Understanding the Performance Increase of Catalysts Supported on N-Functionalized Carbon in PEMFC Catalyst Layers

Applying nitrogen-modified carbon support in PEMFCs has been attracting arising interest due to the resulting performance enhancement. In the present study, we attempt to uncover the origin and gain a deeper understanding of the different N-modification processes, whose influences are responsible fo...

Full description

Saved in:
Bibliographic Details
Published inJournal of the Electrochemical Society Vol. 169; no. 5; pp. 54520 - 54532
Main Authors Ott, Sebastian, Du, Fengmin, Luna, Mauricio Lopez, Dao, Tuan Anh, Cuenya, Beatriz Roldan, Orfanidi, Alin, Strasser, Peter
Format Journal Article
LanguageEnglish
Published IOP Publishing 01.05.2022
Online AccessGet full text

Cover

Loading…
More Information
Summary:Applying nitrogen-modified carbon support in PEMFCs has been attracting arising interest due to the resulting performance enhancement. In the present study, we attempt to uncover the origin and gain a deeper understanding of the different N-modification processes, whose influences are responsible for the performance improvement. By utilizing chemically modified Ketjenblack supports comprising altered fraction of N-functionalities, we investigate the underlying mechanism of the drastically reduced voltage losses under fuel cell operation conditions. In all, we demonstrate the key role of support modification induced by ammonia in strengthened support/ionomer interactions and alter physico-chemical properties of the carbon support contributing towards enhanced MEA performance. With the use of X-ray photoelectron spectroscopy (XPS), we show unambiguous evidences that not all N modified surfaces yield the desired performance increase. Rather, the latter depends on a complex interplay between different electrochemical parameter and catalyst properties. We want to emphasize the ionomer/support interaction as one important factor for enhanced ionomer distribution and present a prove of a direct interaction between the ionomers´ sidechains and N-functional groups of the support.
Bibliography:JES-105018.R2
ISSN:0013-4651
1945-7111
DOI:10.1149/1945-7111/ac6e4d