Ultra-Pure Nanoporous Gold Films for Electrocatalysis

Hyunah Kwon, Hannah Noa Barad, Alex Ricardo Silva Olaya, Mariana Alarcón-Correa, Kersten Hahn, Gunther Richter, Gunther Wittstock, Peer Fischer

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Nanoporous gold (Au) films are self-supported structures that possess a large surface area and extraordinary catalytic activity. Generally, nanoporous gold is obtained by solution-based dealloying where the less noble metal, often silver (Ag), is etched out. However, the residual amounts of the sacrificial metal are not well controlled, the impure samples show restructuring, and the residual metal prevents the study of the catalytic role of Au alone. Here, we fabricate impurity-free nanoporous gold films by a plasma-enabled dry synthetic route. The scheme does not include sacrificial metals or solution processing and is much more general. It is used to obtain self-supported ultra-pure nanoporous gold films with controllable pore sizes. The impurity-free nanoporous gold films possess highly curved ligaments, are remarkably robust, and stable over hundreds of electrochemical cycles. Furthermore, they contain many catalytically active sites, which is highly promising for electrocatalytic applications.

Original languageEnglish
Pages (from-to)11656-11665
Number of pages10
JournalACS Catalysis
Volume13
Issue number17
DOIs
StatePublished - 1 Sep 2023

Bibliographical note

Publisher Copyright:
© 2023 American Chemical Society.

Funding

The authors would like to express their sincere appreciation for access to measurements in the Stuttgart Center for Electron Microscopy (StEM). G.W. and A.R.S.O. acknowledge funding of Deutsche Forschungsgemeinschaft (DFG) through the Research unit FOR 2213 within the subprojects WI 1617/21-2 (G.W.).

FundersFunder number
Deutsche ForschungsgemeinschaftWI 1617/21-2

    Keywords

    • dry synthesis
    • electrocatalysis
    • methanol oxidation
    • nanoporous gold
    • plasma processing
    • purity
    • under-potential deposition

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