Electrochemical properties of Li-excess
electrode materials, Li1.2Co0.13Ni0.13Mn0.54O2, with different primary particle sizes
are studied in Li
cells, and phase transition behavior on continuous electrochemical
cycles is systematically examined. Although the nanosize (<100
nm) sample delivers a large reversible capacity of 300 mAh g–1 at the initial cycle, capacity retention is not sufficient as a
positive electrode material. Moreover, unfavorable phase transition,
gradual enrichment of trivalent manganese ions, and lowering structural
symmetry is not avoidable on electrochemical cycles for a nanosize
sample, which is confirmed by combined techniques of synchrotron X-ray
diffraction, X-ray absorption spectroscopy, and X-ray photoelectron
spectroscopy. A submicrosize sample also delivers a large reversible
capacity of 250 mAh g–1 even though a slow activation
process is observed accompanied with partial oxygen loss and migration
oxide ions in the crystal lattice coupled with transition metal migration
on the initial charge process. Such an unfavorable phase transition
at room temperature is effectively suppressed by the use of a submicrosize
sample with low surface area. However, suppression of the phase transition
is found to be a kinetically controlled phenomena and is, therefore,
unavoidable at elevated temperatures.