Interplay between localized and itinerant magnetism in Co substituted FeGa
arXiv:1311.1501 · doi:10.1103/PhysRevB.89.104426
Abstract
The evolution of the electronic structure and magnetic properties with Co substitution for Fe in the solid solution FeCoGa was studied by means of electrical resistivity, magnetization, ab-initio band structure calculations, and nuclear spin-lattice relaxation of the Ga nuclei. Temperature dependencies of the electrical resistivity reveal that the evolution from the semiconducting to the metallic state in the FeCoGa system occurs at . The was studied as a function of temperature in a wide temperature range of K for the concentrations and . In the parent semiconducting compound FeGa, the temperature dependence of the exhibits a huge maximum at about K indicating the existence of in-gap states. The opposite binary compound, CoGa, demonstrates a metallic Korringa behavior with . In FeCoGa, the relaxation is strongly enhanced due to spin fluctuations and follows , which is a unique feature of weakly and nearly antiferromagnetic metals. This itinerant antiferromagnetic behavior contrasts with both magnetization measurements, showing localized magnetism with a relatively low effective moment of about 0.7 /f.u., and ab initio band structure calculations, where a ferromagnetic state with an ordered moment of 0.5 /f.u. is predicted. The results are discussed in terms of the interplay betwen the localized and itinerant magnetizm including in-gap states and spin fluctuations.
10 pages, 11 figures
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