| Literature DB >> 26295523 |
Minhua Shao1, Amra Peles2, Krista Shoemaker1, Mallika Gummalla2, Peter N Njoki3, Jin Luo3, Chuan-Jian Zhong3.
Abstract
The increase in oxygen binding energy was previously proposed to account for the lower oxygen reduction activity of a Pt monolayer supported on Au(111) single crystal than that on Pd(111) and pure Pt(111) surfaces. This single-crystal based understanding, however, cannot explain the new finding of a 1.6-fold increase of oxygen reduction activity on Pt monolayer-modified 3-nm Au nanoparticles (Pt/Au/C) in comparison with that on Pt/Pd/C with a similar particle size. The Pt/Au/C catalyst also has an activity higher than that of a state-of-the-art 2.8-nm Pt/C catalyst. Our new experimental results and density functional theory calculations demonstrate that a significant compressive strain in the surface of the core nanoparticles plays a role in the observed activity enhancement.Entities:
Keywords: density functional theory; electrocatalyst; gold nanoparticle; oxygen reduction reaction; particle size effect; platinum monolayer; shape control
Year: 2010 PMID: 26295523 DOI: 10.1021/jz1015789
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475