Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells
In this work, the effects of the La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) electrode–yttria stabilized zirconia (YSZ) electrolyte interface on the stability of LSCF electrodes under high-current electrolysis are studied. Six different half-cells with different configurations are tested at 800 °C for 264 h und...
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sg-ntu-dr.10356-1412062021-01-08T06:11:16Z Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells Pan, Zehua Liu, Qinglin Lyu, Renzhi Li, Ping Chan, Siew Hwa School of Mechanical and Aerospace Engineering Energy Research Institute @ NTU (ERI@N) Engineering::Mechanical engineering La0.6Sr0.4Co0.3Fe0.8O3-δ Anodic Polarization In this work, the effects of the La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) electrode–yttria stabilized zirconia (YSZ) electrolyte interface on the stability of LSCF electrodes under high-current electrolysis are studied. Six different half-cells with different configurations are tested at 800 °C for 264 h under an electrolysis current of 1 A cm−2. A few concluding remarks can be drawn by comparing the behaviors of different cells. Firstly, it is confirmed that the formation of SrZrO3 at the interface will lead to the delamination of air electrode. Thus, the formation of SrZrO3 should be strictly prevented. Secondly, increasing sintering temperature can decrease the degradation rate of polarization resistance, RP, for LSCF electrodes. Thirdly, the increase of ohmic resistance, RS, comes from structural changes as the degradation rate in percentage is similar for cells with different electrolytes and electrodes. Fourthly, the LSCF electrode after the electrolysis test shows recrystallization and lattice shrink which could be the reason for the degradation of LSCF electrodes on Gd0.1Ce0.9O2–δ (GDC) electrolytes. Lastly, comparing all the samples, the cell composed of YSZ electrolyte, dense GDC interlayer and LSCF electrode sintered at 1000 °C can be used for future study on the degradation mechanisms of the LSCF air electrode and the electrolyte. 2020-06-05T01:56:51Z 2020-06-05T01:56:51Z 2018 Journal Article Pan, Z., Liu, Q., Lyu, R., Li, P., & Chan, S. H. (2018). Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells. Journal of Power Sources, 378, 571-578. doi:10.1016/j.jpowsour.2018.01.002 0378-7753 https://hdl.handle.net/10356/141206 10.1016/j.jpowsour.2018.01.002 2-s2.0-85040066086 378 571 578 en Journal of Power Sources © 2018 Elsevier B.V. All rights reserved. |
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Engineering::Mechanical engineering La0.6Sr0.4Co0.3Fe0.8O3-δ Anodic Polarization Pan, Zehua Liu, Qinglin Lyu, Renzhi Li, Ping Chan, Siew Hwa Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
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In this work, the effects of the La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) electrode–yttria stabilized zirconia (YSZ) electrolyte interface on the stability of LSCF electrodes under high-current electrolysis are studied. Six different half-cells with different configurations are tested at 800 °C for 264 h under an electrolysis current of 1 A cm−2. A few concluding remarks can be drawn by comparing the behaviors of different cells. Firstly, it is confirmed that the formation of SrZrO3 at the interface will lead to the delamination of air electrode. Thus, the formation of SrZrO3 should be strictly prevented. Secondly, increasing sintering temperature can decrease the degradation rate of polarization resistance, RP, for LSCF electrodes. Thirdly, the increase of ohmic resistance, RS, comes from structural changes as the degradation rate in percentage is similar for cells with different electrolytes and electrodes. Fourthly, the LSCF electrode after the electrolysis test shows recrystallization and lattice shrink which could be the reason for the degradation of LSCF electrodes on Gd0.1Ce0.9O2–δ (GDC) electrolytes. Lastly, comparing all the samples, the cell composed of YSZ electrolyte, dense GDC interlayer and LSCF electrode sintered at 1000 °C can be used for future study on the degradation mechanisms of the LSCF air electrode and the electrolyte. |
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School of Mechanical and Aerospace Engineering |
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School of Mechanical and Aerospace Engineering Pan, Zehua Liu, Qinglin Lyu, Renzhi Li, Ping Chan, Siew Hwa |
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Article |
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Pan, Zehua Liu, Qinglin Lyu, Renzhi Li, Ping Chan, Siew Hwa |
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Pan, Zehua |
title |
Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
title_short |
Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
title_full |
Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
title_fullStr |
Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
title_full_unstemmed |
Effect of La0.6Sr0.4Co0.3Fe0.8O3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
title_sort |
effect of la0.6sr0.4co0.3fe0.8o3-δ air electrode-electrolyte interface on the short-term stability under high-current electrolysis in solid oxide electrolyzer cells |
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2020 |
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https://hdl.handle.net/10356/141206 |
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1688665569849507840 |