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Ionic and Electronic Conductivities and Fuel Cell Performance of Oxygen Excess-Type Lanthanum Silicates.

Authors :
Mineshige, Atsushi
Nakao, Takayuki
Ohnishi, Yoshiki
Sakamoto, Ryuta
Daiko, Yusuke
Kobune, Masafumi
Yazawa, Tetsuo
Yoshioka, Hideki
Fukutsuka, Tomokazu
Uchimoto, Yoshiharu
Source :
Journal of The Electrochemical Society; 2010, Vol. 157 Issue 10, pB1465-B1470, 6p, 2 Diagrams, 7 Graphs
Publication Year :
2010

Abstract

Highly dense pellets of an oxygen excess-type lanthanum silicate (La<subscript>9.333+x</subscript>Si<subscript>6</subscript>O<subscript>26+1.5x</subscript>, x > ca. 0.3, OE-LSO) were successfully fabricated, and their electrical conducting properties were studied. The replacement of Si by Al enhanced its conductivity, and the slightly Al-doped OE-LSO specimen [La<subscript>9.62</subscript>(Si<subscript>5.79</subscript>Al<subscript>0.21</subscript>)O<subscript>26.33</subscript>] had excellent features as a solid electrolyte; that is, it had high ionic conductivity and was highly stable under reducing as well as oxidizing conditions at 873-1073 K. In addition, the ionic transference number was higher than 0.99. In the fuel cell utilizing this electrolyte (0.72 mm thick), (La<subscript>0.6</subscript>Sr<subscript>0.4</subscript>)(Co<subscript>0.2</subscript>Fe<subscript>0.8</subscript>)O<subscript>3-δ</subscript> cathode, and Ni-Ce<subscript>0.9</subscript>Gd<subscript>0.1</subscript>O<subscript>1.95-δ</subscript> anode, good performance with the maximum power density of ca. 0.25 W cm<superscript>-2</superscript> was obtained at 1073 K. In addition, this electrolyte also had high compatibility with these conventional mixed conducting electrodes, according to an analysis near the electrode/electrolyte interfaces after the fuel cell test. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00134651
Volume :
157
Issue :
10
Database :
Supplemental Index
Journal :
Journal of The Electrochemical Society
Publication Type :
Academic Journal
Accession number :
54862651
Full Text :
https://doi.org/10.1149/1.3464803