The structure and electronic effects of ZIF-8 and ZIF-67 supported Pt catalysts for crotonaldehyde selective hydrogenation

Metal organic frameworks (MOFs) have been applied to stabilize metal nanoparticles due to their excellent properties, but there are many different viewpoints about the interaction between MOF and nanoparticles, which...

Atomic level fluxional behavior and activity of CeO2-supported Pt catalysts for CO oxidation

Reducible oxides are widely used catalyst supports that can increase oxidation reaction rates by transferring lattice oxygen at the metal-support interface. There are many outstanding questions regarding the atomic-scale dynamic meta-stability (i.e., fluxional behavior) of the interface during catalysis. Here, we employ aberration-corrected operando electron microscopy to visualize the structural dynamics occurring at and near Pt/CeO2 interfaces during CO oxidation. We show that the catalytic turnover frequency correlates with fluxional behavior that (a) destabilizes the supported Pt particle, (b) marks an enhanced rate of oxygen vacancy creation and annihilation, and (c) leads to increased strain and reduction in the CeO2 support surface. Overall, the results implicate the interfacial Pt-O-Ce bonds anchoring the Pt to the support as being involved also in the catalytically-driven oxygen transfer process, and they suggest that oxygen reduction takes place on the highly reduced CeO2 surface before migrating to the interfacial perimeter for reaction with CO.

Reduction of NOx by H2 on WOx-Promoted Pt/Al2O3/SiO2 Catalysts Under O2-Rich Conditions

This work addresses the reduction of NOx by H2 under O2-rich conditions using Al2O3/SiO2-supported Pt catalysts with different loads of WOx promotor. The samples were thoroughly characterised by N2 physisorption, temperature-programmed desorption of CO, scanning electron microscopy, X-ray diffraction, laser raman spectroscopy, X-ray photoelectron spectroscopy and diffuse reflectance infrared fourier transform spectroscopy with probe molecule CO. The catalytic studies of the samples without WOx showed pronounced NOx conversion below 200 °C, whereas highest efficiency was related to small Pt particles. The introduction of WOx provided increasing deNOx activity as well as N2 selectivity. This promoting effect was referred to an additional reaction path at the Pt-WOx/Al2O3/SiO2 interface, whereas an electronic activation of Pt by strong metal support interaction was excluded. Graphic Abstract