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Eu3Ta2ON5: an n = 2 Ruddlesden-Popper ferromagnetic oxynitride with long-range ordered anion vacancies
Judith Oró-Solé1, Jhonatan Ricardo Guarín1, Carlos Frontera1
1Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus UAB, 08193 Bellaterra, Spain. amparo.fuertes@icmab.es.
Abstract:
The new compound Eu3Ta2ON5 with an n = 2 Ruddlesden-Popper structure has been prepared by solid state reaction between EuN, Eu2O3 and Ta3N5 at 1200 °C under N2. It crystallizes in the I4/mmm space group with unit cell parameters a = 3.98240(1) Å and c = 20.42020(6) Å and has anion vacancies in central A-site layers of the perovskite blocks, where tantalum is in a square pyramidal coordination polyhedron with composition [TaO0.5N4.5] and europium is 8-coordinated. The perovskite blocks intergrow with [EuO0.5N0.5] NaCl-type layers of the Ruddlesden-Popper structure. Electron Energy Loss spectrum imaging shows a mixed Eu2+/Eu3+ valence with preferred occupation of Eu3+ in the 8-coordinated sites. Magnetic susceptibility measurements are consistent with the formal composition Eu22+Eu3+Ta5+2ON5 and indicate ferromagnetic order of Eu2+ ions below TC = 20 K. Interestingly, despite the oxynitride containing non-magnetic Eu3+ ions (7F0), the Curie temperature is found to be much larger than in related Eu2TiO4 and Eu3Ti2O7 Ruddlesden-Popper compounds (≈9-10 K), which is attributed to the covalency-reinforced Eu2+-N/O-Eu2+ superexchange interactions.
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