The calculation of luminescence intensity parameters of rare earth ions doped in Y2O3 crystals

1988 ◽  
Vol 40-41 ◽  
pp. 117-118
Author(s):  
Fei Mei ◽  
Guilin Yang ◽  
You Xu
2016 ◽  
Vol 16 (4) ◽  
pp. 3883-3885 ◽  
Author(s):  
Shihu Liu ◽  
Peng Zhang ◽  
Daguang Li ◽  
Min Lan ◽  
Zhe Wang ◽  
...  

Monodisperse water-soluble LaF3: Yb3+/Er3+ nanocrystals (NCs) have been successfully fabricated via a fast, facile, and environmentally-friendly polyol process with polyvinylpyrrolidone (PVP) as an amphiphilic surfactant. The obtained NCs with a small size of 18 nm can be well dispersed in hydrophilic solutions. Meanwhile, their upconversion (UC) luminescence intensity was increased through Ca2+ doping due to the decrease of symmetry around rare earth ions.


Author(s):  
A. P. Mar`in ◽  
U. A. Mar`ina ◽  
V. A. Vorob`ev ◽  
R. V. Pigulev

The paper presents the results of a study of the luminescent properties of calcium gallate activated by trivalent rare earth ions Yb3+ and Er3+. IR luminescence spectra of samples with a single activator Ca1‑хYbxGa2O4,Ca1‑хErxGa2O4 were studied when excited by radiation sources with a wavelength of 940 and 790 nm, respectively. The dependence of the luminescence intensity of samples on the concentration of rare earth ions is obtained. When the two-activator composition of Ca1‑х‑yYbxEryGa2O4 is excited by a semiconductor laser diode with a wavelength of 940 nm, IR luminescence is registered in the regions of 980-1100 nm and 1450-1670 nm. The radiation in these bands corresponds to electronic transitions in Yb3+ and Er3+ ions, respectively. For a luminescence band with a maximum at a wavelength of 1540 nm, the excitation spectra were measured, the maximum intensity is at the wavelengths: 930, 941, 970, 980 nm. The dependence of the IR luminescence intensity of a solid solution of Ca1‑х‑yYbxEryGa2O4 on the concentration of Er3+ ions was studied. With an increase in the concentration of Er3+ ions in the luminescence spectra, there is a redistribution in the intensity of the bands belonging to Yb3+ and Er3+ ions, which indicates the presence of energy transfer processes between these ions. The kinetics of IR luminescence attenuation was studied for series with one and two activators: Ca1‑хYbxGa2O4,Ca1‑хErxGa2O4, Ca1‑х‑yYbxEryGa2O4. It is established that the luminescence attenuation occurs mainly according to the exponential law, which indicates the predominance of the intracenter luminescence mechanism in the studied structures. Based on the analysis of the excitation and luminescence spectra of experimental samples, conclusions are made about the interaction of Yb3+ and Er3+ activator ions in the crystal lattice of calcium gallate.


2015 ◽  
Vol 137 (6) ◽  
Author(s):  
T. N. Nurakhmetov ◽  
K. A. Kuterbekov ◽  
D. H. Daurenbekov ◽  
A. Zh. Zhanbotin ◽  
A. A. Betekbaev ◽  
...  

Intrinsic and extrinsic nature of the luminescence of pure and Eu3+ and Tb3+ rare-earth ions activated mesoporous silica has been investigated by spectroscopic methods. Increasing the Eu3+ impurity concentration from 0.01 mg to 7 mg, results in an increase of the impurity particles radiation in the luminescent mesoporous colloidal silica (LMCS) matrix by several times. With an increase in the concentration of Tb3+ from 0.01 mg to 3 mg, impurity luminescence intensity increases several times while the intrinsic luminescence intensity maximum at 400 and 460 nm is decreasing. Based on the experimental evidence, it is suggested that the energy of the own electronic matrix excitation is transferred by emitters, i.e., impurities of Eu3+ and Tb3+ ions. Also, it is assumed that the emission band at 610 nm in an LMCS—Eu3+ and emission band at 543 nm in the LMCS—Tb3+ is attributed to the intracenter transitions within the Eu3+ and Tb3+ ions.


2017 ◽  
Vol 268 ◽  
pp. 191-197 ◽  
Author(s):  
Nurhafizah Hasim ◽  
Md Supar Rohani

The modification of absorption characteristics in rare-earth doped tellurite glasses is important in photonics application. The Er3+/Nd3+ doped glasses of the form (69-x)TeO2–15Li2CO3–15Nb2O5–1Er2O3 -(x)Nd2O3 with x =0.2 and 0.6 mol% are successfully made by using conventional melt-quenching technique. The Judd-Ofelt analysis is to determine the local structure and bonding in the vicinity of rare-earth ions. The oscillator strengths are calculated from the absorption spectra and used to evaluate Judd-Ofelt intensity parameters (Ωλ, λ=2, 4 and 6). The values of Ω4 and Ω6 change with the increase of Nd3+ concentration is ascribed to the change in glass network structures. The values of Ω2 are increased from 1.53 to 37.13 (10-22) cm2 with the increase of Nd3+ concentration which indicate an increase in the covalent nature of Nd-O bond and less centrosymmetrical the ion sites. The decrease in τrad for each level with the increase of Nd3+ concentration signifies on how fast a particular level gets depopulated. The values of β for the transitions 4G5/2, 2G7/2 → 4I9/2, 2H11/2 → 4I9/2 and 4F9/2 → 4I9/2 are found to lie in between 99.6 to 100.0%.


Author(s):  
N. M. P. Low ◽  
L. E. Brosselard

There has been considerable interest over the past several years in materials capable of converting infrared radiation to visible light by means of sequential excitation in two or more steps. Several rare-earth trifluorides (LaF3, YF3, GdF3, and LuF3) containing a small amount of other trivalent rare-earth ions (Yb3+ and Er3+, or Ho3+, or Tm3+) have been found to exhibit such phenomenon. The methods of preparation of these rare-earth fluorides in the crystalline solid form generally involve a co-precipitation process and a subsequent solid state reaction at elevated temperatures. This investigation was undertaken to examine the morphological features of both the precipitated and the thermally treated fluoride powders by both transmission and scanning electron microscopy.Rare-earth oxides of stoichiometric composition were dissolved in nitric acid and the mixed rare-earth fluoride was then coprecipitated out as fine granules by the addition of excess hydrofluoric acid. The precipitated rare-earth fluorides were washed with water, separated from the aqueous solution, and oven-dried.


2020 ◽  
Vol 10 (2) ◽  
pp. 152-156 ◽  
Author(s):  
Muhammad Hanif bin Zahari ◽  
Beh Hoe Guan ◽  
Lee Kean Chuan ◽  
Afiq Azri bin Zainudin

Background: Rare earth materials are known for its salient electrical insulation properties with high values of electrical resistivity. It is expected that the substitution of rare earth ions into spinel ferrites could significantly alter its magnetic properties. In this work, the effect of the addition of Samarium ions on the structural, morphological and magnetic properties of Ni0.5Zn0.5SmxFe2-xO4 (x=0.00, 0.02, 0.04, 0.06, 0.08, 0.10) synthesized using sol-gel auto combustion technique was investigated. Methods: A series of Samarium-substituted Ni-Zn ferrite nanoparticles (Ni0.5Zn0.5SmxFe2-xO4 where x=0.00, 0.02, 0.04, 0.06, 0.08, 0.10) were synthesized by sol-gel auto-combustion technique. Structural, morphological and magnetic properties of the samples were examined through X-Ray Diffraction (XRD), Field-Emission Scanning Electron Microscope (FESEM) and Vibrating Sample Magnetometer (VSM) measurements. Results: XRD patterns revealed single-phased samples with spinel cubic structure up to x= 0.04. The average crystallite size of the samples varied in the range of 41.8 – 85.6 nm. The prepared samples exhibited agglomerated particles with larger grain size observed in Sm-substituted Ni-Zn ferrite as compared to the unsubstituted sample. The prepared samples exhibited typical soft magnetic behavior as evidenced by the small coercivity field. The magnetic saturation, Ms values decreased as the Sm3+ concentration increases. Conclusion: The substituted Ni-Zn ferrites form agglomerated particles inching towards more uniform microstructure with each increase in Sm3+ substitution. The saturation magnetization of substituted samples decreases with the increase of samarium ion concentration. The decrease in saturation magnetization can be explained based on weak super exchange interaction between A and B sites. The difference in magnetic properties between the samples despite the slight difference in Sm3+ concentrations suggests that the properties of the NiZnFe2O4 can be ‘tuned’, depending on the present need, through the substitution of Fe3+ with rare earth ions.


Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3717
Author(s):  
Jae-Young Jung ◽  
Soung-Soo Yi ◽  
Dong-Hyun Hwang ◽  
Chang-Sik Son

The precursor prepared by co-precipitation method was sintered at various temperatures to synthesize crystalline manganese tungstate (MnWO4). Sintered MnWO4 showed the best crystallinity at a sintering temperature of 800 °C. Rare earth ion (Dysprosium; Dy3+) was added when preparing the precursor to enhance the magnetic and luminescent properties of crystalline MnWO4 based on these sintering temperature conditions. As the amount of rare earth ions was changed, the magnetic and luminescent characteristics were enhanced; however, after 0.1 mol.%, the luminescent characteristics decreased due to the concentration quenching phenomenon. In addition, a composite was prepared by mixing MnWO4 powder, with enhanced magnetism and luminescence properties due to the addition of dysprosium, with epoxy. To one of the two prepared composites a magnetic field was applied to induce alignment of the MnWO4 particles. Aligned particles showed stronger luminescence than the composite sample prepared with unsorted particles. As a result of this, it was suggested that it can be used as phosphor and a photosensitizer by utilizing the magnetic and luminescent properties of the synthesized MnWO4 powder with the addition of rare earth ions.


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