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Issue 6, 2017
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A combined UHV-STM-flow cell set-up for electrochemical/electrocatalytic studies of structurally well-defined UHV prepared model electrodes

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Abstract

We describe the construction and discuss the performance of a novel combined ultrahigh vacuum (UHV)-electrochemistry set-up, allowing the controlled preparation and structural characterization of complex nanostructured electrode surfaces by high resolution scanning tunnelling microscopy (STM) under UHV conditions on the one hand and, after electrode transfer under clean conditions, electrochemical measurements under continuous, controlled electrolyte mass transport conditions on the other. Electrochemical measurements can be coupled with online product detection, either using an additional collector electrode or by differential electrochemical mass spectrometry (DEMS). The potential of the set-up will be illustrated in two electrocatalytic reactions on complex, but structurally well-defined bimetallic electrode surfaces, O2 reduction on PtxAg1−x/Pt(111) monolayer surface alloys and bulk CO oxidation on Pt monolayer island modified Ru(0001) electrodes. We will particularly demonstrate the importance of structural characterization after the electrochemical measurements for identifying structural modifications induced by the electrochemical environment and thus avoiding misleading conclusions about the structure–activity relationships.

Graphical abstract: A combined UHV-STM-flow cell set-up for electrochemical/electrocatalytic studies of structurally well-defined UHV prepared model electrodes

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The article was received on 01 Sep 2016, accepted on 21 Sep 2016 and first published on 21 Sep 2016


Article type: Paper
DOI: 10.1039/C6CP06051J
Citation: Phys. Chem. Chem. Phys., 2017,19, 4166-4178
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    A combined UHV-STM-flow cell set-up for electrochemical/electrocatalytic studies of structurally well-defined UHV prepared model electrodes

    J. Schnaidt, S. Beckord, A. K. Engstfeld, J. Klein, S. Brimaud and R. J. Behm, Phys. Chem. Chem. Phys., 2017, 19, 4166
    DOI: 10.1039/C6CP06051J

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