Cascos Vanessa, Alonso José Antonio, Fernández-Díaz María Teresa
Instituto de Ciencia de Materiales de Madrid, CSIC, Cantoblanco, 28049 Madrid, Spain.
Institut Laue Langevin, BP 156X, 38042 Grenoble, France.
Materials (Basel). 2016 Jul 15;9(7):579. doi: 10.3390/ma9070579.
SrCoO outperforms as cathode material in solid-oxide fuel cells (SOFC) when the three-dimensional (3C-type) perovskite structure is stabilized by the inclusion of highly-charged transition-metal ions at the octahedral positions. In a previous work we studied the Nb incorporation at the Co positions in the SrCoNbO system, in which the stabilization of a tetragonal / perovskite superstructure was described for the = 0.05 composition. In the present study we extend this investigation to the = 0.10-0.15 range, also observing the formation of the tetragonal / structure instead of the unwanted hexagonal phase corresponding to the 2H polytype. We also investigated the effect of Nb doping on the thermal, electrical, and electrochemical properties of SrCoNbO ( = 0.1 and 0.15) perovskite oxides performing as cathodes in SOFC. In comparison with the undoped hexagonal SrCoO phase, the resulting compounds present high thermal stability and an increase of the electrical conductivity. The single-cell tests for these compositions ( = 0.10 and 0.15) with LaSrGaMgO (LSGM) as electrolyte and SrMoFeCoO as anode gave maximum power densities of 693 and 550 mW∙cm at 850 °C respectively, using pure H₂ as fuel and air as oxidant.
当通过在八面体位置引入高电荷过渡金属离子来稳定三维(3C型)钙钛矿结构时,SrCoO作为固体氧化物燃料电池(SOFC)的阴极材料表现优异。在之前的一项工作中,我们研究了SrCoNbO体系中Nb在Co位置的掺入情况,其中描述了对于x = 0.05组成的四方/钙钛矿超结构的稳定性。在本研究中,我们将此研究扩展到x = 0.10 - 0.15范围,还观察到形成了四方/结构,而不是对应于2H多型的不需要的六方相。我们还研究了Nb掺杂对作为SOFC阴极的SrCoNbO(x = 0.1和0.15)钙钛矿氧化物的热、电和电化学性能的影响。与未掺杂的六方SrCoO相相比,所得化合物具有高的热稳定性和电导率的增加。以LaSrGaMgO(LSGM)作为电解质和SrMoFeCoO作为阳极对这些组成(x = 0.10和0.15)进行的单电池测试,在850°C下分别使用纯H₂作为燃料和空气作为氧化剂时,最大功率密度分别为693和550 mW∙cm²。