The
synthesis of Sr2FeO3 through a hydride reduction
of the Ruddlesden–Popper layered perovskite Sr2FeO4 is reported. Rietveld refinements using synchrotron and neutron
powder diffraction data revealed that the structure contains corner-shared
FeO4 square-planar chains running along the [010] axis,
being isostructural with Sr2CuO3 (Immm space group). Fairly strong Fe–O–Fe and Fe–Fe
interactions along [010] and [100], respectively, make it an S = 2 quasi two-dimensional (2D) rectangular lattice antiferromagnet.
This compound represents the end-member (n = 1) of
the serial system Srn+1FenO2n+1, together with
previously reported Sr3Fe2O5 (n = 2) and SrFeO2 (n = ∞),
thus giving an opportunity to study the 2D-to-3D dimensional crossover.
Neutron diffraction and Mössbauer spectroscopy show the occurrence
of G-type antiferromagnetic order below 179 K, which
is, because of dimensional reduction, significantly lower than those
of the other members, 296 K in Sr3Fe2O5 and 468 K in SrFeO2. However, the temperature dependence
of magnetic moment shows a universal behavior.