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首页> 外文期刊>The journal of physics and chemistry of solids >Spinel-type solid solutions involving Mn~(4+) and Ti ~(4+):Crystal chemistry, magnetic and electrochemical properties
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Spinel-type solid solutions involving Mn~(4+) and Ti ~(4+):Crystal chemistry, magnetic and electrochemical properties

机译:Mn〜(4+)和Ti〜(4+)的尖晶石型固溶体:晶体化学,磁性和电化学性质

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摘要

This study reports the structural and magnetic properties of spinel systems Li_4Mn_(5-x)Ti_xO_(12) ("4-5-12" series) and LiNi_(0.5)Mn_(1.5-x)Ti_xO_4 ("LNMTO" series), both based on Mn~4 substitution by Ti ~4. Intermediate compositions covering the whole range of compositions (0≤x≤5 and 0≤x≤1.5, respectively) were prepared by solid state reaction. The 4-5-12 system forms a continuous spinel solid solution, whereas the spinel phase range in LNMTO stops before the end member "LiNi _(0.5)Ti_(1.5)O_4", which is multi-phased with a major hexagonal phase component. Cell parameters and (Mn,Ti)O distances increase monotonically with titanium content in both series. In the LNMTO series, the end member LiNi_(0.5)Mn_(1.5)O_4 is known to form a superstructure with Ni/Mn cation ordering. Neutron diffraction and Raman spectroscopy show that this order is lost when Ti is substituted, even at low level (x=0.15). The LNMTO crystal chemistry is also complicated by the presence of partial cation inversion, and the presence of a secondary rocksalt-type phase that modifies the spinel stoichiometry. Magnetic properties are characterized by a competition between ferromagnetic and antiferromagnetic interactions; no magnetic ordering is achieved, in agreement with B-site cation frustration and disorder. Electrochemical measurements show that the Ti~(3/4) and Mn~(3/4) redox couples behave independently in the 4-5-12 series, and that titanium decreases the high-potential electrochemical redox activity of LNMTO because of its blocking character for electron transfer to and from the nickel sites in the spinel structure.
机译:这项研究报告了尖晶石系统Li_4Mn_(5-x)Ti_xO_(12)(“ 4-5-12”系列)和LiNi_(0.5)Mn_(1.5-x)Ti_xO_4(“ LNMTO”系列)的结构和磁性。两者均基于Mn〜4被Ti〜4取代。通过固态反应制备覆盖整个组成范围(分别为0≤x≤5和0≤x≤1.5)的中间组合物。 4-5-12系统形成连续的尖晶石固溶体,而LNMTO中的尖晶石相范围在端部件“ LiNi _(0.5)Ti_(1.5)O_4”之前停止,该端部件与主要的六方相组成多相。在两个系列中,电池参数和(Mn,Ti)O距离均随钛含量单调增加。在LNMTO系列中,已知末端成员LiNi_(0.5)Mn_(1.5)O_4形成具有Ni / Mn阳离子有序的上层结构。中子衍射和拉曼光谱表明,即使在低水平(x = 0.15)取代Ti时,也失去了该顺序。由于存在部分阳离子转化和改变尖晶石化学计量的次生岩盐型相,LNMTO晶体化学也变得复杂。磁性质的特征是铁磁性和反铁磁性之间的竞争。与B位阳离子的受挫和无序一致,没有实现磁性排序。电化学测量表明,Ti〜(3/4)和Mn〜(3/4)氧化还原对在4-5-12系列中表现出独立的行为,并且钛由于其阻断而降低了LNMTO的高电势电化学氧化还原活性电子在尖晶石结构中的镍位置上来回转移的特征。

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