Journal
ACS CATALYSIS
Volume 6, Issue 4, Pages 2642-2653Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b02722
Keywords
surface functionalization; graphene; metal-support interaction; catalyst durability; oxygen reduction reaction; PEMFC
Categories
Funding
- U.S. Department of Energy-Basic Energy Sciences
- Canadian Light Source
- University of Washington
- Advanced Photon Source
- U.S. DOE [DE-AC02-06CH11357]
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The enhancement of Pt nanoparticle anchoring strength and dispersion on carbon supports is highly desirable in polymer electrolyte membrane fuel cells (PEMFCs) as well as in other catalysis processes. Presented here is a comprehensive study of the interaction between catalyst nanoparticles and carbon supports in terms of the electronic structure change and its effects on the electrocatalytic performance of supported catalysts. Graphene was chosen as an ideal model support because the unique 2-D structure allows the direct investigation of the interaction with supported metal nanoparticles at their interface. We developed a facile strategy to covalently graft p-phenyl SO3H or p-phenyl NH2-groups onto the graphene surface. The functional groups were found to not only facilitate the homogeneous distribution of Pt nanoparticles on the surface of graphene supports and reduce the Pt average particle size but also strengthen the interaction of the Pt atoms with the functional groups and, consequently, minimize the migration/coalescence of the Pt nanoparticles in the course of accelerated durability tests. The experimental results from both X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) demonstrate the electron density shift from Pt to graphene supports with the strength of the Pt graphene interaction following the trend of Pt/p-phenyl NH2-graphene > Pt/p-phenyl SO3H-graphene > Pt/graphene. This study will shed light on strategies to improve not only the durability but also the activity of the metal nanoparticles via the functionalization of the catalyst supports in the catalysis field.
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