Investigating Li Microstructure Formation on Li Anodes
for Lithium Batteries by in Situ <sup>6</sup>Li/<sup>7</sup>Li NMR
and SEM
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Abstract
The growth of lithium microstructures
during battery cycling has,
to date, prohibited the use of Li metal anodes and raises serious
safety concerns even in conventional lithium-ion rechargeable batteries,
particularly if they are charged at high rates. The electrochemical
conditions under which these Li microstructures grow have, therefore,
been investigated by in situ nuclear magnetic resonance (NMR), scanning
electron microscopy (SEM), and susceptibility calculations. Lithium
metal symmetric bag cells containing LiPF<sub>6</sub> in EC/DMC electrolytes
were used. Distinct <sup>7</sup>Li NMR resonances were observed due
to the Li metal bulk electrodes and microstructures, the changes in
peak positions and intensities being monitored in situ during Li deposition.
The changes in the NMR spectra, observed as a function of separator
thickness and porosity (using Celgard and Whatmann glass microfiber
membranes) and different applied pressures, were correlated with changes
in the type of microstructure, by using SEM. Isotopically enriched <sup>6</sup>Li metal electrodes were used against natural abundance predominantly <sup>7</sup>Li metal counter electrodes to investigate radiofrequency
(rf) field penetration into the Li anode and to confirm the assignment
of the higher frequency peak to Li dendrites. The conclusions were
supported by calculations performed to explore the effect of the different
microstructures on peak position/broadening, the study showing that
Li NMR spectroscopy can be used as a sensitive probe of both the amount
and type of microstructure formation