Effect of binder on the overcharge response in LiFePO4-containing cells

Two types of small pouch cells based on LiFePO4/graphite, one containing a N-methyl pyrrolidinone (NMP)-soluble binder, poly(vinylidene difluoride), and the other an aqueous-soluble binder, styrene-butadiene rubber/carboxymethylcellulose were systematically charged to 100, 120, 140, 160, 180, and 25...

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Bibliographic Details
Published in:Journal of power sources Vol. 450; no. C
Main Authors: Rago, Nancy Dietz, Li, Jianlin, Sheng, Yangping, Wood III, David L., Steele, Leigh Anna, Lamb, Joshua, Grosso, Christopher, Fenton, Kyle, Bloom, Ira
Format: Journal Article
Language:English
Published: United States Elsevier 29-01-2020
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Summary:Two types of small pouch cells based on LiFePO4/graphite, one containing a N-methyl pyrrolidinone (NMP)-soluble binder, poly(vinylidene difluoride), and the other an aqueous-soluble binder, styrene-butadiene rubber/carboxymethylcellulose were systematically charged to 100, 120, 140, 160, 180, and 250% state of charge (SOC). The cells were then discharged to 3.0 V at room temperature before being disassembled for postmortem analysis. Microstructural changes in the anode associated with increasing SOC were more pronounced in the aqueous processed cells in comparison to the NMP-processed cells. Dendrite formation was observed on the aqueous-processed anode at 120% SOC, while the NMP-processed anode surface does not show dendrites until 250% SOC. Overall, the aqueous-processed anode surfaces displayed more evidence of microstructural degradation as a function of increasing SOC. In the NMP-processed cells, four organic compounds on the anode surface were found to show a dependence on SOC, while only two displayed a similar dependency in the aqueous-processed cells. The nature of the binder changed the number and composition of the species found at the anode.
Bibliography:USDOE Office of Science (SC)
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Transportation Office. Vehicle Technologies Office
USDOE National Nuclear Security Administration (NNSA)
AC02-06CH11357; AC05-00OR22725; NA0003525
ISSN:0378-7753
1873-2755