独居石
钆
分子
拉曼光谱
傅里叶变换红外光谱
红外光谱学
化学
粉末衍射
结晶学
光谱学
材料科学
磷酸盐矿物
磷酸盐
有机化学
古生物学
物理
光学
生物
量子力学
锆石
作者
Nicolas Clavier,Adel Mesbah,Stéphanie Szenknect,Nicolas Dacheux
标识
DOI:10.1016/j.saa.2018.07.016
摘要
Rare-earth phosphates with the general formula REEPO4·nH2O belong to four distinct structural types: monazite, rhabdophane, churchite, and xenotime. We report herein the first direct comparison between vibrational spectra of these compounds for the same metal cation i.e. gadolinium. The four GdPO4·nH2O samples were prepared through wet chemistry methods and first characterized by X-ray diffraction. Three distinct spectral domains, associated to the deformation and stretching modes of phosphate tetrahedra (PO4) and to water molecules vibrations were then analyzed from FTIR and Raman data, and discussed regarding the structural characteristics of each sample. The most obvious differences between the spectra were associated to δ(H2O) and δs(PO4) modes and led to propose a simple method to rapidly and unambiguously discriminate the four polymorphs.
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