Acetate adsorption on Pt(111): Implications for copper underpotential deposition and surface oxidation

Acetate stabilizes the Cu underpotential deposition (UPD) on Pt(111) as shown previously for Cu UPD on Au(111). A similar kinetic hindrance of Cu bulk deposition (OPD) for Pt(111) and Au(111) is found. The adsorption of acetate therefore leads to a broad potential window for a stable Cu UPD monolayer. Pt(111) surface oxidation shows a strong kinetic hindrance in the presence of acetate. The processes of Cu UPD and surface oxidation are dependent on the previous Cu deposition for Pt(111). This effect is attributed to the competitive adsorption of hydroxide and acetate. A model for Cu UPD on different Pt(111) surface sites is developed to describe variations of the charges of the two Cu UPD peaks governed by dissimilar anion adlayers. The extent of Pt(111) surface oxidation can be controlled by a specific Cu UPD routine.

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Publication Details

Journal
Electrochimica Acta
Published
2025-09-09
DOI
https://doi.org/10.1016/j.electacta.2025.147354
Primary Topic
Catalytic Processes in Materials Science
Type
article
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article

Acetate adsorption on Pt(111): Implications for copper underpotential deposition and surface oxidation

Ludwig A. Kibler, Timo Jacob, Johannes M. Hermann, Sebastian Fackler
Electrochimica Acta
Catalytic Processes in Materials Science
article

Acetate adsorption on Pt(111): Implications for copper underpotential deposition and surface oxidation

Ludwig A. Kibler, Timo Jacob, Johannes M. Hermann, Sebastian Fackler
article en

Abstract

Acetate stabilizes the Cu underpotential deposition (UPD) on Pt(111) as shown previously for Cu UPD on Au(111). A similar kinetic hindrance of Cu bulk deposition (OPD) for Pt(111) and Au(111) is found. The adsorption of acetate therefore leads to a broad potential window for a stable Cu UPD monolayer. Pt(111) surface oxidation shows a strong kinetic hindrance in the presence of acetate. The processes of Cu UPD and surface oxidation are dependent on the previous Cu deposition for Pt(111). This effect is attributed to the competitive adsorption of hydroxide and acetate. A model for Cu UPD on different Pt(111) surface sites is developed to describe variations of the charges of the two Cu UPD peaks governed by dissimilar anion adlayers. The extent of Pt(111) surface oxidation can be controlled by a specific Cu UPD routine.

Electrochimica ActaVol. 542
Universität Ulm (DE)
Openalex Percentile: Top 81%
Catalytic Processes in Materials Science
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Acetate adsorption on Pt(111): Implications for copper underpotential deposition and surface oxidation — Ludwig A. Kibler, Timo Jacob, et al. · Electrochimica Acta (2025) | TGRS Research Map | TGRS