Tuning Single‐atom Pt1−CeO2 Catalyst for Efficient CO and C3H6 Oxidation: Size Effect of Ceria on Pt Structural Evolution

Abstract

AbstractTo reveal the effect of ceria particle size on dispersion and structure of supported Pt catalysts during preparation, activation, and reaction testing, a unique CeO2/Al2O3 support (CA−c) with smaller CeO2 particle size and more surface defects was prepared using a colloidal CeO2 precursor, comparing with a conventional CeO2/Al2O3 support (CA−n) using cerium nitrate as precursor. More atomically dispersed Pt and abundant Pt−O−Ce structures were observed in the Pt/CA−c catalyst than in the Pt/CA−n catalyst. Both parent catalysts received significant enhancement on their catalytic CO oxidation activities if activated by 10% hydrogen at 400 °C before reaction. Between the two representative catalysts, the extent of activity enhancement upon activation was more pronounced for Pt/CA−c. We found that smaller Pt clusters with more active ionic Pt sites were generated on the activated Pt/CA−c catalyst, while agglomerated larger Pt particles with more metallic sites were formed on the activated Pt/CA−n. The facile formation of Ce3+ was also indicative of more active metal‐support interfaces in the activated Pt/CA−c catalyst. These results highlight the importance of regulating ceria support particles to enable a controlled anchoring and subsequent activation of Pt single atoms for low‐temperature CO oxidation reaction.