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dc.contributor.advisorMcGuinness, Cormac
dc.contributor.authorKennedy, Brian
dc.date.accessioned2019-11-07T15:58:04Z
dc.date.available2019-11-07T15:58:04Z
dc.date.issued2011
dc.identifier.citationBrian Kennedy, 'Resonant soft X-ray spectroscopic studies of certain transition metal oxides', [thesis], Trinity College (Dublin, Ireland). School of Physics, 2011, pp 245
dc.identifier.otherTHESIS 9519
dc.description.abstractRutile-type transition-metal oxides are extremely fertile areas of study both for fundamental and technological reasons due to the range of physical properties they present, such as insulating TiO2, semiconducting Sn02 and metallic RuO2. The chemical bonding of such rutile-type oxides is assumed to have an essentially ionic character despite differences in the outer electronic structures of the cations, from empty outer shell (Ti 4+), to partially filled (Ru 4+) to filled (Sn 4+), but has been shown to become progressively more covalent, and details of their electronic structure are still under intense experimental study and theoretical consideration. To this end, resonant x-ray absorption and emission spectroscopy (RXES) provides a sensitive element-specific and symmetry-selective probe of the unoccupied and occupied electronic bandstructure of these materials.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). School of Physics
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb15116289
dc.subjectPhysics, Ph.D.
dc.subjectPh.D. Trinity College Dublin.
dc.titleResonant soft X-ray spectroscopic studies of certain transition metal oxides
dc.typethesis
dc.type.supercollectionthesis_dissertations
dc.type.supercollectionrefereed_publications
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (Ph.D.)
dc.rights.ecaccessrightsopenAccess
dc.format.extentpaginationpp 245
dc.description.noteTARA (Trinity’s Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie
dc.identifier.urihttp://hdl.handle.net/2262/90269


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