Peculiar Properties of the La0.25Ba0.25Sr0.5Co0.8Fe0.2O3-δ Perovskite as Oxygen Reduction Electrocatalyst

被引:0
|
作者
Aliotta, Chiara [1 ]
Costa, Maria [1 ]
Liotta, Leonarda Francesca [1 ]
La Parola, Valeria [1 ]
Magnacca, Giuliana [2 ]
Deganello, Francesca [1 ]
机构
[1] CNR, Ist Studio Mat Nanostrutturati, I-90146 Palermo, Italy
[2] Univ Torino, Dipartimento Chim, I-10125 Turin, Italy
来源
MOLECULES | 2023年 / 28卷 / 04期
关键词
heterostructure; oxygen vacancies; Ba-doped-LSCF; ORR; co-doping; SOLUTION COMBUSTION SYNTHESIS; OXIDE FUEL-CELLS; TEMPERATURE; CATHODE; STRONTIUM;
D O I
10.3390/molecules28041621
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The electrochemical reduction of molecular oxygen is a fundamental process in Solid Oxide Fuel Cells and requires high efficiency cathode materials. Two La0.25Ba0.25Sr0.5Co0.8Fe0.2O3-delta-based perovskite compounds were prepared by solution combustion synthesis, and characterized for their structural, microstructural, surface, redox and electrochemical properties as potential cathodes in comparison with Ba0.5Sr0.5Co0.8Fe0.2O3-delta and La0.5Sr0.5Co0.8Fe0.2O3-delta perovskites. Results highlighted that calcination at 900 degrees C led to a "bi-perovskite heterostructure", where two different perovskite structures coexist, whereas at higher calcination temperatures a single-phase perovskite was formed. The results showed the effectiveness of the preparation procedures in co-doping the A-site of perovskites with barium and lanthanum as a strategy to optimize the cathode's properties. The formation of nanometric heterostructure co-doped in the A-site evidenced an improvement in oxygen vacancies' availability and in the redox properties, which promoted both processes: oxygen adsorption and oxygen ions drift, through the cathode material, to the electrolyte. A reduction in the total resistance was observed in the case of heterostructured material.
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页数:15
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