journal article·2021-04-03Open access

Preparation of Sm0.2Ce0.8O1.9electrolytes via the chitosan templating method and investigation of the sintering behavior

Dilara Güçtaş, Vedat Sarıboğa, M.A. Faruk Öksüzömer

Abstract

Sm0.2Ce0.8O1.9 electrolytes were prepared using a novel chitosan templating method. To examine the sintering kinetics of the materials, 5 minutes, 1 hour, and 6 hours of sintering processes were carried out at 1200, 1300, and 1400 ⁰C. The phase structure of the sintered samples was clarified by XRD analysis. The morphological structure was examined by SEM and the average grain sizes were calculated with the Linear Intercept Method. The dominant diffusion mechanism and grain growth activation energies during sintering were calculated for the SDC20 electrolytes synthesized by the chitosan templating method for the first time. In addition to the sintering study, the ionic conductivities of the samples were determined by electrochemical impedance spectroscopy. The maximum O2- conductivity value for the 1300–6 sample was found to be 0.052 S.cm−1. The study showed that the chitosan templating method is an effective way of synthesizing SDC20 materials.
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Research context

OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides · Catalysis and Oxidation Reactions

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

Affiliations

Chemical Engineering Department, Istanbul University - Cerrahpasa, Istanbul, Turkey

Funding

Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi · Türkiye Bilimsel ve Teknolojik Araştirma Kurumu

References (31)

Show source-provided references
1. 10.1016/j.jpowsour.2010.11.04110.1016/j.jpowsour.2010.11.041 ↗
2. 10.1016/j.matlet.2005.07.08810.1016/j.matlet.2005.07.088 ↗
3. 10.1016/j.ceramint.2008.06.01410.1016/j.ceramint.2008.06.014 ↗
4. Tian R · Neuroscience · 2011 · 192 · 58010.1016/j.neuroscience.2011.06.066 ↗
5. Fu YP · J Am Ceram Soc · 2008 · 91 · 12710.1111/j.1551-2916.2007.01923.x ↗
6. 10.1016/S1293-2558(03)00123-710.1016/S1293-2558(03)00123-7 ↗
7. 10.1016/j.jeurceramsoc.2013.01.01610.1016/j.jeurceramsoc.2013.01.016 ↗
8. 10.1016/j.jpowsour.2006.07.05010.1016/j.jpowsour.2006.07.050 ↗
9. 10.1016/j.micromeso.2010.12.01210.1016/j.micromeso.2010.12.012 ↗
10. 10.1016/j.materresbull.2011.07.04910.1016/j.materresbull.2011.07.049 ↗
11. 10.1533/978184569994910.1533/9781845699949 ↗
12. 10.1007/s10973-007-8321-310.1007/s10973-007-8321-3 ↗
13. 10.1021/bm060531110.1021/bm0605311 ↗
14. 10.1016/j.ijhydene.2007.10.02610.1016/j.ijhydene.2007.10.026 ↗
15. 10.1016/j.ceramint.2013.02.06910.1016/j.ceramint.2013.02.069 ↗
16. 10.1016/j.jallcom.2011.09.01610.1016/j.jallcom.2011.09.016 ↗
17. 10.1111/j.1151-2916.1970.tb12007.x10.1111/j.1151-2916.1970.tb12007.x ↗
18. 10.1016/j.jpowsour.2012.08.02010.1016/j.jpowsour.2012.08.020 ↗
19. Rahaman MN · 1995
20. 10.1016/j.actamat.2004.01.01410.1016/j.actamat.2004.01.014 ↗
21. 10.1111/j.1551-2916.2010.04233.x10.1111/j.1551-2916.2010.04233.x ↗
22. 10.1016/S0955-2219(01)00240-010.1016/S0955-2219(01)00240-0 ↗
23. 10.1016/0956-7151(90)90185-J10.1016/0956-7151(90)90185-J ↗
24. 10.1002/047171624310.1002/0471716243 ↗
25. 10.1023/B:JMSC.0000007749.72739.bb10.1023/B:JMSC.0000007749.72739.bb ↗
26. 10.1016/S0167-577X(02)00673-010.1016/S0167-577X(02)00673-0 ↗
27. 10.1016/j.ssi.2004.09.04610.1016/j.ssi.2004.09.046 ↗
28. 10.1016/S0167-577X(03)00578-010.1016/S0167-577X(03)00578-0 ↗
29. 10.1016/j.actamat.2005.10.00410.1016/j.actamat.2005.10.004 ↗
30. 10.1016/j.jssc.2003.09.02010.1016/j.jssc.2003.09.020 ↗
31. 10.1016/B978-0-12-655280-5.50010-910.1016/B978-0-12-655280-5.50010-9 ↗