Enhancing the real-time detection of phase changes in lithium-graphite intercalated compounds through derivative operando (dOp) NMR cyclic voltammetry
Journal of Materials Chemistry A, ISSN: 2050-7496, Vol: 6, Issue: 1, Page: 231-243
2017
- 34Citations
- 46Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Article Description
Robust and reliable diagnostic tools that can be employed under operating conditions are crucial to understanding performance and failure mechanisms in battery processes. The operando spectrum of a battery often consists of a strongly overlapping mixture of time dependent and independent resonances due to the compositional complexity. Here we report a new method called derivative operando (dOp) that improves the resolution of operando nuclear magnetic resonance (NMR) spectra by removing time independent signals and further distinguishes between time dependent signals associated with the formation and removal of species. This approach not only provides better resolution but also more clearly reveals correlations between resonances and the chemical transformations occurring at a specific potential. With the dOp-NMR method we detect the formation of lithium graphite intercalation compounds (GICs), including the signatures of LiC and its precursors, which have been previously undetected. We also observe a clear correlation of the dOp Li NMR spectra of lithium metal dendrites on the counter electrode with the chemistry of the working electrode.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85038610468&origin=inward; http://dx.doi.org/10.1039/c7ta07521a; http://xlink.rsc.org/?DOI=C7TA07521A; http://pubs.rsc.org/en/content/articlepdf/2018/TA/C7TA07521A; https://xlink.rsc.org/?DOI=C7TA07521A; https://dx.doi.org/10.1039/c7ta07521a; https://pubs.rsc.org/en/content/articlelanding/2018/ta/c7ta07521a
Royal Society of Chemistry (RSC)
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