Abstract

An original Ruddlesden-Popper phase, La(0.77)Sr(3.23)Co(2.75)C(0.25)O(8.40+δ), was isolated and studied by electron, X-ray, and neutron diffraction. This structure has complex crystal chemistry resulting from a high degree of flexibility in the structure, comprising the disordered introduction of carbonates into a cobalt layer and an important oxygen deficiency with a preferential repartition of vacancies along the layers stacking sequence. The former is necessary for the stabilization of the system, while the latter can be tuned by postsynthetic treatment, yielding in a large variety of cobalt species formal oxidation states ranging from Co(2+)/Co(3+) in the as-made phase to Co(3+)/Co(4+) when annealed under oxygen pressure. The potential richness deriving from this flexibility is illustrated in terms of the magnetotransport properties and includes a resistivity that varies within a range of 5 orders of magnitude after modulation of the oxygen content with the appearance of negative magnetoresistance and ferromagnetic interactions due to Co(3+)/Co(4+) mixed-valence state.

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