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http://hdl.handle.net/123456789/1833
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DC Field | Value | Language |
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dc.contributor.author | Halder, Soumyadip | - |
dc.contributor.author | Sharma, Minaxi | - |
dc.contributor.author | Singh, Inderjit | - |
dc.contributor.author | Venkatesan, A. | - |
dc.date.accessioned | 2020-11-19T04:44:59Z | - |
dc.date.available | 2020-11-19T04:44:59Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Physical Review B, 96 (11) | en_US |
dc.identifier.other | 10.1103/PhysRevB.96.115423 | - |
dc.identifier.uri | https://journals.aps.org/prb/abstract/10.1103/PhysRevB.96.115423 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/1833 | - |
dc.description | Only IISERM authors are available in the record. | - |
dc.description.abstract | Oxygen 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.iso | en_US | en_US |
dc.publisher | APS | en_US |
dc.subject | Oxygen | en_US |
dc.subject | perovskite oxid | en_US |
dc.subject | KTaO3 | en_US |
dc.subject | Ar+ irradiation | en_US |
dc.title | Electronic structure modification of the KTaO3 single-crystal surface by Ar+ bombardment | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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