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Direct Applicability of La0.6Sr0.4CoO3 (-) (delta) Thin Film Cathode to Yttria Stabilised Zirconia Electrolytes at T <= 650 degrees C

Authors
Noh, H. -S.Son, J. -W.Lee, H.Park, J. -S.Lee, H. -W.Lee, J. -H.
Issue Date
Dec-2010
Publisher
WILEY-V C H VERLAG GMBH
Keywords
Lanthanum Strontium Cobalt Oxide (LSC); Micro-Solid Oxide Fuel Cells (Micro-SOFCs); Pulsed Laser Deposition (PLD); Thin Film Cathodes
Citation
FUEL CELLS, v.10, no.6, pp.1057 - 1065
Indexed
SCIE
SCOPUS
Journal Title
FUEL CELLS
Volume
10
Number
6
Start Page
1057
End Page
1065
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/115294
DOI
10.1002/fuce.201000009
ISSN
1615-6846
Abstract
For investigating the direct applicability of highly active cobalt containing cathodes on YSZ electrolytes at a lower processing and operating temperature range (T <= 650 degrees C), we fabricated a thin film lanthanum strontium cobalt oxide (LSC) cathode on an yttria stabilised zirconia (YSZ)-based solid oxide fuel cell (SOFC) via pulsed laser deposition (PLD). Its electrochemical performance (5.9 mW cm(-2) at 0.7 V, 650 degrees C) was significantly inferior to that (595 mW cm(-2) at 0.7 V, 650 degrees C) of an SOFC with a thin (t similar to 200 nm) gadolinium doped ceria (GDC) buffer layer in between the LSC thin film cathode and the YSZ electrolyte. It implies that even though the cathode processing and cell operating temperatures were strictly controlled not to exceed 650 degrees C, the direct application of LSC on YSZ should be avoided. The origin of the cell performance deterioration is thoroughly studied by glancing angle X-ray diffraction (GAXRD) and transmission electron microscopy (TEM), and the decomposition of the cathode and diffusion of La and Sr into YSZ were observed when LSC directly contacted YSZ.
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