Abstract
Li plating/stripping on Cu and Y2O3 (Cu + Y2O3) electrodes was examined in a super-concentrated electrolyte of lithium bis(fluorosulfonyl)amide and methylphenylamino-di(trifluoroethyl) phosphate. In principle, Li+ ions cannot intercalate into a Y2O3 crystal because its intercalation potential obtained from first-principles calculations is −1.02 V vs. Li+/Li. However, a drastic decrease in the electrode potential and a subsequent constant-potential region were observed during Li plating onto a Cu + Y2O3 electrode, suggesting that Li+ interacted with Y2O3. X-ray diffraction (XRD) patterns and X-ray absorption fine structure (XAFS) spectra of the Cu + Y2O3 electrodes after the Li plating were recorded to verify this phenomenon. The XRD and XAFS results indicated that the crystallinity of Y2O3 crystals was lowered because of attack by Li+ ions or that the Y2O3 crystal structure was broken while the +3 valence state of Y was maintained.
Highlights
Li+-ion batteries (LIBs) are one of the most important rechargeable power devices and are essential to hybrid and electric vehicles
Li plating/stripping on Cu and Y2O3 (Cu + Y2O3) electrodes was examined in a super-concentrated electrolyte of lithium bis(fluorosulfonyl)amide and methylphenylamino-di(trifluoroethyl) phosphate
The X-ray diffraction (XRD) and X-ray absorption fine structure (XAFS) results indicated that the crystallinity of Y2O3 crystals was lowered because of attack by Li+ ions or that the Y2O3 crystal structure was broken while the +3 valence state of Y was maintained
Summary
Li+-ion batteries (LIBs) are one of the most important rechargeable power devices and are essential to hybrid and electric vehicles. Li plating/stripping has been investigated in this electrolyte using an electrochemical cell with Cu and Li metal electrodes.
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