Improved Oxygen Reduction Activity on Pt 3 Ni(111) via Increased Surface Site Availability
Author(s) -
Vojislav R. Stamenković,
Ben Fowler,
Bongjin Simon Mun,
Guofeng Wang,
Philip N. Ross,
C. A. Lucas,
Nenad M. Marković
Publication year - 2007
Publication title -
science
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1135941
Subject(s) - proton exchange membrane fuel cell , adsorption , electrolyte , oxygen , catalysis , active layer , layer (electronics) , materials science , surface layer , chemistry , chemical engineering , analytical chemistry (journal) , nanotechnology , electrode , organic chemistry , engineering , thin film transistor
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 Pt3Ni(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 Pt3Ni(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 O2 adsorption.
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