Photoluminescence of GdVO4:Eu3+, Al 3+ Phosphors under VUV Excitation

2012 ◽  
Vol 18-19 ◽  
pp. 257-263 ◽  
Author(s):  
K. Park ◽  
M.H. Heo ◽  
Y. Kim ◽  
J.Y. Kim

The microstructure and photoluminescence properties of Gd0.94-xAlxEu0.06VO4 (0≤x≤0.04) phosphors with various Al3+ contents were investigated. The phosphors showed a nanocrystalline nature and a high-quality powder characteristic. The crystallite sizes of the phosphors were calculated to be 46-48 nm. The annealed Gd0.94-xAlxEu0.06VO4 phosphors crystallized in the tetragonal structure. In the emission spectra, several emission peaks were observed over the measured wavelength range (500-750 nm), which were caused by the difference in the transitions of Eu3+ ions, depending on the local symmetry (5D0 → 7Fj, j = 1, 2, 3, and 4). The strongest emission peak was located at 619 nm, providing a high-purity red emission. The doped Al3+ yielded significantly enhanced the emission intensity. The most intense high-purity red emission was obtained for Gd0.93Al0.01Eu0.06VO4.

2011 ◽  
Vol 399-401 ◽  
pp. 982-986
Author(s):  
Jin Liu ◽  
Dong Mei Shi ◽  
Ying Gang Zhao ◽  
Xiao Feng Wang

The visible and near infrared emission spectra of Er3+/Tm3+-doped Ga2O3-Bi2O3-PbO-GeO2(GBPG) glasses excited at 808 nm are experimentally investigated. The results reveal that 1.53 µm emission were enhanced with an increase of Er3+concentration. Furthermore, the incorporation of Er3+into Tm3+-doped systems has also resulted in intense 522, 545 and 693nm upconversion emission intensity and an weak 660 nm red emission. The possible mechanism and related discussions on this phenomenon have been presented. The results show that Er3+/Tm3+-codoped GBPG glass may be a promising materials for developing laser and fiber optical devices.


Open Physics ◽  
2012 ◽  
Vol 10 (2) ◽  
Author(s):  
Xipu He ◽  
Junli Huang ◽  
Liya Zhou ◽  
Qi Pang ◽  
Fuzhong Gong

AbstractA series of new red phosphors, MZr2(PO4)3:Eu3+; Bi3+ (M=Na; K), were synthesized using the solidstate reaction method, and their photoluminescence spectra were measured. The MZr2(PO4)3:Eu3+; Bi3+ (M=Na; K) phosphors were efficiently excited by an ultraviolet (UV; 395 nm) source, and showed intense orange-red emission at 595 nm. Further investigation of the concentration-dependent emission spectra indicated that the MZr2(PO4)3:Eu3+; Bi3+ (M=Na; K) phosphors exhibit the strongest luminescence intensity when y = 0.01 in NaZr2(0:95−y)(PO4)3:Eu0.103+, Bi2y 3+ and y = 0.09 in NaZr2(0.95−y)(PO4)3:Eu0.103+, Bi2y 3+, whereas the relative PL intensity decreases with increasing Bi3+ concentration due to concentration quenching. The addition of Bi3+ widens the excitation band of NaZr2(0.95−y)(PO4)3:Eu0.103+, Bi2y 3+ around 320 nm, which provides the useful idea of broadening the excitation band around 300–350 nm to fit the ultraviolet chip.


2019 ◽  
Vol 12 (04) ◽  
pp. 1950057 ◽  
Author(s):  
Chao-Chao Guo ◽  
Qun Zeng ◽  
Chun-Feng Yao ◽  
Yan-Zhao Feng ◽  
Xi Chen ◽  
...  

Red phosphors with compositions of Li[Formula: see text]Nb[Formula: see text]Ti[Formula: see text]O3:3[Formula: see text]wt.% Eu[Formula: see text] [Formula: see text] were synthesized by solid-state reaction method. The samples were investigated by using X-ray diffraction (XRD) and photoluminescence spectroscopy, respectively. XRD results showed that all samples were main phase of Li2TiO3. Emission spectra of Li[Formula: see text]Nb[Formula: see text]Ti[Formula: see text]O3:3[Formula: see text]wt.% Eu[Formula: see text] powders showed strong red emission at 612[Formula: see text]nm (5D0–7F[Formula: see text] with 396[Formula: see text]nm excitation. In addition, the excitation and emission intensity increased up to [Formula: see text], and then decreased with further increasing of the x values. And the chromaticity coordinate (CIE) of the component with [Formula: see text] was superior to other components.


2011 ◽  
Vol 311-313 ◽  
pp. 1327-1331 ◽  
Author(s):  
Ling He ◽  
Wei Min Sun ◽  
Yu Tian Ding ◽  
Yu Hua Wang

A novel phosphor, Gd2MoB2O9:Eu3+ has been synthesized by solid-state reaction and its photoluminescence in UV-VUV range are investigated. A sharp excitation band is observed in the region of 120–135 nm, which is related to the charge-transfer (CT) band of Gd3+. The broad band around 135–160 nm can be assigned to the BO3 host absorption. The broad bands around 248 nm are assigned to the CT band of Eu3+-O2-. The phosphors emit strong red luminescence centered at about 591 nm, 614 nm and 626 nm due to the5D0–7F1 and 5D0–7F2 transitions of Eu3+. The main emission peak under 254 and 147 nm excitations also shows different shifts with increasing Eu3+ concentration. This could be due to the different luminescence sites selected at high doping concentrations of Eu3+. Gd2MoB2O9:Eu3+ shows the pure red emission under both 254 and 147 nm excitations.


2013 ◽  
Vol 12 (04) ◽  
pp. 1350023 ◽  
Author(s):  
V. P. HEDAOO ◽  
V. B. BHATKAR ◽  
S. K. OMANWAR

Nanoscale phosphors have superior performance characteristics than the bulk phosphors. This paper explains the synthesis and characterization like XRD, FTIR, SEM and photoluminescence properties of nanocrystalline Sr 4 Al 14 O 25 doped with rare earth elements like europium, dysprosium and samarium by combustion method. XRD showed the nanoscale crystalline nature of as-prepared samples. SEM confirmed size of the particle less than 100 nm. Photoluminescent emission spectra showed strong orange red emission at 593 nm for Sr 4 Al 14 O 25: Sm 3+. The green emission of Eu 2+ was observed at around 490 nm for Sr 4 Al 14 O 25: Eu 2+.


2016 ◽  
Vol 702 ◽  
pp. 57-61 ◽  
Author(s):  
Piyachat Meejitpaisan ◽  
Chittra Kedkaew ◽  
Yotsakit Ruangtaweep ◽  
Jakrapong Kaewkhao

Sm3+-doped gadolinium calcium phosphate glasses of the composition (70-x)P2O5 : 10CaO : 20Gd2O3 : xSm2O3 (PCGSm), where x = 0.05, 0.10, 0.50, 1.00, 1.50, 2.00, 2.50 and 3.00 mol% have been prepared by melt-quenching technique and investigated their photoluminescence properties. The emission spectra of Eu3+-doped glasses recorded in wavelength range 500-750 nm with 402 nm excitation. All the spectra exhibited 4 emission bands corresponding to the 4G5/2→6H5/2, 4G5/2→6H7/2, 4G5/2→6H9/2 and 4G5/2→6H11/2 transition, respectively. The peak intensities increase with the increase of concentration from 0.05 to 0.5 mol% and beyond that the quenching in the emission peak intensities have been observed.


2020 ◽  
Vol 1 (2) ◽  
pp. 5-8
Author(s):  
Komang Gde Suastika, Heri Suyanto, Gunarjo, Sadiana, Darmaji

Abstract - Laser-Induced Breakdown Spectroscopy (LIBS) is one method of atomic emission spectroscopy using laser ablation as an energy source. This method is used to characterize the type of amethysts that originally come from Sukamara, Central Kalimantan. The result of amethyst characterization can be used as a reference for claiming the natural wealth of the amethyst. The amethyst samples are directly taken from the amethyst mining field in the District Gem Amethyst and consist of four color variations: white, black, yellow, and purple. These samples were analyzed by LIBS, using laser energy of 120 mJ, delay time detection of 2 μs and accumulation of 3, with and without cleaning. The purpose of this study is to determine emission spectra characteristics, contained elements, and physical characteristics of each amethyst sample. The spectra show that the amethyst samples contain some elements such as Al, Ca, K, Fe, Gd, Ba, Si, Be, H, O, N, Cl and Pu with various emission intensities. The value of emission intensity corresponds to concentration of element in the sample. Hence, the characteristics of the amethysts are based on their concentration value. The element with the highest concentration in all samples is Si, which is related to the chemical formula of SiO2. The element with the lowest concentration in all samples is Ca that is found in black and yellow amethysts. The emission intensity of Fe element can distinguish between white, purple, and yellow amethyst. If Fe emission intensity is very low, it indicates yellow sample. Thus, we may conclude that LIBS is a method that can be used to characterize the amethyst samples.Key words: amethyst, impurity, laser-induced, breakdown spectroscopy, characteristic, gemstones


Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 115
Author(s):  
Suhail Huzaifa Jaafar ◽  
Mohd Hafiz Mohd Zaid ◽  
Khamirul Amin Matori ◽  
Sidek Hj. Ab Aziz ◽  
Halimah Mohamed Kamari ◽  
...  

This research paper proposes the usage of a simple thermal treatment method to synthesis the pure and Eu3+ doped ZnO/Zn2SiO4 based composites which undergo calcination process at different temperatures. The effect of calcination temperatures on the structural, morphological, and optical properties of ZnO/Zn2SiO4 based composites have been studied. The XRD analysis shows the existence of two major phases which are ZnO and Zn2SiO4 crystals and supported by the finding in the FT-IR. The FESEM micrograph further confirms the existence of both ZnO and Zn2SiO4 crystal phases, with progress in the calcination temperature around 700–800 °C which affects the existence of the necking-like shape particle. Absorption humps discovered through UV-Vis spectroscopy revealed that at the higher calcination temperature effects for higher absorption intensity while absorption bands can be seen at below 400 nm with dropping of absorption bands at 370–375 nm. Two types of band gap can be seen from the energy band gap analysis which occurs from ZnO crystal and Zn2SiO4 crystal progress. It is also discovered that for Eu3+ doped ZnO/Zn2SiO4 composites, the Zn2SiO4 crystal (5.11–4.71 eV) has a higher band gap compared to the ZnO crystal (3.271–4.07 eV). While, for the photoluminescence study, excited at 400 nm, the emission spectra of Eu3+ doped ZnO/Zn2SiO4 revealed higher emission intensity compared to pure ZnO/Zn2SiO4 with higher calcination temperature exhibit higher emission intensity at 615 nm with 700 °C being the optimum temperature. The emission spectra also show that the calcination temperature contributed to enhancing the emission intensity.


Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2753
Author(s):  
Bartosz Fetliński ◽  
Sebastian Turczyński ◽  
Michał Malinowski ◽  
Paweł Szczepański

In this work, we investigate Ce3+ to Yb3+ energy transfer in Y4Al2O9 (YAM) for potential application in solar spectrum down-converting layers for photovoltaic devices. Photoluminescence properties set, of 10 samples, of the YAM host activated with Ce3+ and Yb3+ with varying concentrations are presented, and the Ce3+ to Yb3+ energy transfer is proven. Measurement of highly non-exponential luminescence decays of Ce3+ 5d band allowed for the calculation of maximal theoretical quantum efficiency, of the expected down-conversion process, equal to 123%. Measurements of Yb3+ emission intensity, in the function of excitation power, confirmed the predominantly single-photon downshifting character of Ce3+ to Yb3+ energy transfer. Favorable location of the Ce3+ 5d bands in YAM makes this system a great candidate for down-converting, and down-shifting, luminescent layers for photovoltaics.


Membranes ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 400
Author(s):  
Hajime Kamebuchi ◽  
Satoshi Tamaki ◽  
Atsushi Okazawa ◽  
Norimichi Kojima

The development and the photophysical behavior of a transparent ion-exchange membrane based on a pH-sensitive polypyridyl ruthenium(II) complex, [(bpy)2RuII(H2bpib)RuII(bpy)2](ClO4)4 (bpy = 2,2′-bipyridine, H2bpib = 1,4-bis([1,10]phenanthroline[5,6-d]-imidazol-2-yl)benzene), are experimentally and theoretically reported. The emission spectra of [(bpy)2RuII(H2bpib)RuII(bpy)2]@Nafion film were observed between pH 2 and pH 11 and showed the highest relative emission intensity at pH 5 (λmaxem = 594.4 nm). The relative emission intensity of the film significantly decreased down to 75% at pH 2 and 11 compared to that of pH 5. The quantum yields (Φ) and lifetimes (τ) showed similar correlations with respect to pH, Φ = 0.13 and τ = 1237 ns at pH 5, and Φ = 0.087 and τ = 1014 ns and Φ = 0.069 and τ = 954 ns at pH 2 and pH 11, respectively. These photophysical data are overall considerably superior to those of the solution, with the radiative- (kr) and non-radiative rate constants (knr) at pH 5 estimated to be kr = 1.06 × 105 s−1 and knr = 7.03 × 105 s−1. Density functional theory calculations suggested the contribution of ligand-to-ligand- and intraligand charge transfer to the imidazolium moiety in Ru-H3bpib species, implying that the positive charge on the H3bpib ligand works as a quencher. The Ru-Hbpib species seems to enhance non-radiative deactivation by reducing the energy of the upper-lying metal-centered excited state. These would be responsible for the pH-dependent “off-on-off” emission behavior.


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