Display options
Cite
Sundararaman R, Goddard WA, Arias TA. Grand canonical electronic density-functional theory: Algorithms and applications to electrochemistry. J Chem Phys. 2017;146(11):114104doi: 10.1063/1.4978411.
Sundararaman, R., Goddard, W. A., & Arias, T. A. (2017). Grand canonical electronic density-functional theory: Algorithms and applications to electrochemistry. The Journal of chemical physics, 146(11), 114104. https://doi.org/10.1063/1.4978411
Sundararaman, Ravishankar, et al. "Grand canonical electronic density-functional theory: Algorithms and applications to electrochemistry." The Journal of chemical physics vol. 146,11 (2017): 114104. doi: https://doi.org/10.1063/1.4978411
Sundararaman R, Goddard WA, Arias TA. Grand canonical electronic density-functional theory: Algorithms and applications to electrochemistry. J Chem Phys. 2017 Mar 21;146(11):114104. doi: 10.1063/1.4978411. PMID: 28330356.
Copy Download .nbib Format: NLM
Share it on

J Chem Phys. 2017 Mar 21;146(11):114104. doi: 10.1063/1.4978411.

Grand canonical electronic density-functional theory: Algorithms and applications to electrochemistry.

The Journal of chemical physics

Ravishankar Sundararaman, William A Goddard, Tomas A Arias

Affiliations

  1. Department of Materials Science and Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
  2. Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, California 91125, USA.
  3. Laboratory of Atomic and Solid State Physics, Cornell University, Ithaca, New York 14853, USA.

PMID: 28330356 DOI: 10.1063/1.4978411

Abstract

First-principles calculations combining density-functional theory and continuum solvation models enable realistic theoretical modeling and design of electrochemical systems. When a reaction proceeds in such systems, the number of electrons in the portion of the system treated quantum mechanically changes continuously, with a balancing charge appearing in the continuum electrolyte. A grand-canonical ensemble of electrons at a chemical potential set by the electrode potential is therefore the ideal description of such systems that directly mimics the experimental condition. We present two distinct algorithms: a self-consistent field method and a direct variational free energy minimization method using auxiliary Hamiltonians (GC-AuxH), to solve the Kohn-Sham equations of electronic density-functional theory directly in the grand canonical ensemble at fixed potential. Both methods substantially improve performance compared to a sequence of conventional fixed-number calculations targeting the desired potential, with the GC-AuxH method additionally exhibiting reliable and smooth exponential convergence of the grand free energy. Finally, we apply grand-canonical density-functional theory to the under-potential deposition of copper on platinum from chloride-containing electrolytes and show that chloride desorption, not partial copper monolayer formation, is responsible for the second voltammetric peak.

Publication Types