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  3. The colloidal tool-box approach for fuel cell catalysts: Systematic study of perfluorosulfonate-ionomer impregnation and Pt loading
 

The colloidal tool-box approach for fuel cell catalysts: Systematic study of perfluorosulfonate-ionomer impregnation and Pt loading

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BORIS DOI
10.7892/boris.81567
Date of Publication
March 2016
Publication Type
Article
Division/Institute

Departement für Chemi...

Author
Speder, Jozsef
Zana, Alessandro
Arenz, Matthiasorcid-logo
Departement für Chemie und Biochemie (DCB)
Subject(s)

500 - Science::570 - ...

500 - Science::540 - ...

Series
Catalysis today
ISSN or ISBN (if monograph)
0920-5861
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.cattod.2015.09.021
Description
In this study, the correlation between the impregnation of proton exchange membrane fuel cell catalysts with perfluorosulfonate-ionomer (PFSI) and its electrochemical and electrocatalytic properties is investigated for different Pt loadings and carbon supports using a rotating-disk electrode (RDE) setup. We concentrate on its influence on the electrochemical surface area (ECSA) and the oxygen reduction reaction (ORR) activity. For this purpose, platinum (Pt) nanoparticles are prepared via a colloidal based preparation route and supported on three different carbon supports. Based on RDE experiments, we show that the ionomer has an influence both on the Pt utilization and the apparent kinetic current density of ORR. The experimental data reveal a strong interaction in the microstructure between the electrochemical properties and the surface properties of the carbon supports, metal loading and ionomer content. This study demonstrates that the colloidal synthesis approach offers interesting potential for systematic studies for the optimization of fuel cell catalysts.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/141627
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
1-s2.0-S0920586115005957-main.pdftextAdobe PDF1.67 MBpublisherpublished restricted
speder et al. final.pdftextAdobe PDF1.05 MBAttribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0)acceptedOpen
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