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The structure of water at a Pt(111) electrode and the potential of zero charge studied from first principles.
Sakong, Sung; Forster-Tonigold, Katrin; Groß, Axel.
Afiliación
  • Sakong S; Institute of Theoretical Chemistry, Ulm University, 89069 Ulm, Germany.
  • Forster-Tonigold K; Helmholtz Institute Ulm (HIU), Electrochemical Energy Storage, 89069 Ulm, Germany.
  • Groß A; Institute of Theoretical Chemistry, Ulm University, 89069 Ulm, Germany.
J Chem Phys ; 144(19): 194701, 2016 May 21.
Article en En | MEDLINE | ID: mdl-27208959
The structure of a liquid water layer on Pt(111) has been studied by ab initio molecular dynamics simulations based on periodic density functional theory calculations. First the reliability of the chosen exchange-correlation function has been validated by considering water clusters, bulk ice structures, and bulk liquid water, confirming that the dispersion corrected RPBE-D3/zero functional is a suitable choice. The simulations at room temperature yield that a water layer that is six layers thick is sufficient to yield liquid water properties in the interior of the water film. Performing a statistical average along the trajectory, a mean work function of 5.01 V is derived, giving a potential of zero charge of Pt(111) of 0.57 V vs. standard hydrogen electrode, in good agreement with experiments. Therefore we propose the RPBE-D3/zero functional as the appropriate choice for first-principles calculations addressing electrochemical aqueous electrolyte/metal electrode interfaces.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Chem Phys Año: 2016 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Chem Phys Año: 2016 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos