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 |
|---|---|
| Pages (from-to) | 1670-1673 |
| Number of pages | 4 |
| Journal | Science |
| Volume | 325 |
| Issue number | 5948 |
| DOIs | |
| State | Published - 2009 |