Abstract:Yttrium tungstate precursors with novel 3D hierarchical architectures assembled from nanosheet building blocks were successfully synthesized by a hydrothermal method with the assistance of sodium dodecyl benzenesulfonate (SDBS). After calcination, the precursors were easily converted to Y(2)(WO(4))(3) without an obvious change in morphology. The as-prepared precursors and Y(2)(WO(4))(3) were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy … Show more
“…Therefore, they are recently considered as promising host materials for rare-earth luminescent centers because of the special properties of WO 4 2-& Guixia Liu liuguixia22@163.com group [11][12][13][14]. From the report of Huang et al [15], it was seen that tungstate host essentially showed a little weaker blue emission at room temperature compared to the absorption in excitation spectrum, owing to efficient energy transfer from WO 4 2-group to activators. Liu et al [16] had also discovered that NaY(WO 4 ) 2 exhibited a broad emission centered at approximately 469 nm without doping Ln 3? ions, and the intensity of this emission decreased when Ln 3?…”
Eu 3? and/or Tb 3? doped NaY(WO 4 ) 2 nanomaterials have been successfully synthesized by one-step hydrothermal method. The samples were characterized by X-ray diffraction, field-emission scanning electron microscopy, X-ray energy dispersive spectroscopy, and photoluminescence spectra. The results show that the novel nanoplates with a diameter of 300-600 nm and the thickness of 20-25 nm are observed. Under the excitation of 246 or 230 nm, individual RE 3? ions activated NaY(WO 4 ) 2 phosphors exhibit excellent emission properties in their respective regions. The as-prepared Eu 3? or Tb 3? doped samples show strong red and green emission, originating from the allowed 5 D 0 ? 7 F J (J = 0, 1, 2) transition of the Eu 3? ions and the 5 D 4 ? 7 F J (J = 6, 5, 4, 3) transition of the Tb 3? ions. In addition, by properly tuning the relative concentration of Eu 3? ions in the case of Eu 3? and Tb 3? co-doped systems, tunable emissions in a single component are obtained under the excitation of 230 or 395 nm. Moreover, an energy transfer from Tb 3? to Eu 3? is observed, which has been justified through the luminescence spectra and the fluorescence decay curves. Furthermore, the corresponding luminescence and energy transfer mechanism have been proposed in optical transitions and possible energy transfer scheme. These results indicate that Eu 3? and Tb 3? doped NaY(WO 4 ) 2 phosphors will find potential application in the field of solid-state lighting.
“…Therefore, they are recently considered as promising host materials for rare-earth luminescent centers because of the special properties of WO 4 2-& Guixia Liu liuguixia22@163.com group [11][12][13][14]. From the report of Huang et al [15], it was seen that tungstate host essentially showed a little weaker blue emission at room temperature compared to the absorption in excitation spectrum, owing to efficient energy transfer from WO 4 2-group to activators. Liu et al [16] had also discovered that NaY(WO 4 ) 2 exhibited a broad emission centered at approximately 469 nm without doping Ln 3? ions, and the intensity of this emission decreased when Ln 3?…”
Eu 3? and/or Tb 3? doped NaY(WO 4 ) 2 nanomaterials have been successfully synthesized by one-step hydrothermal method. The samples were characterized by X-ray diffraction, field-emission scanning electron microscopy, X-ray energy dispersive spectroscopy, and photoluminescence spectra. The results show that the novel nanoplates with a diameter of 300-600 nm and the thickness of 20-25 nm are observed. Under the excitation of 246 or 230 nm, individual RE 3? ions activated NaY(WO 4 ) 2 phosphors exhibit excellent emission properties in their respective regions. The as-prepared Eu 3? or Tb 3? doped samples show strong red and green emission, originating from the allowed 5 D 0 ? 7 F J (J = 0, 1, 2) transition of the Eu 3? ions and the 5 D 4 ? 7 F J (J = 6, 5, 4, 3) transition of the Tb 3? ions. In addition, by properly tuning the relative concentration of Eu 3? ions in the case of Eu 3? and Tb 3? co-doped systems, tunable emissions in a single component are obtained under the excitation of 230 or 395 nm. Moreover, an energy transfer from Tb 3? to Eu 3? is observed, which has been justified through the luminescence spectra and the fluorescence decay curves. Furthermore, the corresponding luminescence and energy transfer mechanism have been proposed in optical transitions and possible energy transfer scheme. These results indicate that Eu 3? and Tb 3? doped NaY(WO 4 ) 2 phosphors will find potential application in the field of solid-state lighting.
“…The crystallite size values for Ca 0.5 Y(WO 4 ) 2 doped with Pr 3+ , Sm 3+ , Eu 3+ , Tb 3+ , Dy 3+ and Yb 3+ /Er 3+ are found between 30.0 and 42.0 nm and the cell parameters and its volume are given in Table S1 (Supplementary Material). 7 Scanning electron microscopy and energy dispersive X-ray analysis were used to determine the morphology and chemical composition of elements in the prepared sample. In this context, as a representative candidate for the analysis, 0.…”
Section: Structural and Morphological Studiesmentioning
“…In modern materials science, the ability to prepare nano-and microstructures with well-defined morphology and excellent monodispersity in bulk scale is an essential requirement for applications of materials [1,2]. Till now, it is generally accepted that the morphology, dimensionality, and crystal structure of the materials all play important roles in the electronic, optical, magnetic, catalytic, chemical, and other physical properties [3][4][5].…”
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