Abstract
A La0.75 Sr0.25 Cr0.5 Mn0.5 O3 Gd0.2 Ce0.8 O1.9 (LSCM/GDC) composite electrode was developed and applied as a solid oxide fuel cell (SOFC) anode for the direct oxidation of sulfur-containing methane. The anode was fully activated in wet CH4 at 850°C and a constant potential of -0.5 V with respect to a Pt/air reference before the fuel was shifted to wet 0.5% H2 S+99.5% CH4. In the sulfur-containing methane fuel, the anodic current dropped from 0.233 A cm-2 to 0.2 A cm-2 in a 10 h period, showing a performance degradation rate of ca. 1.4%/hr possibly due to sulfur poisoning. In the subsequent 110 h period, the anodic current tended to be relatively stable with a very small degradation rate of 0.017%/h, which is most likely attributed to the coarsening of the electrode microstructure. Though some impurities, such as MnS, La2 O2 S, and α-MnOS, were detected in the X-ray diffraction analysis of the anode after 120 h of stability test, the scanning electron microscopy micrographs and energy-dispersive X-ray analysis showed that no carbon and sulfur deposition was found on the cross-sectional surface of the anode. The results suggest that the LSCM/GDC composite is a promising candidate material for an anode and has much better hydrocarbon stability and sulfur tolerance under the anodic polarization than Ni-based cermets.
Original language | English |
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Pages (from-to) | B1206-B1210 |
Journal | Journal of the Electrochemical Society |
Volume | 154 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2007 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Electronic, Optical and Magnetic Materials
- Renewable Energy, Sustainability and the Environment
- Surfaces, Coatings and Films
- Electrochemistry
- Materials Chemistry