TY - JOUR
T1 - Magnetic properties of the ordered double perovskite Sr 2MnTeO6
AU - Ortega-San Martin, Luis
AU - Chapman, Jon P.
AU - Lezama, Luis
AU - Sánchez Marcos, Jorge
AU - Rodríguez-Fernández, Jesús
AU - Arriortua, María I.
AU - Rojo, Teófilo
PY - 2006/4/3
Y1 - 2006/4/3
N2 - The ordered double perovskite Sr2MnTeO6 was prepared by the freeze-drying method. The nuclear and magnetic structures were determined by both X-ray and neutron (D2B and D1B) powder diffraction. A distorted, double perovskite structure type described by the monoclinic P121/n1 space group is observed at room temperature and down to 4 K. The room temperature EPR spectrum shows an isotropic signal centered at a g value of 1.998 indicating that manganese ions are in the +2 oxidation state. At low temperature the EPR signal broadens as the exchange and dipolar interactions between Mn2+ cations increase. Below 25 K no signal is observed, indicating that the sample is magnetically ordered. The dc magnetic susceptibility shows the existence of antiferromagnetic interactions with an ordering temperature around 20 K. A sharp λ-type anomaly observed at 19 K in the specific heat curve and refinement of low-temperature neutron diffraction data confirm the presence of a three-dimensional, antiferromagnetic ordered structure with an ordering temperature of ca. 23 K. The propagation vector of the magnetic structure is k = [0,0,0], yielding a type I antiferromagnetic ordering between Mn2+ (S = 5/2) cations. At 2 K, each manganese ion is antiferromagnetically aligned to 8 out of 12 nearest-neighbors at an approximate distance of 5.6 Å. This magnetic structure can be viewed as being composed of ferromagnetic arrangement of Mn2+ moments in the ab plane, coupled antiferromagnetically along the c axis.
AB - The ordered double perovskite Sr2MnTeO6 was prepared by the freeze-drying method. The nuclear and magnetic structures were determined by both X-ray and neutron (D2B and D1B) powder diffraction. A distorted, double perovskite structure type described by the monoclinic P121/n1 space group is observed at room temperature and down to 4 K. The room temperature EPR spectrum shows an isotropic signal centered at a g value of 1.998 indicating that manganese ions are in the +2 oxidation state. At low temperature the EPR signal broadens as the exchange and dipolar interactions between Mn2+ cations increase. Below 25 K no signal is observed, indicating that the sample is magnetically ordered. The dc magnetic susceptibility shows the existence of antiferromagnetic interactions with an ordering temperature around 20 K. A sharp λ-type anomaly observed at 19 K in the specific heat curve and refinement of low-temperature neutron diffraction data confirm the presence of a three-dimensional, antiferromagnetic ordered structure with an ordering temperature of ca. 23 K. The propagation vector of the magnetic structure is k = [0,0,0], yielding a type I antiferromagnetic ordering between Mn2+ (S = 5/2) cations. At 2 K, each manganese ion is antiferromagnetically aligned to 8 out of 12 nearest-neighbors at an approximate distance of 5.6 Å. This magnetic structure can be viewed as being composed of ferromagnetic arrangement of Mn2+ moments in the ab plane, coupled antiferromagnetically along the c axis.
KW - EPR spectroscopy
KW - Magnetic structure
KW - Neutron diffraction
KW - Perovskite phases
UR - http://www.scopus.com/inward/record.url?scp=33645795043&partnerID=8YFLogxK
U2 - 10.1002/ejic.200500880
DO - 10.1002/ejic.200500880
M3 - Article
AN - SCOPUS:33645795043
SN - 1434-1948
SP - 1362
EP - 1370
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 7
ER -