This research demonstrates the synthesis of a cation-ordered perovskite, showing significant charge ordering below 50 K, indicating its unique properties.
Many cation-ordered perovskites have been reported, exploiting differences in cation size and valence. They are mostly double perovskite structures with rock-salt ordering, while cation ordering with periodicity longer than three primitive perovskite cells is relatively rare. Here, we successfully synthesized a 5-fold cation-ordered perovskite oxide, Sr₅V1.5Fe3.5O₁₅, through topochemical oxidation of oxygen-deficient perovskite Sr₅V1.5Fe3.5O₁₄. The cation ordering in the precursor, with 5-fold periodicity of triple 100% Fe layers and double 75% V and 25% Fe layers along the [111] direction of the primitive perovskite cell, is preserved during topochemical oxidation, as evidenced by synchrotron and neutron diffraction analyses. Mössbauer spectroscopy measurements for Sr₅V1.5Fe3.5O₁₅ suggest a sign of charge ordering to Fe³⁺ and Fe⁴⁺ below ∼50 K, where a short-range order is a plausible picture due to the existence of the iron-poor double layers.
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Nagase et al. (2026) studied this question.
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