4.6 Article

Comparison of the Electrochemical Lithiation/Delitiation Mechanisms of FePx (x=1, 2, 4) Based Electrodes in Li-Ion Batteries

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 113, Issue 51, Pages 21441-21452

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp906080j

Keywords

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Funding

  1. European Union [SES6 - CT-2003-503532]
  2. ADEME (Agence de l'Environnement et de la Maitrise de l'Energie, France)

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The electrochemical reaction mechanisms of FePx (x = 1, 2, 4) as electrode materials in Li batteries were analyzed by Fe-57 Mossbauer spectroscopy, magnetic and NMR measurements. Depending on their stoichiometry, iron phosphides react with lithium along different pathways. FeP and FeP2 are fully or partially converted to a composite electrode of Li3P and Fe. For both, the same intermediate phases, namely FeP and LixFeP, were identified in cycling and FeP is partially regenerated on charge. Surprisingly, FeP4 reacts with Li through an insertion type process previously identified for earlier transition metal phosphides (Ti, V, and Mn), and no conversion reaction to Li3P/Fe is observed. The long-term stability of the composite electrode Li3P/Fe-0 and of the intermediate phase LixFeP is analyzed.

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