Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7856398 | Carbon | 2013 | 14 Pages |
Abstract
Graphite is used in the lithium-ion batteries as a negative electrode. We use continuous, in situ, operando 7Li nuclear magnetic resonance (NMR) to show, in real time, the progressive intercalation and de-intercalation of lithium in graphite when a battery is charged and discharged. We obtain all the Li-graphite intercalation compound stages through an electrochemical path. We explain the overvoltages by transient entropic and Peltier effects. The sample is a plastic cell, NMR compatible, made of commercial graphite, commercial electrolyte and lithium metal foil. We analyze the NMR characteristics of the Li-GIC stages: line shift, quadrupolar frequencies, line width (Li diffusion), line intensity and area as a function of x = Li/C6. This allows us to estimate the lithium quantities in each stage at each step. Two facts differ from the theoretical stage n formation: for the C/20 cycling rate, we find an hysteresis in the filling/emptying of the dilute (LiC9n) stages, and we find another NMR line synchronous with LiC6. The lithium metal line also provides quantitative information on the lithium deposited as dendrites when x diminishes, in de-intercalation. This paper presents experimental NMR data over two cycles, and is an extension of the first cycle analysis published earlier.
Related Topics
Physical Sciences and Engineering
Energy
Energy (General)
Authors
Frédéric Chevallier, Fabrizia Poli, Bénédicte Montigny, Michel Letellier,