Synergized Tri‐Phase Anode via Purposive Ba 2+ Doping at the La 3+ Site in LaFe 0.7 Ni 0.3 O 3‐δ for Improved SOFC Performance
Source abstract
Abstract
ABSTRACT Although perovskites are promising anode materials for solid oxide fuel cells (SOFCs), poor hydrogen oxidation reaction (HOR) kinetics and low peak power density (PPD) are usually limited by the single‐phase composition. Herein, purposive doping of Ba 2+ at the La 3+ site of La 0.5 Ba 0.5 Fe 0.7 Ni 0.3 O 3‐δ under reducing atmosphere triggers the formation of Ruddlesden‐Popper perovskite (La 2 Ba)Fe 2 O 7 , hexagonal Ba 6 La 2 Fe 4 O 15 , and exsolved cubic Ni 3 Fe nanoparticles, which facilitates excellent ionic and electronic conductivity, extra oxygen vacancies, and accelerated HOR kinetics. The as‐fabricated SOFC containing a tri‐phase anode made from the above composite leads to 57% polarization resistance reduction (from 0.28 to 0.12 Ω cm 2 ), doubled PPD with a record value of 1.25 W cm −2 at 800 °C of that without Ba 2+ doping, negligible voltage decrease rate of ∼8.9 × 10 −5 ·V h −1 , and 300‐h durability operated at 750°C.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electrocatalysts for Energy Conversion · Magnetic and transport properties of perovskites and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources College of Chemistry Xinjiang University Urumqi China
School of Materials Science and Engineering Nanjing Tech University Nanjing China
Funding
National Natural Science Foundation of China
References (45)
Show source-provided references
1. 10.1038/2322010.1038/23220 ↗
2. 10.1038/nmat104010.1038/nmat1040 ↗
3. 10.1038/nature0286310.1038/nature02863 ↗
4. 10.1002/advs.20170033710.1002/advs.201700337 ↗
5. 10.1002/smll.20200185910.1002/smll.202001859 ↗
6. 10.1039/C3EE23791E10.1039/C3EE23791E ↗
7. 10.1126/science.112587710.1126/science.1125877 ↗
8. 10.1002/aenm.20110010810.1002/aenm.201100108 ↗
9. 10.1038/s41563‐020‐00854‐810.1038/s41563‐020‐00854‐8 ↗
10. 10.1002/adfm.20240875610.1002/adfm.202408756 ↗
11. 10.1126/science.aam709210.1126/science.aam7092 ↗
12. 10.1002/aenm.20180006210.1002/aenm.201800062 ↗
13. 10.1016/j.electacta.2017.03.04610.1016/j.electacta.2017.03.046 ↗
14. 10.1016/j.jpowsour.2013.03.02510.1016/j.jpowsour.2013.03.025 ↗
15. 10.1016/j.nanoen.2014.12.00110.1016/j.nanoen.2014.12.001 ↗
16. 10.1002/adma.20190619310.1002/adma.201906193 ↗
17. 10.1038/s41467‐021‐26739‐110.1038/s41467‐021‐26739‐1 ↗
18. 10.1021/acs.energyfuels.4c0053810.1021/acs.energyfuels.4c00538 ↗
19. 10.1016/j.cej.2021.13261510.1016/j.cej.2021.132615 ↗
20. 10.1021/acs.jpcc.5b0601410.1021/acs.jpcc.5b06014 ↗
21. 10.1021/cm103489r10.1021/cm103489r ↗
22. 10.1021/ja300831k10.1021/ja300831k ↗
23. 10.1016/j.apsusc.2010.10.05110.1016/j.apsusc.2010.10.051 ↗
24. 10.1016/j.ijhydene.2014.06.00910.1016/j.ijhydene.2014.06.009 ↗
25. 10.1021/acsami.9b0766810.1021/acsami.9b07668 ↗
26. 10.1039/C5TA07178J10.1039/C5TA07178J ↗
27. 10.1016/j.joule.2024.04.00910.1016/j.joule.2024.04.009 ↗
28. 10.1038/s41560‐022‐01098‐310.1038/s41560‐022‐01098‐3 ↗
29. 10.1039/C7TA08249E10.1039/C7TA08249E ↗
30. 10.1002/slct.20180090810.1002/slct.201800908 ↗
31. 10.1021/acs.iecr.7b0217410.1021/acs.iecr.7b02174 ↗
32. 10.1016/j.electacta.2018.09.10210.1016/j.electacta.2018.09.102 ↗
33. 10.1021/jacs.3c1212110.1021/jacs.3c12121 ↗
34. 10.1039/C9TA00467J10.1039/C9TA00467J ↗
35. 10.1002/aenm.20160189010.1002/aenm.201601890 ↗
36. 10.1039/C8EE00449H10.1039/C8EE00449H ↗
37. 10.1039/D1TA04044H10.1039/D1TA04044H ↗
38. 10.1016/j.jechem.2025.08.06910.1016/j.jechem.2025.08.069 ↗
39. 10.1021/jacs.5c0353610.1021/jacs.5c03536 ↗
40. 10.1002/adma.20190502510.1002/adma.201905025 ↗
41. 10.1021/jacs.5c0066510.1021/jacs.5c00665 ↗
42. 10.1021/jacs.4c0864310.1021/jacs.4c08643 ↗
43. 10.1038/nchem.12110.1038/nchem.121 ↗
44. 10.1002/aenm.20240012410.1002/aenm.202400124 ↗
45. 10.1002/adma.20240156810.1002/adma.202401568 ↗