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Partial PdAu nanoparticle embedding into TiO 2 support accentuates catalytic contributions from the Au/TiO 2 interface.

Authors :
Lim KRG
Kaiser SK
Herring CJ
Kim TS
Perich MP
Garg S
O'Connor CR
Aizenberg M
van der Hoeven JES
Reece C
Montemore MM
Aizenberg J
Source :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2025 Jan 14; Vol. 122 (2), pp. e2422628122. Date of Electronic Publication: 2025 Jan 09.
Publication Year :
2025

Abstract

Despite the broad catalytic relevance of metal-support interfaces, controlling their chemical nature, the interfacial contact perimeter (exposed to reactants), and consequently, their contributions to overall catalytic reactivity, remains challenging, as the nanoparticle and support characteristics are interdependent when catalysts are prepared by impregnation. Here, we decoupled both characteristics by using a raspberry-colloid-templating strategy that yields partially embedded PdAu nanoparticles within well-defined SiO <subscript>2</subscript> or TiO <subscript>2</subscript> supports, thereby increasing the metal-support interfacial contact compared to nonembedded catalysts that we prepared by attaching the same nanoparticles onto support surfaces. Between nonembedded PdAu/SiO <subscript>2</subscript> and PdAu/TiO <subscript>2</subscript> , we identified a support effect resulting in a 1.4-fold higher activity of PdAu/TiO <subscript>2</subscript> than PdAu/SiO <subscript>2</subscript> for benzaldehyde hydrogenation. Notably, partial nanoparticle embedding in the TiO <subscript>2</subscript> raspberry-colloid-templated support increased the metal-support interfacial perimeter and consequently, the number of Au/TiO <subscript>2</subscript> interfacial sites by 5.4-fold, which further enhanced the activity of PdAu/TiO <subscript>2</subscript> by an additional 4.1-fold. Theoretical calculations and in situ surface-sensitive desorption analyses reveal facile benzaldehyde binding at the Au/TiO <subscript>2</subscript> interface and at Pd ensembles on the nanoparticle surface, explaining the connection between the number of Au/TiO <subscript>2</subscript> interfacial sites (via the metal-support interfacial perimeter) and catalytic activity. Our results demonstrate partial nanoparticle embedding as a synthetic strategy to produce thermocatalytically stable catalysts and increase the number of catalytically active Au/TiO <subscript>2</subscript> interfacial sites to augment catalytic contributions arising from metal-support interfaces.<br />Competing Interests: Competing interests statement:C.R. and G.J.H. participated in a Faraday Discussion together in 2021 (Faraday Discuss. 229, 378–421 (2021)].

Details

Language :
English
ISSN :
1091-6490
Volume :
122
Issue :
2
Database :
MEDLINE
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
39786932
Full Text :
https://doi.org/10.1073/pnas.2422628122