Closed-Pore Formation in Oxygen Electrodes for Solid Oxide Electrolysis Cells Investigated by Impedance Spectroscopy
Research output: Contribution to journal › Article › Research › peer-review
Standard
In: ACS Applied Materials and Interfaces, Vol. 15.2023, No. 6, 02.02.2023, p. 8076–8092.
Research output: Contribution to journal › Article › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex - Download
}
RIS (suitable for import to EndNote) - Download
TY - JOUR
T1 - Closed-Pore Formation in Oxygen Electrodes for Solid Oxide Electrolysis Cells Investigated by Impedance Spectroscopy
AU - Krammer, Martin
AU - Schmid, Alexander
AU - Nenning, Andreas
AU - Bumberger, Andreas Ewald
AU - Siebenhofer, Matthäus
AU - Herzig, Christopher
AU - Limbeck, Andreas
AU - Rameshan, Christoph
AU - Kubicek, Markus
AU - Fleig, Juergen
N1 - Publisher Copyright: © 2023 The Authors. Published by American Chemical Society.
PY - 2023/2/2
Y1 - 2023/2/2
N2 - Electrochemical impedance spectroscopy was used to investigate the chemical capacitance of La0.6Sr0.4CoO3−δ (LSC) thin-film electrodes under anodic polarization (i.e., in the electrolysis mode). For this purpose, electrodes with different microstructures were prepared via pulsed-laser deposition. Analysis of dense electrodes and electrodes with open porosity revealed decreasing chemical capacitances with increasing anodic overpotentials, as expected from defect chemical considerations. However, extremely high chemical capacitance peaks with values in the range of 104 F/cm3 at overpotentials of >140 mV were obtained after annealing for several hours in synthetic air and/or after applying high anodic bias voltages of >750 mV. From the results of several surface analysis techniques and transmission electron microscopy, it is concluded that closed pores develop upon both of these treatments: (i) During annealing, initially open pores get closed by SrSO4, which forms due to strontium segregation in measurement gases with minute traces of sulfur. (ii) The bias treatment causes mechanical failure and morphological changes including closed pores in the bulk of dense films. Under anodic polarization, high-pressure oxygen accumulates in those closed pores, and this causes the capacitance peak. Model calculations based on a real-gas equation allow us to properly predict the experimentally obtained capacitance increase.
AB - Electrochemical impedance spectroscopy was used to investigate the chemical capacitance of La0.6Sr0.4CoO3−δ (LSC) thin-film electrodes under anodic polarization (i.e., in the electrolysis mode). For this purpose, electrodes with different microstructures were prepared via pulsed-laser deposition. Analysis of dense electrodes and electrodes with open porosity revealed decreasing chemical capacitances with increasing anodic overpotentials, as expected from defect chemical considerations. However, extremely high chemical capacitance peaks with values in the range of 104 F/cm3 at overpotentials of >140 mV were obtained after annealing for several hours in synthetic air and/or after applying high anodic bias voltages of >750 mV. From the results of several surface analysis techniques and transmission electron microscopy, it is concluded that closed pores develop upon both of these treatments: (i) During annealing, initially open pores get closed by SrSO4, which forms due to strontium segregation in measurement gases with minute traces of sulfur. (ii) The bias treatment causes mechanical failure and morphological changes including closed pores in the bulk of dense films. Under anodic polarization, high-pressure oxygen accumulates in those closed pores, and this causes the capacitance peak. Model calculations based on a real-gas equation allow us to properly predict the experimentally obtained capacitance increase.
KW - chemical capacitance
KW - degradation mechanism
KW - impedance spectroscopy
KW - LaSrCoO (LSC)
KW - oxygen electrode
KW - pore formation
KW - solid oxide electrolysis cell (SOEC)
KW - thin film
UR - http://www.scopus.com/inward/record.url?scp=85147573181&partnerID=8YFLogxK
U2 - 10.1021/acsami.2c20731
DO - 10.1021/acsami.2c20731
M3 - Article
AN - SCOPUS:85147573181
VL - 15.2023
SP - 8076
EP - 8092
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
SN - 1944-8244
IS - 6
ER -