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This study was financially supported by the University of Akron and the Natural Sciences and Engineering Research Council of Canada (NSERC) through grants to Z.C. and the University of Waterloo.
A.G. Kashkooli, et al., 2016. , J Power Sources.
An LiFePO4 (LFP) sample from a commercial LFP/graphite cell which was disassembled and scanned using nanoXCT. The obtained 2D stack was imported in Simpleware ScanIP and segmented utilizing thresholding technique to convert the greyscale stack to a binary stack. The process included segmenting the active material particles and pore-PVDF-carbon regions from the scan. If the weight percentage of the active material is high, the carbon material and polymer binder are randomly distributed in the electrode. To reconstruct the connected solid matrix, it was assumed that the carbon material is randomly distributed among the active material to provide electronic connectivity. A morphological close filter was used in Simpleware ScanIP on the active material region to fuse the neighboring active material together.
Reconstructed nanoXCT image data in Simpleware ScanIP
A mesh of the model was then generated using Simpleware FE and exported directly to COMSOL Multiphysics? for solving governing partial differential equations related to developed LIB multiscale model. In microscale, the model is based on the real 3D microstructure data, taking advantage of the traditional homogenous 1D model in macro-scale to characterize discharge/charge performance. This framework was used for the multi-scale - multiphysics study of LIB.
Simulation-ready volume mesh generated in Simpleware FE and exported directly to COMSOL Multiphysics?
It is shown that this model can predict the experimental performance of LiFePO4 cathode at different discharge rates more accurately than the conventional homogenous models. The simulation results could predict the experimental discharge voltage of LFP cathodes at different rates. The simulation showed that the lithium ion concentration in the electrode active material structure is much higher in the region with smaller cross-section area perpendicular to the lithium intercalation pathway. Such low area regions would intercalate ca. 10 times higher than the area with an average concentration. The approach used in this study can provide valuable insight into the spatial distribution of lithium ions inside the microstructure of LIB electrodes. The inhomogeneous microstructure of LFP causes a wide range of physical and electrochemical properties compared to the homogeneous model.
Distribution of lithium concentration (mol m-3) inside the electrode microstructure during discharge at c-rate = 1 for different SOCs (3D electrode microstructure represents geometry in microscale and 1D x-coordinate describe geometry in macro-scale along the electrode thickness direction).
(Reproduced with permission from Journal of Power sources, doi:10.1016/j.jpowsour.2015.12.134)
Distribution of the overpotential (unit:V) on the solid/electrolyte interface during discharge at c-rate = 1 for different SOCs.
(Reproduced with permission from Journal of Power sources, doi:10.1016/j.jpowsour.2015.12.134)
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