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Inhibition of Jahn–Teller cooperative distortion in LiMn2O4 spinel by transition metal ion doping
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Citations
19
References
2001
Year
Magnetic PropertiesEngineeringMagnetic ResonanceLimn2o4 SpinelSolid-state ChemistryChemistryMinimum AmountMagnetic MaterialsMagnetoresistanceMagnetismDopant IonMaterials ScienceInorganic ChemistryPhysicsMagnetic MaterialTransition Metal ChalcogenidesRoom TemperatureFerromagnetismNatural SciencesApplied PhysicsCondensed Matter PhysicsBatteriesJahn–teller Cooperative DistortionFunctional Materials
The aim of this study is to determine the minimum amount of dopant that prevents the occurrence, near room temperature, of a Jahn–Teller (J–T) transition in the M-doped lithium manganese spinel of composition Li1.02MxMn1.98−xO4 with 0.00<x⩽0.06 and M = Ni2+, Co3+, Cr3+ or Ti4+. EPR spectra and magnetic susceptibility data are related to the valence state of M and Mn, and the homogeneous distribution of the dopant. We find that the spinel framework is remarkably sensitive to displaying low electronic and magnetic changes in its cationic sublattice due to cation substitution. The J–T distortion, which is associated with a sudden drop in conductivity with decreasing temperature, is suppressed by substituting 3% of Mn with Co3+ or Cr3+, or by adding an even smaller amount of Ni2+ (x = 0.02, or 1% substitution). However, this inhibition occurs only in samples with a ratio r = [Mn4+]/[Mn3+]1.18, i.e., a value larger than the ratio r = 1.106 we have with no doping (x = 0). As a consequence, doping with the tetravalent cation Ti4+, which always decreases the r value, does not suppress the J–T transition. We suggest that both the dopant ion and the Li+ in excess over the stoichiometric composition are located in 16d sites. The removal of the J–T transition in the Co3+ (x = 0.06) sample is also due to local disorder.
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