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Preparation of High Surface Area Ni-SDC Cermets Using a Surfactant-Assisted Co-Precipitation Method

Published online by Cambridge University Press:  01 February 2011

Sang Joon Park
Affiliation:
[email protected], Kyungwon University, Chemical & Bio Engineering, Soojung-Ku, Bokjungdong, San 65, Dept. of Chemical & Bio Engineering, Seongnam, N/A, N/A, Korea, Republic of
Tae Wook Eom
Affiliation:
[email protected], Kyungwon University, Chemical & Bio Engineering, Seongnam, N/A, N/A, Korea, Republic of
Jae Eun Oh
Affiliation:
[email protected], Kyungwon University, Chemical & Bio Engineering, Seongnam, N/A, N/A, Korea, Republic of
Hae Kwang Yang
Affiliation:
[email protected], Kyungwon University, Chemical & Bio Engineering, Seongnam, N/A, N/A, Korea, Republic of
Kyung Hwan Kim
Affiliation:
[email protected], Kyungwon University, Electrical Engineering, Seongnam, N/A, Korea, Republic of
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Abstract

A surfactant-assisted co-precipitation method was employed for obtaining high surface area Ni-SDC with improved structural properties for SOFC applications. In the work, a cationic surfactant, cetyltrimethylammonium bromide(CTAB) was employed with NiCl2, SmCl3 and CeCl3 as precursors and NH4OH as mineralizer. The elimination of surfactants upon calcination gives rise to the formation of high surface area NiO-SDC. When calcined at 600°C, the powders with surface area of 249 m2/g, were obtained and the pore size was 14.45 nm. The powders consist of two phases, the cubic NiO and SDC confirmed with X-ray diffraction identification.

Type
Research Article
Copyright
Copyright © Materials Research Society 2006

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References

1 Stambouli, A. Boudghene, Traversa, E., Renewable and Sustainable Energy Reviews. 6, 433 (2002).Google Scholar
2 Williford, R.E., Journal of Electron Spectroscopy and related pheomena. 150, 171 (2006).Google Scholar
3 Berkel, F. P. F. van, Heuveln, F. H. van and Huijsmans, J. P. P., Solid State Ionic. 72, 240 (1994).Google Scholar
4 Steele, B. C. H.. Solid State Ionics. 94, 239 (1997).Google Scholar
5 Kharton, V.V., Marques, F.M.B., Atkinson, A., Solid State Ionics. 174, 135 (2004).Google Scholar
6 Mamak, Marc, Coombs, Neil, Ozin, Geoffrey A., Chem. Mater. 13, 3564 (2001).Google Scholar
7 Lenormand, Pascal, Castillo, Simone, Gonzalez, Jose-Ramon, Laberty-Robert, Christel, Ansart, Florence, Solid State Sciences. 7, 159 (2005).Google Scholar
8 Zhu, Bin, Liu, Xiangrong, Schober, T., Electrochem. Communication. 6, 278 (2004).Google Scholar
9 Fang, Xiaohong, Zhu, Guangyan, Xia, Changrong, Liu, Xingqin, Meng, Guangyao, Solid State Ionics. 168, 31 (2004).Google Scholar
10 Li, Ji-Guang, Ikegami, Takayasu, Mori, Toshiyuki, Wada, Toshiaki, Chem. Mater. 13, 2913 (2001).Google Scholar
11 Jenkins, R., and Snyder, R. L. in Introduction to X-ray Powder Diffractometry, edited by Winefordner, J. D. (Wiley Interscince, 1996) pp. 8990.Google Scholar
12 Terribile, Daniela, Trovarelli, Alessandro, Llorca, Jordi, Leitenburg, Carla de, Dolcetti, Giuliano, Catalysis Today. 43, 79 (1998).Google Scholar