TY - JOUR
T1 - Boron deposition and poisoning of La0.8Sr0.2MnO3 oxygen electrodes of solid oxide electrolysis cells under accelerated operation conditions
AU - Chen, Kongfa
AU - Hyodo, Junji
AU - Ai, Na
AU - Ishihara, Tatsumi
AU - Jiang, San Ping
N1 - Funding Information:
The project is supported by Curtin University Research Fellowship and Australian Research Council ( DP150102025 ). The authors thank the technical assistance of Dr Kane O'Donnell on XPS analysis and acknowledge the facilities, scientific and technical assistance of the Curtin University Microscopy & Microanalysis Facility, which is partially funded by the University, State and Commonwealth Governments, and the WA X-Ray Surface Analysis Facility, funded by the Australian Research Council LIEF grant ( LE120100026 ).
Publisher Copyright:
© 2015 Hydrogen Energy Publications, LLC.
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2016/1/21
Y1 - 2016/1/21
N2 - The effect of boron species from borosilicate glass sealant on the electrocatalytic activity and microstructure of La0.8Sr0.2MnO3 (LSM) oxygen electrodes is studied for the first time under accelerated solid oxide electrolysis cell (SOEC) operation conditions at 800 °C. The presence of volatile boron species has remarkable detrimental effect on the electrochemical activity of LSM oxygen electrode for the O2 evolution reaction (OER). After polarization at 200 mA cm-2 for 2 h, the electrode polarization and ohmic resistances increase rapidly from ∼40 and 1.2 cm2 to 614 and 33 cm2, respectively. Under the anodic polarization conditions, there is an accelerated Sr segregation and boron deposition preferentially occurs at the electrode/electrolyte interface, forming lanthanum borates and manganese oxide. Boron deposition and reaction is driven to the interface region due to the increased activity and energetics of lanthanum at LSM lattice sites at the electrode/electrolyte interface under anodic polarization conditions, accelerating the disintegration and delamination of the LSM electrode. The results indicate the potential detrimental effect of volatile boron on the electrochemical activity and stability of LSM oxygen electrodes of solid oxide electrolyzers.
AB - The effect of boron species from borosilicate glass sealant on the electrocatalytic activity and microstructure of La0.8Sr0.2MnO3 (LSM) oxygen electrodes is studied for the first time under accelerated solid oxide electrolysis cell (SOEC) operation conditions at 800 °C. The presence of volatile boron species has remarkable detrimental effect on the electrochemical activity of LSM oxygen electrode for the O2 evolution reaction (OER). After polarization at 200 mA cm-2 for 2 h, the electrode polarization and ohmic resistances increase rapidly from ∼40 and 1.2 cm2 to 614 and 33 cm2, respectively. Under the anodic polarization conditions, there is an accelerated Sr segregation and boron deposition preferentially occurs at the electrode/electrolyte interface, forming lanthanum borates and manganese oxide. Boron deposition and reaction is driven to the interface region due to the increased activity and energetics of lanthanum at LSM lattice sites at the electrode/electrolyte interface under anodic polarization conditions, accelerating the disintegration and delamination of the LSM electrode. The results indicate the potential detrimental effect of volatile boron on the electrochemical activity and stability of LSM oxygen electrodes of solid oxide electrolyzers.
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U2 - 10.1016/j.ijhydene.2015.11.013
DO - 10.1016/j.ijhydene.2015.11.013
M3 - Article
AN - SCOPUS:84954571706
SN - 0360-3199
VL - 41
SP - 1419
EP - 1431
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
IS - 3
ER -