Degradation behaviours of Fe-doped La 0.8 Sr 0.2 CoO 3- δ by thermal stress
Source abstract
Abstract
The improvement in durability by Fe doping to La0.8Sr0.2CoO3-δ (LSC) and its degradation mechanism were investigated in terms of structural and morphological analyses. Polarisation resistance of LSC was increased approximately by 65.7% after exposure to thermal stress at 900°C for 100 h because the oxygen reduction reaction was declined by particle coarsening and aggregation of LSC powders. The polarisation resistance of La0.8Sr0.2Co0.8Fe0.2O3-δ (LSCF) was increased from 0.269 to 0.328 Ωcm2 after the heat treatment. Increasing rate of polarisation resistance of LSCF was 21.9%, which was three times lower than that of LSC due to reduced particle coarsening and aggregation by Fe doping. Particle size of LSCF powders was maintained about 0.5–3 μm, and morphologies were also similar before and after the heat treatment. Chemical reaction between the LSCF and Sm-doped Ceria electrolyte powders did not occur despite the thermal stress, indicating the interface between the cathode and electrolyte is chemically stable.
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
School of Materials Science & Engineering, Pusan National University, Busan, South Korea
Funding
Ministry of Science, ICT and Future Planning
References (19)
Show source-provided references
1. 10.1007/s00706-009-0153-310.1007/s00706-009-0153-3 ↗
2. 10.1021/jz400595z10.1021/jz400595z ↗
3. 10.1016/j.jallcom.2013.01.00210.1016/j.jallcom.2013.01.002 ↗
4. 10.1007/s10008-009-0932-010.1007/s10008-009-0932-0 ↗
5. 10.1016/j.ssi.2007.11.01010.1016/j.ssi.2007.11.010 ↗
6. 10.1007/BF0172912210.1007/BF01729122 ↗
7. 10.1016/j.materresbull.2007.03.00610.1016/j.materresbull.2007.03.006 ↗
8. 10.1149/1.183878910.1149/1.1838789 ↗
9. 10.1149/1.217257210.1149/1.2172572 ↗
10. 10.1016/j.jpowsour.2009.09.03910.1016/j.jpowsour.2009.09.039 ↗
11. 10.1016/0167-2738(94)00244-M10.1016/0167-2738(94)00244-M ↗
12. 10.1016/j.ssi.2008.01.00910.1016/j.ssi.2008.01.009 ↗
13. 10.1016/j.ssi.2013.03.02310.1016/j.ssi.2013.03.023 ↗
14. 10.1016/j.ijhydene.2014.03.07710.1016/j.ijhydene.2014.03.077 ↗
15. 10.1016/j.ijhydene.2015.08.07310.1016/j.ijhydene.2015.08.073 ↗
16. 10.6028/jres.058.01010.6028/jres.058.010 ↗
17. 10.1149/2.0851607jes10.1149/2.0851607jes ↗
18. 10.1016/j.electacta.2007.06.01010.1016/j.electacta.2007.06.010 ↗
19. 10.1016/j.jpowsour.2005.09.05710.1016/j.jpowsour.2005.09.057 ↗