Evidence of strong antiferromagnetic coupling between localized and itinerant electrons in ferromagnetic Sr2FeMoO6
Abstract
Magnetic dc susceptibility () and electron spin resonance (ESR) measurements in the paramagnetic regime, are presented. We found a Curie-Weiss (CW) behavior for (T) with a ferromagnetic = 446(5) K and μeff = 4.72(9) μB/f.u., this being lower than that expected for either Fe3+(5.9μB) or Fe2+(4.9μB) ions. The ESR g-factor g = 2.01(2), is associated with Fe3+. We obtained an excellent description of the experiments in terms of two interacting sublattices: the localized Fe3+ (3d5) cores and the delocalized electrons. The coupled equations were solved in a mean-field approximation, assuming for the itinerant electrons a bare susceptibility independent on T. We obtained e0 = 3.7 10-4 emu/mol. We show that the reduction of μeff for Fe3+ arises from the strong antiferromagnetic (AFM) interaction between the two sublattices. At variance with classical ferrimagnets, we found that is ferromagnetic. Within the same model, we show that the ESR spectrum can be described by Bloch-Hasegawa type equations. Bottleneck is evidenced by the absence of a g-shift. Surprisingly, as observed in CMR manganites, no narrowing effects of the ESR linewidth is detected in spite of the presence of the strong magnetic coupling. These results provide evidence that the magnetic order in Sr2FeMoO6 does not originates in superexchange interactions, but from a novel mechanism recently proposed for double perovskites.
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