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LnPO4·nH2O(Ln = La、Ce、Gd、Tb、Dy)纳米棒和纳米线的合成与表征

Synthesis and characterization of LnPO4 x nH2O (Ln = La, Ce, Gd, Tb, Dy) nanorods and nanowires.

作者信息

Di Weihua, Wang Xiaojun, Zhao Haifeng

机构信息

Key Laboratory of Excited State Processes, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, People's Republic of China.

出版信息

J Nanosci Nanotechnol. 2007 Oct;7(10):3624-8. doi: 10.1166/jnn.2007.847.

Abstract

Aqueous precipitation method has been used to synthesize lanthanide orthophosphates LnPO4 x nH2O (Ln = La, Ce, Gd, Tb, Dy) with high purity and yield. It has been shown by XRD, TGA, and FTIR characterization that the as-synthesized samples are the LnPO4 hydrates (LnPO4 x nH2O) with hexagonal rhabdophane-type structure. The X-ray diffraction peaks and absorption of PO4(3-) groups show a systematic shift from LaPO4 x nH2O to DyPO4 x nH2O due to the effect of lanthanide ionic contraction. The value of n in LnPO4 x nH2O depends on the lanthanide element and synthetic condition. Field-emission scanning electron microscopy observations show the morphology of as-synthesized samples, which consist entirely of nanorods/nanowires with diameters of 30-100 nm and lengths ranging from several hundreds of nanometers to several micrometers. The anisotropic growth of crystals should be responsible for the formation of nanorods/nanowires, which is related to the hexagonal crystal structure.

摘要

采用水相沉淀法合成了高纯度、高产率的稀土正磷酸盐LnPO₄·nH₂O(Ln = La、Ce、Gd、Tb、Dy)。XRD、TGA和FTIR表征表明,合成的样品为具有六方水磷铈矿型结构的LnPO₄水合物(LnPO₄·nH₂O)。由于镧系离子收缩效应,PO₄³⁻基团的X射线衍射峰和吸收峰从LaPO₄·nH₂O到DyPO₄·nH₂O呈现出系统性的位移。LnPO₄·nH₂O中n的值取决于镧系元素和合成条件。场发射扫描电子显微镜观察显示了合成样品的形貌,其完全由直径为30 - 100 nm、长度从几百纳米到几微米不等的纳米棒/纳米线组成。晶体的各向异性生长应是纳米棒/纳米线形成的原因,这与六方晶体结构有关。

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