Complex structural ordering of the oxygen deficiency in La_0.5Ca_2.5Mn₂O_7−δ Ruddlesden–Popper phases

Ruddlesden–Popper oxides, (AO)(ABO₃)_n, occupy a prominent place in the landscape of materials research because of their intriguing potential applications. Compositional modifications to the cation sublattices, A or B, have been explored in order to achieve enhanced functionalities. However, changes to the anionic sublattice have been much less explored. In this work, new oxygen-deficient manganese Ruddlesden–Popper-related phases, La_0.5Ca_2.5Mn₂O_6.5 and La_0.5Ca_2.5Mn₂O_6.25, have been synthesized by controlled reduction of the fully oxidized n = 2 term La_0.5Ca_2.5Mn₂O₇. A complete structural and compositional characterization, by means of neutron diffraction, electron diffraction and atomically resolved scanning transmission electron microscopy and electron energy-loss spectroscopy techniques, allows the proposition of a topotactic reduction pathway through preferential oxygen removal in the [MnO₂] layers along [031] and [] directions. The gradual decrease of the Mn oxidation state, accommodated by short-range ordering of anionic vacancies, reasonably explains the breaking of ferromagnetic interactions reinforcing the emergence of antiferromagnetic ones. Additional short-range order–disorder phenomena of La and Ca cations have been detected in the reduced La_0.5Ca_2.5Mn₂O_7−δ, as previously reported in the parent compound.