Oxygen deficiency-induced anomalous enhancement of Neel temperature and magnetic coupling for Bi0.9Ca0.1FeO3−δ and Bi0.9Pb0.1FeO3−δ

Abstract

Temperature dependent neutron diffraction patterns of the Ca-doped BiFeO3 and Pb-doped BiFeO3 show that their Neel temperatures (TN) increase to 710 K and 680 K, while pure BiFeO3 has a TN ∼ 643 K. This anomalous increase in TN was investigated in detail by probing near edge X-ray absorption fine spectroscopy, X-ray photoemission spectroscopy techniques and structural refinement of the neutron diffraction pattern. Room temperature X-ray absorption spectroscopy clearly shows that there is no evidence of mixed valence states despite divalent cation doping in trivalent Bi-sites. A room temperature X-ray photoemission spectroscopy study revealed that instead of mixed valences, divalent doping has introduced oxygen vacancies in the system. Structural refinement of neutron diffraction patterns also supports the presence of oxygen vacancies in Bi0.9Ca0.1FeO3−δ and Bi0.9Pb0.1FeO3−δ. Oxygen deficiency plays a pivotal role in reducing FeO bond length in FeO6 octahedra and hence increasing the FeOFe bond angle in Bi0.9Ca0.1FeO3−δ and Bi0.9Pb0.1FeO3−δ. This decreased FeO bond length and increased FeOFe bond angle favors the Goodenough-Kanamori-Anderson (GKA) coupling. The GKA coupling increases the magnetic interaction between the spins and hence increases the TN. Additionally, doping of divalent cations (Ca2+ and Pb2+) results in the destruction of cycloidal spin structure and formation of a simple antiferromagnetic (AFM) structure. This structure can easily be canted near the heterogeneous interface with a ferromagnetic layer to induce the Dzyaloshinskii-Moriya (DM) interaction and enhance the magneto-electric (M–E) coupling.