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Comparison of PVDF and PVDF-TFE-P as Binders for Electrode Materials Showing Large Volume Changes in Lithium-Ion Batteries
120
Citations
7
References
2003
Year
Electrode MaterialsEngineeringCarbon Black-filled CompositesAqueous BatteryCarbon-filled CompositesConducting PolymerChemical EngineeringMaterials ScienceElectrical EngineeringDyneon Corp.Battery Electrode MaterialsAdvanced Electrode MaterialLithium-ion BatteryLithium-ion BatteriesEnergy StoragePolymer MembranesSolid-state BatteryLarge Volume ChangesEnergy MaterialElectrochemistryElectric BatteryLi-ion Battery MaterialsPolymer ScienceCathode MaterialsElectrochemical Energy StorageBatteriesAnode Materials
The mechanical and electrical properties of a terpolymer, poly(vinylidene fluoride-tetrafluoroethylene-propylene) (PVDF-TFE-P, BRE-7131X, Dyneon Corp.) and its carbon black-filled composites (without active anode material) have been investigated carefully and are compared to those of PVDF (Solef 1008). High capacity anode materials such as a-Si and have up to 250% volumetric changes during charge/discharge cycling which challenges the mechanical properties of standard binders used in Li-ion battery electrodes. The measurements were carried out on dry polymer films and on films immersed in a nonaqueous solvent commonly used in Li-ion cells (ethylene carbonate/diethyl carbonate, EC/DEC, 1:2 by volume). PVDF and its carbon-filled composites show a maximum elongation before break of less than 10%. However, triethylenetetramine crosslinked BRE-7131X and its carbon-filled composites can be stretched to more than 100% strain before breaking in air and in EC/DEC (1:2 by volume). Furthermore, the stress and the resistivity of the carbon-filled crosslinked BRE-7131X films changes reversibly during elongation/contraction cycles. © 2003 The Electrochemical Society. All rights reserved.
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