2011
DOI: 10.1021/ie201799x
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Characterization of LiFePO4/C Cathode for Lithium Ion Batteries

Abstract: LiFePO 4 /C was synthesized from a mixture of different precursors of Li, Fe, and C by solid-state reaction. The initial mixture obtained was heated in different calcination conditions under inert atmosphere. The precursor of LiFePO 4 doped with carbon was studied using different techniques such as thermal analysis, chemical and physical characterizations, and M€ osbauer spectroscopy. A calculation of the crystallinity of the final product with two different methods is also presented. The chemical analysis tec… Show more

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Cited by 14 publications
(6 citation statements)
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“…The Fe/P ratio is equal to 1 and O/Fe, O/P equal to 4. The precursor formation of LiFePO 4 is in good agreement with the report of Lyczko et al [37].…”
Section: Resultssupporting
confidence: 92%
“…The Fe/P ratio is equal to 1 and O/Fe, O/P equal to 4. The precursor formation of LiFePO 4 is in good agreement with the report of Lyczko et al [37].…”
Section: Resultssupporting
confidence: 92%
“…The Energy dispersive X-ray spectra of both samples (Fig. 3 (c, d) demonstrate the Fe/P ratio is equal to 1; Also, O/Fe and O/P equal to 4 that are calculated by observed atomic weight percentage of the prepared material, which is in good agreement with the report of Lyczko et al [46]. It is clearly seen from the spectra that the carbon content is increased upon encrusting the multi-walled carbon nanotube on LiFePO 4 /C sample.…”
Section: Morphological and Elemental Analysessupporting
confidence: 90%
“…The interdependent nature of the various degradation mechanisms in Li‐ion batteries makes the study of the degradation mechanisms challenging and often requires the employment of novel in‐situ and ex‐situ characterization techniques to elucidate the degradation mechanisms at the nanoscale. The most important characterization techniques for understanding the degradation mechanism in Li‐ion batteries are in‐situ and ex‐situ transmission electron microscopy (TEM) , in‐situ atomic force microscopy (AFM) , ex‐situ X‐ray diffraction (XRD), Raman spectroscopy, X‐ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM) . The better understanding of the degradation mechanism would lead to prolonged cycle life, development of improved materials as well as help in identifying the optimal control strategies to limit degradation.…”
Section: Introductionmentioning
confidence: 99%