Structure, conductivity and redox reversibility of Ca-doped cerium metavanadate

被引:17
|
作者
Petit, Christophe T. G. [1 ]
Lan, Rong [1 ]
Cowin, Peter I. [1 ]
Irvine, John T. S. [2 ]
Tao, Shanwen [1 ]
机构
[1] Univ Strathclyde, Fac Engn, Dept Chem & Proc Engn, Glasgow G1 1XJ, Lanark, Scotland
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
基金
英国工程与自然科学研究理事会;
关键词
OXIDE FUEL-CELLS; TRANSPORT-PROPERTIES; ANODE; STABILITY; PEROVSKITES; CEVO4; CRYSTAL; PR; CE;
D O I
10.1039/c1jm10960j
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
A-site substituted cerium metavanadates, Ce1-xCaxVO3, were synthesised by solid-state reactions from single-phase powders of the corresponding orthovanadates. All metavanadate samples were found to exhibit either an orthorhombic and/or monoclinic phase of space group Pnma (62) with a = 5.5067 (4), b = 7.7904 (5) and c = 5.4814(7) angstrom for Ce0.8Ca0.2VO3. X-Ray diffraction patterns and thermal analyses have shown that the reduction of Ca-doped CeVO3 from the equivalent orthovanadate is redox phase reversible without formation of parasitic phases at x = 0.2, 0.3. Conductivity measurements were performed in air and in dry 5% H-2-Ar with conductivity of Ce1-xCaxVO3 ranging from 1.5 to 13 S cm(-1) at 700 degrees C in a reducing atmosphere. Sample Ce0.7Ca0.3VO3 exhibits the highest conductivity in a reducing atmosphere in all the measured samples which could be a potential anode or as a part of composite anode for SOFCs. The conductivity of Ce0.7Ca0.3VO3 is higher than that for Ce0.85Sr0.15VO3 which could be related to the higher doping level.
引用
收藏
页码:8854 / 8861
页数:8
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