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3D architectures of iron molybdate: Phase selective synthesis, growth mechanism, and magnetic properties

机译:钼酸铁的3D体系结构:相选择合成,生长机理和磁性

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摘要

Monoclinic and orthorhombic Fe,(MoO4)(3) microsized particles with complex 3D architectures have been selectively prepared by a template-free hydrothermal process. The pH value, reaction time, temperature, and molybdenian source have crucial influence on the phase formation, shape evolution, and microstructures. Monoclinic Fe-2(MoO4)(3) particles obtained at pH I and pH 1.65 display ferromagnetic ordering at 10.4 K and 10.5 K, respectively, and the ferromagnetic component is determined to be 0.0458 mu(B) and 0.0349 mu(B), per Fe-ion at 10 K, respectively. For orthorhombic beta-Fe-2(MoO4)(3), antiferromagnetic ordering. was observed about 12 K. At higher temperatures, beta-Fe-2(MoO4)(3) began to follow the Curie-Weiss law with theta = -70 K. Such 3D architectures of monoclinic and orthorhombic beta-Fe-2(MoO4)(3) microparticles with unique shapes and structural characteristics may find applications as catalysts and as well as in other fields.
机译:已经通过无模板水热工艺选择性地制备了具有复杂3D结构的单斜晶和正交晶Fe,(MoO4)(3)微尺寸颗粒。 pH值,反应时间,温度和钼源对相形成,形状演变和微观结构具有至关重要的影响。在pH I和pH 1.65下获得的单斜晶Fe-2(MoO4)(3)颗粒分别显示10.4 K和10.5 K的铁磁有序性,确定铁磁成分为0.0458 mu(B)和0.0349 mu(B),铁离子在10 K时分别对于斜方β-Fe-2(MoO4)(3),反铁磁有序。观测到大约12K。在更高的温度下,β-Fe-2(MoO4)(3)开始遵循居里-魏斯定律,θ= -70K。这种单斜和正交的β-Fe-2(MoO4)的3D架构)(3)具有独特形状和结构特征的微粒可作为催化剂以及其他领域的应用。

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