TY - JOUR
T1 - Chemical stability of La 1-xSr xCrO 3 in oxidizing atmospheres
AU - Miyoshi, Shogo
AU - Onuma, Shigenori
AU - Kaimai, Atsushi
AU - Matsumoto, Hiroshige
AU - Yashiro, Keiji
AU - Kawada, Tatsuya
AU - Mizusaki, Junichiro
AU - Yokokawa, Harumi
N1 - Funding Information:
The authors acknowledge the financial support from the Ministry of Education, Culture, Science, Sports and Technology, Grant-in-Aid for Scientific Research (A), 13305046, 2002. Part of this study was also supported by NEDO of JAPAN.
PY - 2004/11
Y1 - 2004/11
N2 - The single-phase region of La 1-xSr xCrO 3 (x=0.1, 0.2, 0.3) was precisely determined as a function of temperature, P O2 and Sr content. The powders with the nominal composition of La 1-xSr xCrO 3 were equilibrated under various conditions, and then identified by XRD analyses. To confirm the equilibration, two independent experiments were performed for each composition observing (i) the precipitation of the second phase from a single-phase solid solution, and (ii) the formation of the single phase from the constituent oxides. Two kinds of second phases, SrCrO 4 and an unknown phase, were observed depending on the conditions. The second phases tended to appear at low temperature, in high P O2 and with a large Sr content. The single-phase regions obtained via the two equilibration routes were in good agreement with each other. The thermodynamic calculations on the supposition of ideality of the solid solution essentially reproduced the experimental results. When this material is used as the interconnects of solid oxide fuel cells, much attention should be paid to its relatively narrow solubility range of Sr; for example, the solubility limit is approximately 0.1 under a typical cathode-side condition (1273K, air).
AB - The single-phase region of La 1-xSr xCrO 3 (x=0.1, 0.2, 0.3) was precisely determined as a function of temperature, P O2 and Sr content. The powders with the nominal composition of La 1-xSr xCrO 3 were equilibrated under various conditions, and then identified by XRD analyses. To confirm the equilibration, two independent experiments were performed for each composition observing (i) the precipitation of the second phase from a single-phase solid solution, and (ii) the formation of the single phase from the constituent oxides. Two kinds of second phases, SrCrO 4 and an unknown phase, were observed depending on the conditions. The second phases tended to appear at low temperature, in high P O2 and with a large Sr content. The single-phase regions obtained via the two equilibration routes were in good agreement with each other. The thermodynamic calculations on the supposition of ideality of the solid solution essentially reproduced the experimental results. When this material is used as the interconnects of solid oxide fuel cells, much attention should be paid to its relatively narrow solubility range of Sr; for example, the solubility limit is approximately 0.1 under a typical cathode-side condition (1273K, air).
UR - http://www.scopus.com/inward/record.url?scp=8844250740&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=8844250740&partnerID=8YFLogxK
U2 - 10.1016/j.jssc.2004.04.054
DO - 10.1016/j.jssc.2004.04.054
M3 - Article
AN - SCOPUS:8844250740
SN - 0022-4596
VL - 177
SP - 4112
EP - 4118
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
IS - 11
ER -