Langmuir · 2005 · 58 citations · 12 references
Natural SciencesChemistryMaterials ScienceCatalysisNanomaterialsSurface ScienceCatalysis At SurfacesCatalytic MaterialsCatalytic MechanismsSupported CatalystsSurface CatalysisSurface Functionalization Of NanomaterialsActivation TreatmentCatalytic ActivityCo OxidationDendrimersNanoparticle CatalysisNanoparticlesOxidation CatalysisOxidation Treatment
Surface immobilized polyamidoamine (PAMAM) dendrimer templated Pt nanoparticles were employed as precursors to heterogeneous catalysts. CO oxidation catalysis and in situ infrared spectroscopy were used to evaluate conditions for dendrimer removal. Infrared spectroscopy showed that PAMAM dendrimer amide bonds begin decomposing at temperatures as low as 75 degrees C. Although the amide stretches are completely removed after 3 h of oxidation at 300 degrees C, 16 h were required to reach maximum catalytic activity. Further treatment under oxidizing or reducing atmospheres did not cause substantial changes in activity. Infrared spectroscopy of the activated materials indicated that organic residues, probably surface carboxylates, are formed during oxidation. These surface species passivate the Pt NPs, and their removal was required to fully activate the catalyst. Substantially less forcing activation conditions were possible by employing a CO/O(2)/He oxidation treatment. At appropriate temperatures, CO acts as a protecting group for the Pt surface, helping to prevent fouling of the nanoparticle by organic residues. CO oxidation catalysis and infrared spectroscopy of adsorbed CO indicated that the low temperature activation treatment yielded supported nanoparticles that were substantially similar to those prepared with more forcing conditions.
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Mechanisms of catalyst deactivation
Calvin H. Bartholomew · Applied Catalysis A General · 2001 · 3K citations
Pio Forzatti · Catalysis Today · 1999 · 778 citations