Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5351
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKar, Indranien_US
dc.contributor.authorHARNAGEA, LUMINITAen_US
dc.contributor.authorBanik, Somaen_US
dc.contributor.authorSINGH, SURJEETen_US
dc.contributor.authorThirupathaiah, Settien_US
dc.coverage.spatialJodhpur, Indiaen_US
dc.date.accessioned2020-11-09T09:49:52Z
dc.date.available2020-11-09T09:49:52Z
dc.date.issued2020-11en_US
dc.identifier.citationAIP Conference Proceedings, 2265(1).en_US
dc.identifier.isbn9780735420250en_US
dc.identifier.issn0094-243Xen_US
dc.identifier.issn1551-7616en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5351-
dc.identifier.urihttps://aip.scitation.org/doi/abs/10.1063/5.0016745en_US
dc.description.abstractUsing angle resolved photoemission spectroscopy (ARPES) we studied the low energy electronic structure of transition metal dichalcogenide (TMDC), NiTe2, single crystal. Our ARPES data clearly show a surface Dirac point observed at a binding energy of 1.45 eV which is consistent with an earlier prediction. Thus, our results for the first time experimentally prove that NiTe2is a topological TMDC. Our ARPES data further suggest a metallic nature of NiTe2. We found that overall the electronic structure of NiTe2has similarities with the other topological TMDCs like PdTe2, PtTe2 and PtSe2.en_US
dc.language.isoenen_US
dc.publisherAIP Publishingen_US
dc.subjectPhysicsen_US
dc.subject2020en_US
dc.subject2020-NOV-WEEK1en_US
dc.subjectTOC-NOV-2020en_US
dc.titleObservation of surface Dirac state in transition metal dichalcogenide NiTe2 using ARPESen_US
dc.typeConference Papersen_US
dc.contributor.departmentDept. of Physicsen_US
dc.identifier.doihttps://doi.org/10.1063/5.0016745en_US
dc.identifier.sourcetitleAIP Conference Proceedingsen_US
dc.publication.originofpublisherForeignen_US
Appears in Collections:CONFERENCE PAPERS

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.