Kinetic Studies on State of the Art Solid Oxide Cells: A Comparison between Hydrogen/Steam and Reformate Fuels

Abstract

© The Author(s) 2016. Published by ECS. All rights reserved. Electrochemical reaction kinetics at the electrodes of Solid Oxide Cells (SOCs) were investigated at 700°C for two cells with different fuel electrode microstructures as well as on a third cell with a reduced active electrode area. Three fuel mixtures were investigated - hydrogen/steam and model reformate fuels-hydrogen/carbon-dioxide and hydrogen/methane/steam. It was found that the electrode kinetics at the fuel electrode were exactly the same in both reformates. The hydrogen/steam fuel displayed 5-7% faster kinetics than the reformate fuels. 19% faster kinetics were recorded for the cell with a finer microstructure. The measured gas conversion impedance was compared with models in literature for both the 16- and the 2 cm 2 cells. The continuously stirred tank reactor (CSTR) AC model approximated the overpotential of the smaller cells (2 cm 2 ) with greater accuracy in the current density range 0-0.5 A/cm 2 while the plug flow reactor (PFR) model although derived for the case of zero DC bias predicted the 16 cm 2 cell ASR better than the zero bias CSTR model. Furthermore, the gas conversion impedance in the hydrogen/steam fuel split into two processes with opposing temperature behavior in the reformate fuels. By using a 87.5% smaller active electrode area the gas conversion impedance was diminished in the hydrogen/steam fuel at (the same absolute) high fuel flow rates. In both reformates, the second and third lowest frequency processes merged into a single process as the gas conversion was reduced. The SOC with finer electrode microstructure displayed improved kinetics.