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dc.contributor.authorKarabulut B.
dc.contributor.authorTapramaz R.
dc.contributor.authorKöksal F.
dc.date.accessioned2020-06-21T09:23:57Z
dc.date.available2020-06-21T09:23:57Z
dc.date.issued2004
dc.identifier.issn0932-0784
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3704
dc.description.abstractEPR spectra of VO2+ ions in di-sodium tartrate, [Na 2C4H4O6], single crystal and powder spectra have been studied at room temperature. The angular variation of the EPR spectra has shown that three different VO2+ complexes are located in different chemical environments, and each environment contains two magnetically inequvalent sites. The spin Hamiltonian parameters are determined, and these parameters have been used to assess the bonding coefficients of the VO 2+ ion in the di-sodium tartrate lattice. The parallel and perpendicular components of axially symmetric g and hyperfine tensors are evaluated. The results are discussed.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDi-sodium Tartrateen_US
dc.subjectEPRen_US
dc.subjectVanadil Ionen_US
dc.titleEPR spectra of VO2+ doped in Na2C4H 4O6 single crystalsen_US
dc.typereviewen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume59en_US
dc.identifier.issue10en_US
dc.identifier.startpage669en_US
dc.identifier.endpage673en_US
dc.relation.journalZeitschrift fur Naturforschung - Section A Journal of Physical Sciencesen_US
dc.relation.publicationcategoryDiğeren_US


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