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Photogenerated Defects in Shape-Controlled TiO2 Anatase Nanocrystals: A Probe To Evaluate the Role of Crystal Facets in Photocatalytic Processes

dc.contributor.authorD’Arienzo, Massimiliano
dc.contributor.authorCarbajo Olleros, Jaime
dc.contributor.authorBahamonde, Ana
dc.contributor.authorCrippa, Maurizio
dc.contributor.authorPolizzi, Stefano
dc.contributor.authorScotti, Roberto
dc.contributor.authorWahba, Laura
dc.contributor.authorMorazzoni, Franca
dc.date.accessioned2024-01-23T12:10:52Z
dc.date.available2024-01-23T12:10:52Z
dc.date.issued2011
dc.description.abstractThe promising properties of anatase TiO2 nanocrystals exposing specific surfaces have been investigated in depth both theoretically and experimentally. However, a clear assessment of the role of the crystal faces in photocatalytic processes is still under debate. In order to clarify this issue, we have comprehensively explored the properties of the photogenerated defects and in particular their dependence on the exposed crystal faces in shape-controlled anatase. Nanocrystals were synthesized by solvothermal reaction of titanium butoxide in the presence of oleic acid and oleylamine as morphology-directing agents, and their photocatalytic performances were evaluated in the phenol mineralization in aqueous media, using O2 as the oxidizing agent. The charge-trapping centers, Ti3+, O–, and O2–, formed by UV irradiation of the catalyst were detected by electron spin resonance, and their abundance and reactivity were related to the exposed crystal faces and to the photoefficiency of the nanocrystals. In vacuum conditions, the concentration of trapped holes (O– centers) increases with increasing {001} surface area and photoactivity, while the amount of Ti3+ centers increases with the specific surface area of {101} facets, and the highest value occurs for the sample with the worst photooxidative efficacy. These results suggest that {001} surfaces can be considered essentially as oxidation sites with a key role in the photoxidation, while {101} surfaces provide reductive sites which do not directly assist the oxidative processes. Photoexcitation experiments in O2 atmosphere led to the formation of Ti4+–O2– oxidant species mainly located on {101} faces, confirming the indirect contribution of these surfaces to the photooxidative processes. Although this work focuses on the properties of TiO2, we expect that the presented quantitative investigation may provide a new methodological tool for a more effective evaluation of the role of metal oxide crystal faces in photocatalytic processes.
dc.description.departmentDepto. de Ingeniería Química y de Materiales
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipCariplo Foundation of Milan (Italia)
dc.description.statuspub
dc.identifier.citationMassimiliano D’Arienzo, Jaime Carbajo, Ana Bahamonde, Maurizio Crippa, Stefano Polizzi, Roberto Scotti, Laura Wahba, and Franca Morazzoni Journal of the American Chemical Society 2011 133 (44), 17652-17661 DOI: 10.1021/ja204838s
dc.identifier.doi10.1021/ja204838s
dc.identifier.issn0002-7863
dc.identifier.officialurlhttps://doi.org/10.1021/ja204838s
dc.identifier.urihttps://hdl.handle.net/20.500.14352/94730
dc.issue.number44
dc.journal.titleJournal of the American Chemical Society
dc.language.isoeng
dc.page.final17661
dc.page.initial17652
dc.publisherACS publications
dc.rights.accessRightsopen access
dc.subject.cdu54
dc.subject.ucmCiencias
dc.subject.unesco23 Química
dc.titlePhotogenerated Defects in Shape-Controlled TiO2 Anatase Nanocrystals: A Probe To Evaluate the Role of Crystal Facets in Photocatalytic Processes
dc.typejournal article
dc.type.hasVersionAO
dc.volume.number133
dspace.entity.typePublication
relation.isAuthorOfPublication4aee7b9d-806f-481c-a6d8-fc22bcf369bb
relation.isAuthorOfPublication.latestForDiscovery4aee7b9d-806f-481c-a6d8-fc22bcf369bb

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