Structure and properties of the CaFe2O4-type cobalt oxide CaCo2O4

The calcium cobalt oxide CaCo2O4 was synthesized for the first time and characterized from a powder X-ray diffraction study, measuring magnetic susceptibility, specific heat, electrical resistivity, and thermoelectric power. CaCo2O4 crystallizes in the CaFe2O4 (calcium ferrite)-type structure, consisting of an edge- and corner-shared CoO6 octahedral network. The structure of CaCo2O4 belongs to an orthorhombic system (space group: Pnma) with lattice parameters, a=8.789(2) Å, b=2.9006(7) Å and c=10.282(3) Å. Curie–Weiss-like behavior in magnetic susceptibility with the nearly trivalent cobalt low-spin state (Co3+, 3d  t2g6, S=0), semiconductor-like temperature dependence of resistivity (ρ=3×10−1 Ω cm at 380 K) with dominant hopping conduction at low temperature, metallic-temperature-dependent large thermoelectric power (Seebeck coefficient: S=+147 μV/K at 380 K), and Schottky-type specific heat with a small Sommerfeld constant (γ=4.48(7) mJ/Co mol K2), were observed. These results suggest that the compound possesses a metallic electronic state with a small density of states at the Fermi level. The doped holes are localized at low temperatures due to disorder in the crystal. The carriers probably originate from slight off-stoichiometry of the phase. It was also found that S tends to increase even more beyond 380 K. The large S is possibly attributed to residual spin entropy and orbital degeneracy coupled with charges by strong electron correlation in the cobalt oxides.

A new calcium cobalt oxide CaCo2O4 phase, which crystallizes in the calcium-ferrite-type structure (space group: Pnma; a=8.789(2) Å, b=2.9006(7) Å, and c=10.282(3) Å), has been synthesized for the first time under high temperature and high pressure (1500 °C, 6 GPa). This compound exhibits large thermoelectric power (Seebeck coefficient: S=+147 μV/K at 380 K) and an unsaturated temperature dependence of S around 380 K.Figure optionsDownload as PowerPoint slide