Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6601
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dc.contributor.authorJog, Harshvardhanen_US
dc.contributor.authorHARNAGEA, LUMINITAen_US
dc.contributor.authorMele, Eugene J.en_US
dc.contributor.authorAgarwal, Riteshen_US
dc.date.accessioned2022-02-25T10:24:45Z
dc.date.available2022-02-25T10:24:45Z
dc.date.issued2022-02en_US
dc.identifier.citationScience Advances, 8(7).en_US
dc.identifier.issn2375-2548en_US
dc.identifier.urihttps://doi.org/10.1126/sciadv.abl9020en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6601
dc.description.abstractIn low–electron density materials, interactions can lead to highly correlated quantum states of matter. Ta2NiSe5, an excitonic insulator (EI) candidate, exists in a novel broken-symmetry phase below 327 K, characterized by robust exchange interaction and electron-lattice coupling. We study this phase of Ta2NiSe5 using the quadrupole circular photogalvanic effect (QCPGE). Light matter interaction in Ta2NiSe5 mediated by electric quadrupole/magnetic dipole coupling produces helicity-dependent DC response even with centrosymmetry, making it particularly sensitive to certain other broken symmetries. We show that the exchange interaction in Ta2NiSe5 can lead to a triclinic structure with a broken C2 symmetry. Our results provide an incisive probe of the symmetries of the low-temperature phase of Ta2NiSe5 and add new symmetry constraints to the identification of a strongly correlated EI phase. The high sensitivity of QCPGE to subtle symmetry breaking in centrosymmetric systems will enable its use in studying other complex crystalline systems.en_US
dc.language.isoenen_US
dc.publisherAmerican Association for the Advancement of Scienceen_US
dc.subjectPhysicsen_US
dc.subject2022-FEB-WEEK4en_US
dc.subjectTOC-FEB-2022en_US
dc.subject2022en_US
dc.titleExchange coupling–mediated broken symmetries in Ta2NiSe5 revealed from quadrupolar circular photogalvanic effecten_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Physicsen_US
dc.identifier.sourcetitleScience Advancesen_US
dc.publication.originofpublisherForeignen_US
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