New method for analysis of nanoparticle geometry in supported fee metal catalysts with scanning transmission electron microscopy

To apply the knowledge of reaction mechanisms of heterogeneously catalyzed reactions on the atomic scale to supported catalyst systems, a detailed description of the structure of active particles on the atomic scale is required. In this article, a method is developed to construct atomic-scale geometric models for supported active fee metal nanoparticles, based on a measurement of particle sizes and particle volumes by Scanning Transmission Electron Microscopy (STEM) and the M-M coordination number determined from EXAFS. The method is applied to supported Au/TiO2, Au/MgAl2O4-, and Au/Al2O3 catalysts. These geometric models allow for estimation of geometric properties, such as specific Au surface area, metal-support contact perimeter, metal-Support contact surface area, edge length, and number of Au atoms located at the corners of the particles, with an error on the order of 20%. In the three catalysts studied here we find that the Au particles in the Al2O3 supported catalyst are small. The Au particles in the Au/TiO2 catalyst are smaller in diameter than those for the Au/MgAl2O4, but also thicker. The differences in particle size and shape seem to reflect the differences in the metal-support interface energy in the three catalyst systems.