Y. Naveen Kumar, A. Paul Blessington Selvadurai, N. Aparnadevi, C. Venkateswaran
{"title":"Negative Magnetization and Spin-Phonon Coupling in Faceted Nd2FeCrO6 Double Perovskite","authors":"Y. Naveen Kumar, A. Paul Blessington Selvadurai, N. Aparnadevi, C. Venkateswaran","doi":"10.1016/j.jallcom.2024.177901","DOIUrl":null,"url":null,"abstract":"The magnetic feature of a faceted double perovskite Nd<sub>2</sub>FeCrO<sub>6,</sub> synthesized by the solid-state reaction method, is investigated. Nd<sub>2</sub>FeCrO<sub>6</sub> exhibits an orthorhombic structure with Fe and Cr ions in 3<sup>+</sup> oxidation states. These ions are shifted away from the centre of FeO<sub>6</sub>/CrO<sub>6</sub> octahedral sublattice, indicating distortion. The Isomer shift in the Mössbauer spectrum correlates with the 3<sup>+</sup> oxidation state of Fe, and the existence of magnetic fraction leading to magnetic frustration in Nd<sub>2</sub>FeCrO<sub>6</sub> is established. The superexchange Fe<sup>3+</sup> -O- Fe<sup>3+</sup> and Cr<sup>3+</sup> -O- Cr<sup>3+</sup> interactions favour antiferromagnetic ordering, while Fe<sup>3+</sup> -O- Cr<sup>3+</sup> interactions promote weak ferromagnetic ordering. The low-temperature magnetic study traces negative magnetization in FC mode for the applied external fields of 100<!-- --> <!-- -->Oe and 1000<!-- --> <!-- -->Oe, attributed to the paramagnetic effect of Nd<sup>3+</sup> ions aligning antiparallel to the ferromagnetic component of the |Fe+Cr| sublattice internal field. Also, the negative magnetization of FC mode is found to be field-dependent. The deviation of the B<sub>2g</sub> phonon around the magnetic ordering temperature T<sub>N</sub>~250<!-- --> <!-- -->K provides evidence of spin-phonon coupling. This variation in the B<sub>2g</sub> phonon is analysed in terms of the full width at half maximum (FWHM), peak position, intensity, and height.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"19 1","pages":""},"PeriodicalIF":5.8000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jallcom.2024.177901","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The magnetic feature of a faceted double perovskite Nd2FeCrO6, synthesized by the solid-state reaction method, is investigated. Nd2FeCrO6 exhibits an orthorhombic structure with Fe and Cr ions in 3+ oxidation states. These ions are shifted away from the centre of FeO6/CrO6 octahedral sublattice, indicating distortion. The Isomer shift in the Mössbauer spectrum correlates with the 3+ oxidation state of Fe, and the existence of magnetic fraction leading to magnetic frustration in Nd2FeCrO6 is established. The superexchange Fe3+ -O- Fe3+ and Cr3+ -O- Cr3+ interactions favour antiferromagnetic ordering, while Fe3+ -O- Cr3+ interactions promote weak ferromagnetic ordering. The low-temperature magnetic study traces negative magnetization in FC mode for the applied external fields of 100 Oe and 1000 Oe, attributed to the paramagnetic effect of Nd3+ ions aligning antiparallel to the ferromagnetic component of the |Fe+Cr| sublattice internal field. Also, the negative magnetization of FC mode is found to be field-dependent. The deviation of the B2g phonon around the magnetic ordering temperature TN~250 K provides evidence of spin-phonon coupling. This variation in the B2g phonon is analysed in terms of the full width at half maximum (FWHM), peak position, intensity, and height.
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.