Sm 0.5 Sr 0.5 CoO 3−δ Surface Modification of La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3−δ -Ce 0.9 Gd0.1 2−δ Composite Oxygen Electrodes for Solid Oxide Electrochemical Cells
La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3− δ -Ce 0.9 Gd 0.1 O 2− δ (LSCF-GDC) composite oxygen electrodes have been widely used in intermediate temperature (<700 °C) solid oxide cells, with composite usually providing better electrochemical performance than single-phase LSCF. However, LSCF-based electrodes...
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Published in | Journal of the Electrochemical Society Vol. 167; no. 16; p. 164504 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.12.2020
|
Online Access | Get full text |
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Summary: | La
0.6
Sr
0.4
Co
0.2
Fe
0.8
O
3−
δ
-Ce
0.9
Gd
0.1
O
2−
δ
(LSCF-GDC) composite oxygen electrodes have been widely used in intermediate temperature (<700 °C) solid oxide cells, with composite usually providing better electrochemical performance than single-phase LSCF. However, LSCF-based electrodes are often observed to degrade over time due to Sr segregation. Here we present an impedance spectroscopy study comparing the degradation behaviors of LSCF-GDC and Sm
0.5
Sr
0.5
CoO
3−
δ
(SSC) infiltrated LSCF-GDC electrodes. The LSCF-GDC polarization resistance increases by ∼5 times over ∼1000 h at 650 °C. In contrast, the SSC-infiltrated electrode shows similar initial polarization resistance but much more stable performance. The impedance modeling results show that the improved stability is associated with the low frequency oxygen dissociative adsorption/desorption process. The results suggest that this adsorption/desorption process slows due to increased Sr segregation on LSCF over time, and that SSC does not degrade significantly due to Sr surface segregation. |
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ISSN: | 0013-4651 1945-7111 |
DOI: | 10.1149/1945-7111/abca6f |