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首页> 外文期刊>Journal of Materials Chemistry: An Interdisciplinary Journal dealing with Synthesis, Structures, Properties and Applications of Materials, Particulary Those Associated with Advanced Technology >Structural, magnetic and lithium insertion properties of spinel-type Li2Mn3MO8 oxides (M = Mg, Co, Ni, Cu)
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Structural, magnetic and lithium insertion properties of spinel-type Li2Mn3MO8 oxides (M = Mg, Co, Ni, Cu)

机译：尖晶石型Li2Mn3MO8氧化物（M = Mg，Co，Ni，Cu）的结构，磁性和锂插入特性

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摘要

Single-phase compounds Li2Mn3MO8 (M = Mg, Co, Ni, Cu) have been synthesized and investigated as replacements of LiMn2O4 for lithium intercalation below 3 V. They all retain the spinel structure, with cation ordering on the octahedral M (16d) site for M = Mg only. Cell parameters vary as Co < Ni < Mg approximate to Cu < Mn and average M-O bond lengths as Co approximate to Ni < Cu < Mg < Mn. Lithium was intercalated both chemically and electrochemically. Electrochemical potential step spectroscopy shows features typical of a two-phase intercalation reaction, in spite of a manganese valence range mostly above the accepted Jahn-Teller distortion limit (50% Mn3+). The tetragonal distortion is only noticeable at high intercalation levels. It yields c/a distortion values much lower for M = Co or Ni than for unsubstituted LiMn2O4. However, no improvement in electrochemical cyclability was obtained. Magnetic susceptibility measurements show features typical of frustrated systems, as expected for the 16d sublattice, and confirm that chemical intercalation reaches lithium contents close to the theoretical limit (one additional Li per AB(2)O(4) formula unit). For cobalt substitution, bond length and Curie constant analysis both lead to a charge distribution Li-2[(Mn4+)(2)Mn3+Co3+]O-8 rather than Li-2[(Mn4+)(3)Co2+]O-8. [References: 33]
机译：合成并研究了单相化合物Li2Mn3MO8（M = Mg，Co，Ni，Cu）作为LiMn2O4在3 V以下锂嵌入的替代物。它们都保留了尖晶石结构，阳离子在八面体M（16d）上有序仅对于M = Mg。电池参数随Co

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