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CO Oxidation at the Interface of Au Nanoclusters and the Stepped-CeO2(111) Surface by the Mars–van Krevelen Mechanism
DFT+U calculations of CO oxidation by Au12 nanoclusters supported on a stepped-CeO2(111) surface show that lattice oxygen at the step edge oxidizes CO bound to Au NCs by the Mars–van Krevelen (M-vK) mechanism. We found that CO2 desorption determines the rate of CO oxidation, and the vacancy formatio...
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Published in: | The journal of physical chemistry letters 2013-01, Vol.4 (1), p.216-221 |
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container_title | The journal of physical chemistry letters |
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creator | Kim, Hyun You Henkelman, Graeme |
description | DFT+U calculations of CO oxidation by Au12 nanoclusters supported on a stepped-CeO2(111) surface show that lattice oxygen at the step edge oxidizes CO bound to Au NCs by the Mars–van Krevelen (M-vK) mechanism. We found that CO2 desorption determines the rate of CO oxidation, and the vacancy formation energy is a reactivity descriptor for CO oxidation. Our results suggest that the M-vK mechanism contributes significantly to CO oxidation activity at Au particles supported on the nano- or meso-structured CeO2 found in industrial catalysts. |
doi_str_mv | 10.1021/jz301778b |
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We found that CO2 desorption determines the rate of CO oxidation, and the vacancy formation energy is a reactivity descriptor for CO oxidation. Our results suggest that the M-vK mechanism contributes significantly to CO oxidation activity at Au particles supported on the nano- or meso-structured CeO2 found in industrial catalysts.</description><identifier>ISSN: 1948-7185</identifier><identifier>EISSN: 1948-7185</identifier><identifier>DOI: 10.1021/jz301778b</identifier><identifier>PMID: 26291234</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Surfaces, Interfaces, Porous Materials, and Catalysis</subject><ispartof>The journal of physical chemistry letters, 2013-01, Vol.4 (1), p.216-221</ispartof><rights>Copyright © 2012 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26291234$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Hyun You</creatorcontrib><creatorcontrib>Henkelman, Graeme</creatorcontrib><title>CO Oxidation at the Interface of Au Nanoclusters and the Stepped-CeO2(111) Surface by the Mars–van Krevelen Mechanism</title><title>The journal of physical chemistry letters</title><addtitle>J. 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Phys. Chem. Lett</addtitle><date>2013-01-03</date><risdate>2013</risdate><volume>4</volume><issue>1</issue><spage>216</spage><epage>221</epage><pages>216-221</pages><issn>1948-7185</issn><eissn>1948-7185</eissn><abstract>DFT+U calculations of CO oxidation by Au12 nanoclusters supported on a stepped-CeO2(111) surface show that lattice oxygen at the step edge oxidizes CO bound to Au NCs by the Mars–van Krevelen (M-vK) mechanism. We found that CO2 desorption determines the rate of CO oxidation, and the vacancy formation energy is a reactivity descriptor for CO oxidation. Our results suggest that the M-vK mechanism contributes significantly to CO oxidation activity at Au particles supported on the nano- or meso-structured CeO2 found in industrial catalysts.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>26291234</pmid><doi>10.1021/jz301778b</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Surfaces, Interfaces, Porous Materials, and Catalysis |
title | CO Oxidation at the Interface of Au Nanoclusters and the Stepped-CeO2(111) Surface by the Mars–van Krevelen Mechanism |
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