2003
DOI: 10.1016/s1293-2558(03)00134-1
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Cation ordering in Li2Mn3MO8 spinels: structural and vibration spectroscopy studies

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Cited by 79 publications
(56 citation statements)
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“…A small amount of Sn 4+ doping could stabilize the structure of the material, whereas the existence of too many Sn 4+ cations in the crystal lattice may induce large changes to the structure and cause irreversible phase transfer [17,41]. The capacity increases slightly at the outset, which is attributed to the expansion of the electrode materials and the electrolyte wetting the electrode material during the charge-discharge progress [35]. .…”
Section: Resultsmentioning
confidence: 99%
“…A small amount of Sn 4+ doping could stabilize the structure of the material, whereas the existence of too many Sn 4+ cations in the crystal lattice may induce large changes to the structure and cause irreversible phase transfer [17,41]. The capacity increases slightly at the outset, which is attributed to the expansion of the electrode materials and the electrolyte wetting the electrode material during the charge-discharge progress [35]. .…”
Section: Resultsmentioning
confidence: 99%
“…Despite the replacement of a fraction of Mn ions by bigger Ni 2+ ions, the Mn valence change effect prevails [5]. Recently, Strobel et al [6] suggested that the occurrence of cation ordering corresponds to the largest valence difference ΔZ (Mn−M)≥2. The net result is thus a significant optimization of space occupation, leading to a reduced unit cell volume.…”
Section: Resultsmentioning
confidence: 99%
“…1. Recently, the formation of the ordered spinel has been confirmed by combining X-ray diffraction (XRD) and Fourier transform infrared (FTIR) measurements [6,15].…”
Section: Introductionmentioning
confidence: 99%
“…Even in the x = 1 case (50 % Mn dilution), the frustration remains, probably because the substitution is random. In Li(Mn 1.5 M 0.5 )O 4 compositions with other magnetic as well as non-magnetic M substituents, the Weiss constants are less negative than in unsubstituted LiMn 2 O 4 , and cation ordering, which has been shown to occur for M = Mg, Ni or Cu [12], does not suppress the frustration either [13]. The M = Ni case shows particularly strong magnetic interactions starting at 120 K resembling the ferrimagnetic behaviour previously observed in NiMn 2 O 4 [14].…”
Section: Magnetism In Manganese Compounds With Intermediate Anglesmentioning
confidence: 98%