Stability of metallo-porphyrin networks under oxygen reduction and evolution conditions in alkaline media
- verfasst von
- Diana Hötger, Markus Etzkorn, Claudius Morchutt, Benjamin Wurster, Jan Dreiser, Sebastian Stepanow, Doris Grumelli, Rico Gutzler, Klaus Kern
- Abstract
Transition metal atoms stabilised by organic ligands or as oxides exhibit promising catalytic activity for the electrocatalytic reduction and evolution of oxygen. Built-up from earth-abundant elements, they offer affordable alternatives to precious-metal based catalysts for application in fuel cells and electrolysers. For the understanding of a catalyst's activity, insight into its structure on the atomic scale is of highest importance, yet commonly challenging to experimentally access. Here, the structural integrity of a bimetallic iron tetrapyridylporphyrin with co-adsorbed cobalt electrocatalyst on Au(111) is investigated using scanning tunneling microscopy and X-ray absorption spectroscopy. Topographic and spectroscopic characterization reveals structural changes of the molecular coordination network after oxygen reduction, and its decomposition and transformation into catalytically active Co/Fe (oxyhydr)oxide during oxygen evolution. The data establishes a structure-property relationship for the catalyst as a function of electrochemical potential and, in addition, highlights how the reaction direction of electrochemical interconversion between molecular oxygen and hydroxyl anions can have very different effects on the catalyst's structure.
- Externe Organisation(en)
-
Max-Planck-Institut für Festkörperforschung
Technische Universität Braunschweig
Eidgenössische Technische Hochschule Lausanne (ETHL)
Paul Scherrer Institut (PSI)
ETH Zürich
Universidad Nacional de La Plata
- Typ
- Artikel
- Journal
- Physical Chemistry Chemical Physics
- Band
- 21
- Seiten
- 2587-2594
- Anzahl der Seiten
- 8
- ISSN
- 1463-9076
- Publikationsdatum
- 2019
- Publikationsstatus
- Veröffentlicht
- Peer-reviewed
- Ja
- ASJC Scopus Sachgebiete
- Allgemeine Physik und Astronomie, Physikalische und Theoretische Chemie
- Elektronische Version(en)
-
https://doi.org/10.1039/c8cp07463a (Zugang:
Offen)