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Electrochemical performance and stability of SrTi0.3Fe0.6Co0.1O3-δ infiltrated La0.8Sr0.2MnO3Zr0.92Y0.16O2-δ oxygen electrodes for intermediate-temperature solid oxide electrochemical cells

We report that the La0.8Sr0.2MnO3-Zr0.92Y0.16O2-δ (LSM-YSZ) composite is the most widely used oxygen electrode for solid oxide electrochemical cells (SOCs). However, operating temperatures > 700 degrees C are required for good performance since oxygen reactions are limitied to three-phase boundar...

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Bibliographic Details
Published in:Journal of power sources 2019-04, Vol.426 (C)
Main Authors: Zhang, Shan-Lin, Wang, Hongqian, Lu, Matthew Y., Li, Cheng-Xin, Li, Chang-Jiu, Barnett, Scott A.
Format: Article
Language:English
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Summary:We report that the La0.8Sr0.2MnO3-Zr0.92Y0.16O2-δ (LSM-YSZ) composite is the most widely used oxygen electrode for solid oxide electrochemical cells (SOCs). However, operating temperatures > 700 degrees C are required for good performance since oxygen reactions are limitied to three-phase boundaries (TPBs) because of poor ionic conductivity of LSM. Furthermore, LSM-YSZ electrodes typically delaminate during electrolysis operation leading to cell degradation. One strategy to improve SOCs with LSM-YSZ electrodes is to infiltrate a mixed ionically and electronically conducting (MIEC) material that promotes oxygen exchange. However, infiltrated materials have a nano-scale structure that may not be stable under SOC operating temperatures. Here, we report results on the infiltration of SrTi0.3Fe0.6Co0.1O3-δ(STFC), a recently reported high performance MIEC, into LSM-YSZ to improve its electrochemical performance and stability at intermediate temperatures. The infiltrated STFC enhances LSM-YSZ and cell performance, typically yielding a decrease in electrode polarization resistance by a factor > 3 times, resulting in an increase in fuel cell maximum power density and electrolysis current density (at 1.3 V) by a factor > 2 times. Perhaps more significantly, the infiltrated electrodes show good performance stability, with suppression of electrode delamination during electrolysis and no evidence of coarsening or segregation induced degradation.
ISSN:0378-7753
1873-2755