Intrinsic magnetic properties of BixCo2−xMnO4 spinels obtained by short-time etching
We report the structural and magnetic properties of Co2MnO4, partially substituted by Bi at the octahedral site. Bismuth enhances ferromagnetism due to a decrease of the Co2+–Co2+ antiferromagnetic interactions and an increase of the Mn3+–Mn4+ exchanges. Spurious phases (magnetic and/or nonmagnetic...
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Veröffentlicht in: | Journal of magnetism and magnetic materials 2013-08, Vol.339, p.157-162 |
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Sprache: | eng |
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Zusammenfassung: | We report the structural and magnetic properties of Co2MnO4, partially substituted by Bi at the octahedral site. Bismuth enhances ferromagnetism due to a decrease of the Co2+–Co2+ antiferromagnetic interactions and an increase of the Mn3+–Mn4+ exchanges. Spurious phases (magnetic and/or nonmagnetic oxides) can easily form because of the large differences between the ionic radii of Bi3+ and Co3+, hiding or altering the intrinsic physical properties of the main BixCo2−xMnO4 phase. An easy way to eliminate the secondary phases is using acid reagents. Short-time etching of Bi0.1Co1.9MnO4 using nitric acid was successfully used, keeping most of the properties of the initial compound, with no alteration of the crystallographic structure. Final stoichiometry was respected (∼Bi0.08Co1.82MnO4), meaning that the material after etching definitely contains bismuth elements in its structure and the observed properties are intrinsic to the oxide spinel. Additional experiments were performed as a function of the synthesis conditions, showing that an optimal pH value of 7 allowed the best magnetic response of the non-doped material.
•Optimal synthesis conditions of Co2MnO4 spinel were obtained by a pH of 7.•Enhancement of magnetic properties by Bi incorporation in BixCo2−xMnO4 due to oxide impurities.•Short-time etching eliminates spurious phases but keep the properties of the starting material.•Intrinsic properties correspond to a Bi-substituted cobalt-based manganite spinel. |
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ISSN: | 0304-8853 1873-4766 |
DOI: | 10.1016/j.jmmm.2013.02.047 |