Stability of metallo-porphyrin networks under oxygen reduction and evolution conditions in alkaline media
- authored by
- 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.
- External Organisation(s)
-
Max Planck Institute for Solid State Research (MPI-FKF)
Technische Universität Braunschweig
École polytechnique fédérale de Lausanne (EPFL)
Paul Scherrer Institut (PSI)
ETH Zurich
Universidad Nacional de La Plata
- Type
- Article
- Journal
- Physical Chemistry Chemical Physics
- Volume
- 21
- Pages
- 2587-2594
- No. of pages
- 8
- ISSN
- 1463-9076
- Publication date
- 2019
- Publication status
- Published
- Peer reviewed
- Yes
- ASJC Scopus subject areas
- General Physics and Astronomy, Physical and Theoretical Chemistry
- Electronic version(s)
-
https://doi.org/10.1039/c8cp07463a (Access:
Open)