TY - JOUR
T1 - Degradation of La0.6Sr0.4Fe0.8Co0.2O3-δ oxygen electrodes on Ce0.9Gd0.1O2-δ electrolytes during reversing current operation
AU - Railsback, Justin G.
AU - Wang, Hongqian
AU - Liu, Qinyuan
AU - Lu, Matthew Y.
AU - Barnett, Scott A.
N1 - Funding Information:
The authors gratefully acknowledge support from NSF PIRE grant # 1545907, and NSF grant # DMR-1506925 for support of the 3D tomography work. This work made use of the EPIC facility of North-western University’s NUANCE Center, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205); the MRSEC program (NSF DMR-1121262) at the Materials Research Center; the International Institute for Nanotechnology (IIN); the Keck Foundation; and the State of Illinois, through the IIN. This work made use of the MatCI Facility which receives support from the MRSEC Program (NSF DMR-1121262) of the Materials Research Center at Northwestern University. The authors thank Gareth A. Hughes for his early input on the cell testing and helpful discussions.
Publisher Copyright:
© The Author(s) 2017.
PY - 2017
Y1 - 2017
N2 - In order to assess the durability of La0.6Sr0.4Co0.2Fe0.8O3 oxygen electrodes in reversible solid oxide cells, current switched ~1000 h galvanostatic (0.7, 1.0, and 1.5 A/cm2) life tests were performed on symmetrical Ce0.9Gd0.1O2-electrolyte cells at 700°C. Cell operating voltage and resistance, the latter measured by impedance spectroscopy, were monitored throughout. Degradation was minimal for the 0.7 A/cm2 case. For the higher current densities, the cell voltage and resistance increased with time, although the cell appeared to stabilize after ~500 h in the 1.5 A/cm2 case. Post-test analyses showed no evidence of electrolyte cracking or delamination for any current. However, 3D imaging revealed measureable microstructural coarsening after 1.5 A/cm2 operation that was not present after 0.7 A/cm2 operation. Furthermore, the amount of Sr segregated onto LSCF surfaces was higher for the cells operated with current switching versus the as-prepared and zero-current cells. Analysis of the results suggest that much of the degradation was due to decreased oxygen surface exchange rate due to current-enhanced Sr segregation, with a smaller contribution due to microstructural coarsening. The possibility of extrapolating these accelerated tests to longer times is discussed.
AB - In order to assess the durability of La0.6Sr0.4Co0.2Fe0.8O3 oxygen electrodes in reversible solid oxide cells, current switched ~1000 h galvanostatic (0.7, 1.0, and 1.5 A/cm2) life tests were performed on symmetrical Ce0.9Gd0.1O2-electrolyte cells at 700°C. Cell operating voltage and resistance, the latter measured by impedance spectroscopy, were monitored throughout. Degradation was minimal for the 0.7 A/cm2 case. For the higher current densities, the cell voltage and resistance increased with time, although the cell appeared to stabilize after ~500 h in the 1.5 A/cm2 case. Post-test analyses showed no evidence of electrolyte cracking or delamination for any current. However, 3D imaging revealed measureable microstructural coarsening after 1.5 A/cm2 operation that was not present after 0.7 A/cm2 operation. Furthermore, the amount of Sr segregated onto LSCF surfaces was higher for the cells operated with current switching versus the as-prepared and zero-current cells. Analysis of the results suggest that much of the degradation was due to decreased oxygen surface exchange rate due to current-enhanced Sr segregation, with a smaller contribution due to microstructural coarsening. The possibility of extrapolating these accelerated tests to longer times is discussed.
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U2 - 10.1149/2.0111710jes
DO - 10.1149/2.0111710jes
M3 - Article
AN - SCOPUS:85047065785
SN - 0013-4651
VL - 164
SP - F3083-F3090
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 10
ER -