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Confined-space alloying of nanoparticles for the synthesis of efficient PtNi fuel-cell catalysts

MPG-Autoren
http://pubman.mpdl.mpg.de/cone/persons/resource/persons125037

Baldizzone,  Claudio
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons132869

Mezzavilla,  Stefano
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons125275

Meier,  Josef Christian
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons125382

Schuppert,  Anna Katharina
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons58560

Galeano Nuñez,  Diana Carolina
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons58985

Schüth,  Ferdi
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons125274

Mayrhofer,  Karl J. J.
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;

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Zitation

Baldizzone, C., Mezzavilla, S., Carvalho, H. W. P., Meier, J. C., Schuppert, A. K., Heggen, M., et al. (2014). Confined-space alloying of nanoparticles for the synthesis of efficient PtNi fuel-cell catalysts. Angewandte Chemie International Edition, 53(51), 14250-14254. doi:10.1002/anie.201406812.


Zitierlink: http://hdl.handle.net/11858/00-001M-0000-0024-C67C-B
Zusammenfassung
The efficiency of polymer electrolyte membrane fuel cells is strongly depending on the electrocatalyst performance, that is, its activity and stability. We have designed a catalyst material that combines both, the high activity for the decisive cathodic oxygen reduction reaction associated with nanoscale Pt alloys, and the excellent durability of an advanced nanostructured support. Owing to the high specific activity and large active surface area, the catalyst shows extraordinary mass activity values of 1.0 Amg Pt-1. Moreover, the material retains its initial active surface area and intrinsic activity during an extended accelerated aging test within the typical operation range. This excellent performance is achieved by confined-space alloying of the nanoparticles in a controlled manner in the pores of the support.