Ak. Padhi et al., PHOSPHO-OLIVINES AS POSITIVE-ELECTRODE MATERIALS FOR RECHARGEABLE LITHIUM BATTERIES, Journal of the Electrochemical Society, 144(4), 1997, pp. 1188-1194
Reversible extraction of lithium from LiFePO4 (triphylite) and inserti
on of lithium into FePO4 at 3.5 V vs. lithium at 0.05 mA/cm(2) shows t
his material to be an excellent candidate for the cathode oi a low-pow
er, rechargeable Lithium battery that is inexpensive, nontoxic, and en
vironmentally benign. Electrochemical extraction was limited to simila
r to 0.6 Li/formula unit; but even with this restriction the specific
capacity is 100 to 110 mAh/g. Complete extraction of lithium was perfo
rmed chemically; it gave a new phase, FePO4, isostructural with hetero
site, Fe0.65Mn0.35PO4. The FePO4 framework of the ordered olivine LiFe
PO4 is retained with minor displacive adjustments. Nevertheless the in
sertion/extraction reaction eless proceeds via a two-phase process, an
d a reversible loss in capacity with increasing current density appear
s to be associated with a diffusion-limited transfer of lithium across
the two-phase interface. Electrochemical extraction of lithium from i
sostructural LiMPO4 (M = Mn, Co, or Ni) with an LiClO4 electrolyte was
not possible; but successful extraction of lithium from LiFe1-xMnxPO4
was accomplished with maximum oxidation of the Mn3+/Mn2+ occurring at
x = 0.5. The Fe3+/Fe2+ couple was oxidized first at 3.5 V followed by
oxidation of the Mn3+/Mn2+ couple at 4.1 V vs. lithium. The Fe3+-O-Mn
2+ interactions appear to destabilize the Mn2+ level and stabilize the
Fe3+ level so as to make the Mn3+/Mn2+ energy accessible.