Please use this identifier to cite or link to this item:
|Title:||Spectral, magnetic and electrochemical studies of layered manganese oxides with P2 and O2 structure|
|Authors:||Shaju, K.M. |
Subba Rao, G.V.
|Source:||Shaju, K.M., Ramanujachary, K.V., Lofland, S.E., Subba Rao, G.V., Chowdari, B.V.R. (2003-10). Spectral, magnetic and electrochemical studies of layered manganese oxides with P2 and O2 structure. Journal of Materials Chemistry 13 (10) : 2633-2640. ScholarBank@NUS Repository. https://doi.org/10.1039/b301043k|
|Abstract:||X-Ray photoelectron spectroscopy (XPS), infrared spectroscopy and magnetic susceptibility studies were performed on layered O2-phase compounds, Li 2/3(Ni1/3Mn2/3)O2, Li (2/3)+x(Ni1/3Mn2/3)O2, Li 2/3(Co0.15Mn0.85)O2 and Li (2/3)+x(Co0.15Mn0.85)O2 and their respective P2 phases, Na2/3(Ni1/3Mn2/3)O 2 and Na2/3(Co0.15Mn0.85)O 2. The observed electrochemical performance was correlated with the oxidation states of the M ions (M = Mn, Ni, Co). Li(2/3)+x(Ni 1/3Mn2/3)O2 and Li(2/3)+x(Co 0.15Mn0.85)O2 show significant improvement in their first-charge capacity over Li2/3(Ni1/3Mn 2/3)O2 and Li2/3(Co0.15Mn 0.85)O2 when used as cathodes vs. Li. Chemical analysis and XPS data indicate that the incorporation of x ∼ 1/3 in the above two compounds is accompanied by the reduction of a corresponding amount of Mn 4+ to Mn3+ ions in the lattice. The magnetic moments obtained in the paramagnetic region are in fair agreement with the oxidation state of the ions derived from the XPS data for the Ni-system but show deviations for the Co-system. Below 100 K, weak ferrimagnetic ordering is observed in Li(2/3)+x(Ni1/3Mn2/3)O2 and Li(2/3)+x(Co0.15Mn0.85)O2.|
|Source Title:||Journal of Materials Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 15, 2018
WEB OF SCIENCETM
checked on Feb 7, 2018
checked on Feb 20, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.