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dc.contributor.authorTELANG, PRACHIen_US
dc.contributor.authorMISHRA, KSHITIen_US
dc.contributor.authorSINGH, SURJEETen_US
dc.coverage.spatialMumbai, Indiaen_US
dc.date.accessioned2021-02-05T06:14:07Z-
dc.date.available2021-02-05T06:14:07Z-
dc.date.issued2018-04en_US
dc.identifier.citationDAE Solid State Physics Symposium 2017.en_US
dc.identifier.isbn9780740000000en_US
dc.identifier.issn-en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5605-
dc.identifier.urihttps://aip.scitation.org/doi/10.1063/1.5029034en_US
dc.description.abstractWe investigate the structural and physical properties of the pyrochlores Eu2-xBi2xIr2O7 (x = 0, 0.05, 0.1, 0.25, 0.5, 0.75 and 1). We found that the lattice parameters of the compositions close to Eu2Ir2O7 end (i.e., x < 0.1) do not follow a regular increase as expected due the bigger ionic size of Bi3+ compared to Eu3+. Measurement of physical properties, including, resistivity and magnetic susceptibility showed a strong structure-property correlation in the x < 0.1 doping range. Above this doping level, the lattice parameters show a linear increase, and the physical behavior of the series quickly approaches that of the end member Bi2Ir2O7 which exhibits a metallic conductivity with no magnetic transitionen_US
dc.language.isoenen_US
dc.publisherAIP Publishingen_US
dc.subjectPhysicsen_US
dc.subject2018en_US
dc.titleOn the effect of isovalent Bi substitution at the Eu site in the pyrochlore Eu2Ir2O7en_US
dc.typeConference Papersen_US
dc.contributor.departmentDept. of Physicsen_US
dc.identifier.doihttps://doi.org/10.1063/1.5029034en_US
dc.identifier.sourcetitleDAE Solid State Physics Symposium 2017.en_US
dc.publication.originofpublisherForeignen_US
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