TY - JOUR
T1 - Cation ordering in the perovskite-type Sr2-xLaxCo1-yTa1+yO6
AU - Kato, Sumio
AU - Kawase, Tatsuhiro
AU - Ohshima, Yozo
AU - Sugai, Mikio
AU - Takizawa, Hirotsugu
AU - Endo, Tadashi
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1999/6/30
Y1 - 1999/6/30
N2 - Perovskite-related solid solutions, Sr2-xLaxCu1-yTa1+yOz, were synthesized by solid-state reaction at 1200°C in air. The crystalline phases were identified by powder X-ray diffraction. The perovskite-type solid solutions with different ordering types were observed including simple cubic perovskite-type (random), the Ba(Sr1/3Ta2/3)O3-type (1:2 ordering) and the (NH4)3FeF6-type (1:1 ordering). The 1:2 ordering phase formed near the Sr2(Co0.67Ta1.33)O6 composition. In the composition range, 0≤y≤0.2, the random and the 1:1 ordered phases formed. In the higher La3+ content region, the 1:1 ordering phase was observed. The valency state of Co decreased with increasing La3+ content and the perovskite cell expanded resulting from the increase of the average ionic radii on (Co,Ta) site The 1:1 ordering of the ions on the octahedral site was found to be affected by the size difference of the ions more than the charge difference in this system.
AB - Perovskite-related solid solutions, Sr2-xLaxCu1-yTa1+yOz, were synthesized by solid-state reaction at 1200°C in air. The crystalline phases were identified by powder X-ray diffraction. The perovskite-type solid solutions with different ordering types were observed including simple cubic perovskite-type (random), the Ba(Sr1/3Ta2/3)O3-type (1:2 ordering) and the (NH4)3FeF6-type (1:1 ordering). The 1:2 ordering phase formed near the Sr2(Co0.67Ta1.33)O6 composition. In the composition range, 0≤y≤0.2, the random and the 1:1 ordered phases formed. In the higher La3+ content region, the 1:1 ordering phase was observed. The valency state of Co decreased with increasing La3+ content and the perovskite cell expanded resulting from the increase of the average ionic radii on (Co,Ta) site The 1:1 ordering of the ions on the octahedral site was found to be affected by the size difference of the ions more than the charge difference in this system.
UR - http://www.scopus.com/inward/record.url?scp=0345476709&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0345476709&partnerID=8YFLogxK
U2 - 10.1016/S0925-8388(99)00004-3
DO - 10.1016/S0925-8388(99)00004-3
M3 - Article
AN - SCOPUS:0345476709
SN - 0925-8388
VL - 285
SP - 64
EP - 68
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
IS - 1-2 Complete
ER -