1998
DOI: 10.1016/s0008-6223(98)00119-5
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Electrochemical intercalation of lithium into graphite: influence of the solvent composition and of the nature of the lithium salt

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Cited by 39 publications
(20 citation statements)
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“…In agreement with the well-known mechanism of formation of LiF with the reduction of CF x [8,12,13,41], these particles can be attributed to LiF. By analogy to lithium-graphite intercalation compounds, such as LiC 6 , F À ions, which are formed during the fluorocarbon reduction, diffuse within the interlayer and combine with solvated Li þ on the sheet's edges [42,43]. A recent study on the discharge mechanism of fluorinated carbon nanofibres showed that such particles made of LiF, are formed outside the carbonaceous matrix [8,13].…”
Section: Electrochemical Propertiessupporting
confidence: 78%
“…In agreement with the well-known mechanism of formation of LiF with the reduction of CF x [8,12,13,41], these particles can be attributed to LiF. By analogy to lithium-graphite intercalation compounds, such as LiC 6 , F À ions, which are formed during the fluorocarbon reduction, diffuse within the interlayer and combine with solvated Li þ on the sheet's edges [42,43]. A recent study on the discharge mechanism of fluorinated carbon nanofibres showed that such particles made of LiF, are formed outside the carbonaceous matrix [8,13].…”
Section: Electrochemical Propertiessupporting
confidence: 78%
“…Carbonaceous materials have been widely used as anode materials for Li-ion batteries because of their high-initial columbic efficiency and good cyclic stability [1][2][3][4]. However, new anode materials with higher discharge capacity and better reversibility capacity are still strongly demanded for expanding applications to the large energyconsuming devices such as electric vehicles and other various digital portable equipments of next generation [5,6].…”
Section: Introductionmentioning
confidence: 99%
“…Many NG's have been studied electrochemically to characterize their reversible capacity and first cycle irreversible capacity loss (ICL), or first cycle coulombic inefficiency. The dependence of performance on the particle size [1], surface area [2], surface modification [3,4], and mechanical milling [5,6], in various organic electrolytes has been studied, as well as the dependence on the composition of the electrolyte [7,8]. The ICL is due to primarily to the formation of a passivating solid electrolyte interface (SEI) layer by the decomposition of the electrolyte to form both as SEI layer and gaseous products on the surface of graphite during the initial charge/discharge cycles [9].…”
Section: Introductionmentioning
confidence: 99%