Abstract
In many heterogeneous catalysts, the interaction of metal particles with their oxide support can alter the electronic properties of the metal and can play a critical role in determining particle morphology and maintaining dispersion. We used a combination of ultrahigh magnetic field, solid-state magic-angle spinning nuclear magnetic resonance spectroscopy, and high-angle annular dark-field scanning transmission electron microscopy coupled with density functional theory calculations to reveal the nature of anchoring sites of a catalytically active phase of platinum on the surface of a γ-Al 2O3 catalyst support material. The results obtained show that coordinatively unsaturated pentacoordinate Al3+ (AL 3+Penta) centers present on the (100) facets of the Y-Al2O3 surface are anchoring Pt. At low loadings, the active catalytic phase is ato mica Hy dispersed on the support surface (Pt/Al3+peta = 1), whereas two-dimensional Pt rafts form at higher coverages.
Original language | English |
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Pages (from-to) | 1670-1673 |
Number of pages | 4 |
Journal | Science |
Volume | 325 |
Issue number | 5948 |
DOIs | |
State | Published - 2009 |