Metastable and nanosize cation-disordered rocksalt-type oxides: revisit of stoichiometric LiMnO2 and NaMnO2Electronic supplementary information (ESI) available. See DOI: 10.1039/c8ta03667e

Stoichiometric LiMnO 2 and NaMnO 2 with a cation-disordered rocksalt-type structure as metastable polymorphs were successfully prepared by mechanical milling. Although cation-disordered rocksalt phases with a stoichiometric composition (Li : Mn molar ratio = 1 : 1) are expected to be electrochemical...

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Bibliographic Details
Main Authors Sato, Takahito, Sato, Kei, Zhao, Wenwen, Kajiya, Yoshio, Yabuuchi, Naoaki
Format Journal Article
LanguageEnglish
Published 17.07.2018
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Summary:Stoichiometric LiMnO 2 and NaMnO 2 with a cation-disordered rocksalt-type structure as metastable polymorphs were successfully prepared by mechanical milling. Although cation-disordered rocksalt phases with a stoichiometric composition (Li : Mn molar ratio = 1 : 1) are expected to be electrochemically less active, both samples show superior performance as electrode materials when compared with thermodynamically stable layered phases in Li/Na cells. Both metastable samples deliver large reversible capacities, which correspond to >80% of their theoretical capacities, with relatively small polarization on the basis of reversible Mn 3+ /Mn 4+ redox. Moreover, for rocksalt LiMnO 2 , the phase transition into a spinel phase is effectively suppressed compared with a thermodynamically stable phase. The electrode reversibility of NaMnO 2 is also drastically improved by the use of the metastable phase with good capacity retention. Metastable phases with unique nanostructures open a new path for the design of advanced electrode materials with high energy density, and thus a broad impact is anticipated for rechargeable Li/Na battery applications. Stoichiometric LiMnO 2 and NaMnO 2 with a cation-disordered rocksalt-type structure as metastable polymorphs were successfully prepared by mechanical milling.
Bibliography:10.1039/c8ta03667e
Electronic supplementary information (ESI) available. See DOI
ISSN:2050-7488
2050-7496
DOI:10.1039/c8ta03667e