ACS Applied Materials & Interfaces · 2015 · 126 citations · 34 references
Natural SciencesMaterials EngineeringMaterials ScienceElectrochemistryMaterials ChemistryPolymer ChemistryBattery MaterialsConducting PolymersConductive PolymersElectrochemical CellsGelsIonic PolymersCapacity FadingElectrolytesFlexible ElectrolytesGel ElectrolytesGel Polymer ElectrolytesIonic TransportLiquid ElectrolytesPolymer Electrolytes
LiMn2O4-based batteries exhibit severe capacity fading during cycling or storage in LiPF6-based liquid electrolytes, especially at elevated temperatures. Herein, a novel rigid-flexible gel polymer electrolyte is introduced to enhance the cyclability of LiMn2O4/graphite battery at elevated temperature. The polymer electrolyte consists of a robust natural cellulose skeletal incorporated with soft segment poly(ethyl α-cyanoacrylate). The introduction of the cellulose effectively overcomes the drawback of poor mechanical integrity of the gel polymer electrolyte. Density functional theory (DFT) calculation demonstrates that the poly(ethyl α-cyanoacrylate) matrices effectively dissociate the lithium salt to facilitate ionic transport and thus has a higher ionic conductivity at room temperature. Ionic conductivity of the gel polymer electrolyte is 3.3 × 10(-3) S cm(-1) at room temperature. The gel polymer electrolyte remarkably improves the cycling performance of LiMn2O4-based batteries, especially at elevated temperatures. The capacity retention after the 100th cycle is 82% at 55 °C, which is much higher than that of liquid electrolyte (1 M LiPF6 in carbonate solvents). The polymer electrolyte can significantly suppress the dissolution of Mn(2+) from surface of LiMn2O4 because of strong interaction energy of Mn(2+) with PECA, which was investigated by DFT calculation.
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Synthesis and Electrochemistry of LiNi x Mn2 − x O 4
Qiming Zhong, Arman Bonakdarpour, Meijie Zhang et al. · Journal of The Electrochemical Society · 1997 · 1.1K citations