Mathilde Rieu

Investigation of Graded La2NiO4+δ Cathodes to Improve SOFC Electrochemical Performance

Mixed ionic and electronic conducting MIEC oxides are promising materials for use as cathodes in solid oxide fuel cells SOFCs due to their enhanced electrocatalytic activity compared with electronic conducting oxides. In this paper, the MIEC oxide La2NiO4+ was prepared by the sol-gel route. Graded cathodes were deposited onto yttria-stabilized zirconia YSZ pellets by dip-coating, and electrochemical impedance spectroscopy studies were performed to characterize the symmetrical cell performance. By adapting the slurries, cathode layers with different porosities and thicknesses were obtained. A ceria gadolinium oxide CGO barrier layer was introduced, avoiding insulating La2Zr2O7 phase formation and thus reducing resistance polarization of the cathode. A systematic correlation between microstructure, composition, and electrochemical performance of these cathodes has been performed. An improvement of the electrochemical performance has been demonstrated, and a reduction in the area specific resistance ASR by a factor of 4.5 has been achieved with a compact interlayer of La2NiO4+ between the dense electrolyte and the porous La2NiO4+ cathode layer. The lowest observed ASR of 0.11 cm2 at 800°C was obtained from a symmetrical cell composed of a YSZ electrolyte, a CGO interlayer, an intermediate compact La2NiO4+ layer, a porous La2NiO4+ electrode layer, and a current collection layer of platinum paste.

Investigation of Graded La[sub 2]NiO[sub 4+δ] Cathodes to Improve SOFC Electrochemical Performance

Mixed ionic and electronic conducting MIEC oxides are promising materials for use as cathodes in solid oxide fuel cells SOFCs due to their enhanced electrocatalytic activity compared with electronic conducting oxides. In this paper, the MIEC oxide La2NiO4+ was prepared by the sol-gel route. Graded cathodes were deposited onto yttria-stabilized zirconia YSZ pellets by dip-coating, and electrochemical impedance spectroscopy studies were performed to characterize the symmetrical cell performance. By adapting the slurries, cathode layers with different porosities and thicknesses were obtained. A ceria gadolinium oxide CGO barrier layer was introduced, avoiding insulating La2Zr2O7 phase formation and thus reducing resistance polarization of the cathode. A systematic correlation between microstructure, composition, and electrochemical performance of these cathodes has been performed. An improvement of the electrochemical performance has been demonstrated, and a reduction in the area specific resistance ASR by a factor of 4.5 has been achieved with a compact interlayer of La2NiO4+ between the dense electrolyte and the porous La2NiO4+ cathode layer. The lowest observed ASR of 0.11 cm2 at 800°C was obtained from a symmetrical cell composed of a YSZ electrolyte, a CGO interlayer, an intermediate compact La2NiO4+ layer, a porous La2NiO4+ electrode layer, and a current collection layer of platinum paste.

New route to prepare anodic coatings on dense and porous metallic supports for SOFC application

Metallic cell supports have been developed for the new generation of fuel cells. A sol—gel process has been used to prepare anodic coatings on these supports at moderate thermal treatment temperature, in order to keep good support mechanical behavior and limit metallic corrosion. Indeed, we take advantage of the numerous reaction routes that the sol—gel method can offer to first synthesize NiO—YSZ (yttria-stabilized zirconia) homogeneous composites, and then to process films of different thicknesses on metallic supports by dip-coating. In this work, the metallic supports could be either dense or porous. To begin with, duplex microstructured anodes were prepared from both thin and thick layers, directly deposited on dense metallic supports. The interfacial anodic layer, around 100 nm thick, improves adhesion and accommodates stresses between the metallic interconnect and active thick anode. Moreover, by dipping the substrate into an optimized slurry containing sol—gel composite powders, films a few microns thick have been obtained, and constitute the active anodic part. A heat treatment at only 800°C leads to a coherent anodic duplex stacking which is continuous, homogeneous and adherent. Subsequently, thick anodic films have also been deposited on two different porous supports, with both the dip-coating process and slurry routes. These thick anodic coatings were characterized after thermal treatment at 800°C.