Structural characterization of water-metal interfaces

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DOIResolve DOI: https://doi.org/10.1103/PhysRevB.96.064104
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  1. National Research Council of Canada. Security and Disruptive Technologies
FormatText, Article
Journal titlePhysical Review B
ISSN2469-9950
2469-9969
Volume96
Issue6
Article number064104
Abstract
We analyze and compare the structural, dynamical, and electronic properties of liquid water next to prototypical metals including Pt, graphite, and graphene. Our results are built on Born-Oppenheimer molecular dynamics (BOMD) generated using density functional theory (DFT) which explicitly include van der Waals (vdW) interactions within a first principles approach. All calculations reported use large simulation cells, allowing for an accurate treatment of the water-electrode interfaces. We have included vdW interactions through the use of the optB86b-vdW exchange correlation functional. Comparisons with the Perdew-Burke-Ernzerhof (PBE) exchange correlation functional are also shown. We find an initial peak, due to chemisorption, in the density profile of the liquid water-Pt interface not seen in the liquid water-graphite interface, liquid water-graphene interface, nor interfaces studied previously. To further investigate this chemisorption peak, we also report differences in the electronic structure of single water molecules on both Pt and graphite surfaces. We find that a covalent bond forms between the single water molecule and the Pt surface but not between the single water molecule and the graphite surface. We also discuss the effects that defects and dopants in the graphite and graphene surfaces have on the structure and dynamics of liquid water.
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PublisherAmerican Physical Society
LanguageEnglish
Peer reviewedYes
NPARC number23003151
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Record created2018-05-02
Record modified2020-05-30
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