Anisotropic Oxygen Diffusion Properties in Pr2NiO4+δ and Nd2NiO4+δ Single Crystals

被引:87
作者
Bassat, Jean-Marc [1 ,2 ]
Burriel, Monica [3 ]
Wahyudi, Olivia [1 ,2 ,5 ]
Castaing, Remi [1 ,2 ,3 ]
Ceretti, Monica [4 ]
Veber, Philippe [1 ,2 ]
Weill, Isabelle [1 ,2 ]
Villesuzanne, Antoine [1 ,2 ]
Grenier, Jean-Claude [1 ,2 ]
Paulus, Werner [4 ]
Kilner, John A. [3 ]
机构
[1] CNRS, ICMCB, UPR 9048, F-33600 Pessac, France
[2] Univ Bordeaux, ICMCB, UPR 9048, F-33600 Pessac, France
[3] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[4] Inst Charles Gerhardt, UMR 5253, F-34095 Montpellier 5, France
[5] Univ Rennes 1, UMR 6226, F-35042 Rennes, France
关键词
FUEL-CELL CATHODE; ELECTROCHEMICAL OXIDATION; TRANSPORT-PROPERTIES; NEUTRON-DIFFRACTION; LA2NIO4; OXIDES;
D O I
10.1021/jp409057k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The anisotropy of the oxygen anionic conductivity was measured for two mixed ionic electronic conducting (MIEC) oxides with the 2D K2NiF4-type structure, i.e., Nd2NiO4+delta and Pr2NiO4+delta, using high quality single crystals. Measurements of the oxygen diffusivity and surface exchange performed parallel and perpendicularly to the [001] direction, from 450 to 700 degrees C, using the isotope exchange depth profile (IEDP) technique, combining O-16/O-18 exchange and secondary ion mass spectroscopy (SIMS) are reported. For both materials the diffusion is about 3 orders of magnitude higher along the (a,b)-plane compared to the perpendicular (c-axis) direction. These values are among the highest when compared to several state-of-the-art MIEC materials. The diffusion along the (a,b)-plane for Pr2NiO4+delta is higher than that of Nd2NiO4+delta due to a much lower diffusion activation energy (0.5 and 1.4 eV for Pr2NiO4+delta and Nd2NiO4+delta, respectively). A large anisotropy is also observed in the surface exchange coefficient (k*) values for both materials, with (a,b)-plane coefficients being 1 to 1.5 orders of magnitude larger than those for the c-axis.
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页码:26466 / 26472
页数:7
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