Abstract

The partial substitution of Cu2+ for Pb4+, rather than occurring in the BaPbO3 perovskite as claimed previously, has been identified in the triple-perovskite-slab Intergrowth plumbate Ba4Pb3O10. New non-stoichiometric phases, barium–copper–lead mixed oxides Ba4–xPb3–xCuxO10–δ(x⩽0.33; δ⩽0.67), were prepared at 1243 K in flowing oxygen. They exhibit both barium and oxygen vacancies and Pb4+/Cu2+ ordering in the external perovskite layers of the triple slab, as deduced from X-ray powder structure calculations. Magnetic susceptibility measurements in the range 77–400 K point to the existence of weak ferromagnetic interactions within the perovskite slab. From the value of µ, 30% of the total Cu content is assumed to be oxidized to Cu3+, in agreement with the structural data. Water intercalation is characterized from crystallographic and thermal analysis. The intercalation–deintercalation process is shown to be irreversible. A similar trend with respect to water intercalation is evidenced for the double-perovskite-slab Intergrowth plumbate Ba3Pb2O7.

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