Agglomerative Sintering of an Atomically Dispersed Ir1/Zeolite Y Catalyst: Compelling Evidence Against Ostwald Ripening but for Bimolecular and Autocatalytic Agglomeration Catalyst Sintering Steps

Agglomerative sintering of an atomically dispersed, zeolite Y-supported catalyst, Ir1/zeolite Y, formed initially from the well-characterized precatalyst [Ir­(C2H4)2]/zeolite Y and in the presence of liquid-phase reactants, was monitored over three cycles of 3800 turnovers (TTOs) of cyclohexene hydrogenation at 72 °C. The catalyst evolved and sintered during each cycle, even at the relatively mild temperature of 72 °C in the presence of the cyclohexene plus H2 reactants and cyclohexane solvent. Post each of the three cycles of catalysis, the resultant sintered catalyst was characterized by extended X-ray absorption fine structure spectroscopy and atomic-resolution high-angle annular dark-field scanning transmission electron microscopy. The results show that higher-nuclearity iridium species, Ir n , are formed during each successive cycle. The progression from the starting mononuclear precursor, Ir1, is first to Ir∼4–6; then, on average, Ir∼40; and finally, on average, Ir∼70, the latter more accurately described as a bimodal dispersion of on-average Ir∼40–50 and on-average Ir∼1600 nanoparticles. The size distribution and other data disprove Ostwald ripening during the initial and final stages of the observed catalyst sintering. Instead, the diameter-dispersion data plus quantitative fits to the cluster or nanoparticle diameter vs time data provide compelling evidence for the underlying, pseudoelementary steps of bimolecular agglomeration, B + B → C, and autocatalytic agglomeration, B + C → 1.5C, where B represents the smaller, formally Ir(0) nanoparticles, and C is the larger (more highly agglomerated) nanoparticles (and where the 1.5 coefficient in the autocatalytic agglomeration of B + C necessarily follows from the definition, in the bimolecular agglomeration step, that 1C contains the Ir from 2B). These two specific, balanced chemical reactions are of considerable significance in going beyond the present state-of-the-art, but word-only, “mechanism”that is, actually and instead, just a collection of phenomenafor catalyst sintering of “Particle Migration and Coalescence”. The steps of bimolecular plus autocatalytic agglomeration provide two specific, balanced chemical equations useful for fitting sintering kinetics data, as is done herein, thereby quantitatively testing proposed sintering mechanisms. These two pseudoelementary reactions also define the specific words and concepts for sintering of bimolecular agglomeration and autocatalytic agglomeration