential-dependent
energetics is critical
to the investigation of mechanisms for electrochemical reactions.
While methodology for evaluating reaction thermodynamics is established,
simulation techniques for the corresponding kinetics is still a major
challenge owing to a lack of potential control, finite cell size effects,
or computational expense. In this work, we develop a model that allows
for computing electrochemical activation energies from just a handful
of density functional theory (DFT) calculations. The sole input into
the model are the atom-centered forces obtained from DFT calculations
performed on a homogeneous grid composed of varying field strengths.
We show that the activation energies as a function of the potential
obtained from our model are consistent for different supercell sizes
and proton concentrations for a range of electrochemical reactions.