RESUMEN
Studies on magnetic oxyhydrides have been almost limited to perovskite-based lattices with corner-sharing octahedra with a M-H-M (M: transition metal) angle of θ â¼ 180°. Using a high-pressure method, we prepared BaCrO2H with a 6H-type hexagonal perovskite structure with corner- and face-sharing octahedra, offering a unique opportunity to investigate magnetic interactions based on a θ â¼ 90° case. Neutron diffraction for BaCrO2H revealed an antiferromagnetic (AFM) order at TN â¼ 375 K, which is higher than â¼240 K in BaCrO3-xFx. The relatively high TN of BaCrO2H can be explained by the preferred occupancy of H- at the face-sharing site that provides AFM superexchange in addition to AFM direct exchange interactions. First-principles calculations on BaCrO2H in comparison with BaCrO2F and BaMnO3 further reveal that the direct Cr-Cr interaction is significantly enhanced by shortening the Cr-Cr distance due to the covalent nature of H-. This study provides a useful strategy for the extensive control of magnetic interactions by exploiting the difference in the covalency of multiple anions.
RESUMEN
We report the epitaxial thin-film synthesis of SrCu3O4 with infinitely stacked Cu3O4 layers composed of edge-sharing CuO4 square planes, using molecular-beam epitaxy. Experimental and theoretical characterizations showed that this material is a metastable phase that can exist by applying tensile biaxial strain from the (001)-SrTiO3 substrate. SrCu3O4 shows an insulating electrical resistivity in accordance with the Cu2+ valence state revealed by X-ray photoelectron spectroscopy. First-principles calculations also indicated that the unoccupied d3z2-r2 band becomes substantially stabilized owing to the absence of apical anions, in contrast to A2Cu3O4Cl2 (A = Sr, Ba) with an A2Cl2 block layer and therefore a trans-CuO4Cl2 octahedron. These results suggest that SrCu3O4 is a suitable parent material for electron-doped superconductivity based on the Cu3O4 plane.