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Synthesis and characterization of reduced ternary alkali metal molybdenum oxides

机译:还原性三元碱金属钼氧化物的合成与表征

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摘要

A series of novel layered reduced Na and Li Mo-oxides is reported. The two dimensional framework is quite unique among the structure types previously observed for reduced molybdenum oxides;Synthetic exploration of oxides related to Na[subscript]2Mo[subscript]3O[subscript]6 (Hubert, P. H. C. R. Acad. Sc. Paris 1966, 262, 1189) led to the isolation of a series of monoclinic layered Na-Mo-oxides, Na[subscript]0.41MoO[subscript]2, Na[subscript]0.51MoO[subscript]2, and Na[subscript]0.66MoO[subscript]2. The basic framework of these compounds consists of oxide layers alternating with sheets of Na and Mo atoms. Within the Mo layers, the metal atoms shift from ideal octahedral sites toward neighboring Mo atoms to form extended chains of fused rhomboidal clusters;Structurally, from Na[subscript]0.41MoO[subscript]2 to Na[subscript]0.66MoO[subscript]2, the Na ions shift from octahedral to trigonal prismatic sites; and oxygen packing changes from nonsequential to ABBCCA;The stacking of layers toward cubic close packing, ABCABC, was realized in the analogous Li-Mo-oxide system. A material with ccp oxygen layers, LiMoO[subscript]2, was isolated as the product from the high temperature reaction between Li[subscript]2MoO[subscript]4 and Mo metal. Neutron powder diffraction Rietveld analysis shows that LiMoO[subscript]2 is isomorphous with [alpha]-NaFeO[subscript]2 and reveals for Mo-Mo bonded compounds an unprecedented arrangement, an infinite hexagonal sheet. DOS and COOP curves from extended Huckel band calculations indicate that all Mo-Mo bonding states are filled within the O-Mo-O layers;The results of the extended Huckel calculations suggest that as the Mo bonding states are emptied, via oxidation by delithiation, the Mo sheet should rearrange to form Mo ribbons or some other type of clustering favored by the lower electron to Mo ratio. Indeed, such a structural transition of the hexagonal structure, in partially delithiated Li[subscript] 1-xMoO[subscript]2, to a monoclinic framework with infinite Mo bonded zig-zag chains has been observed;Synthetic efforts in the heavier alkali metal ternary system, K-Mo-oxide, have led to a novel compound containing Mo octahedral clusters. Partial characterization through single crystal diffraction data suggests the structure contains discrete segments of chains comprised of edged shared Mo[subscript]6 units. ftn*DOE Report IS-T-1330. This work was performed under contract No. W-7405-Eng-82 with the U.S. Department of Energy.
机译:报道了一系列新颖的层状还原Na和Li Mo-氧化物。在先前观察到的还原钼氧化物的结构类型中,二维框架是非常独特的;与Na [下标] 2Mo [下标] 3O [下标] 6相关的氧化物的合成勘探(Hubert,PHCR Acad。Sc。Paris 1966,262, 1189)导致一系列单斜层Na-Mo-氧化物,Na [下标] 0.41MoO [下标] 2,Na [下标] 0.51MoO [下标] 2和Na [下标] 0.66MoO [下标]的分离2。这些化合物的基本骨架由交替排列的Na和Mo原子的氧化物层组成。在Mo层中,金属原子从理想的八面体位置移向相邻的Mo原子,以形成融合的菱形簇的延伸链;结构上,从Na [下标] 0.41MoO [下标] 2到Na [下标] 0.66MoO [下标] 2 ,Na离子从八面体移动到三棱柱形位置;在类似的Li-Mo-氧化物体系中实现了层向立方密堆积ABCABC的堆叠。从Li [2] MoO [4]和Mo金属之间的高温反应中分离出具有ccp氧层的材料LiMoO [2]作为产物。中子粉末衍射Rietveld分析表明,LiMoO 2与α-NaFeO2是同构的,并且对于Mo-Mo键合的化合物显示出前所未有的排列,无限的六边形片。扩展的Huckel带计算得出的DOS和COOP曲线表明,所有Mo-Mo键合状态都填充在O-Mo-O层内;扩展的Huckel计算结果表明,随着Mo键合状态被清空,通过脱锂氧化, Mo片应重新排列以形成Mo带或其他类型的簇,这些簇受较低的电子与Mo比率所青睐。确实,已经观察到部分脱锂的Li [下标] 1-xMoO [下标] 2中的六边形结构向具有无限Mo键合之字形链的单斜构架的这种结构转变;在较重的碱金属三元中的合成作用K-Mo-氧化物是一种新的化合物,它含有Mo八面体簇。通过单晶衍射数据的部分表征表明该结构包含由有边的共享的Mo 6单元组成的离散链段。 ftn * DOE报告IS-T-1330。这项工作是根据与美国能源部签订的W-7405-Eng-82合同进行的。

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    Aleandri, Lorraine Esther;

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  • 年度 1987
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  • 原文格式 PDF
  • 正文语种 en
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