Journal of Materials Chemistry · 2011 · 100 citations · 26 references
Natural SciencesChemistryMaterials ScienceElectrochemistryInterface ScienceMaterials ChemistryBattery MaterialsElectrochemical Energy StorageElectrode MaterialsElectrode-electrolyte InterfacesSolid ElectrolytesSolid-state ElectrolytesCharge Transfer ResistanceElectrode - Electrolyte InterphasesExtended X-ray Absorption Fine StructureLithium-ion BatteriesLocal Electronic StructureLocal StructurePower DensitySolid-state Lithium Batteries
Depth-resolved X-ray absorption spectroscopy (DR-XAS) measurements were performed for the direct observation of the chemical state and local structure at the LiCoO2 electrode–solid electrolyte model interface, which can contribute towards the enhancement of the power density in all solid-state lithium batteries. The charge transfer resistance, measured by AC impedance spectroscopy, of the LiCoO2 electrode–solid electrolyte interface decreased with the introduction of a NbO2 interlayer at the interface, while the resistance increased with ZrO2 and MoO2 interlayers. Using DR-XAS with a depth resolution of about 7 nm, the changes in electronic structure and local structure of the LiCoO2 electrode were clarified. The extended X-ray absorption fine structure of DR-XAS revealed that the introduction of the NbO2 layer is effective for restricting the large Co–O bond change at the interface during delithiation. This interlayer relieved the stress at the interface due to the volume change of LiCoO2 during delithiation and then decreased the activation energy for the charge transfer process.
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Theoretical approaches to x-ray absorption fine structure
J. J. Rehr, R. C. Albers · Reviews of Modern Physics · 2000 · 3.2K citations