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Origin of unusual spinel-to-layered phase transformation by crystal water

It is well known that many layered transition metal oxides can transform into a spinel structure upon repeated battery cycling, but a phase transition in the opposite direction is rare. Recently, the transformation from spinel Mn(3)O(4) to layered MnO(2) was observed during the operation of a Mg bat...

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Detalles Bibliográficos
Autores principales: Yang, Eunjeong, Kim, Heejin, Kim, Sangryun, Kim, In, Kim, Jaehoon, Ji, Hyunjun, Choi, Jang Wook, Jung, Yousung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868318/
https://www.ncbi.nlm.nih.gov/pubmed/29629114
http://dx.doi.org/10.1039/c7sc04114d
Descripción
Sumario:It is well known that many layered transition metal oxides can transform into a spinel structure upon repeated battery cycling, but a phase transition in the opposite direction is rare. Recently, the transformation from spinel Mn(3)O(4) to layered MnO(2) was observed during the operation of a Mg battery in aqueous conditions, resulting in high performance Mg batteries. We hereby use ab initio calculations to unveil the mechanism by which crystal water plays a critical role in this unique transformation. Once inserted into the spinel form, a water molecule donates an electron, offering a key structural and thermodynamic driving force to initiate the transformation process. These crystal water molecules then get favorably clustered into a planar form in the layered structure and act as a stabilizing agent for birnessite. Kinetically, the inserted crystal water dramatically promotes the necessary rearrangement of Mn during the transition by lowering the activation barrier by >2 eV. The present structural, thermodynamic and kinetic understanding of the crystal water-driven phase transition provides novel insights to further the design of related low dimensional hydrated materials for multi-valent cathodes.