I am running tubular cells Ni-YSZ | YSZ | Nd-Ni at low T (600 C). The operating condition is as below:
Fuel: H2 50 sccm/min
Air: 100 sccm/min
T: 600 C
Active cell area: 2 cm2
potentiostatic voltage = 0.7 V
I am facing a continuous degradation (current drop) at the initial 100 hours of operation. Post-morterm SEM analysis shows no sign of microstrtuctural degradation (Ni migration, agglomeration, oxidation | layers delamination, etc.) and polarization resistance is low before the test (low ohmic, activation, concentration) + the support contains enough porosity. This is what happens to all of the cells. The cells have closed caps. Cells are inside a zirconia tube. I'm afraid there is a systematic error in my long-term tests. Like the type of silver/gold paste I use for my cathode side or the position of the cell for better removal of produced water (I noticed some groups use vertical furnaces) or maybe making tubes open ended (not closed end).
I am trying to change the current collector or change the design for better removal of water inside zirconia tube holder.
I would appreciate if anyone experiencing similar problem, share their ideas with me.