Publication | Open Access
Direct Experimental Probe of the Ni(II)/Ni(III)/Ni(IV) Redox Evolution in LiNi<sub>0.5</sub>Mn<sub>1.5</sub>O<sub>4</sub> Electrodes
166
Citations
35
References
2015
Year
EngineeringChemistryLini0.5mn1.5o4 SpinelRedox ChemistryElectrochemical InterfaceRedox EvolutionElectrode Reaction MechanismMaterials ScienceInorganic ChemistryElectrode SurfaceBattery Electrode MaterialsSurface ElectrochemistryAdvanced Electrode MaterialLithium-ion BatteryEnergy StorageDirect Experimental ProbeElectrochemistryLi-ion Battery MaterialsNi-based Battery ElectrodesCathode MaterialsElectrochemical Energy StorageBatteriesElectrochemical Surface Science
The LiNi0.5Mn1.5O4 spinel is an appealing cathode material for next generation rechargeable Li-ion batteries due to its high operating voltage of ∼4.7 V (vs Li/Li+). Although it is widely believed that the full range of electrochemical cycling involves the redox of Ni(II)/(IV), it has not been experimentally clarified whether Ni(III) exists as the intermediate state or a double-electron transfer takes place. Here, combined with theoretical calculations, we show unambiguous spectroscopic evidence of the Ni(III) state when the LiNi0.5Mn1.5O4 electrode is half charged. This provides a direct verification of single-electron-transfer reactions in LiNi0.5Mn1.5O4 upon cycling, namely, from Ni(II) to Ni(III), then to Ni(IV). Additionally, by virtue of its surface sensitivity, soft X-ray absorption spectroscopy also reveals the electrochemically inactive Ni2+ and Mn2+ phases on the electrode surface. Our work provides the long-awaited clarification of the single-electron transfer mechanism in LiNi0.5Mn1.5O4 electrodes. Furthermore, the experimental results serve as a benchmark for further spectroscopic characterizations of Ni-based battery electrodes.
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