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Electrocatalytic Properties of Mixed-Oxide-Containing Composite-Supported Platinum for Polymer Electrolyte Membrane (PEM) Fuel Cells.

Authors :
Ayyubov I
Tálas E
Salmanzade K
Kuncser A
Pászti Z
Neațu Ș
Mirea AG
Florea M
Tompos A
Borbáth I
Source :
Materials (Basel, Switzerland) [Materials (Basel)] 2022 May 20; Vol. 15 (10). Date of Electronic Publication: 2022 May 20.
Publication Year :
2022

Abstract

TiO <subscript>2</subscript> -based mixed oxide-carbon composite supports have been suggested to provide enhanced stability for platinum (Pt) electrocatalysts in polymer electrolyte membrane (PEM) fuel cells. The addition of molybdenum (Mo) to the mixed oxide is known to increase the CO tolerance of the electrocatalyst. In this work Pt catalysts, supported on Ti <subscript>1-x</subscript> Mo <subscript>x</subscript> O <subscript>2</subscript> -C composites with a 25/75 oxide/carbon mass ratio and prepared from different carbon materials (C: Vulcan XC-72, unmodified and functionalized Black Pearls 2000), were compared in the hydrogen oxidation reaction (HOR) and in the oxygen reduction reaction (ORR) with a commercial Pt/C reference catalyst in order to assess the influence of the support on the electrocatalytic behavior. Our aim was to perform electrochemical studies in preparation for fuel cell tests. The ORR kinetic parameters from the Koutecky-Levich plot suggested a four-electron transfer per oxygen molecule, resulting in H <subscript>2</subscript> O. The similarity between the Tafel slopes suggested the same reaction mechanism for electrocatalysts supported by these composites. The HOR activity of the composite-supported electrocatalysts was independent of the type of carbonaceous material. A noticeable difference in the stability of the catalysts appeared only after 5000 polarization cycles; the Black Pearl-containing sample showed the highest stability.

Details

Language :
English
ISSN :
1996-1944
Volume :
15
Issue :
10
Database :
MEDLINE
Journal :
Materials (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
35629708
Full Text :
https://doi.org/10.3390/ma15103671