| Literature DB >> 31570820 |
Sebastian Ott1, Alin Orfanidi2, Henrike Schmies1, Björn Anke3, Hong Nhan Nong1,4, Jessica Hübner1, Ulrich Gernert5, Manuel Gliech1, Martin Lerch3, Peter Strasser6.
Abstract
The reduction of Pt content in the cathode for proton exchange membrane fuel cells is highly desirable to lower their costs. However, lowering the Pt loading of the cathodic electrode leads to high voltage losses. These voltage losses are known to originate from the mass transport resistance of O2 through the platinum-ionomer interface, the location of the Pt particle with respect to the carbon support and the supports' structures. In this study, we present a new Pt catalyst/support design that substantially reduces local oxygen-related mass transport resistance. The use of chemically modified carbon supports with tailored porosity enabled controlled deposition of Pt nanoparticles on the outer and inner surface of the support particles. This resulted in an unprecedented uniform coverage of the ionomer over the high surface-area carbon supports, especially under dry operating conditions. Consequently, the present catalyst design exhibits previously unachieved fuel cell power densities in addition to high stability under voltage cycling. Thanks to the Coulombic interaction between the ionomer and N groups on the carbon support, homogeneous ionomer distribution and reproducibility during ink manufacturing process is ensured.Entities:
Year: 2019 PMID: 31570820 DOI: 10.1038/s41563-019-0487-0
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841