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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Main Authors | , , , , |
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Format | Journal Article |
Language | English |
Published |
17.07.2018
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Online Access | Get full text |
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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 |