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hal.structure.identifierMatériaux Inorganiques
dc.contributor.authorHIDOURI, Mourad
hal.structure.identifierMatériaux Inorganiques
dc.contributor.authorLAJMI, Besma
hal.structure.identifierMatériaux Inorganiques
dc.contributor.authorGMATI, Nadia
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorWATTIAUX, Alain
hal.structure.identifierInstitut Laue-Langevin [ILL]
dc.contributor.authorNENERT, Gwilherm
hal.structure.identifierInstitut Laue-Langevin [ILL]
dc.contributor.authorRITTER, Clemens
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorFOURNÈS, Léopold
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDARRIET, Jacques
hal.structure.identifierDepartamento de Química Inorgánica I
dc.contributor.authorLOPEZ MARIA, Luisa
hal.structure.identifierDepartamento de Química Inorgánica I
dc.contributor.authorPICO, Carlos
hal.structure.identifierMatériaux Inorganiques
dc.contributor.authorBEN AMARA, Mongi
dc.date.issued2010
dc.identifier.issn0025-5408
dc.description.abstractEnA new iron oxophosphate of composition Rb<sub>7</sub>Fe<sub>7</sub>(PO<sub>4</sub>)<sub>8</sub>O<sub>2</sub>·2H<sub>2</sub>O has been synthesized and studied by X-ray diffraction, TG and DTA analysis, magnetic susceptibility, neutron diffraction, Mössbauer spectroscopy and ionic conductivity. This compound crystallizes in the monoclinic system with the <i>P</i>2<sub>1</sub>/<i>c</i> space group and the unit cell parameters <i>a</i> = 8.224(8) Å, <i>b</i> = 22.162(6) Å, <i>c</i> = 9.962(6) Å and <i>β</i> = 109.41(8)°. Its structure is built up from Fe<sub>7</sub>O<sub>32</sub> clusters of edge- and corner-sharing FeO<sub>5</sub> and FeO<sub>6</sub> polyhedra. Neighboring clusters are connected by the phosphate tetrahedra to form a three-dimensional framework. The Rb<sup>+</sup> cations and the water molecules are occupying intersecting tunnels parallel to <i>a</i> and <i>c</i>. The presence of water molecules was confirmed by TG and DTA analysis. The magnetic susceptibility measurements have shown the existence of antiferromagnetic ordering below 22 K with a weak ferromagnetic component. Additionally, these measurements show evidence for a strong magnetic frustration characterized by |<i>θ</i>/<i>T</i><sub>N</sub>| ≈ 12. Powder neutron diffraction study confirms the presence of a long range antiferromagnetic order coupled to a weak ferromagnetic component along the <i>b</i>-axis. The strongly reduced magnetic moments extracted from the refinement support the existence of a magnetically frustrated ground state. The Mössbauer spectroscopy results confirmed the presence of only Fe<sup>3+</sup> ions in both five and six coordination. The ionic conductivity measurements led to activation energy of 0.81 eV, a value that agrees with the obtained for other rubidium phosphates.
dc.language.isoen
dc.publisherElsevier
dc.subject.enChemical synthesis
dc.subject.enMössbauer spectroscopy
dc.subject.enImpedance spectroscopy
dc.subject.enNeutron scattering
dc.subject.enMagnetic structure
dc.title.enStructural, thermal, magnetic and electrical studies of the iron oxophosphate Rb<sub>7</sub>Fe<sub>7</sub>(PO<sub>4</sub>)<sub>8</sub>O<sub>2</sub>·2H<sub>2</sub>O
dc.typeArticle de revue
dc.identifier.doi10.1016/j.materresbull.2010.05.008
dc.subject.halChimie/Matériaux
bordeaux.journalMaterials Research Bulletin
bordeaux.page1255-1262
bordeaux.volume45
bordeaux.issue9
bordeaux.peerReviewedoui
hal.identifierhal-00528351
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00528351v1
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