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Size of the rare-earth ions: a key factor in phase tuning and morphology control of binary and ternary rare-earth fluoride materials

机译:稀土离子的大小:二元和三元稀土氟化物材料的相位调整和形态控制的关键因素

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In an ionic liquid assisted solvothermal synthesis developed by us for the synthesis of rare-earth (RE) fluorides, it is possible to control the product formation by the choice of the rare earth ion. For rare-earth cations with smaller ionic radii (below 1.075 ?), cubic NaREF4 with a spherical morphology is obtained, whilst for rare-earth cations with radii between 1.08 ? and 1.13 ?, the formation of hexagonal NaREF4 with a nanorod-like morphology is observed. For rare earth ions with a larger radius than that of La3+ (1.216 ?), instead of ternary fluorides, binary fluorides REF3 in the trigonal modification is obtained. The growth mechanism behind this morphology change is explained from atomistic origin using electron microscope studies. The lattice strain changes with the rare-earth fluoride phase. For cubic NaREF4 a tensile strain is observed, whilst for the hexagonal and trigonal binary fluoride a compressive strain is observed. The optical properties of the obtained materials promises use for various optoelectronic applications.
机译:在我们开发的用于合成稀土(RE)氟化物的离子液体辅助溶剂热合成中,可以通过选择稀土离子来控制产物的形成。对于具有较小离子半径(小于1.075?)的稀土阳离子,可获得具有球形形态的立方NaREF 4 ,而对于半径介于1.08?3的稀土阳离子则可获得球形。和1.13Ω,观察到形成具有纳米棒状形态的六方NaREF 4 。对于半径大于La 3 + (1.216?)半径的稀土离子,代替三元氟化物,而是二元氟化物REF 3 。使用电子显微镜研究从原子起源解释了这种形态变化背后的生长机理。晶格应变随稀土氟化物相而变化。对于立方NaREF 4 ,观察到拉伸应变,而对于六方和三角二元氟化物,观察到压缩应变。所获得的材料的光学性质有望用于各种光电应用。

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