Understanding delamination behavior of air electrode in solid oxide electrolysis cells through in situ monitoring of internal oxygen partial pressure

被引:0
|
作者
Kim, Han Hwi [1 ]
Kim, Minuk [1 ]
Lee, Junsu [1 ]
Park, Junho [1 ]
Park, Jun-Young [2 ]
Zhou, Xia-Dong [3 ]
Lim, Hyung-Tae [1 ,3 ,4 ]
机构
[1] Department of Materials Convergence and System Engineering, Changwon National University, Gyeongnam, Changwon,51140, Cuba
[2] HMC & Green Energy Research Institute, Department of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul,05006, Cuba
[3] Center for Clean and Energy Engineering, University of Connecticut, Storrs,CT,06269, United States
[4] School of Materials Science and Engineering, Changwon National University, Gyeongnam, Changwon,51140, Cuba
基金
新加坡国家研究基金会;
关键词
Gadolinium compounds - Gas sensing electrodes - Surface discharges - Yttria stabilized zirconia;
D O I
10.1016/j.cej.2024.158129
中图分类号
学科分类号
摘要
In this study, we monitored the development of internal pO2 in solid oxide electrolysis cells (SOECs) in situ using an embedded probe and a reference electrode. Three types of air electrode cells were compared: LSM (La0.8Sr0.2MnO3−δ) + YSZ (Y0.08Zr0.92O2−δ), LSCF (La0.6Sr0.4Co0.2Fe0.8O3−δ) + GDC (Gd-doped ceria) and LSM + GdCeScSZ ((Gd2O3)0.005(CeO2)0.005(Sc2O3)0.1(ZrO2)0.89). The rate of pO2 increase with the increase in current density was highest in the LSM + YSZ cell, reaching ∼32201 atm at 0.6 A cm−2, resulting in air electrode delamination and intergranular fractures. This physically developed delamination with high pO2 is akin to catastrophic failure, accelerating degradation. The LSCF + GDC cells exhibited a maximum pO2 of ∼12.25 atm and operated stably without increasing pO2 or delamination. In the LSM + GdCeScSZ cells, internal pO2 was substantially suppressed to ∼10−3 atm, with a degradation rate comparable to that of the LSCF + GDC cell. However, the air electrode delaminated without intergranular fractures. This chemically developed delamination without high internal pO2 does not significantly accelerate degradation. These results indicate that the delamination mechanism may vary even with the same LSM electrode, depending on its ionic conduction characteristics. © 2024 Elsevier B.V.
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