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Spatial Distribution of Electrochemical Performance in a Segmented SOFC: A Combined Modeling and Experimental Study
Author(s) -
Bessler W. G.,
Gewies S.,
Willich C.,
Schiller G.,
Friedrich K. A.
Publication year - 2010
Publication title -
fuel cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.485
H-Index - 69
eISSN - 1615-6854
pISSN - 1615-6846
DOI - 10.1002/fuce.200900083
Subject(s) - anode , cathode , materials science , polarization (electrochemistry) , triple phase boundary , electrochemistry , solid oxide fuel cell , electrode , gas composition , voltage , current density , analytical chemistry (journal) , chemical engineering , nuclear engineering , thermodynamics , chemistry , electrical engineering , physics , engineering , quantum mechanics , chromatography
Spatially inhomogeneous distribution of current density and temperature in solid oxide fuel cells (SOFC) contributes to accelerated electrode degradation, thermomechanical stresses, and reduced efficiency. This paper presents a combined experimental and modeling study of the distributed electrochemical performance of a planar SOFC. Experimental data were obtained using a segmented cell setup that allows the measurement of local current‐voltage characteristics, gas composition and temperature in 4 × 4 segments. Simulations were performed using a two‐dimensional elementary kinetic model that represents the experimental setup in a detailed way. Excellent agreement between model and experiment was obtained for both global and local performance over all investigated operating conditions under varying H 2 /H 2 O/N 2 compositions at the anode, O 2 /N 2 compositions at the cathode, temperature, and fuel utilization. A strong variation of the electrochemical performance along the flow path was observed when the cell was operated at high fuel utilization. The simulations predict a considerable gradient of gas‐phase concentrations along the fuel channel and through the thickness of the porous anode, while the gradients are lower at the cathode side. The anode dominates polarization losses. The cell may operate locally in critical operating conditions (low H 2 /H 2 O ratios, low local segment voltage) without notably affecting globally observed electrochemical behavior.