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This paper addresses the use of Ce 0.8 Gd 0.2 O 2−δ (GDC) infiltration into the Ni–(Y 2 O 3 ) 0.08 (ZrO 2 ) 0.92 (YSZ) fuel electrode of solid oxide cells (SOCs) for improving their electrochemical performance in fuel cell and electrolysis operation. Although doped ceria infiltration into Ni–YSZ has recently been shown to improve the electrode performance and stability, the mechanisms defining how GDC impacts electrochemical characteristics are not fully delineated. Furthermore, the electrochemical characteristics have not yet been determined over the full range of conditions normally encountered in fuel cell and electrolysis operation. Here we present a study of both symmetric and full cells aimed at understanding the electrochemical mechanisms of GDC-modified Ni–YSZ over a wide range of fuel compositions and temperatures. Single-step GDC infiltration at an appropriate loading substantially reduced the polarization resistance of Ni–YSZ electrodes in electrolyte-supported cells, as measured using electrochemical impedance spectroscopy (EIS) at various temperatures (600–800 °C) in a range of H 2 O–H 2 mixtures (3–90 vol% H 2 O). Fuel-electrode-supported cells had significant concentration polarization due to the thick Ni–YSZ supports. A distribution of relaxation times approach is used to develop a physically-based electrochemical model; the results show that GDC reduces the reaction resistance associated with three-phase boundaries, but also appears to improve oxygen transport in the electrode. Increasing the H 2 O fraction in the H 2 –H 2 O fuel mixture reduced both the three-phase boundary resistance and the gas diffusion resistance for Ni–YSZ; with GDC infiltration, the electrode resistance showed less variation with fuel composition. GDC infiltration improved the performance of fuel-electrode-supported full cells, which yielded a maximum power density of 2.28 W cm −2 in fuel cell mode and an electrolysis current density at 1.3 V of 2.22 A cm −2 , both at 800 °C.
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A Method for Time-Resolved Characterization of Polarization-Induced Solid Oxide Cell Microstructure Evolution
Solid oxide cell long-term durability experiments are resource-intensive and have limited ability to capture the interdependence of microstructural evolution and electrochemical performance. Studies of microstructural degradation mechanisms are usually limited to before and after life-test images. Here we describe a life testing method that simultaneously operates multiple symmetric cells under different conditions, simultaneously providing information on electrolysis and fuel cell operation, while sampling the microstructure during operation. The method utilizes laser-cutting to exactly define different cell areas, allowing testing under different current densities with a single current source, and facilitating removal of segments of the cellsduringlife tests, allowing for microstructural evaluation at intermediate times. The method is demonstrated in Ni-YSZ / YSZ / Ni-YSZ fuel-electrode-supported cells at low H2O/H2ratios. Characterization using SEM-based imaging techniques shows pronounced microstructural damage that increases rapidly with increasing current density and time, mirroring observed electrochemical degradation. The present results agree with prior reports for SOC operation under such conditions but reveal new features of the degradation process via the unique capability of time-resolved imaging.
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- Award ID(s):
- 1912530
- PAR ID:
- 10406917
- Publisher / Repository:
- The Electrochemical Society
- Date Published:
- Journal Name:
- Journal of The Electrochemical Society
- Volume:
- 170
- Issue:
- 2
- ISSN:
- 0013-4651
- Page Range / eLocation ID:
- Article No. 024514
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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