On the importance of metal–oxide interface sites for the water–gas shift reaction over Pt/CeO2 catalysts

• Published in: Journal of catalysis 2014-01, Vol.309, p.314-324
• Main Authors: Aranifard, Sara, Ammal, Salai Cheettu, Heyden, Andreas
• Format: Article
• Language: English
• Subjects: Catalysis; Catalysts; Chemical bonds; Chemistry; DFT; Exact sciences and technology; General and physical chemistry; Interface reaction; Kinetics; Microkinetic modeling; Redox pathway; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Three-phase boundary; Water–gas shift reaction
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2013.10.012

[Display omitted] •WGS reaction on CeO2 (111)-supported Pt cluster follow both redox and associative carboxyl with redox regeneration mechanisms.•High activity of Pt/CeO2 interface sites originates from a significantly enhanced water activation and dissociation at interfacial oxygen vacancies.•First principles-based microkinetic modeling analysis provides insights on the unique activity of Pt/CeO2 interface. The mechanism of water–gas shift reaction at the three-phase boundary of Pt/CeO2 catalysts has been investigated using density functional theory and microkinetic modeling to better understand the importance of metal–oxide interface sites in heterogeneous catalysis. Analysis of a microkinetic model based on parameters obtained from first principles suggests that both the “Redox pathway” and the “Associative carboxyl pathway with redox regeneration” could operate on Pt/CeO2 catalysts. Although (1) only few interfacial Pt atoms are found to be catalytically active at low temperatures due to strong adsorption of CO and (2) interfacial O–H bond breakage is difficult due to the high reducibility of ceria, interface sites are 2–3 orders of magnitude more active than Pt (111) and stepped Pt surface sites and therefore effectively determine the overall activity of Pt/CeO2. The high activity of Pt/CeO2 interface sites originates from a significantly enhanced water activation and dissociation at interfacial oxygen vacancies.