A Novel Blue-Green-Emitting Phosphor Gd4.67Si3O13:Tb3+

2016 ◽  
Vol 16 (4) ◽  
pp. 3861-3864
Author(s):  
Ye Jin ◽  
Qingping Wang

A novel blue-green-emitting phosphor Gd4.67Si3O13:Tb3+ has been synthesized by a conventional high temperature solid-state method at 1350 °C for 6 h. X-ray diffraction and photoluminescence spectra were used to characterize the as-synthesized phosphor. The excitation spectrum is composed of a broadband and two sharp peaks, at 274 nm, and 311 nm, respectively. The emission spectrum is composed of multiple sharp peaks, of which the strongest peak is at 544 nm (5D4 →7F5). The critical doping content of Tb3+ is 5%, with the emission intensity increasing proportionally with Tb3+ concentration increase until it reaches 5%. As doping concentration from 5% to 7%, the luminescence intensity gradually reduces. Concentration quenching mechanism for Tb3+ is demonstrated to be dipole–dipole interaction. The Commission Internationale de L’Eclairage (CIE) coordinates are also investigated in this work. The CIE coordinates of the Gd4.67Si3O13:0.03Tb3+ phosphor upon 311 nm excitation are (0.242, 0.323). All the results indicate that the blue-green-emitting phosphor Gd4.67Si3O13:Tb3+ has potential research value.

2021 ◽  
Vol 267 ◽  
pp. 02018
Author(s):  
Jianhua Li ◽  
Jinyu Huang ◽  
Jing Liao ◽  
Jinjin Fu ◽  
Bin Deng

A series of Ca2YTaO6: Tm3+ blue-emitting phosphors were firstly prepared by the solid-state method. The phase formations and purity of Ca2YTaO6: xTm3+ (x = 0.3%-5% mol) were verified by X-ray powder diffraction. The morphological characteristics of Ca2YTaO6: 0.005Tm3+ were detected by scanning electron microscopy (SEM). Photoluminescence properties were discussed by emission (λem = 460 nm) and excitation (λex = 359 nm) spectra. The critical doping concentration of the products was 0.005 mol. The proposed concentration quenching mechanism in Ca2YTaO6 materials was the electric multipole interaction. Besides, the color coordinates (0.1408, 0.0891) of Ca2YTaO6: 0.005Tm3+ were located in blue region. The results suggested the Ca2YTaO6: Tm3+ phosphors can be promising blue-emitting components for the WLED applications.


2020 ◽  
Vol 213 ◽  
pp. 01034
Author(s):  
Sumeng Jiang ◽  
Fanhua Zeng ◽  
Hui Liu ◽  
Yan Duan ◽  
Bin Deng

Various novel Ca2MgTeO6:Tm3+ blue-emitting tellurate materials were synthesized via solid-state reaction. The structure and phase purity of prepared Ca2MgTeO6:xTm3+ (x = 0.0025-0.10 mol) were examined by X-ray powder diffraction. The Ca2MgTeO6:Tm3+ phosphors emit blue emission at 359 nm excitation. The optimum doping concentration was 0.02 mol. The concentration quenching mechanism in the Ca2MgTeO6 host was due to the electric dipole-dipole interaction. The The CIE chromaticity coordinates of Ca2MgTeO6:Tm3+ phosphors located in the blue region. These results validated the Ca2MgTeO6:Tm3+ tellurate phosphor can be used as good blue-emitting candidate for W-LEDs.


2013 ◽  
Vol 28 (S1) ◽  
pp. S41-S44 ◽  
Author(s):  
Ming He ◽  
Z.H. Zhang ◽  
Y.Z. Zhu ◽  
Y.G. Tang ◽  
Z. Song

Eu3+-doped SmBa3B9O18 luminescent materials were synthesized by high temperature solid state reactions. The structure and photoluminescence properties of Sm(1−x)EuxBa3B9O18 (x = 0.2, 0.4, and 0.6) were investigated by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, and photoluminescence spectra. The results show that doping of Eu3+ ions does not change the structure of SmBa3B9O18. The luminescence is mainly the characteristic Eu3+ ion luminescence. No concentration quenching processes occur with the increment of Eu3+ concentration. The work implies that SmBa3B9O18 is a potential host material and europium-doped SmBa3B9O18 may find application in display and optical devices.


2015 ◽  
Vol 815 ◽  
pp. 301-303
Author(s):  
Jing Jing Ru ◽  
Mei Zhen Zhou ◽  
Bing Zhao ◽  
Gui Yang Yan ◽  
Shao Ming Ying

A series of novel reddish-orange phosphors Ca3Y2-xSmxWO9were synthesized by solid-state method and characterized by X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR) and photoluminescence (PL) spectra. The results showed that these phosphors are tetragonal structures. The optimum calcining temperature was 1100°C, and the sintering time was 3h. The results demonstrated that the optimal doping concentration of Sm3+in Ca3Y2WO9was about 1 mol%. The main emission line was4G5/2→6H7/2transition of Sm3+at 593nm, and showed intense reddish-orange.


Nanomaterials ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 1023 ◽  
Author(s):  
Ashish Chhaganlal Gandhi ◽  
Chia-Liang Cheng ◽  
Sheng Yun Wu

We report the synthesis of room temperature (RT) stabilized γ–Bi2O3 nanoparticles (NPs) at the expense of metallic Bi NPs through annealing in an ambient atmosphere. RT stability of the metastable γ–Bi2O3 NPs is confirmed using synchrotron radiation powder X-ray diffraction and Raman spectroscopy. γ–Bi2O3 NPs exhibited a strong red-band emission peaking at ~701 nm, covering 81% integrated intensity of photoluminescence spectra. Our findings suggest that the RT stabilization and enhanced red-band emission of γ‒Bi2O3 is mediated by excess oxygen ion vacancies generated at the octahedral O(2) sites during the annealing process.


Author(s):  
Mingqiang Zhong ◽  
Qin Feng ◽  
Changlai Yuan ◽  
Xiao Liu ◽  
Baohua Zhu ◽  
...  

AbstractIn this work, the (1−x)Bi0.5Na0.5TiO3-xBaNi0.5Nb0.5O3 (BNT-BNN; 0.00 ⩽ x ⩽ 0.20) ceramics were prepared via a high-temperature solid-state method. The crystalline structures, photovoltaic effect, and electrical properties of the ceramics were investigated. According to X-ray diffraction, the system shows a single perovskite structure. The samples show the normal ferroelectric loops. With the increase of BNN content, the remnant polarization (Pr) and coercive field (Ec) decrease gradually. The optical band gap of the samples narrows from 3.10 to 2.27 eV. The conductive species of grains and grain boundaries in the ceramics are ascribed to the double ionized oxygen vacancies. The open-circuit voltage (Voc) of ∼15.7 V and short-circuit current (Jsc) of ∼1450 nA/cm2 are obtained in the 0.95BNT-0.05BNN ceramic under 1 sun illumination (AM1.5G, 100 mW/cm2). A larger Voc of 23 V and a higher Jsc of 5500 nA/cm2 are achieved at the poling field of 60 kV/cm under the same light conditions. The study shows this system has great application prospects in the photovoltaic field.


2012 ◽  
Vol 217-219 ◽  
pp. 733-736
Author(s):  
Xiu Mei Han ◽  
Shu Ai Hao ◽  
Ying Ling Wang ◽  
Gui Fang Sun ◽  
Xi Wei Qi

Zn2SiO4:Eu3+, Dy3+ phosphors have been prepared through the sol-gel process. X-ray diffraction (XRD), thermogravimetric and ddifferential thermal analysis (TG-DTA), FT-IR spectra and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicated that the phosphors crystallized completely at 1000oC. In Zn2SiO4:Eu3+,Dy3+ phosphors, the Eu3+ and Dy3+ show their characteristic red(613nm, 5D0-7F2), blue (481nm, 4F9/2–6H15/2) and yellow (577nm, 4F9/2–6H13/2) emissions.


2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.


2021 ◽  
Vol 19 (11) ◽  
pp. 108-115
Author(s):  
Nihad Ali Shafeek

This research contains preparing the superconducting compound Bi2-xAgxSr2Ca2Cu3O10+δ and studying its structural and electrical characteristics. The samples were prepared using the solid-state method in two stages, and different concentrations of x were (x= 0.2,0.4,0.6,0.8) replaced instead of bismuth Bi. Then, using a hydraulic press 9 ton/cm2 and sintering with a temperature of 850°C, the samples were pressed. Next, x-ray diffraction is used to study the structural properties. The study of these samples was presented in different proportions of x values, where x = 0.4 is the best compensation ratio of x. A critical temperature of 1400C and the Tetragonal structure was got. After that, the effect of laser nidinium _ yak (Nd: YAG laser) was used on the compositional. It was found that the temperature value increased, so we got the best critical temperature, which is 142 0C.


2006 ◽  
Vol 11-12 ◽  
pp. 159-162 ◽  
Author(s):  
Yong Ge Cao ◽  
Lei Miao ◽  
Sakae Tanemura ◽  
Yasuhiko Hayashi ◽  
Masaki Tanemura

Transparent indium-doped ZnO (IZO) films with low In content (<6at%) were fabricated through radio-frequency (rf) helicon magnetron sputtering. Formation of In-Zn-O solid solution was confirmed by X-ray diffraction (XRD) patterns. Incorporation of indium into ZnO films enhances the optical transmission in the visible wavelength. The optical band-gaps slightly increase from 3.25eV (ZnO) to 3.28eV (In0.04Zn0.96O) and to 3.30eV (In0.06Zn0.94O) due to Burstain-Moss effect. The Urbach tail parameter E0, which is believed to be a function of structural disorder, increases from 79meV (ZnO), to 146meV (In0.04Zn0.96O), and to 173meV (In0.06Zn0.94O), which is consistent with increase of Full-Width Half-Maximum (FWHM) in corresponding XRD patterns. Decreasing in crystal quality with increasing indium concentration is also confirmed by photoluminescence spectra.


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