Geometric and disorder -- type magnetic frustration in ferrimagnetic "114" Ferrites: Role of diamagnetic Li+ and Zn2+ cation substitution

Details Geometric and disorder -- type magnetic frustration in ferrimagnetic "114" Ferrites: Role of diamagnetic Li+ and Zn2+ cation substitution Geometric and disorder -- type magnetic frustration in ferrimagnetic "114" Ferrites: Role of diamagnetic Li+ and Zn2+ cation substitution

2012-03-28

arxiv.org/abs/1203.6220v1

Journal of superconductivity and Novel Magnetism, Vol. 25, Pg. 627 - 632 (2012)

Physics

Condensed Matter

Materials Science

2 tables, 7 figures

Scientific paper

10.1007/s10948-012-1474-8

The comparative study of the substitution of zinc and lithium for iron in the "114" ferrites, YBaFe4O7 and CaBaFe4O7, shows that these diamagnetic cations play a major role in tuning the competition between ferrimagnetism and magnetic frustration in these oxides. The substitution of Li or Zn for Fe in the cubic phase YBaFe4O7 leads to a structural transition to a hexagonal phase YBaFe4-xMxO7, for M = Li (0.30 < x < 0.75) and for M = Zn (0.40 < x < 1.50). It is seen that for low doping values i.e. x = 0.30 (for Li) and x = 0.40 (for Zn), these diamagnetic cations induce a strong ferrimagnetic component in the samples, in contrast to the spin glass behaviour of the cubic phase. In all the hexagonal phases, YBaFe4-xMxO7 and CaBaFe4-xMxO7 with M = Li and Zn, it is seen that in the low doping regime (x ~ 0.3 to 0.5), the competition between ferrimagnetism and 2 D magnetic frustration is dominated by the average valency of iron. In contrast, in the high doping regime (x ~ 1.5), the emergence of a spin glass is controlled by the high degree of cationic disorder, irrespective of the iron valency.

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