Namba M, Takatsu H, Mikita R, Sijia Y, Murayama K, Li HB, Terada R, Tassel C, Ubukata H, Ochi M, Saez-Puche R, Latasa EP, Ishimatsu N, Shiga D, Kumigashira H, Kinjo K, Kitagawa S, Ishida K, Terashima T, Fujita K, Mashiko T, Yanagisawa K, Kimoto K, and Kageyama H
Perovskite oxides AB O 3 continue to be a major focus in materials science. Of particular interest is the interplay between A and B cations as exemplified by intersite charge transfer (ICT), which causes novel phenomena including negative thermal expansion and metal-insulator transition. However, the ICT properties were achieved and optimized by cationic substitution or ordering. Here we demonstrate an anionic approach to induce ICT using an oxyhydride perovskite, EuVO 2 H, which has alternating layers of EuH and VO 2 . A bulk EuVO 2 H behaves as a ferromagnetic insulator with a relatively high transition temperature ( T C ) of 10 K. However, the application of external pressure to the Eu II V III O 2 H bulk or compressive strain from the substrate in the thin films induces ICT from the Eu II H layer to the V III O 2 layer due to the extended empty V d xy orbital. The ICT phenomenon causes the VO 2 layer to become conductive, leading to an increase in T C that is dependent on the number of carriers in the d xy orbitals (up to a factor of 4 for 10 nm thin films). In addition, a large perpendicular magnetic anisotropy appears with the ICT for the films of <100 nm, which is unprecedented in materials with orbital-free Eu 2+ , opening new perspectives for applications. The present results provide opportunities for the acquisition of novel functions by alternating transition metal/rare earth layers with heteroanions.