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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >High-Pressure Phase Relations and Crystal Structures of Postspinel Phases in MgV2O4, FeV2O4, and MnCr2O4: Crystal Chemistry of AB(2)O(4) Postspinel Compounds
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High-Pressure Phase Relations and Crystal Structures of Postspinel Phases in MgV2O4, FeV2O4, and MnCr2O4: Crystal Chemistry of AB(2)O(4) Postspinel Compounds

机译:MgV2O4,FEV2O4和MNCR2O4中晶柱阶段的高压相位关系和晶体结构:AB(2)O(4)晶体化合物的晶体化学

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We have investigated high-pressure, high-temperature phase transitions of spinel (Sp)-type MgV2O4, FeV2O4, and MnCr(2)O(4)w. At 1200-1800 degrees C, MgV2O4 Sp decomposes at 4-7 GPa into a phase assemblage of MgO periclase + corundum (Cor)-type V2O3, and they react at 10-15 GPa to form a phase with a calcium titanite (CT) -type structure. FeV2O4 Sp transforms to CT -type FeV2O4 at 12 GPa via decomposition phases of FeO wustite + Cor-type V2O3. MnCr2O4 Sp directly transforms to the calcium ferrite (CF)-structured phase at 10 GPa and 1000-1400 degrees C. Rietveld refinements of CT-type MgV2O4 and FeV2O4 and CF -type MnCr2O4 confirm that both the CT- and CF-type structures have frameworks formed by double chains of edge-shared B3+O6 octahedra (B3+ = V3+ and Cr3+) running parallel to one of orthorhombic cell axes. A relatively large A(2+) cation (A(2+) = Mg2+, Fe2+, and Mn2+) occupies a tunnel shaped space formed by corner-sharing of four double chains. Effective coordination numbers calculated from eight neighboring oxygen A(2+) cation distances of CT-type MgV2O4 and FeV2O4 and CF-type MnCr2O4 are 5.50, 5.16, and 7.52, respectively. This implies that the CT- and CF-type structures practically have trigonal prism (six-coordinated) and bicapped trigonal prism (eight coordinated) sites for the A(2+) cations, respectively. A relationship between cation sizes of (VIII)A(2+) and B-VI(3+) and crystal structures (CF- and CT-types) of A(2+)B(2)(3+)O(4) is discussed using the above new data and available previous data of the postspinel phases. We found that CF-type A(2)B(2)(3+)O(4) crystallize in wide ionic radius ranges of 0.9-1.4 angstrom for (VIII)A(2+) and 0.55-1.1 angstrom for B-VI(3+), whereas CT -type phases crystallize in very narrow ionic radius ranges of similar to 0.9 angstrom for (VIII)A(2+) and 0.6-0.65 angstrom for B-VI(3+). This would be attributed to the fact that the tunnel space of CT-type structure is geometrically less flexible due to the smaller coordination
机译:我们研究了尖晶石(SP)型MgV2O4,FEV2O4和MNCR(2)O(4)W的高压,高温相转变。在1200-1800℃下,MgV2O4 SP在4-7GPa中分解成MgO Periclase +刚玉(Cor)-Type V2O3的相位组件,它们在10-15GPa下反应以形成钙二钛矿(CT)的相位-type结构。 FEV2O4 SP通过Feo Wustite + Cor型V2O3的分解相,在12GPa变换到CT -TYPE FEV2O4。 MnCr2O4 SP在10GPa和1000-1400℃下直接转化为10gpa和1000-1400℃的CT型MgV2O4和FEV2O4和CF -TYPE MNCR2O4的RIETVELDEDEMETION确认CT和CF型结构都有边缘共用B3 + O6八面体(B3 + = = V3 +和CR3 +)双链组成的框架,平行于正交电池轴。相对较大的A(2+)阳离子(A(2+)= Mg2 +,Fe2 +和Mn2 +)占据由四个双链的角落共享形成的隧道形空间。根据CT型MGVV2O4和FEV2O4和CF型MNCR2O4的八个相邻氧A(2+)阳离子距离计算的有效配位数分别为5.50,5.16和7.52。这意味着CT-和CF型结构几乎具有分别具有Trigonal棱镜(六个协调的)和A(2+)阳离子的偏相的三角棱镜(八个协调)位点。阳离子尺寸(vIII)A(2+)和B-VI(3+)和晶体结构(CF-和CT型)的关系(2+)B(2)(3+)O(4)(4使用上述新数据讨论和可用的Postpinel阶段的先前数据进行讨论。我们发现,CF型A(2)B(2)(3+)O(4)在宽离子半径范围内结晶0.9-1.4埃(VIII)A(2+)和0.55-1.1埃的宽度VI(3+),而CT -TYPE相位在非常窄的离子半径范围内结晶,类似于0.9埃(VIII)A(2+)和0.6-0.65埃的0.9埃(3 +)。这将归因于由于CT型结构的隧道空间由于较小的协调而具有几何上的灵活性

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