EVIDENCE FOR MULTIPLE M SITES IN AMO(2) COMPOUNDS - CO-59 SOLID-STATENMR-STUDIES ON LICOO2

Citation
P. Ganguly et al., EVIDENCE FOR MULTIPLE M SITES IN AMO(2) COMPOUNDS - CO-59 SOLID-STATENMR-STUDIES ON LICOO2, JOURNAL OF PHYSICAL CHEMISTRY B, 101(51), 1997, pp. 11099-11105
Citations number
35
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
101
Issue
51
Year of publication
1997
Pages
11099 - 11105
Database
ISI
SICI code
1089-5647(1997)101:51<11099:EFMMSI>2.0.ZU;2-8
Abstract
The layered AMO(2) compounds (A = alkali metal, M = trivalent octahedr al site cations) derived from the simple rock-salt structure have alwa ys been considered to have only one crystallographic site for the A an d the M atoms. These structures are described in terms of close-packed oxygen layers with interstitial A and M atoms, especially when A = Li . This gives a layer sequence (AO)(-) and (MO)(+). The AMO(2) compound s are part of the compounds in the A-M-O systems such as A(2)MO(3) and A(5)MO(6), which are derived from the rock-salt structure with altern ating layers of pure (AO)(-) and mixed [(A,M)O](+) layers with multipl e interstitial octahedral sites in the (A,M)O layer for occupation by the different A and M cations. Evidence is presented from Co-59 NMR ex periments on LiCoO2 for the existence of at least two sites in the (Co O)(+) layer. Several NMR methodologies, such as the use of various pul se sequence, nutation experiments, and magic angle sample spinning (MA SS) are employed. Magic-angle-sample-spinning experiments show only on e isotropic peak. However, an analysis of spinning sidebands envelope at various spinning speeds clearly shows the presence of at least two sites. One of these has orthorhombic symmetry and another has axial sy mmetry, with closely related chemical shift anisotropy components that result in the observation of nearly identical isotropic chemical shif ts. The possible importance of the absence or presence of holes on oxy gen has been discussed in accounting for the two sites.