Design criteria for stable Pt/C fuel cell catalysts

Platinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different st...

Full description

Bibliographic Details
Main Authors: Josef C. Meier, Carolina Galeano, Ioannis Katsounaros, Jonathon Witte, Hans J. Bongard, Angel A. Topalov, Claudio Baldizzone, Stefano Mezzavilla, Ferdi Schüth, Karl J. J. Mayrhofer
Format: Article
Language:English
Published: Beilstein-Institut 2014-01-01
Series:Beilstein Journal of Nanotechnology
Subjects:
Online Access:https://doi.org/10.3762/bjnano.5.5
_version_ 1819275446141845504
author Josef C. Meier
Carolina Galeano
Ioannis Katsounaros
Jonathon Witte
Hans J. Bongard
Angel A. Topalov
Claudio Baldizzone
Stefano Mezzavilla
Ferdi Schüth
Karl J. J. Mayrhofer
author_facet Josef C. Meier
Carolina Galeano
Ioannis Katsounaros
Jonathon Witte
Hans J. Bongard
Angel A. Topalov
Claudio Baldizzone
Stefano Mezzavilla
Ferdi Schüth
Karl J. J. Mayrhofer
author_sort Josef C. Meier
collection DOAJ
description Platinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different structural characteristics were investigated in depth: a conventional Pt/Vulcan catalyst with a particle size of 3–4 nm and two Pt@HGS catalysts with different particle size, 1–2 nm and 3–4 nm. Specifically, Pt@HGS corresponds to platinum nanoparticles incorporated and confined within the pore structure of the nanostructured carbon support, i.e., hollow graphitic spheres (HGS). All three materials are characterized by the same platinum loading, so that the differences in their performance can be correlated to the structural characteristics of each material. The comparison of the activity and stability behavior of the three catalysts, as obtained from thin film rotating disk electrode measurements and identical location electron microscopy, is also extended to commercial materials and used as a basis for a discussion of general fuel cell catalyst design principles. Namely, the effects of particle size, inter-particle distance, certain support characteristics and thermal treatment on the catalyst performance and in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested.
first_indexed 2024-12-23T23:24:27Z
format Article
id doaj.art-38900b9fb55a4927ad8171b87887893b
institution Directory Open Access Journal
issn 2190-4286
language English
last_indexed 2024-12-23T23:24:27Z
publishDate 2014-01-01
publisher Beilstein-Institut
record_format Article
series Beilstein Journal of Nanotechnology
spelling doaj.art-38900b9fb55a4927ad8171b87887893b2022-12-21T17:26:16ZengBeilstein-InstitutBeilstein Journal of Nanotechnology2190-42862014-01-0151446710.3762/bjnano.5.52190-4286-5-5Design criteria for stable Pt/C fuel cell catalystsJosef C. Meier0Carolina Galeano1Ioannis Katsounaros2Jonathon Witte3Hans J. Bongard4Angel A. Topalov5Claudio Baldizzone6Stefano Mezzavilla7Ferdi Schüth8Karl J. J. Mayrhofer9Department of Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Strasse 1, 40237 Düsseldorf, GermanyDepartment of Heterogeneous Catalysis, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, GermanyDepartment of Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Strasse 1, 40237 Düsseldorf, GermanyDepartment of Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Strasse 1, 40237 Düsseldorf, GermanyDepartment of Heterogeneous Catalysis, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, GermanyDepartment of Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Strasse 1, 40237 Düsseldorf, GermanyDepartment of Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Strasse 1, 40237 Düsseldorf, GermanyDepartment of Heterogeneous Catalysis, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, GermanyDepartment of Heterogeneous Catalysis, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, GermanyDepartment of Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Strasse 1, 40237 Düsseldorf, GermanyPlatinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different structural characteristics were investigated in depth: a conventional Pt/Vulcan catalyst with a particle size of 3–4 nm and two Pt@HGS catalysts with different particle size, 1–2 nm and 3–4 nm. Specifically, Pt@HGS corresponds to platinum nanoparticles incorporated and confined within the pore structure of the nanostructured carbon support, i.e., hollow graphitic spheres (HGS). All three materials are characterized by the same platinum loading, so that the differences in their performance can be correlated to the structural characteristics of each material. The comparison of the activity and stability behavior of the three catalysts, as obtained from thin film rotating disk electrode measurements and identical location electron microscopy, is also extended to commercial materials and used as a basis for a discussion of general fuel cell catalyst design principles. Namely, the effects of particle size, inter-particle distance, certain support characteristics and thermal treatment on the catalyst performance and in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested.https://doi.org/10.3762/bjnano.5.5catalyst design criteriadegradation mechanismsfuel cell catalystnanoparticlesstability
spellingShingle Josef C. Meier
Carolina Galeano
Ioannis Katsounaros
Jonathon Witte
Hans J. Bongard
Angel A. Topalov
Claudio Baldizzone
Stefano Mezzavilla
Ferdi Schüth
Karl J. J. Mayrhofer
Design criteria for stable Pt/C fuel cell catalysts
Beilstein Journal of Nanotechnology
catalyst design criteria
degradation mechanisms
fuel cell catalyst
nanoparticles
stability
title Design criteria for stable Pt/C fuel cell catalysts
title_full Design criteria for stable Pt/C fuel cell catalysts
title_fullStr Design criteria for stable Pt/C fuel cell catalysts
title_full_unstemmed Design criteria for stable Pt/C fuel cell catalysts
title_short Design criteria for stable Pt/C fuel cell catalysts
title_sort design criteria for stable pt c fuel cell catalysts
topic catalyst design criteria
degradation mechanisms
fuel cell catalyst
nanoparticles
stability
url https://doi.org/10.3762/bjnano.5.5
work_keys_str_mv AT josefcmeier designcriteriaforstableptcfuelcellcatalysts
AT carolinagaleano designcriteriaforstableptcfuelcellcatalysts
AT ioanniskatsounaros designcriteriaforstableptcfuelcellcatalysts
AT jonathonwitte designcriteriaforstableptcfuelcellcatalysts
AT hansjbongard designcriteriaforstableptcfuelcellcatalysts
AT angelatopalov designcriteriaforstableptcfuelcellcatalysts
AT claudiobaldizzone designcriteriaforstableptcfuelcellcatalysts
AT stefanomezzavilla designcriteriaforstableptcfuelcellcatalysts
AT ferdischuth designcriteriaforstableptcfuelcellcatalysts
AT karljjmayrhofer designcriteriaforstableptcfuelcellcatalysts