TU Darmstadt / ULB / TUbiblio

Time-resolved potential-induced changes in Fe/N/C-catalysts studied by in situ modulation excitation x-ray absorption spectroscopy

Ebner, Kathrin ; Clark, Adam H. ; Saveleva, Viktoriia A. ; Smolentsev, Grigory ; Chen, Jingfeng ; Ni, Lingmei ; Zitolo, Andrea ; Jaouen, Frédéric ; Kramm, Ulrike I. ; Schmidt, Thomas J. ; Herranz, Juan (2022)
Time-resolved potential-induced changes in Fe/N/C-catalysts studied by in situ modulation excitation x-ray absorption spectroscopy.
In: Advanced Energy Materials, 12 (14)
doi: 10.1002/aenm.202103699
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

To advance the widespread implementation of electrochemical energy storage and conversion technologies, the development of inexpensive electrocatalysts is imperative. In this context, Fe/N/C-materials represent a promising alternative to the costly noble metals currently used to catalyze the oxygen reduction reaction (ORR), and also display encouraging activities for the reduction of CO2. Nevertheless, the application of these materials in commercial devices requires further improvements in their performance and stability that are currently hindered by a lack of understanding of the nature of their active sites and the associated catalytic mechanisms. With this motivation, herein the authors exploit the high sensitivity of modulation excitation X-ray absorption spectroscopy toward species undergoing potential-induced changes to elucidate the operando local geometry of the active sites in two sorts of Fe/N/C-catalysts. While the ligand environment of a part of both materials' sites appears to change from six-/five- to fourfold coordination upon potential decrease, they differ substantially when it comes to the geometry of the coordination sphere, with the more ORR-active material undergoing more pronounced restructuring. Furthermore, these time-resolved spectroscopic measurements yield unprecedented insights into the kinetics of Fe-based molecular sites' structural reorganization, identifying the oxidation of iron as a rate-limiting process for the less ORR-active catalyst.

Typ des Eintrags: Artikel
Erschienen: 2022
Autor(en): Ebner, Kathrin ; Clark, Adam H. ; Saveleva, Viktoriia A. ; Smolentsev, Grigory ; Chen, Jingfeng ; Ni, Lingmei ; Zitolo, Andrea ; Jaouen, Frédéric ; Kramm, Ulrike I. ; Schmidt, Thomas J. ; Herranz, Juan
Art des Eintrags: Bibliographie
Titel: Time-resolved potential-induced changes in Fe/N/C-catalysts studied by in situ modulation excitation x-ray absorption spectroscopy
Sprache: Englisch
Publikationsjahr: April 2022
Verlag: Wiley-VCH
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Advanced Energy Materials
Jahrgang/Volume einer Zeitschrift: 12
(Heft-)Nummer: 14
DOI: 10.1002/aenm.202103699
Kurzbeschreibung (Abstract):

To advance the widespread implementation of electrochemical energy storage and conversion technologies, the development of inexpensive electrocatalysts is imperative. In this context, Fe/N/C-materials represent a promising alternative to the costly noble metals currently used to catalyze the oxygen reduction reaction (ORR), and also display encouraging activities for the reduction of CO2. Nevertheless, the application of these materials in commercial devices requires further improvements in their performance and stability that are currently hindered by a lack of understanding of the nature of their active sites and the associated catalytic mechanisms. With this motivation, herein the authors exploit the high sensitivity of modulation excitation X-ray absorption spectroscopy toward species undergoing potential-induced changes to elucidate the operando local geometry of the active sites in two sorts of Fe/N/C-catalysts. While the ligand environment of a part of both materials' sites appears to change from six-/five- to fourfold coordination upon potential decrease, they differ substantially when it comes to the geometry of the coordination sphere, with the more ORR-active material undergoing more pronounced restructuring. Furthermore, these time-resolved spectroscopic measurements yield unprecedented insights into the kinetics of Fe-based molecular sites' structural reorganization, identifying the oxidation of iron as a rate-limiting process for the less ORR-active catalyst.

ID-Nummer: Artikel-ID: 2103699
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Anorganische Chemie > Fachgruppe Katalysatoren und Elektrokatalysatoren
07 Fachbereich Chemie
07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Anorganische Chemie
07 Fachbereich Chemie > Eduard Zintl-Institut
Hinterlegungsdatum: 07 Mai 2024 06:05
Letzte Änderung: 07 Mai 2024 08:59
PPN: 517915359
Export:
Suche nach Titel in: TUfind oder in Google
Frage zum Eintrag Frage zum Eintrag

Optionen (nur für Redakteure)
Redaktionelle Details anzeigen Redaktionelle Details anzeigen