Abstract

A novel quadruple perovskite oxide YMn3Co4O12 has been synthesized in high-pressure and high-temperature conditions of 16 GPa and 1473 K, respectively. Rietveld refinement of synchrotron X-ray powder diffraction data reveals that this oxide crystallizes in a cubic quadruple perovskite structure in a space group of Im3 (No. 204) with a 1:3-type atomic ordering of Y and Mn at A-sites, and the bond valence analysis suggests the valence state of YMn3+3Co3+4O12. A ferromagnetic-like transition is observed at ~125 K and the magnetization value reaches up to ~3 µB per formula unit at 5 K. The low-temperature magnetic state can be interpreted as ferrimagnetism with antiparallel alignment of A'-site Mn3+ (S = 2) and B-site Co3+ (high-spin, S = 2), which is in contrast to the antiferromagnetism in other A'-Mn-containing quadruple perovskite oxides. This finding proposes that the coexistence of A’-Mn3+ and B-Co3+ leading to ferrimagnetic state is realized in the specific structure with distinct crystallographic sites.

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