Thermal aging stability of infiltrated solid oxide fuel cell electrode microstructures: A three-dimensional kinetic Monte Carlo simulation

2015 ◽  
Vol 299 ◽  
pp. 578-586 ◽  
Author(s):  
Yanxiang Zhang ◽  
Meng Ni ◽  
Mufu Yan ◽  
Fanglin Chen
2011 ◽  
Vol 8 (5) ◽  
Author(s):  
Andrew Martinez ◽  
Jacob Brouwer

A previously developed microstructure model of a solid oxide fuel cell (SOFC) electrode-electrolyte interface has been applied to study the impacts of particle properties on these interfaces through the use of a Monte Carlo simulation method. Previous findings that have demonstrated the need to account for gaseous phase percolation have been confirmed through the current investigation. In particular, the effects of three-phase percolation critically affect the dependence of TPB formation and electrode conductivity on (1) conducting phase particle size distributions, (2) electronic:ionic conduction phase contrast, and (3) the amount of mixed electronic-ionic conductor (MEIC) included in the electrode. In particular, the role of differing percolation effectiveness between electronic and ionic phases has been shown to counteract and influence the role of the phase contrast. Porosity, however, has been found to not be a significant factor for active TPB formation in the range studied, but does not obviate the need for modeling the gas phase. In addition, the current work has investigated the inconsistencies in experimental literature results concerning the optimal particle size distribution. It has been found that utilizing smaller particles with a narrow size distribution is the preferable situation for electrode-electrolyte interface manufacturing. These findings stress the property-function relationships of fuel cell electrode materials.


2010 ◽  
Vol 94 (2) ◽  
pp. 620-627 ◽  
Author(s):  
Danijel Gostovic ◽  
Nicholas J. Vito ◽  
Kathryn A. O'Hara ◽  
Kevin S. Jones ◽  
Eric D. Wachsman

2014 ◽  
Vol 2 (33) ◽  
pp. 13407-13414 ◽  
Author(s):  
David S. D. Gunn ◽  
Neil L. Allan ◽  
John A. Purton

Millisecond length simulations have been performed to directly calculate accurate ionic conductivities in solid oxide fuel cell (SOFC) electrolyte and cathode materials using adaptive kinetic Monte Carlo (aKMC).


2009 ◽  
Vol 15 (1) ◽  
pp. 71-77 ◽  
Author(s):  
James R. Wilson ◽  
Marcio Gameiro ◽  
Konstantin Mischaikow ◽  
William Kalies ◽  
Peter W. Voorhees ◽  
...  

AbstractA method is described for quantitatively analyzing the level of interconnectivity of solid-oxide fuel cell electrode phases. The method was applied to the three-dimensional microstructure of a Ni–Y2O3-stabilized ZrO2 (Ni-YSZ) anode active layer measured by focused ion beam scanning electron microscopy. Each individual contiguous network of Ni, YSZ, and porosity was identified and labeled according to whether it was contiguous with the rest of the electrode. It was determined that the YSZ phase was 100% connected, whereas at least 86% of the Ni and 96% of the pores were connected. Triple-phase boundary (TPB) segments were identified and evaluated with respect to the contiguity of each of the three phases at their locations. It was found that 11.6% of the TPB length was on one or more isolated phases and hence was not electrochemically active.


Author(s):  
Andrew Martinez ◽  
Jacob Brouwer

A previously-developed microstructure model of the Solid Oxide Fuel Cell (SOFC) electrode-electrolyte interface has been applied to the study of particle properties in these devices through the use of the Monte Carlo simulation method. Previous findings that have demonstrated the necessity of accounting for the gaseous phase percolation have been re-emphasized through the current investigation. In particular, the effects of three-phase percolation critically affect the dependence of TPB formation and electrode conductivity on: 1) conducting phase particle size distributions, 2) electronic:ionic conduction phase contrast, and 3) the amount of Mixed Electronic-Ionic Conductor (MEIC) included in the electrode. In particular, the role of differing percolation effectiveness between electronic and ionic phases has been shown to counteract and influence the role of the phase contrast. Porosity, however, has been found to not be a significant factor for the range studied, but does not obviate the necessity of modeling the gas phase. In addition, the current work has investigated the inconsistencies in experimental literature results concerning the optimal particle size distribution. It has been found that utilizing smaller particles with a narrow size distribution is the preferable situation for electrode manufacturing. These findings stress the property-function relationships of fuel cell electrode materials.


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