Microfocused X-ray Study on Precipitate Formation in the Separator Region of Nonaqueous Li-O2 Batteries

Using a microfocused synchrotron X‐ray diffraction (μ‐XRD) method, we systematically investigated the distributions of insoluble lithium precipitates, which formed through electrolyte decomposition, separately in all three regions (cathode, separator, and anode) of failed batteries with a spatial re...

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Bibliographic Details
Published inChemSusChem Vol. 5; no. 12; pp. 2421 - 2426
Main Authors Shui, Jiang-Lan, Okasinski, John S., Zhao, Dan, Almer, Jonathan D., Liu, Di-Jia
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.12.2012
WILEY‐VCH Verlag
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Summary:Using a microfocused synchrotron X‐ray diffraction (μ‐XRD) method, we systematically investigated the distributions of insoluble lithium precipitates, which formed through electrolyte decomposition, separately in all three regions (cathode, separator, and anode) of failed batteries with a spatial resolution of 20 μm. We found unexpectedly that there was a significantly higher concentration (almost twice as much) of precipitates in the separator than in the cathode. SEM revealed that the precipitates grew on the separator fiber surface, ultimately obstructing the pores serving as the ion‐transport channel. A “refurbished” battery, which was composed of a spent separator from a failed battery, showed a much higher overpotential and shorter cycle life than that found in a new battery. Rejuvenation: Unexpectedly high concentrations of precipitates (mainly Li2CO3) with unique spatial and morphological distributions are detected in the separator region of Li–O2 batteries by microfocused XRD and SEM techniques, revealing the need for a stable electrolyte to minimize the deleterious effect of insoluble lithium salt (see picture).
Bibliography:US Department of Energy - No. DE-AC02-06CH11357
ArticleID:CSSC201200555
Grand Challenge program of Argonne National Laboratory
ark:/67375/WNG-PXM4CH15-N
istex:68C25EA08D6C5F6AF27EBA4169C3C440634DC87F
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.201200555