journal article·2024-02-12Open access

SrCo0.50Fe0.40Ir0.10O3−δ Decorated with Pd and La0.8Sr0.2Ga0.83Mg0.17O3−δ: A Cleaner Electrode for Intermediate-Temperature Solid Oxide Fuel Cells with Reduced Cobalt Content

Mónica Chivite-Lacaba, Jesús Prado-Gonjal, Loreto Troncoso, José Antonio Alonso, Vanessa Cascos

ACS Applied Energy Materials· Volume 7· Issue 3

Abstract

High Resolution Image Download MS PowerPoint Slide Recent studies related to cathode materials for solid oxide fuel cells (SOFCs) have showcased the feasibility of stabilizing cubic or tetragonal perovskite phases in the SrCoO 3−δ system at room temperature. This achievement has been facilitated by partially substituting Co atoms with small amounts of highly charged cations such as Ir 4+ in SrCo 0.90 Ir 0.10 O 3−δ . This specific material exhibits exceptional performance as a cathode for SOFCs operating at intermediate temperatures (800–850 °C). However, it contains a high amount of cobalt, which is both costly and toxic. In this study, our focus has been on further improving this material by reducing its cobalt content, resulting in a cleaner and more cost-effective cathode for SOFCs. The resulting SrCo 0.50 Fe 0.40 Ir 0.10 O 3−δ perovskite, synthesized by the citrate method, introduces a 40% composition of Fe in the sites of Co and Ir, effectively decreasing the amount of Co in the material. The crystal structure of this perovskite oxide has been analyzed using X-ray diffraction (XRD) and neutron powder diffraction (NPD), allowing us to establish correlations with its mechanical and electrical properties. In the single-cell test, this material gave reasonable performances as a cathode at intermediate temperatures (800–850 °C), with La 0.8 Sr 0.2 Ga 0.83 Mg 0.17 O 3−δ (LSGM) as the electrolyte. An analysis of the chemical compatibility between the cathode and the electrolyte, LSGM, demonstrated no interaction at elevated temperatures. Thermal expansion coefficient (TEC) measurements exhibited consistent linear expansion across the entire temperature range. Lastly, the perovskite displayed commendable electrical conductivity along with a promising power density measurement of 384 mW/cm 2 at 850 °C. These findings collectively suggest the potential of this material as a viable cleaner cathode option for intermediate-temperature SOFCs. Moreover, the cathode was further optimized and the performance of the cell improved, by either infiltrating SrCo 0.50 Fe 0.40 Ir 0.10 O 3−δ with a Pd(NO 3 ) 2 solution or mixing it with 30% of LSGM electrolyte, resulting in higher power densities (568 and 675 mW/cm 2, respectively) in test cells fed with pure H 2 as a fuel.
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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

Departamento de Química Inorgánica, Universidad Complutense de Madrid, Madrid E-28040, Spain

Instituto de Ciencia de Materiales de Madrid, C.S.I.C., Cantoblanco, Madrid E-28049, Spain

Instituto de Ingeniería Mecánica, MIGA Millennium Institute, Universidad Austral de Chile, General Lagos, 2086, Valdivia 5111187, Chile

Funding

Comunidad de Madrid · Ministerio de Ciencia e Innovaci?n · Fondo Nacional de Desarrollo Cient?fico y Tecnol?gico · Agencia Nacional de Investigaci?n y Desarrollo

References (41)

Show source-provided references
2. Ritchie, H.; Roser, M.; Rosado, P. “Energy”, 2022. Published online at OurWorldInData.org. Retrieved from: https://ourworldindata.org/energy (accessed July, Nov 22, 2023).
3. Mead, N. Fuel of the future: How to realize the potential of hydrogen. Published online at ‘World Economic Forum’. Retrieved from: https://www.weforum.org/agenda/2022/03/hydrogen-decarbonization-climate-change-energy/ (accessed Aug 11, 2023).
4. 10.1016/j.est.2021.10267610.1016/j.est.2021.102676 ↗
5. 10.1007/s41825-020-00029-810.1007/s41825-020-00029-8 ↗
6. 10.1007/s10853-011-6213-110.1007/s10853-011-6213-1 ↗
7. 10.1021/acsami.5b0035810.1021/acsami.5b00358 ↗
8. 10.1016/j.jpowsour.2009.12.08110.1016/j.jpowsour.2009.12.081 ↗
9. 10.1149/1.179939110.1149/1.1799391 ↗
10. 10.1016/S0167-2738(01)01015-310.1016/S0167-2738(01)01015-3 ↗
11. 10.1016/S0167-2738(03)00027-410.1016/S0167-2738(03)00027-4 ↗
12. 10.1016/S0167-2738(98)00270-710.1016/S0167-2738(98)00270-7 ↗
13. 10.1016/j.jpowsour.2011.04.02510.1016/j.jpowsour.2011.04.025 ↗
14. 10.1021/am501297z10.1021/am501297z ↗
15. 10.1002/zaac.1986540092910.1002/zaac.19865400929 ↗
16. 10.1021/acsaem.0c0084810.1021/acsaem.0c00848 ↗
17. 10.1016/j.ijhydene.2016.01.07110.1016/j.ijhydene.2016.01.071 ↗
18. 10.1016/j.ijhydene.2010.04.02110.1016/j.ijhydene.2010.04.021 ↗
19. 10.1016/j.jpowsour.2018.06.02710.1016/j.jpowsour.2018.06.027 ↗
20. 10.1016/j.ijhydene.2016.02.14210.1016/j.ijhydene.2016.02.142 ↗
21. 10.1016/j.ijhydene.2019.01.22310.1016/j.ijhydene.2019.01.223 ↗
22. 10.1039/C9TA12208G10.1039/C9TA12208G ↗
23. 10.1016/S0378-7753(96)02361-010.1016/S0378-7753(96)02361-0 ↗
24. 10.1149/1.358110910.1149/1.3581109 ↗
25. 10.1107/S002188986900655810.1107/S0021889869006558 ↗
26. 10.1016/0921-4526(93)90108-I10.1016/0921-4526(93)90108-I ↗
27. 10.1080/1044863920821877010.1080/10448639208218770 ↗
28. 10.1016/j.jpowsour.2012.02.00210.1016/j.jpowsour.2012.02.002 ↗
29. 10.1107/S056773947600155110.1107/S0567739476001551 ↗
30. 10.1149/1.139388510.1149/1.1393885 ↗
31. 10.1021/acsaem.2c0356910.1021/acsaem.2c03569 ↗
32. 10.1016/j.renene.2018.09.07310.1016/j.renene.2018.09.073 ↗
33. 10.1016/j.solidstatesciences.2008.03.01510.1016/j.solidstatesciences.2008.03.015 ↗
34. 10.1016/j.ceramint.2014.05.08910.1016/j.ceramint.2014.05.089 ↗
35. 10.1016/j.jallcom.2021.15970110.1016/j.jallcom.2021.159701 ↗
36. 10.1021/acsaem.8b0037610.1021/acsaem.8b00376 ↗
37. 10.1039/C7CS00120G10.1039/C7CS00120G ↗
38. 10.1039/C8TA01104D10.1039/C8TA01104D ↗
39. 10.3390/ma907057910.3390/ma9070579 ↗
40. 10.1016/j.ijhydene.2015.03.13410.1016/j.ijhydene.2015.03.134 ↗
41. 10.1016/j.ijhydene.2014.03.10010.1016/j.ijhydene.2014.03.100 ↗