| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1593338 | Solid State Communications | 2012 | 5 Pages |
The title compounds have been synthesized by a citrate technique. The crystal structure of these materials has been studied at room temperature from high-resolution neutron powder diffraction data. In, Ru, and M=Mn,Fe are distributed at random over the metal sites of a C-M2O3 bixbyite-type structure, space group Ia3̄, with a=9.89000(3)Å for M=Mn and a=10.07536(4)Å for M=Fe. It is well known that In2O3 is able to dissolve certain amounts of transition metals but, at ambient pressure, the solubility is rather small, lower than s=0.5s=0.5 in In2−sMsO3. Here, we describe a substantial incorporation of magnetic transition metals into In2O3 of half of the metal positions (s=1s=1), by simple thermal treatment at temperatures in the 1300–1400 °C range. Although a bond-valence study shows unrealistically low valences for Ru ions, which statistically occupy the metal positions, replacing In, the magnetic properties suggest a valence equilibrium Ru3+/M3+↔Ru4+/M2+. In2RuFeO6 shows antiferromagnetic interactions below TN≈95K, with a very weak ferromagnetism effect at low temperatures.
► The crystal structure of In2RuMnO6 and In2RuFeO6 was studied from neutron powder diffraction data. ► Incorporation of magnetic transition metals into In2O3 of half of the metal positions was obtained. ► In, Ru, and M are distributed at random over the metal sites of a bixbyite-type structure. ► The magnetic properties of these phases suggest a valence equilibrium Ru3+/M3+↔Ru4+/M2+.
