Transmission Electron Microscopy Study of Ba0.5Sr0.5Co0.8Fe0.2O3-δ Perovskite Decomposition at Intermediate Temperatures

被引:153
作者
Efimov, Konstantin [1 ]
Xu, Qiang [2 ,3 ]
Feldhoff, Armin [1 ]
机构
[1] Leibniz Univ Hannover, Inst Phys Chem & Electrochem, D-30167 Hannover, Germany
[2] Delft Univ Technol, Natl Ctr HREM, Kavli Inst Nanosci, NL-2628 CJ Delft, Netherlands
[3] Univ Antwerp, Vis Lab, B-2020 Antwerp, Belgium
关键词
IN-SITU; OXYGEN; OXIDE; CO; PERFORMANCE; STABILITY; OXIDATION; FE;
D O I
10.1021/cm101745v
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 cubic perovskite Ba0.5Sr0.5Co0.8Fe0.2O3-delta (denoted BSCF) is the state-of-the-art ceramic membrane material used for oxygen separation technologies above 1150 K. BSCF is a mixed oxygen-ion and electron conductor (MIEC) and exhibits one of the highest oxygen permeabilities reported so far for dense oxides. Additionally, it has excellent phase stability above 1150 K. In the intermediate temperature range (750-1100 K), however, BSCF suffers from a slow decomposition of the cubic perovskite into variants with hexagonal stacking that are barriers to oxygen transport. To elucidate details of the decomposition process, both sintered BSCF ceramic and powder were annealed for 180-240 h in ambient air at temperatures below 1123 K and analyzed by different transmission electron microscopy techniques. Aside from hexagonal perovskite Ba0.5Sr0.5CoO3-delta , the formation of lamellar noncubic phases was observed in the quenched samples. The structure of the lamellae with the previously unknown composition Ba1-xSrxCo2-yFeyO5-delta was found to be related to the 15R hexagonal perovskite polytype. The valence and spin-state transition of cobalt leading to a considerable diminution of its ionic radius can be considered a reason for BSCF's inherent phase instability at intermediate temperatures.
引用
收藏
页码:5866 / 5875
页数:10
相关论文
共 38 条
[1]   Correlation of the formation and the decomposition process of the BSCF perovskite at intermediate temperatures [J].
Arnold, Mirko ;
Gesing, Thorsten M. ;
Martynczuk, Julia ;
Feldhoff, Armin .
CHEMISTRY OF MATERIALS, 2008, 20 (18) :5851-5858
[2]   In situ study of the reaction sequence in the sol-gel synthesis of a (Ba0.5Sr0.5)(Co0.8Fe0.2)O3-δ perovskite by x-ray diffraction and transmission electron microscopy [J].
Arnold, Mirko ;
Wang, Haihui ;
Martynczuk, Julia ;
Feldhoff, Armin .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2007, 90 (11) :3651-3655
[3]   Local Charge Disproportion in a High-Performance Perovskite [J].
Arnold, Mirko ;
Xu, Qiang ;
Tichelaar, Frans D. ;
Feldhoff, Armin .
CHEMISTRY OF MATERIALS, 2009, 21 (04) :635-640
[4]   Evaluation of perovskites in hollow fibre and disk geometry in catalytic membrane reactors and in oxygen separators [J].
Caro, J. ;
Wang, H. H. ;
Tablet, C. ;
Kleinert, A. ;
Feldhoff, A. ;
Schiestel, T. ;
Kilgus, M. ;
Koelsch, P. ;
Werth, S. .
CATALYSIS TODAY, 2006, 118 (1-2) :128-135
[5]   Conversion of methane to syngas by a membrane-based oxidation-reforming process [J].
Chen, CS ;
Feng, SJ ;
Ran, S ;
Zhu, DC ;
Liu, W ;
Bouwmeester, HJM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (42) :5196-5198
[6]   15R SrMn1-xFexO3-δ (x≈0.1);: A new perovskite stacking sequence [J].
Cussen, EJ ;
Sloan, J ;
Vente, JP ;
Battle, PD ;
Gibb, TC .
INORGANIC CHEMISTRY, 1998, 37 (23) :6071-6077
[7]   Novel Cobalt-Free Oxygen-Permeable Perovskite-Type Membrane [J].
Efimov, Konstantin ;
Halfer, Torben ;
Kuhn, Alexander ;
Heitjans, Paul ;
Caro, Juergen ;
Feldhoff, Armin .
CHEMISTRY OF MATERIALS, 2010, 22 (04) :1540-1544
[8]   Spin-state transition of iron in (Ba0.5Sr0.5)(Fe0.8Zn0.2)O3-δ perovskite [J].
Feldhoff, Armin ;
Martynczuk, Julia ;
Arnold, Mirko ;
Myndyk, Maxym ;
Bergmann, Ingo ;
Sepelak, Vladimir ;
Gruner, Wolfgang ;
Vogt, Ulrich ;
Haehnel, Angelika ;
Woltersdorf, Joerg .
JOURNAL OF SOLID STATE CHEMISTRY, 2009, 182 (11) :2961-2971
[9]  
GOLDSCHMIDT VM, 1926, M NATURTVISSENSCHAFT, V14, P477
[10]   THE PREPARATION OF A BARIUM COBALT OXIDE AND OTHER PHASES WITH SIMILAR STRUCTURES [J].
GUSHEE, BE ;
KATZ, L ;
WARD, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1957, 79 (21) :5601-5603