Structural studies of a mixed-valence state in the incommensurate composite crystal Sr1.261CoO3

Abstract

The incommensurate modulated crystal structure of the hexagonal cobalt oxide Sr_1.261CoO₃ has been studied using a four-dimensional (4D) superspace profile analysis of neutron powder diffraction data. Sr_1.261CoO₃ is a composite crystal that consists of the CoO₃] and 2Sr] subsystems. The CoO₃] subsystem forms 1D chains that run parallel to the c-axis and consist of face-sharing CoO₆ polyhedra with octahedral (Oh) and trigonal prismatic (TP) coordinations. The structure analysis reveals that the CoO₃] chains contain 73.9% Oh and 26.1% TP sites, and that the TP sites have longer Co–O bonds than the Oh sites: d_av. =2.039(4) Å (TP) and 1.895(3) Å (Oh). The averaged Co bond valences are Co^3.56(3)+ in the Oh sites and Co^2.45(3)+ in the TP sites, suggesting that a considerable amount of Co³⁺ ions are mixed with Co⁴⁺ions in the Oh sites and with Co²⁺ ions in the TP sites. The observed magnetic susceptibility can be well explained assuming that the compound has the Co mixed-valence state with the spin configurations of S=0 low-spin state for Co³⁺(dε⁶), S=1/2 low-spin state for Co⁴⁺(dε⁵) and S=3/2 high-spin state for Co²⁺(dε⁵dγ²). The Weiss temperature, approximately 0.8 K, implies that Sr_1.261CoO₃ naturally assumes a Curie paramagnetic state, probably owing to the obstruction of the intrachain magnetic interaction by the nonmagnetic Co³⁺ ions. These results suggest that the nonmagnetic Co³⁺ ions play an essential role in the magnetism of Sr_2γCoO₃ systems.