Publication | Open Access
Band Diagram and Rate Analysis of Thin Film Spinel LiMn<sub>2</sub>O<sub>4</sub> Formed by Electrochemical Conversion of ALD‐Grown MnO
45
Citations
46
References
2016
Year
Limn 2EngineeringThin Film Process TechnologyChemistryElectrochemical ConversionElectronic StatesSodium BatteryThin Film ProcessingMaterials ScienceBattery Electrode MaterialsOxide ElectronicsRate AnalysisAdvanced Electrode MaterialEnergy StorageBand DiagramO 4Solid-state BatteryElectrochemical ProcessElectrochemistryMaterial AnalysisLi-ion Battery MaterialsApplied PhysicsCathode MaterialsElectrochemical Energy StorageBatteriesThin FilmsFunctional Materials
Nanoscale spinel lithium manganese oxide is of interest as a high‐rate cathode material for advanced battery technologies among other electrochemical applications. In this work, the synthesis of ultrathin films of spinel lithium manganese oxide (LiMn 2 O 4 ) between 20 and 200 nm in thickness by room‐temperature electrochemical conversion of MnO grown by atomic layer deposition (ALD) is demonstrated. The charge storage properties of LiMn 2 O 4 thin films in electrolytes containing Li + , Na + , K + , and Mg 2+ are investigated. A unified electrochemical band‐diagram (UEB) analysis of LiMn 2 O 4 informed by screened hybrid density functional theory calculations is also employed to expand on existing understanding of the underpinnings of charge storage and stability in LiMn 2 O 4 . It is shown that the incorporation of Li + or other cations into the host manganese dioxide spinel structure (λ‐MnO 2 ) stabilizes electronic states from the conduction band which align with the known redox potentials of LiMn 2 O 4 . Furthermore, the cyclic voltammetry experiments demonstrate that up to 30% of the capacity of LiMn 2 O 4 arises from bulk electronic charge‐switching which does not require compensating cation mass transport. The hybrid ALD‐electrochemical synthesis, UEB analysis, and unique charge storage mechanism described here provide a fundamental framework to guide the development of future nanoscale electrode materials for ion‐incorporation charge storage.
| Year | Citations | |
|---|---|---|
Page 1
Page 1