Studies on structural, morphological and electrical properties of Ce0.8Ln0.2O2-δ (Ln = Y3+, Gd3+, Sm3+, Nd3+ and La3+) solid solutions prepared by citrate complexation method

被引:59
|
作者
Anjaneya, K. C. [1 ]
Nayaka, G. P. [1 ]
Manjanna, J. [1 ]
Govindaraj, G. [2 ]
Ganesha, K. N. [2 ]
机构
[1] Kuvempu Univ, Dept Ind Chem, Shankarghatta 577451, India
[2] Pondicherry Univ, Dept Phys, Pondicherry 605001, India
关键词
Fuel cells; Ceramics; Chemical synthesis; Vacancy formation; Electrochemical impedance spectroscopy; FUEL-CELL ELECTROLYTE; DOPED CERIA; GRAIN-BOUNDARIES; TEMPERATURE; CEO2; RAMAN; COPRECIPITATION; CONDUCTIVITY; PERFORMANCE; TRANSPORT;
D O I
10.1016/j.jallcom.2013.09.101
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 modified sol-gel method which is also known as citrate complexation is used here to prepare Ce(0.8)Ln(0.2)O(2) (delta) (Ln = Y3+, Gd3+, Sm3+, Nd3+ and La3+) solid solutions for their proposed application in intermediate-temperature solid oxide fuel cells (IT-SOFCs) as electrolytes. All the samples exhibit the fluorite type crystalline structure without any phase segregation, characteristics of CeO2, as revealed in XRD pattern. The lattice parameters and densities calculated based on the oxygen vacancy model agreed well with the experimental (Archimedes method) values. The formation of solid solution is also confirmed by Raman spectroscopy. The microstructural features of the samples are recorded by using FE-SEM/TEM. The ionic conductivities of various Ln-doped samples at 623 K as obtained from electrochemical impedance measurement are as follows: Ce0.8Sm0.2O2 (delta) > Ce0.8Gd0.2O2 (delta) > Ce0.8Nd0.2O2 (delta) > Ce0.8La0.2O2 (delta) > Ce0.8Y0.2O2 (delta). The activation energy for total conductivity are found to be 0.86, 0.87, 0.89, 0.96 and 1.02 eV for Sm, Gd, Nd, La and Y doped ceria, respectively. The relationship between the dopant radius, chemical composition, lattice parameters, morphology and electric properties are discussed here. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:594 / 601
页数:8
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