A computational study of hydrogen doping induced metal-to-insulator transition in CaFeO, SrFeO, BaFeO and SmMnO

The metal-to-insulator transition (MIT) in rare earth perovskite oxides has drawn significant research interest for decades to unveil the underlying physics and develop novel electronic materials. Recently, chemical doping induced MIT in SmNiO 3 has been observed experimentally, with its resistivity changed by eight orders of magnitude. The mechanism of switching from one singly occupied Ni e g orbital to two singly occupied e g orbitals upon doping has been proposed by experimentalists and verified by computation. Here, we tested if this mechanism can be generally applied to other perovskite oxides with non-Ni B site elements. We applied first principles density functional theory (DFT) to study a series of perovskite oxides, CaFeO 3 , SrFeO 3 , BaFeO 3 and SmMnO 3 . We investigated the geometry and electronic structures of pure and hydrogen doped oxides. We found that pure CaFeO 3 , SrFeO 3 and BaFeO 3 are metallic while pure SmMnO 3 has a small band gap of 0.69 eV. Upon hydrogen doping, band gap opening was predicted for all four oxides: HSE06 predicted band gap values of 1.58 eV, 1.40 eV, 1.20 eV and 2.55 eV for H-doped CaFeO 3 , SrFeO 3 , BaFeO 3 and SmMnO 3 , respectively. This finding opens up research opportunities for exploring a broader range of materials for MIT to be used in optical and electronic devices. First principles density functional theory calculations were performed to identify transition metal perovskites CaFeO 3 , SrFeO 3 , BaFeO 3 and SmMnO 3 as promising candidates with large band gap opening upon hydrogen doping.