Structural characterizations of water-metal interfaces

TL;DR

This study uses first-principles molecular dynamics to compare water's structural, electronic, and dynamical properties at metal interfaces, revealing unique chemisorption behavior on platinum surfaces.

Contribution

It provides detailed insights into water-metal interface structures, especially highlighting chemisorption on platinum and the effects of defects on graphene and graphite.

Findings

Chemisorption peak observed at water-Pt interface.

Covalent bond formation between water and Pt surface.

Defects and dopants influence water's interface behavior.

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.