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  The Common Intermediates of Oxygen Evolution and Dissolution Reactions during Water Electrolysis on Iridium

Kasian, O., Grote, J.-P., Geiger, S., Cherevko, S., & Mayrhofer, K. J. J. (2018). The Common Intermediates of Oxygen Evolution and Dissolution Reactions during Water Electrolysis on Iridium. Angewandte Chemie International Edition, 57(9), 2488-2491. doi:10.1002/anie.201709652.

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 Creators:
Kasian, Olga1, Author           
Grote, Jan-Philipp1, Author           
Geiger, Simon1, Author           
Cherevko, Serhiy1, 2, Author           
Mayrhofer, Karl Johann Jakob1, 2, 3, Author           
Affiliations:
1Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society, ou_1863354              
2Helmholtz-Institute Erlangen-Nuremberg for Renewable Energy (IEK-11), Forschungszentrum Jülich, Egerlandstrasse 3, 91058 Erlangen, Germany, ou_persistent22              
3Department of Chemical and Biological Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany, ou_persistent22              

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Free keywords: Degradation; Dissolution; Electrolysis; Hydrogen; Inductively coupled plasma; Mass spectrometry; Oxygen; Photodegradation; Reaction intermediates, Catalyst degradation; Degradation products; Dissolution mechanism; Dissolution reactions; Electrochemical mass spectrometry; Oxygen evolution reaction; Reaction mechanism; Water electrolysis, Iridium
 Abstract: Understanding the pathways of catalyst degradation during the oxygen evolution reaction is a cornerstone in the development of efficient and stable electrolyzers, since even for the most promising Ir based anodes the harsh reaction conditions are detrimental. The dissolution mechanism is complex and the correlation to the oxygen evolution reaction itself is still poorly understood. Here, by coupling a scanning flow cell with inductively coupled plasma and online electrochemical mass spectrometers, we monitor the oxygen evolution and degradation products of Ir and Ir oxides in situ. It is shown that at high anodic potentials several dissolution routes become possible, including formation of gaseous IrO3. On the basis of experimental data, possible pathways are proposed for the oxygen-evolution-triggered dissolution of Ir and the role of common intermediates for these reactions is discussed. © 2018 The Authors. Published by Wiley-VCH Verlag GmbH Co. KGaA.

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Language(s): eng - English
 Dates: 2018-12-08
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.201709652
BibTex Citekey: Kasian20182488
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Title: Angewandte Chemie International Edition
  Other : Angew. Chem. Int. Ed.
  Other : Angewandte Chemie, International Edition
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 57 (9) Sequence Number: - Start / End Page: 2488 - 2491 Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851