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  Autocatalysis by the intermediate surface hydroxide formed during hydrogen peroxide reduction on silver electrodes

Doblhofer, K., Flätgen, G., Horswell, S. L., Pettinger, B., Wasle, S., & Weil, K. G. (2009). Autocatalysis by the intermediate surface hydroxide formed during hydrogen peroxide reduction on silver electrodes. Surface Science, 603(10-12), 1900-1903. doi:10.1016/j.susc.2008.11.047.

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 Creators:
Doblhofer, Karl1, Author           
Flätgen, Georg1, Author           
Horswell, Sarah L.1, Author           
Pettinger, Bruno1, Author           
Wasle, Sabine1, Author           
Weil, Konrad G.1, Author           
Affiliations:
1Physical Chemistry, Fritz Haber Institute, Max Planck Society, ou_634546              

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Free keywords: Models of non-equilibrium phenomena; Electrochemical methods; Surface chemical reactions; Hydrogen peroxide; Silver electrode
 Abstract: Recent electrochemical studies of the cathodic reduction of hydrogen peroxide (H2O2) on silver electrodes in acidic electrolyte (HClO4) revealed a novel autocatalytic reaction path. Adsorbed hydroxyl groups, OHad, were proposed to act as the catalyst. To gather further clarity about this mechanism, in particular about the presence and nature of the postulated adsorbate formed as an intermediate, constitute the autocatalytically active species. In order to obtain a clearer conception of the species OHad, in the present work surface science experiments on Ag(111) electrodes are evaluated. It is concluded that the species OHad is identical with the surfaceAgOH formed in alkaline solution as a relatively stable intermediate in the anodic oxidation of OH– to surface-Ag2O.

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Language(s): eng - English
 Dates: 2009-06-01
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 362557
DOI: 10.1016/j.susc.2008.11.047
 Degree: -

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Title: Surface Science
  Alternative Title : Surf. Sci.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 603 (10-12) Sequence Number: - Start / End Page: 1900 - 1903 Identifier: -