Inter-network magnetic interactions in GdMexMn1−xO3 perovskites (Me=transition metal) |
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Authors: | O. Peñ a,A.B. Antunes,G. Martí nez,V. Gil,C. Moure |
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Affiliation: | 1. Unité de Sciences Chimiques de Rennes, UMR-CNRS 6226, Université de Rennes 1, 35042 Rennes, France;2. GEMA, Centro Universitário FEEVALE, Novo Hamburgo, RS, Brazil;3. Institute of Physics, UFRGS, 91501-970, Porto Alegre, RS, Brazil;4. Electroceramics Department. Instituto de Cerámica y Vidrio, CSIC. 28049 Madrid, Spain |
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Abstract: | The gadolinium-based manganite GdMnO3 of perovskite structure has been partially substituted at the manganese site by transition metal elements Me like Cu, Ni and Co, leading to a general formula GdMexMn1−xO3, in which different magnetic entities (e.g., Gd3+, Cu2+, Ni2+, Co2+, Co3+, Mn3+, Mn4+) can coexist, depending on charge equilibrium conditions. For divalent cations such as Cu2+ and Ni2+, the solid solution extends from x (Me)=0–0.5, with O-type orthorhombic symmetry (a(a<c/√2<b). When the substituting element is cobalt, the solid solution extends over the whole range [0?x ?1], changing from O′-type symmetry (c/√2(c/√2<a<b) to O-type for x>0.5. In this latter case, the synthesis is performed under oxygen flow, which allows the cobalt ion to take a 3+ oxidation state. |
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Keywords: | 61.66.Fn 75.25.+z 75.30.Et 75.50.Gg |
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