Impurity diffusion of 141Pr in LaMnO3, LaCoO3 and LaFeO3 materials

被引:34
作者
Palcut, Marian [1 ]
Christensen, Jens S. [2 ]
Wiik, Kjell [1 ]
Grande, Tor [1 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Mat Sci & Engn, N-7491 Trondheim, Norway
[2] Univ Oslo, Dept Phys, N-0316 Oslo, Norway
关键词
D O I
10.1039/b808789j
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 impurity diffusion of Pr3+ in dense polycrystalline LaMnO3, LaCoO3 and LaFeO3 was studied at 1373-1673 K in air in order to investigate cation diffusion in these materials. Cation distribution profiles were measured by secondary-ion mass spectrometry and it was found that penetration profiles of Pr3+ had two distinct regions with different slopes. The first, shallow region was used to evaluate the bulk diffusion coefficients. The activation energies for bulk diffusion of Pr3+ in LaMnO3, LaCoO3 and LaFeO3 were 126 +/- 6, 334 +/- 68 and 258 +/- 75 kJ mol(-1), respectively, which are significantly lower than previously predicted by atomistic simulations. The bulk diffusion of Pr3+ in LaMnO3 was enhanced compared to LaCoO3 and LaFeO3 due to higher concentrations of intrinsic point defects in LaMnO3, especially La site vacancies. Grain-boundary diffusion coefficients of Pr3+ in LaCoO3 and LaFeO3 materials were evaluated according to the Whipple-Le Claire equation. Activation energies for grain-boundary diffusion of Pr3+ in LaCoO3 and LaFeO3 materials were 264 +/- 41 kJ mol(-1) and 290 +/- 36 kJ mol(-1) respectively. Finally, a correlation between activation energies for cation diffusion in bulk and along grain boundaries in pure and substituted LaBO3 materials (B = Cr, Fe, Co) is discussed.
引用
收藏
页码:6544 / 6552
页数:9
相关论文
共 57 条
[1]   Determination of diffusion coefficient of Nd3+ in NdCrO3 based on solid state reaction [J].
Akashi, T ;
Mizuno, Y ;
Nanko, M ;
Maruyama, T ;
Saiki, A ;
Tsukui, K ;
Tanabe, J .
MATERIALS TRANSACTIONS, 2001, 42 (07) :1411-1416
[2]   Solid-state reaction kinetics of LaCrO3 from the oxides and determination of La3+ diffusion coefficient [J].
Akashi, T ;
Nanko, M ;
Maruyama, T ;
Shiraishi, Y ;
Tanabe, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (06) :2090-2094
[3]   REVIEW OF P-TYPE DOPED PEROVSKITE MATERIALS FOR SOFC AND OTHER APPLICATIONS [J].
ANDERSON, HU .
SOLID STATE IONICS, 1992, 52 (1-3) :33-41
[4]   A simple approach to lattice effects in conducting perovskite-type oxides [J].
Attfield, JP .
CHEMISTRY OF MATERIALS, 1998, 10 (11) :3239-3248
[5]  
Aylward G.H., 1971, SI CHEM DATA
[6]   Stability of solid oxide fuel cell components [J].
Badwal, SPS .
SOLID STATE IONICS, 2001, 143 (01) :39-46
[7]   Diffusion in nanocrystalline materials [J].
Belova, IV ;
Murch, GE .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2003, 64 (05) :873-878
[8]   Recent advances in materials for fuel cells [J].
Brandon, NP ;
Skinner, S ;
Steele, BCH .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2003, 33 :183-213
[9]   Growth of ternary oxides in the Gd2O3-Fe2O3 system.: A diffusion couple study [J].
Buscaglia, V ;
Buscaglia, MT ;
Giordano, L ;
Martinelli, A ;
Viviani, M ;
Bottino, C .
SOLID STATE IONICS, 2002, 146 (3-4) :257-271
[10]   Reaction diffusion in the Y2O3-Fe2O3 system [J].
Buscaglia, V ;
Caracciolo, F ;
Bottino, C ;
Leoni, M ;
Nanni, P .
ACTA MATERIALIA, 1997, 45 (03) :1213-1224