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首页> 外文期刊>Crystal growth & design >Generalized low-temperature synthesis of nanocrystalline rare-earth orthoferrites LnFeO(3) (Ln = La, Pr, Nd, Sm, Eu, Gd)
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Generalized low-temperature synthesis of nanocrystalline rare-earth orthoferrites LnFeO(3) (Ln = La, Pr, Nd, Sm, Eu, Gd)

机译:纳米晶稀土正铁氧体LnFeO(3)的广义低温合成(Ln = La,Pr,Nd,Sm,Eu,Gd)

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摘要

Rare-earth orthoferrite LnFeO(3) nanocrystals were traditionally synthesized at temperatures higher than 700 degrees C. In this study, we developed a general nanosized heterobimetallic precursors approach for the synthesis of nanocrystalline rare-earth orthoferrite LnFeO(3) (Ln = La, Pr, Nd, Sm, Eu, Gd) at 500 degrees C. The nanosized heterobimetallic precursors were obtained via the reaction between the Ln and Fe oleates synthesized from their corresponding metal nitrates and sodium oleate. Subsequently, the calcination of the nanosized heterobimetallic precursors at a relatively low temperature (500 degrees C) produced nanocrystalline rare-earth orthoferrites. The precursors and products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), nitrogen adsorption, thermal analysis (TGA/DSC), and Fourier transform infrared absorption spectroscopy (FT-IR). On the basis of characterization results, we attributed the low temperature formation of nanocrystalline rare-earth orthoferrites to the reduced diffusion distance between the nanosized heterobimetallic precursors. We thought these heterobimetallic precursors ensured the desirable stoichiometry ratio of the orthoferrite products and avoided the formation of garnet. The magnetization features of the orthoferrites were evaluated at room temperature. The M-H curves revealed that EuFeO3 and GdFeO3 exhibit better weak ferromagnetic behavior, corresponding to the antisymmetric-exchange anisotropy. Our method may be extended to prepare other ternary metal oxides at relatively low temperatures.
机译:传统上在高于700摄氏度的温度下合成稀土正铁氧体LnFeO(3)纳米晶体。在这项研究中,我们开发了一种用于合成纳米晶稀土正铁氧体LnFeO(3)的通用纳米异质双金属前体方法(Ln = La, Pr,Nd,Sm,Eu,Gd)在500摄氏度下进行。通过从相应的金属硝酸盐和油酸钠合成的Ln和Fe油酸盐之间的反应,获得了纳米级异双金属前体。随后,在相对较低的温度(500摄氏度)下煅烧纳米尺寸的异双金属前驱体,生成了纳米晶稀土正铁酸盐。通过X射线衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM),高分辨率透射电子显微镜(HRTEM),氮吸附,热分析(TGA / DSC)对前体和产物进行表征和傅立叶变换红外吸收光谱(FT-IR)。根据表征结果,我们将纳米晶稀土正铁氧体的低温形成归因于纳米级异双金属前体之间减小的扩散距离。我们认为这些异双金属前体确保了正铁氧体产品的理想化学计量比,并避免了石榴石的形成。在室温下评估了正铁氧体的磁化特征。 M-H曲线表明,EuFeO3和GdFeO3表现出更好的弱铁磁性能,对应于反对称交换各向异性。我们的方法可以扩展到在相对较低的温度下制备其他三元金属氧化物。

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