Enhancing oxygen reaction kinetics in lanthanum nickelate Ruddlesden-Popper electrodes via praseodymium oxide infiltration for solid oxide cells

被引:0
|
作者
Farias, Morena B. [1 ]
Araujo, Allan J. M. [2 ,3 ]
Paskocimas, Carlos A. [1 ]
Fagg, Duncan P. [2 ,3 ]
Loureiro, Francisco J. A. [2 ,3 ]
机构
[1] Fed Univ Rio Grande Norte UFRN, Mat Sci & Engn Postgrad Program PPGCEM, BR- 59078970 Natal, Brazil
[2] Univ Aveiro, TEMA Ctr Mech Technol & Automat, Dept Mech Engn, P-3810193 Aveiro, Portugal
[3] LASI Intelligent Syst Associate Lab, P-4800058 Guimaraes, Portugal
关键词
FUEL-CELLS; CATHODE MATERIALS; REDUCTION; PERFORMANCE; MICROSTRUCTURE; LA2NIO4+DELTA; CONDUCTIVITY; THICKNESS; TRANSPORT; EXCHANGE;
D O I
10.1039/d4dt02277g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This study explores the effect of praseodymium oxide (PrOx) impregnation in lanthanum nickelate Ruddlesden-Popper (RP) type materials for use in oxygen electrodes of solid oxide cells (SOCs). These mixed conductors are free of cobalt and strontium, which are increasingly being avoided in solid oxide cell applications. We investigate two compositions, La2NiO4+delta (L2N1) and La4Ni3O10-delta (L4N3), demonstrating distinct electrical and oxygen kinetic properties. The L2N1 material exhibits superior performance due to its higher bulk oxygen-ion diffusion, which governs the enhanced ambipolar conduction, crucial for the oxygen exchange process. In the PrOx-impregnated samples, at 700 degrees C, the total polarization resistance (Rpol) values decrease to similar to 0.6 Omega cm(2) for L2N1 + PrOx and similar to 0.8 Omega cm(2) for L4N3 + PrOx, representing reductions by factors of similar to 7 and similar to 17, respectively, compared to the non-impregnated counterparts. Electrochemical measurements as a function of oxygen partial pressure suggest that surface-exchange processes may be rate-limiting. The impregnated PrOx acts as a catalyst for the dissociative adsorption of oxygen and improves the charge transfer, leading to significant enhancements in the polarization processes. The electrochemical properties and stability of these RP phases in oxidizing conditions, combined with the oxygen transport capabilities and mixed oxidation state of praseodymium oxide (Pr4+/Pr3+), offer promising Co- and Sr-free oxygen electrodes for SOC applications.
引用
收藏
页码:16610 / 16620
页数:11
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