journal article·2003-01Open access

Low-temperature fabrication and electrical property of 10 mol% Sm2O3-doped CeO2 ceramics

Yarong Wang, Toshiyuki Mori, Ji-Guang Li, Yoshiyuki Yajima

Abstract

Ten mol% Sm2O3-doped CeO2 solid-solution (20SDC) powders have been synthesized via carbonate coprecipitation using ammonium hydrogen carbonate (AHC) and urea as the precipitants, respectively. Characterizations were achieved by elemental analysis, X-ray diffractometry, differential thermal analysis/thermogravimetry, and FESEM. An amorphous hydroxyl carbonate precursor (Ce,Sm)(OH)CO3·2H2O having nanosized (~10 nm) spherical particles was formed with AHC, while a mixture of crystalline (Ce,Sm)2(CO3)2(OH)2·H2O and (Ce,Sm)2O(CO3)2·H2O phases exhibiting irregular particle morphologies was obtained with urea. Both the precursors convert to oxide solid solutions without any phase detected corresponding to Sm2O3 during calcination. The oxide powder processed via the AHC method can be sintered to >99% of the theoretical at a low temperature of 1200 ˚C, due to the good dispersion and ultrafine size (~15 nm) of the particles, while that from the urea method can only reach ,67.2% dense at the same temperature. Electrical conductivity of the densified ceramic was measured in air in the range 400—700 ˚C by the DC three-point method, and an activation energy of ~60.5 kJ/mol was derived from the experimental data.© 2003 Elsevier Ltd. All rights reserved.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Catalytic Processes in Materials Science · Catalysis and Oxidation Reactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Eco-materials Research Center, National Institute for Materials Science, Namiki 1-1,, Tsukuba, Ibaraki, 305-0044, Japan

Advanced Materials Laboratory, National Institute for Materials Sciencea, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan

References (28)

Show source-provided references
1. 10.1111/j.1151-2916.1993.tb03645.x10.1111/j.1151-2916.1993.tb03645.x ↗
2. 10.1016/0167-2738(95)00229-410.1016/0167-2738(95)00229-4 ↗
3. 10.1016/0167-2738(89)90061-110.1016/0167-2738(89)90061-1 ↗
4. 10.1149/1.213414310.1149/1.2134143 ↗
5. 10.1557/JMR.1999.012710.1557/JMR.1999.0127 ↗
6. 10.1007/BF0035131810.1007/BF00351318 ↗
7. 10.1016/0167-2738(95)99031-H10.1016/0167-2738(95)99031-H ↗
8. Y. Wang · J. Am. Ceram. Soc. · 2002 · 85 · 310510.1111/j.1151-2916.2002.tb00591.x ↗
9. 10.1111/j.1151-2916.2002.tb00465.x10.1111/j.1151-2916.2002.tb00465.x ↗
10. 10.1246/bcsj.52.42810.1246/bcsj.52.428 ↗
11. K. Hayashi · J. Ceram. Soc. Jpn · 1990 · 98 · 44410.2109/jcersj.98.444 ↗
12. S. Kato · Yogyo-Kyokai-Shi · 1976 · 84 · 21510.2109/jcersj1950.84.969_215 ↗
13. K. Hayashi · J. Ceram. Soc. Jpn · 1991 · 99 · 55010.2109/jcersj.99.550 ↗
14. S. Kato · Yogyo-Kyokai-Shi · 1976 · 84 · 25510.2109/jcersj1950.84.970_255 ↗
15. 10.1016/0021-9797(87)90486-310.1016/0021-9797(87)90486-3 ↗
16. M. Akinc · Adv. Ceram. Mater. · 1987 · 2 · 23210.1111/j.1551-2916.1987.tb00087.x ↗
17. 10.1016/0021-9797(88)90286-X10.1016/0021-9797(88)90286-X ↗
18. D.E. Williams · 1964
19. 10.1021/ja01623a01110.1021/ja01623a011 ↗
20. N.E. Topp · The Chemistry of Rare-Earth Elements · 1965
21. 10.1021/cm010148x10.1021/cm010148x ↗
22. E.L. Head · Rare Earth Research II · 1964 · 51
23. 10.1107/S056774086900322010.1107/S0567740869003220 ↗
24. M. Akinc · Fourth Euro Ceramics · 1995 · 3
25. 10.1111/j.1151-2916.1988.tb07534.x10.1111/j.1151-2916.1988.tb07534.x ↗
26. 10.1021/cm970425t10.1021/cm970425t ↗
27. 10.1016/S0167-2738(97)00309-310.1016/S0167-2738(97)00309-3 ↗
28. 10.1149/1.212901810.1149/1.2129018 ↗