4.7 Article

Phase-Dependent Enhancement of the Green-Emitting Upconversion Fluorescence in LaVO4:Yb3+, Er3+

期刊

INORGANIC CHEMISTRY
卷 54, 期 15, 页码 7325-7334

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.5b00851

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资金

  1. National Natural Science Foundation of China [51402088]
  2. Postdoctoral Science Foundation of China [2013M531671]
  3. Science and Technology Research Foundation by Educational Commission of Henan Province of China [13A430096]
  4. Fundamental Research Fund of provincial universities for young scientific talents [0000A40545]

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The phase-dependent upconversion luminescence properties of LaVO4:Er3+ were studied to provide new insights into the design of new upconversion materials with high efficiency. Er3+-, Yb3+/Er3+-doped t-LaVO4 microcrystals were successfully synthesized by the disodium ethylenediaminetetraacetic acid (Na(2)EDTA)-assisted hydrothermal method. X-ray diffraction (XRD), inductively coupled plasma optical emission spectrometer (ICP-OES), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, luminescence spectroscopy, and thermogravimetric analysis (TGA) were used to characterize the samples. The results indicated that t-LaVO4 presents sheaf-like morphology, and the possible formation mechanism for these sheaves was proposed on the basis of time-dependent experiments. Furthermore, the phase-dependence (i.e., monoclinic- and tetragonal-type) upconversion luminescence properties were systematically studied, and the upconversion mechanisms were proposed according to spectral, pump power, and the concentration of Yb3+ dependence analyses. It is worthwhile pointing out that the Er3+-doped t-LaVO4 exhibits a brighter green emission, which is approximately 10 times that of m-LaVO4:Er3+ using a continuous 980 nm laser diode as the excitation source. This remarkable improvement was rationally analyzed on the basis of the composition, crystal structures, Raman spectra, morphology, and size. The comparative experiments suggest that the local structure of Er3+ was considered as an important reason for the higher fluorescence intensity of t-LaVO4:Er3+, which was also confirmed by the results of density functional theory (DFT) calculations.

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