Stable, Low Polarization Resistance Solid Oxide Fuel Cell Anodes: La1–xSrxCr1–xFexO3-δ (x = 0.2–0.67)
Source abstract
Abstract
The perovskite series, La 1– x Sr x Cr 1– x Fe x O 3-δ ( x = 0.2, 0.3, 0.4, 0.5, 0.67, LSCrFe), was synthesized and examined as both single phase and LSCrFe–Gd 0.1 Ce 0.9 O 2-β (GDC) composite solid oxide fuel cell anodes in full cells with La 0.9 Sr 0.1 Ga 0.8 Mg 0.2 O 3-ε /La 0.4 Ce 0.6 O 2 bilayer electrolytes. Each anode demonstrated marked improvement in polarization resistance compared to prior studies on Fe-free La 1– x Sr x CrO 3-δ -based anodes and in stability compared to studies on more Fe-rich compositions. Higher Fe content anodes yielded lower polarization resistances, with the x = 0.67 anodes obtaining resistances of 0.275 Ω·cm 2 for LSCrFe and 0.333 Ω·cm 2 for LSCrFe-GDC in humidified H 2 at 800 °C. The lower polarization resistance with increasing Fe content can be attributed to oxygen loss, which introduces significant ionic conductivity into these perovskites. Substitution of an intermediate amount of Fe and Sr into the perovskites can thus optimize anode performance.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides · Magnetic and transport properties of perovskites and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States
Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States
References (26)
Show source-provided references
1. Ramos T. · Solid State Ionics · 2004 · 170 · 27510.1016/j.ssi.2004.03.001 ↗
2. Atkinson A. · J. Power Sources · 2004 · 130 · 12910.1016/j.jpowsour.2003.11.047 ↗
3. Ramos T. · Chem. Mater. · 2006 · 18 · 386010.1021/cm060689s ↗
4. Carvalho M. D. · Solid State Sci. · 2010 · 12 · 47610.1016/j.solidstatesciences.2009.12.011 ↗
5. Zhang X.-H. · Chem. Ind. Eng. Prog. · 2009 · 28 · 788
6. Tao S. W. · Chem. Mater. · 2004 · 16 · 411610.1021/cm049341s ↗
7. Peña-Martínez J. · Electrochim. Acta · 2007 · 52 · 295010.1016/j.electacta.2006.09.004 ↗
8. Danilovic N. · Chem. Mater. · 2010 · 22 · 95710.1021/cm901875u ↗
9. Kozhevnikov V. L. · Chem. Mater. · 2004 · 16 · 501410.1021/cm031084o ↗
10. Haag J. M. · Electrochem. Solid-State Lett. · 2008 · 11 · B5110.1149/1.2836484 ↗
11. Gong M. · J. Power Sources · 2010 · 195 · 401310.1016/j.jpowsour.2009.12.117 ↗
12. Haag J. M. · Solid State Ionics · 2012 · 212 · 110.1016/j.ssi.2012.01.037 ↗
13. Chen M. · J. Power Sources · 2013 · 236 · 6810.1016/j.jpowsour.2013.02.024 ↗
14. Haag J. M. · Chem. Mater. · 2010 · 22 · 328310.1021/cm100609e ↗
15. Bierschenk D. M. · J. Electrochem. Soc. · 2013 · 160 · F9010.1149/2.032302jes ↗
16. Madsen B. · Solid State Ionics · 2005 · 176 · 254510.1016/j.ssi.2005.08.004 ↗
17. Mizusaki J. · Solid State Ionics · 1984 · 12 · 11910.1016/0167-2738(84)90138-3 ↗
18. Mizusaki J. · J. Solid State Chem. · 1985 · 58 · 25710.1016/0022-4596(85)90243-9 ↗
19. Cho S. · Energy Environ. Sci. · 2013 · 6 · 185010.1039/c3ee23791e ↗
20. Cronin J. S. · J. Electrochem. Soc. · 2012 · 159 · B38510.1149/2.053204jes ↗
21. Patrakeev M. V. · J. Solid State Chem. · 2003 · 172 · 21910.1016/S0022-4596(03)00040-9 ↗
22. Madsen B. D. · J. Power Sources · 2007 · 166 · 6410.1016/j.jpowsour.2006.12.080 ↗
23. Bierschenk D. M. · J. Power Sources · 2012 · 201 · 9510.1016/j.jpowsour.2011.10.119 ↗
24. Fu Q. X. · J. Electrochem. Soc. · 2006 · 153 · D7410.1149/1.2170585 ↗
25. Adler S. B. · J. Electrochem. Soc. · 1996 · 143 · 355410.1149/1.1837252 ↗
26. Vernoux P. · Ionics · 1997 · 3 · 27010.1007/BF02375628 ↗