A Comparison of Molten Sn and Bi for Solid Oxide Fuel Cell Anodes

被引:68
作者
Jayakumar, A. [1 ]
Lee, S. [1 ]
Hornes, A. [2 ]
Vohs, J. M. [1 ]
Gorte, R. J. [1 ]
机构
[1] Univ Penn, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
[2] CSIC, Inst Catalysis & Petrochem, E-28049 Madrid, Spain
关键词
bismuth; electric impedance; electrochemical electrodes; electrolytes; liquid metals; oxidation; scanning electron microscopy; solid oxide fuel cells; thermodynamics; tin; yttrium compounds; zirconium compounds; LIQUID-TIN; CARBON; OXIDATION; OXYGEN;
D O I
10.1149/1.3282443
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Molten Sn and Bi were examined at 973 and 1073 K for use as anodes in solid oxide fuel cells with yttria-stabilized zirconia (YSZ) electrolytes. Cells were operated under "battery" conditions, with dry He flow in the anode compartment, to characterize the electrochemical oxidation of the metals at the YSZ interface. For both metals, the open-circuit voltages (OCVs) were close to that expected based on their oxidation thermodynamics, similar to 0.93 V for Sn and similar to 0.48 V for Bi. With Sn, the cell performance degraded rapidly after the transfer of approximately 0.5-1.5 C/cm(2) of charge due to the formation of a SnO2 layer at the YSZ interface. At 973 K, the anode impedance at OCV for freshly reduced Sn was approximately 3 cm(2) but this increased to well over 250 cm(2) after the transfer of 1.6 C/cm(2) of charge. Following the transfer of 8.2 C/cm(2) at 1073 K, the formation of a 10 mu m thick SnO2 layer was confirmed by scanning electron microscopy. With Bi, the OCV anode impedance at 973 K was less than 0.25 cm(2) and remained constant until essentially all of the Bi had been oxidized to Bi2O3. Some implications of these results for direct carbon fuel cells are discussed.
引用
收藏
页码:B365 / B369
页数:5
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