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Coulombic self-ordering upon charging a large-capacity layered cathode material for rechargeable batteries

Lithium- and sodium-rich layered transition-metal oxides have recently been attracting significant interest because of their large capacity achieved by additional oxygen-redox reactions. However, layered transition-metal oxides exhibit structural degradation such as cation migration, layer exfoliati...

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Detalles Bibliográficos
Autores principales: Mortemard de Boisse, Benoit, Reynaud, Marine, Ma, Jiangtao, Kikkawa, Jun, Nishimura, Shin-ichi, Casas-Cabanas, Montse, Delmas, Claude, Okubo, Masashi, Yamada, Atsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522540/
https://www.ncbi.nlm.nih.gov/pubmed/31097700
http://dx.doi.org/10.1038/s41467-019-09409-1
Descripción
Sumario:Lithium- and sodium-rich layered transition-metal oxides have recently been attracting significant interest because of their large capacity achieved by additional oxygen-redox reactions. However, layered transition-metal oxides exhibit structural degradation such as cation migration, layer exfoliation or cracks upon deep charge, which is a major obstacle to achieve higher energy-density batteries. Here we demonstrate a self-repairing phenomenon of stacking faults upon desodiation from an oxygen-redox layered oxide Na(2)RuO(3), realizing much better reversibility of the electrode reaction. The phase transformations upon charging A(2)MO(3) (A: alkali metal) can be dominated by three-dimensional Coulombic attractive interactions driven by the existence of ordered alkali-metal vacancies, leading to counterintuitive self-repairing of stacking faults and progressive ordering upon charging. The cooperatively ordered vacancy in lithium-/sodium-rich layered transition-metal oxides is shown to play an essential role, not only in generating the electro-active nonbonding 2p orbital of neighbouring oxygen but also in stabilizing the phase transformation for highly reversible oxygen-redox reactions.