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LiPF[sub 3](CF[sub 2]CF[sub 3])[sub 3]: A Salt for Rechargeable Lithium Ion Batteries
104
Citations
32
References
2003
Year
EngineeringMerck KgaaComposite GraphiteLifap SolutionsChemistryAqueous BatteryChemical EngineeringSub 3Sodium BatteryMaterials ScienceBiochemistryLithium-ion BatteryLithium-ion BatteriesBattery AdditivesEnergy StorageSolid-state BatteryElectrochemistryElectric BatteryLi-ion Battery MaterialsNatural SciencesCathode MaterialsElectrochemical Energy StorageBatteriesAnode Materials
from Merck KGaA (LiFAP) was tested as a new electrolyte for Li-ion batteries that can replace the commonly used The latter salt is known to be unstable, to decompose thermally to LiF and and to readily undergo hydrolysis with protic species to form HF contamination in solutions. The latter contamination may have a detrimental impact on the performance of both anodes and cathodes for Li-ion batteries. Solutions comprising LiFAP, and (LiBETI) in mixtures of ethylene, dimethyl, and diethyl carbonates were tested with composite graphite and electrodes. The tools for this study included voltammetry (fast and slow scan rates), chronopotentiometry, impedance spectroscopy, Fourier transform infrared, and X-ray and photoelectron spectroscopies. It was found that LiFAP is superior to as an electrolyte for both graphite anodes and cathodes. This should be attributed to the different surface chemistry developed on these electrodes when is replaced by LiFAP. An important impact of such a replacement is probably the absence of possible pronounced HF contamination in LiFAP solutions. © 2003 The Electrochemical Society. All rights reserved.
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