Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9760325 | Journal of Power Sources | 2005 | 6 Pages |
Abstract
It has been demonstrated previously that Li may be removed electrochemically from Mn containing oxides beyond the maximum oxidation state of 4+ for Mn in an octahedral oxygen environment. Here we present a comparison of such overcharge behavior in a series of different layered lithium manganese oxides including Li2MnO3, Lix[Mn1 â yLiy]O2, (y â¤Â 0.2), and Li[NixLi1/3 â 2x/3Mn2/3 â x/3]O2 (0 â¤Â x â¤Â 0.5). We show that there are two competing mechanisms by which electrochemical extraction of lithium can occur in Mn (4+) systems. In the first Li removal is accompanied by O2â loss (effective removal of Li2O) whilst the second involves oxidation of the non-aqueous electrolyte thus generating H+ ions which exchange for Li+. At 30 °C the first mechanism is dominant in all examples studied, whilst at 55 °C the proton exchange mechanism becomes more important. At 30 °C H+ exchange is more prevalent in Li2MnO3 than in the other two cases. The preference for O loss in the Mn/Ni system may be understood in terms of the ease with which MnO2 will lose oxygen.
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Physical Sciences and Engineering
Chemistry
Electrochemistry
Authors
A.R. Armstrong, A.D. Robertson, P.G. Bruce,