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Spinel–rock salt transformation in LiCoMnO(4−δ)

The transformation on heating LiCoMnO(4), with a spinel structure, to LiCoMnO(3), with a cation-disordered rock salt structure, accompanied by loss of 25% of the oxygen, has been followed using a combination of diffraction, microscopy and spectroscopy techniques. The transformation does not proceed...

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Detalles Bibliográficos
Autores principales: Reeves-McLaren, Nik, Sharp, Joanne, Beltrán-Mir, Héctor, Rainforth, W. Mark, West, Anthony R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786028/
https://www.ncbi.nlm.nih.gov/pubmed/26997883
http://dx.doi.org/10.1098/rspa.2014.0991
Descripción
Sumario:The transformation on heating LiCoMnO(4), with a spinel structure, to LiCoMnO(3), with a cation-disordered rock salt structure, accompanied by loss of 25% of the oxygen, has been followed using a combination of diffraction, microscopy and spectroscopy techniques. The transformation does not proceed by a topotactic mechanism, even though the spinel and rock salt phases have a similar, cubic close-packed oxygen sublattice. Instead, the transformation passes through two stages involving, first, precipitation of Li(2)MnO(3), leaving behind a Li-deficient, Co-rich non-stoichiometric spinel and, second, rehomogenization of the two-phase assemblage, accompanied by additional oxygen loss, to give the homogeneous rock salt final product; a combination of electron energy loss spectroscopy and X-ray absorption near edge structure analyses showed oxidation states of Co(2+) and Mn(3+) in LiCoMnO(3). Subsolidus phase diagram determination of the Li(2)O-CoO(x)-MnO(y) system has established the compositional extent of spinel solid solutions at approximately 500°C.