Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1833
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dc.contributor.authorHalder, Soumyadip-
dc.contributor.authorSharma, Minaxi-
dc.contributor.authorSingh, Inderjit-
dc.contributor.authorVenkatesan, A.-
dc.date.accessioned2020-11-19T04:44:59Z-
dc.date.available2020-11-19T04:44:59Z-
dc.date.issued2017-
dc.identifier.citationPhysical Review B, 96 (11)en_US
dc.identifier.other10.1103/PhysRevB.96.115423-
dc.identifier.urihttps://journals.aps.org/prb/abstract/10.1103/PhysRevB.96.115423-
dc.identifier.urihttp://hdl.handle.net/123456789/1833-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractOxygen vacancies play an important role in controlling the physical properties of a perovskite oxide. We report alterations in the electronic properties of a cubic perovskite oxide, namely, KTaO3, as a function of oxygen vacancies. The conducting surface of the KTaO3 single-crystal substrate has been realized via Ar+ irradiation. The band gap changes as a function of conductivity which is controlled by irradiation time, indicating the formation of defect states. Kelvin probe force microscopy suggests a sharp increase in the work function upon Ar+ irradiation for a short period of time followed by a monotonic decrease, as we increase the irradiation time. Our experimental findings along with theoretical simulations suggest a significant surface dipole contribution and an unusual change in the electronic band line-up of KTaO3 due to oxygen vacancies.en_US
dc.language.isoen_USen_US
dc.publisherAPSen_US
dc.subjectOxygenen_US
dc.subjectperovskite oxiden_US
dc.subjectKTaO3en_US
dc.subjectAr+ irradiationen_US
dc.titleElectronic structure modification of the KTaO3 single-crystal surface by Ar+ bombardmenten_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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