Promoter effect of BaO on CO oxidation on PdO surfaces
The effect of bulk BaO promoter on CO oxidation activity of palladium oxide phase was studied by density functional calculations. A series of BaO(100) supported Pd x O y thin layer models were constructed, and energy profiles for CO oxidation on the films were calculated and compared with correspond...
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Veröffentlicht in: | The Journal of chemical physics 2012-02, Vol.136 (8), p.084704-084704-7 |
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container_start_page | 084704 |
container_title | The Journal of chemical physics |
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creator | Hirvi, Janne T. Kallinen, Kauko Kinnunen, Toni-Jani J. Suvanto, Mika Pakkanen, Tapani A. |
description | The effect of bulk BaO promoter on CO oxidation activity of palladium oxide phase was studied by density functional calculations. A series of BaO(100) supported Pd
x
O
y
thin layer models were constructed, and energy profiles for CO oxidation on the films were calculated and compared with corresponding profiles for the most stable PdO bulk surfaces PdO(100) and PdO(101). The most stable of the thin films typically exhibit the same PdO(100) and PdO(101) surface planes; the PdO(100) dominates already with double layer thickness. The supporting promoter improves the CO oxidation activity of the Pd
x
O
y
phase via a direct electronic effect and introduced structural strain and corrugation. Changes in CO adsorption strength are reflected in oxidation energy barriers, and the promoting effect of even 0.3 eV can be seen locally. Easier oxygen vacancy formation may partially facilitate the reaction. |
doi_str_mv | 10.1063/1.3685849 |
format | Article |
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x
O
y
thin layer models were constructed, and energy profiles for CO oxidation on the films were calculated and compared with corresponding profiles for the most stable PdO bulk surfaces PdO(100) and PdO(101). The most stable of the thin films typically exhibit the same PdO(100) and PdO(101) surface planes; the PdO(100) dominates already with double layer thickness. The supporting promoter improves the CO oxidation activity of the Pd
x
O
y
phase via a direct electronic effect and introduced structural strain and corrugation. Changes in CO adsorption strength are reflected in oxidation energy barriers, and the promoting effect of even 0.3 eV can be seen locally. Easier oxygen vacancy formation may partially facilitate the reaction.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.3685849</identifier><identifier>PMID: 22380056</identifier><identifier>CODEN: JCPSA6</identifier><language>eng</language><publisher>United States: American Institute of Physics</publisher><ispartof>The Journal of chemical physics, 2012-02, Vol.136 (8), p.084704-084704-7</ispartof><rights>2012 American Institute of Physics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-c389dc02dc3655e71cca1d3a956b689789ab9c28319bc7c077e84af01c071dc23</citedby><cites>FETCH-LOGICAL-c339t-c389dc02dc3655e71cca1d3a956b689789ab9c28319bc7c077e84af01c071dc23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,794,1559,4512,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22380056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hirvi, Janne T.</creatorcontrib><creatorcontrib>Kallinen, Kauko</creatorcontrib><creatorcontrib>Kinnunen, Toni-Jani J.</creatorcontrib><creatorcontrib>Suvanto, Mika</creatorcontrib><creatorcontrib>Pakkanen, Tapani A.</creatorcontrib><title>Promoter effect of BaO on CO oxidation on PdO surfaces</title><title>The Journal of chemical physics</title><addtitle>J Chem Phys</addtitle><description>The effect of bulk BaO promoter on CO oxidation activity of palladium oxide phase was studied by density functional calculations. A series of BaO(100) supported Pd
x
O
y
thin layer models were constructed, and energy profiles for CO oxidation on the films were calculated and compared with corresponding profiles for the most stable PdO bulk surfaces PdO(100) and PdO(101). The most stable of the thin films typically exhibit the same PdO(100) and PdO(101) surface planes; the PdO(100) dominates already with double layer thickness. The supporting promoter improves the CO oxidation activity of the Pd
x
O
y
phase via a direct electronic effect and introduced structural strain and corrugation. Changes in CO adsorption strength are reflected in oxidation energy barriers, and the promoting effect of even 0.3 eV can be seen locally. Easier oxygen vacancy formation may partially facilitate the reaction.</description><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKAzEUhoMotlYXvoDMTlxMPUk6uWwEW7xBoV3oOmRygZFOU5MZ0Lc3Oq074XAu8PHD-RC6xDDFwOgtnlImKjGTR2iMQciSMwnHaAxAcCkZsBE6S-kdADAns1M0IoQKgIqNEVvH0IbOxcJ570xXBF_M9aoI22KR-2djddfkI9farorUR6-NS-foxOtNchf7OUFvjw-vi-dyuXp6WdwvS0Op7HIX0hog1lBWVY5jYzS2VMuK1UxILqSupSGCYlkbboBzJ2baA84rtobQCboecncxfPQudaptknGbjd660CclCcNVld_K5M1AmhhSis6rXWxaHb8UBvVjSWG1t5TZq31qX7fO_pEHLRm4G4Bkmu5XwP9pB4FqEKiCV3P6DTGjdKo</recordid><startdate>20120228</startdate><enddate>20120228</enddate><creator>Hirvi, Janne T.</creator><creator>Kallinen, Kauko</creator><creator>Kinnunen, Toni-Jani J.</creator><creator>Suvanto, Mika</creator><creator>Pakkanen, Tapani A.</creator><general>American Institute of Physics</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120228</creationdate><title>Promoter effect of BaO on CO oxidation on PdO surfaces</title><author>Hirvi, Janne T. ; Kallinen, Kauko ; Kinnunen, Toni-Jani J. ; Suvanto, Mika ; Pakkanen, Tapani A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-c389dc02dc3655e71cca1d3a956b689789ab9c28319bc7c077e84af01c071dc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirvi, Janne T.</creatorcontrib><creatorcontrib>Kallinen, Kauko</creatorcontrib><creatorcontrib>Kinnunen, Toni-Jani J.</creatorcontrib><creatorcontrib>Suvanto, Mika</creatorcontrib><creatorcontrib>Pakkanen, Tapani A.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirvi, Janne T.</au><au>Kallinen, Kauko</au><au>Kinnunen, Toni-Jani J.</au><au>Suvanto, Mika</au><au>Pakkanen, Tapani A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Promoter effect of BaO on CO oxidation on PdO surfaces</atitle><jtitle>The Journal of chemical physics</jtitle><addtitle>J Chem Phys</addtitle><date>2012-02-28</date><risdate>2012</risdate><volume>136</volume><issue>8</issue><spage>084704</spage><epage>084704-7</epage><pages>084704-084704-7</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><coden>JCPSA6</coden><abstract>The effect of bulk BaO promoter on CO oxidation activity of palladium oxide phase was studied by density functional calculations. A series of BaO(100) supported Pd
x
O
y
thin layer models were constructed, and energy profiles for CO oxidation on the films were calculated and compared with corresponding profiles for the most stable PdO bulk surfaces PdO(100) and PdO(101). The most stable of the thin films typically exhibit the same PdO(100) and PdO(101) surface planes; the PdO(100) dominates already with double layer thickness. The supporting promoter improves the CO oxidation activity of the Pd
x
O
y
phase via a direct electronic effect and introduced structural strain and corrugation. Changes in CO adsorption strength are reflected in oxidation energy barriers, and the promoting effect of even 0.3 eV can be seen locally. Easier oxygen vacancy formation may partially facilitate the reaction.</abstract><cop>United States</cop><pub>American Institute of Physics</pub><pmid>22380056</pmid><doi>10.1063/1.3685849</doi><tpages>1</tpages></addata></record> |
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language | eng |
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source | AIP Journals Complete; AIP Digital Archive; Alma/SFX Local Collection |
title | Promoter effect of BaO on CO oxidation on PdO surfaces |
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