TY - JOUR
T1 - Simulation of oxygen diffusion process on electrical conductivity relaxation
AU - Kudo, Honami
AU - Yashiro, Keiji
AU - Hashimoto, Shin Ichi
AU - Amezawa, Koji
AU - Kawada, Tatsuya
N1 - Funding Information:
This research was partly supported by JST-CREST, “Phase Interface Science for Highly Efficient Energy Utilization”. The simulation software of MSC.Marc/Mentat 2012 used in this research was obtained from supercomputing resources at Cyberscience Center, Tohoku University.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Finite element method (FEM) simulations were carried out for modeling the electrical conductivity relaxation (ECR) process of a mixed ionic electronic conductor upon abrupt change of oxygen partial pressure. Oxygen diffusion pathway was simulated considering enhanced surface exchange rate on the current and voltage terminals formed on the specimen. The results suggested that the vacancy diffusion coefficient, DV, ECR, obtained from ECR method appears to be dependent on vacancy concentration, δ, even though the true DV is constant. The effects of the following parameters were investigated; degree of catalytic effect, surface reaction rate constant and sample dimension. Change in the sample dimension in a realistic range did not effectively suppress the modification of diffusion paths, and the change of apparent chemical diffusion coefficient, Dchem, app, was inevitable when surface reaction rate constant, kchem, and Dchem are in the same range. The results of the FEM simulation were confirmed by ECR experiments with catalytic active (Pt) and inactive (Au) electrodes.
AB - Finite element method (FEM) simulations were carried out for modeling the electrical conductivity relaxation (ECR) process of a mixed ionic electronic conductor upon abrupt change of oxygen partial pressure. Oxygen diffusion pathway was simulated considering enhanced surface exchange rate on the current and voltage terminals formed on the specimen. The results suggested that the vacancy diffusion coefficient, DV, ECR, obtained from ECR method appears to be dependent on vacancy concentration, δ, even though the true DV is constant. The effects of the following parameters were investigated; degree of catalytic effect, surface reaction rate constant and sample dimension. Change in the sample dimension in a realistic range did not effectively suppress the modification of diffusion paths, and the change of apparent chemical diffusion coefficient, Dchem, app, was inevitable when surface reaction rate constant, kchem, and Dchem are in the same range. The results of the FEM simulation were confirmed by ECR experiments with catalytic active (Pt) and inactive (Au) electrodes.
KW - Catalytic effect
KW - Oxide ion diffusion
KW - Surface exchange coefficient
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U2 - 10.1016/j.ssi.2014.01.009
DO - 10.1016/j.ssi.2014.01.009
M3 - Article
AN - SCOPUS:84903274941
SN - 0167-2738
VL - 262
SP - 696
EP - 700
JO - Solid State Ionics
JF - Solid State Ionics
ER -