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Magnetic compensation, field-dependent magnetization reversal, and complex magnetic ordering in Co2TiO4
Indian Inst Technol, Dept Phys, Gauhati 781039, Assam, India..
Indian Inst Technol, Dept Phys, Gauhati 781039, Assam, India..
Indian Inst Technol, Dept Phys, Gauhati 781039, Assam, India..
IFW Dresden, Inst Complex Mat, D-01171 Dresden, Germany..
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2015 (English)In: Physical Review B. Condensed Matter and Materials Physics, ISSN 1098-0121, E-ISSN 1550-235X, Vol. 92, no 21, 214434Article in journal (Refereed) PublishedText
Abstract [en]

The complex nature of magnetic ordering in the spinel Co2TiO4 is investigated by analyzing the temperature and magnetic field dependence of its magnetization (M), specific heat (C-p), and ac magnetic susceptibilities chi' and chi ''. X-ray diffraction of the sample synthesized by the solid-state reaction route confirmed the spinel structure whereas x-ray photoelectron spectroscopy shows its electronic structure to be Co2TiO4 = [Co2+][Co3+ Ti3+]O-4. From analysis of the temperature dependence of the dc paramagnetic susceptibility, the magnetic moments mu(A) = 3.87 mu(B) and mu(B) = 5.19 mu B on the A and B sites are determined with mu(B) in turn yielding mu(Ti3+) = 1.73 mu(B) and mu(Co3+) = 4.89 mu(B). Analysis of the dc and ac susceptibilities combined with the weak anomalies observed in the C-p vs T data shows the existence of a quasi-long-range ferrimagnetic state below T-N similar to 47.8K and a compensation temperature T-comp similar to 32 K, the latter characterized by sign reversal of magnetization with its magnitude depending on the applied magnetic field and the cooling protocol. Analysis of the temperature dependence of M (field cooled) and M (zero field cooled) data and the hysteresis loop parameters is interpreted in terms of large spin clusters. These results in Co2TiO4, significantly different from those reported recently in isostructural Co2SnO4 = [Co2+][Co2+ Sn4+]O-4, warrant further investigations of its magnetic structure using neutron diffraction.

Place, publisher, year, edition, pages
2015. Vol. 92, no 21, 214434
National Category
Condensed Matter Physics Engineering and Technology
URN: urn:nbn:se:uu:diva-274437DOI: 10.1103/PhysRevB.92.214434ISI: 000367058700004OAI: oai:DiVA.org:uu-274437DiVA: diva2:896504
Swedish Research Council
Available from: 2016-01-21 Created: 2016-01-21 Last updated: 2016-01-22Bibliographically approved

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Sarkar, TapatiAndersson, Mikael S.Mathieu, Roland
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