Creating single-atom Pt-ceria catalysts by surface step decoration

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作者
Filip Dvořák
Matteo Farnesi Camellone
Andrii Tovt
Nguyen-Dung Tran
Fabio R. Negreiros
Mykhailo Vorokhta
Tomáš Skála
Iva Matolínová
Josef Mysliveček
Vladimír Matolín
Stefano Fabris
机构
[1] Charles University in Prague,
[2] Faculty of Mathematics and Physics,undefined
[3] CNR-IOM DEMOCRITOS,undefined
[4] Istituto Officina dei Materiali,undefined
[5] Consiglio Nazionale delle Ricerche,undefined
[6] SISSA,undefined
[7] Scuola Internazionale Superiore di Studi Avanzati,undefined
[8] Present address: Universidade Federal do ABC. Av. dos Estados,undefined
[9] 5001 Bairro Bangu,undefined
[10] Santo André SP CEP 09210-580,undefined
[11] Brasil,undefined
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摘要
Single-atom catalysts maximize the utilization of supported precious metals by exposing every single metal atom to reactants. To avoid sintering and deactivation at realistic reaction conditions, single metal atoms are stabilized by specific adsorption sites on catalyst substrates. Here we show by combining photoelectron spectroscopy, scanning tunnelling microscopy and density functional theory calculations that Pt single atoms on ceria are stabilized by the most ubiquitous defects on solid surfaces—monoatomic step edges. Pt segregation at steps leads to stable dispersions of single Pt2+ ions in planar PtO4 moieties incorporating excess O atoms and contributing to oxygen storage capacity of ceria. We experimentally control the step density on our samples, to maximize the coverage of monodispersed Pt2+ and demonstrate that step engineering and step decoration represent effective strategies for understanding and design of new single-atom catalysts.
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