TU Darmstadt / ULB / TUbiblio

Synthesis and characterisation of ternary Pt/Ru/Mo catalysts for the anode of the PEM fuel cell

Benker, Nathalie ; Roth, Christina ; Mazurek, Marian ; Fuess, Hartmut (2006)
Synthesis and characterisation of ternary Pt/Ru/Mo catalysts for the anode of the PEM fuel cell.
In: Journal of new materials for electrochemical systems, 9 (2)
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

Miscellaneous compositions of carbon-supported Pt/Ru/Mo catalysts were synthesised via reductive precipitation using hydrazine. The precipitation of the different Pt/Ru/Mo catalysts was carried out with H2PtCl6, RuCl3 and Mo(CO)6 as precursors for synthesis I and (NH4)6Mo7O24 for synthesis II. The home-made catalysts were structurally characterised with different methods before and after electrochemical investigation in a membrane fuel cell. Furthermore cyclic voltammetry was perfomed to determine the catalytic activity of the different Pt/Ru/Mo catalysts. X-ray fluorescence analysis (XFA), X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDXS) demonstrate that the precursor used in synthesis I is not adequate for the preparation of ternary Pt/Ru/Mo catalysts. Transmission electron microscopy (TEM) images of the differently prepared catalysts show the formation of 20 nm agglomerates composed of 2-3 nm crystallites, which separate into individual nanoparticles during fuel cell operation. The particle size was determined with TEM and X-ray diffraction (XRD), and is independent of the Pt/Ru/Mo ratio. No significant particle growth is observed after operation.

Typ des Eintrags: Artikel
Erschienen: 2006
Autor(en): Benker, Nathalie ; Roth, Christina ; Mazurek, Marian ; Fuess, Hartmut
Art des Eintrags: Bibliographie
Titel: Synthesis and characterisation of ternary Pt/Ru/Mo catalysts for the anode of the PEM fuel cell
Sprache: Englisch
Publikationsjahr: April 2006
Verlag: ECOLE POLYTECHNIQUE MONTREAL, C P 6079, SUCC CENTRE-VILLE, MONTREAL, PQ H3C 3A7, CANADA
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Journal of new materials for electrochemical systems
Jahrgang/Volume einer Zeitschrift: 9
(Heft-)Nummer: 2
Kurzbeschreibung (Abstract):

Miscellaneous compositions of carbon-supported Pt/Ru/Mo catalysts were synthesised via reductive precipitation using hydrazine. The precipitation of the different Pt/Ru/Mo catalysts was carried out with H2PtCl6, RuCl3 and Mo(CO)6 as precursors for synthesis I and (NH4)6Mo7O24 for synthesis II. The home-made catalysts were structurally characterised with different methods before and after electrochemical investigation in a membrane fuel cell. Furthermore cyclic voltammetry was perfomed to determine the catalytic activity of the different Pt/Ru/Mo catalysts. X-ray fluorescence analysis (XFA), X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDXS) demonstrate that the precursor used in synthesis I is not adequate for the preparation of ternary Pt/Ru/Mo catalysts. Transmission electron microscopy (TEM) images of the differently prepared catalysts show the formation of 20 nm agglomerates composed of 2-3 nm crystallites, which separate into individual nanoparticles during fuel cell operation. The particle size was determined with TEM and X-ray diffraction (XRD), and is independent of the Pt/Ru/Mo ratio. No significant particle growth is observed after operation.

Freie Schlagworte: Platinum, Ruthenium, Molybdenum, PEMFC, FC Anode, TEM, XRD, Electrocatalysis
Fachbereich(e)/-gebiet(e): 11 Fachbereich Material- und Geowissenschaften
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Erneuerbare Energien
11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Strukturforschung
Hinterlegungsdatum: 20 Nov 2008 08:25
Letzte Änderung: 20 Feb 2020 13:23
PPN:
Sponsoren: Financial support of the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie is gratefully acknowledged.
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