Improved Oxygen Reduction Activity on Pt 3 Ni(111) via Increased Surface Site Availability

Author:

Stamenkovic Vojislav R.1234,Fowler Ben1234,Mun Bongjin Simon1234,Wang Guofeng1234,Ross Philip N.1234,Lucas Christopher A.1234,Marković Nenad M.1234

Affiliation:

1. Materials Science Division, Argonne National Laboratory, Argonne, IL 60439, USA.

2. Materials Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720, USA.

3. Oliver Lodge Laboratory, Department of Physics, University of Liverpool, Liverpool, L69 7ZE, UK.

4. Department of Chemistry and Physics, University of South Carolina, Aiken, SC 29801, USA.

Abstract

The slow rate of the oxygen reduction reaction (ORR) in the polymer electrolyte membrane fuel cell (PEMFC) is the main limitation for automotive applications. We demonstrated that the Pt 3 Ni(111) surface is 10-fold more active for the ORR than the corresponding Pt(111) surface and 90-fold more active than the current state-of-the-art Pt/C catalysts for PEMFC. The Pt 3 Ni(111) surface has an unusual electronic structure ( d -band center position) and arrangement of surface atoms in the near-surface region. Under operating conditions relevant to fuel cells, its near-surface layer exhibits a highly structured compositional oscillation in the outermost and third layers, which are Pt-rich, and in the second atomic layer, which is Ni-rich. The weak interaction between the Pt surface atoms and nonreactive oxygenated species increases the number of active sites for O 2 adsorption.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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