Source:http://linkedlifedata.com/resource/pubmed/id/20028144
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
51
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pubmed:dateCreated |
2009-12-23
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pubmed:abstractText |
For the case of one-third of a monolayer of tungsten grown by atomic layer deposition on a hematite alpha-Fe(2)O(3)(0001) surface, we report direct atomic-scale observations of the structural and chemical changes that occur as this model interfacial system evolves from the as-deposited state to the oxidized state, then to the reduced state, and finally back to the oxidized state. In situ X-ray standing-wave atomic images relative to the hematite lattice show dramatic (but redox-reversible) changes to the W cation locations with respect to the occupied and unoccupied Fe surface sites. These structural changes are concurrent with X-ray photoelectron spectroscopy chemical shift changes, where W is observed to go from the 6+ to 5+ oxidation state. These novel observations of redox-induced cation dynamics in an oxide-supported catalyst are explained by models that account for W incorporation at the interface in Fe sites with various coordination schemes. Our proposed structure models are supported by our X-ray absorption fine structure measurements.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1520-5126
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
30
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pubmed:volume |
131
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
18200-1
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pubmed:year |
2009
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pubmed:articleTitle |
Direct atomic-scale observation of redox-induced cation dynamics in an oxide-supported monolayer catalyst: WO(x)/alpha-Fe(2)O(3)(0001).
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pubmed:affiliation |
Department of Materials Science and Engineering, Institute for Catalysis in Energy Processes, and DND-CAT, Synchrotron Research Center, Northwestern University, Evanston, Illinois 60208, USA.
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pubmed:publicationType |
Journal Article
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