Anode- versus electrolyte-supported Ni-YSZ/YSZ/Pt SOFCs: Effect of cell design on OCV, performance and carbon formation for the direct utilization of dry methane

被引:55
作者
Buccheri, Marco A. [1 ]
Singh, Anand [1 ]
Hill, Josephine M. [1 ]
机构
[1] Univ Calgary, Dept Chem & Petr Engn, Calgary, AB T2N 1N4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Solid oxide fuel cell; Ni/YSZ anode; Carbon deposition; Direct methane utilization; Anode-supported cell; Electrolyte-supported cell; OXIDE FUEL-CELLS; DIRECT-OXIDATION; ELECTROCHEMICAL OXIDATION; THERMODYNAMIC ANALYSIS; DEPOSITION; HYDROCARBONS; POLARIZATION; CONVERSION; OPERATION; ETHANOL;
D O I
10.1016/j.jpowsour.2010.08.073
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
In this study, anode- and electrolyte-supported Ni-YSZ/YSZ/Pt solid oxide fuel cells (SOFC) are compared in terms of performance and carbon formation when operated on dry methane. Although anode-supported SOFCs are typically used in industry, electrolyte-supported cells may be required for certain laboratory experiments. Thermodynamic calculations were performed to calculate the equilibrium gas-phase composition. The measured open circuit voltages (OCV) in dry methane were 1.15V and 0.92V for anode- and electrolyte-supported cells, respectively. The difference in these OCV values reflects the different gas-phase compositions at the electrochemically active region of the two cell designs. The conduction layer in the anode-supported SOFC provides the catalytic sites to produce more hydrogen, which results in a higher OCV and a larger limiting current density. Over time, carbon is also produced and results in a higher degradation rate on the anode-supported cell. Carbon also forms on the electrolyte-supported cell but has less of a negative impact on the operation of the electrolyte-supported cell. Temperature-programmed oxidation (TPO) studies indicate that the carbon formed in the conduction layer of an anode-supported cell is much more stable and difficult to remove than carbon formed on the functional layer. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:968 / 976
页数:9
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