TY - JOUR
T1 - Orthorhombic superstructures within the rare earth strontium-doped cobaltate perovskites
T2 - Ln1-xSrxCoO3- δ (Ln=Y3+, Dy3+-Yb3+; 0.750≤x≤0.875)
AU - James, Michael
AU - Avdeev, Maxim
AU - Barnes, Paris
AU - Morales, Liliana
AU - Wallwork, Kia
AU - Withers, Ray
PY - 2007/8
Y1 - 2007/8
N2 - A combination of electron, synchrotron X-ray and neutron powder diffraction reveals a new orthorhombic structure type within the Sr-doped rare earth perovskite cobaltates Ln1-xSrxCoO3- δ (Ln=Y3+, Dy3+, Ho3+, Er3+, Tm3+and Yb3+). Electron diffraction shows a C-centred cell based on a 2√2ap×4ap×4√2ap superstructure of the basic perovskite unit. Not all of these very weak satellite reflections are evident in the synchrotron X-ray and neutron powder diffraction data and the average structure of each member of this series could only be refined based on Cmma symmetry and a 2√2ap×4ap×2√2ap cell. The nature of structural and magnetic ordering in these phases relies on both oxygen vacancy and cation distribution. A small range of solid solution exists where this orthorhombic structure type is observed, centred roughly around the compositions Ln0.2Sr0.8CoO3-δ. In the case of Yb3+ the pure orthorhombic phase was only observed for 0.850≤x≤0.875. Tetragonal (I4/mmm; 2ap×2ap×4ap) superstructures were observed for compositions having higher or lower Sr-doping levels, or for compounds with rare earth ions larger than Dy3+. These orthorhombic phases show mixed valence (3+/4+) cobalt oxidation states between 3.2+ and 3.3+. DC magnetic susceptibility measurements show an additional magnetic transition for these orthorhombic phases compared to the associated tetragonal compounds with critical temperatures > 330 K.
AB - A combination of electron, synchrotron X-ray and neutron powder diffraction reveals a new orthorhombic structure type within the Sr-doped rare earth perovskite cobaltates Ln1-xSrxCoO3- δ (Ln=Y3+, Dy3+, Ho3+, Er3+, Tm3+and Yb3+). Electron diffraction shows a C-centred cell based on a 2√2ap×4ap×4√2ap superstructure of the basic perovskite unit. Not all of these very weak satellite reflections are evident in the synchrotron X-ray and neutron powder diffraction data and the average structure of each member of this series could only be refined based on Cmma symmetry and a 2√2ap×4ap×2√2ap cell. The nature of structural and magnetic ordering in these phases relies on both oxygen vacancy and cation distribution. A small range of solid solution exists where this orthorhombic structure type is observed, centred roughly around the compositions Ln0.2Sr0.8CoO3-δ. In the case of Yb3+ the pure orthorhombic phase was only observed for 0.850≤x≤0.875. Tetragonal (I4/mmm; 2ap×2ap×4ap) superstructures were observed for compositions having higher or lower Sr-doping levels, or for compounds with rare earth ions larger than Dy3+. These orthorhombic phases show mixed valence (3+/4+) cobalt oxidation states between 3.2+ and 3.3+. DC magnetic susceptibility measurements show an additional magnetic transition for these orthorhombic phases compared to the associated tetragonal compounds with critical temperatures > 330 K.
KW - Neutron diffraction
KW - Oxygen vacancy ordering
KW - Perovskite superstructure
KW - Phase diagram
KW - Strontium-doped cobaltate
UR - http://www.scopus.com/inward/record.url?scp=34548095068&partnerID=8YFLogxK
U2 - 10.1016/j.jssc.2007.04.029
DO - 10.1016/j.jssc.2007.04.029
M3 - Article
SN - 0022-4596
VL - 180
SP - 2233
EP - 2247
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
IS - 8
ER -