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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2016
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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 |
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. |
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