Characterization of Cu, Ag and Pt added La0.6Sr0.4Co0.2Fe0.8O3-δ and gadolinia-doped ceria as solid oxide fuel cell electrodes by temperature-programmed techniques

被引:61
作者
Huang, Ta-Jen [1 ]
Shen, Xian-De [1 ]
Chou, Chien-Liang [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 30013, Taiwan
关键词
Temperature-programmed oxidation; Temperature-programmed reduction; Characterization; Cathode; Anode; Solid oxide fuel cell; ANODE-SUPPORTED SOFCS; DIRECT-METHANE SOFCS; ELECTROCHEMICAL PERFORMANCE; DIRECT OXIDATION; CARBON-DIOXIDE; COMPOSITE CATHODES; OXYGEN REDUCTION; NICKEL-CATALYSTS; COPPER-OXIDE; VACANCY;
D O I
10.1016/j.jpowsour.2008.11.019
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
Cu, Ag and Pt added La0.6Sr0.4Co0.2Fe0.8O3-delta (LSCF) and gadolinia-doped ceria (GDC) were analyzed by the temperature-programmed techniques for their characteristics as either the cathode or the anode of the solid oxide fuel cells (SCFCs). Temperature-programmed oxidation using CO2 was used to characterize the cathode materials while temperature-programmed reduction (TPR) using H-2 and TPR using CO were used to characterize the anode materials. These techniques can offer an easy screening of the materials as the SOFC electrodes. The effects of adding Cu, Ag and [It to LSCF for the cathodic reduction activity and the anodic oxidation activity are different-Cu > Ag > Pt for reduction and Pt > Cu > Ag for oxidation. The CO oxidation activities are higher than the H-2 Oxidation activities. Adding GDC to LSCF can increase both reduction and oxidation activities. The LSCF-GDC composite has a maximum activity for either reduction or oxidation when LSCF/GDC is 2 in weight. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:348 / 355
页数:8
相关论文
共 44 条
[1]   Impedance spectroscopic study on well-defined (La,Sr)(Co,Fe)O3-δ model electrodes [J].
Baumann, Frank S. ;
Fleig, Juergen ;
Habermeier, Hanns-Ulrich ;
Maier, Joachim .
SOLID STATE IONICS, 2006, 177 (11-12) :1071-1081
[2]   OXYGEN-TRANSPORT IN SELECTED NONSTOICHIOMETRIC PEROVSKITE-STRUCTURE OXIDES [J].
CARTER, S ;
SELCUK, A ;
CHATER, RJ ;
KAJDA, J ;
KILNER, JA ;
STEELE, BCH .
SOLID STATE IONICS, 1992, 53 :597-605
[3]  
Chang CL, 1996, J APPL ELECTROCHEM, V26, P311, DOI 10.1007/BF00242101
[4]   Cathode performance and oxygen-ion transport mechanism of copper oxide for solid-oxide fuel cells [J].
Chang, CL ;
Hsu, CC ;
Huang, TJ .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2003, 7 (03) :125-128
[5]   Oxygen reduction mechanism and performance of Y1Ba2Cu3O7-δ as a cathode material in a high-temperature solid-oxide fuel cell [J].
Chang, CL ;
Lee, TC ;
Huang, TJ .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 1998, 2 (05) :291-298
[6]   High performance cathode-supported SOFC with perovskite anode operating in weakly humidified hydrogen and methane [J].
Chen, X. J. ;
Liu, Q. L. ;
Chan, S. H. ;
Brandon, N. P. ;
Khor, Khiam Aik .
ELECTROCHEMISTRY COMMUNICATIONS, 2007, 9 (04) :767-772
[7]   EFFECTS OF OXYGEN VACANCY OF YTTRIA-STABILIZED ZIRCONIA SUPPORT ON CARBON-MONOXIDE OXIDATION OVER COPPER CATALYST [J].
DOW, WP ;
HUANG, TJ .
JOURNAL OF CATALYSIS, 1994, 147 (01) :322-332
[8]   THE EFFECT OF IONIC RADIUS OF METAL ELEMENT (M) ON (PB,M)-1212 SUPERCONDUCTORS (M=SR, CA, MG, HG, CD, CU) [J].
FENG, QR ;
GUO, JD ;
XU, XL ;
ZHANG, I ;
ZHU, X ;
FENG, SQ .
SOLID STATE COMMUNICATIONS, 1995, 94 (01) :21-25
[9]   Carbon structures obtained by the disproportionation of carbon monoxide over nickel catalysts [J].
Govindaraj, A ;
Sen, R ;
Santra, AK ;
Nagaraju, BV .
MATERIALS RESEARCH BULLETIN, 1998, 33 (04) :663-667
[10]   The influence of ion size on the binding of a charge compensating cobalt vacancy to M3+ dopant ions in CoO [J].
Grimes, RW ;
Chen, SP .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2000, 61 (08) :1263-1268