Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1288493 | Journal of Power Sources | 2011 | 10 Pages |
The full oxidation of Ni–YSZ anode-supported cells at high temperatures (>700 °C) is shown here to lead to much more severe degradation (larger quantity and wider cracks in the electrolyte) than at lower temperatures. This correlates with the linear mass gain/time profile observed in TGA experiments at high temperatures, indicative of diffusion controlled Ni oxidation and thus the presence of O2 (and Ni/NiO) concentration gradients into the depth of the anode layer. At low partial pressures of O2, the severity of cracking also increases. SEM studies of partially oxidized anode layers confirmed that Ni oxidation is non-homogeneous when carried out at either high temperatures or low pO2, in which case the outer regions of the anode (near the anode/air interface) become almost fully oxidized, while the inner regions (near the electrolyte) remain metallic. Under these conditions, the continued volume expansion associated with NiO formation can then only occur towards the electrolyte, increasing the compressive stress inside the anode as the Ni continues to be oxidized, leading to electrolyte cracking and warping (convex to the electrolyte). To prevent severe degradation to the cell, efforts should therefore be made to avoid gradients in NiO/Ni content during oxygen exposure of Ni–YSZ anode-supported cells at high temperatures.