Thermodynamics and Kinetics of the Interaction of Carbon and Sulfur with Solid Oxide fuel Cell Anodes

被引:74
作者
Offer, Gregory J. [1 ]
Mermelstein, Joshua [1 ]
Brightman, Edward [1 ]
Brandon, Nigel P. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
DENSITY-FUNCTIONAL THEORY; CURRENT-VOLTAGE CHARACTERISTICS; LIQUID-HYDROCARBON FUELS; NI-BASED ANODES; IN-SITU RAMAN; HYDROGEN-SULFIDE; DEEP DESULFURIZATION; OXIDATION-KINETICS; SEALING TECHNOLOGY; OXYGEN REDUCTION;
D O I
10.1111/j.1551-2916.2009.02980.x
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Fuel cells are likely to play a key role in any low-carbon economy. Solid oxide fuel cells (SOFCs) are currently capable of sustained and continuous operation on high-purity fuels, but they must demonstrate that they can overcome a number of challenges before they are commercially viable on a large scale. Fuels such as natural gas, and those derived from renewable sources such as gasified biomass, contain many contaminants, typically sulfur- and carbon-containing compounds. To address this it will be necessary to improve our understanding of failure modes in operating SOFCs, and act on this to reduce degradation rates. A combination of techniques will be needed to develop a rigorous approach to understanding and mitigating degradation. The intent of this article is to present a synopsis of the current state of the art in our understanding of the effect of carbon and sulfur on SOFC anodes. Emphasis is placed on the comparison between thermodynamic and kinetic models, and experimental validation of these. In particular the applicability of thermodynamic models to the study of such contaminants is questioned. Additionally the uses of multiscale kinetic models capable of predicting transient conditions are reviewed alongside recent analytical techniques necessary for their validation.
引用
收藏
页码:763 / 780
页数:18
相关论文
共 137 条
[1]   Mechanism and kinetics of oxygen reduction on porous La1-xSrxCoO3-δ electrodes [J].
Adler, SB .
SOLID STATE IONICS, 1998, 111 (1-2) :125-134
[2]   Factors governing oxygen reduction in solid oxide fuel cell cathodes [J].
Adler, SB .
CHEMICAL REVIEWS, 2004, 104 (10) :4791-4843
[3]   Density functional theory study of hydrogen sulfide dissociation on bi-metallic Ni-Mo catalysts [J].
Albenze, Erik J. ;
Shamsi, Abolghasem .
SURFACE SCIENCE, 2006, 600 (16) :3202-3216
[4]   First-principles studies of H2S adsorption and dissociation on metal surfaces [J].
Alfonso, Dominic R. .
SURFACE SCIENCE, 2008, 602 (16) :2758-2768
[5]   Hydrogen oxidation and proton transport at the Ni-zirconia interface in solid oxide fuel cell anodes: Quantum chemical predictions [J].
Anderson, Alfred B. ;
Vayner, Ellen .
SOLID STATE IONICS, 2006, 177 (15-16) :1355-1359
[6]  
[Anonymous], 2003, HDB FUEL CELLS FUNDA
[7]   Thermodynamic analysis of carbon formation in a solid oxide fuel cell with a direct internal reformer fuelled by methanol [J].
Assabumrungrat, S ;
Laosiripojana, N ;
Pavarajarn, V ;
Sangtongkitcharoen, W ;
Tangjitmatee, A ;
Praserthdam, P .
JOURNAL OF POWER SOURCES, 2005, 139 (1-2) :55-60
[8]   Thermodynamic analysis for a solid oxide fuel cell with direct internal reforming fueled by ethanol [J].
Assabunrungrat, S ;
Pavarajarn, V ;
Charojrochkul, S ;
Laosiripojana, N .
CHEMICAL ENGINEERING SCIENCE, 2004, 59 (24) :6015-6020
[9]  
Bard A. J., 2001, ELECTROCHEMICAL METH
[10]  
Barin I., 2008, Thermochemical Data of Pure Substances, VThird