Luminescence in the Visible Region from Annealed Thin ALD-ZnO Films Implanted with Different Rare Earth Ions

2018 ◽  
Vol 215 (16) ◽  
pp. 1700889 ◽  
Author(s):  
Renata Ratajczak ◽  
Elzbieta Guziewicz ◽  
Slawomir Prucnal ◽  
Grzegorz Łuka ◽  
Roman Böttger ◽  
...  
1986 ◽  
Vol 41 (6) ◽  
pp. 866-870 ◽  
Author(s):  
H.-D. Autenrieth ◽  
S. Kemmler-Sack

By activation of the new host lattices Ba2La2B2+Te2O12 (B = Zn, Mg) with trivalent rare earth ions Ln3+ = Pr. Sm, Eu, Tb, Dy, Ho, Tm an emission in the visible region is observed. The influence of the electronic structure and concentration on the relative emission efficiency as well as the host lattice participation in the energy transfer processes are discussed.


1985 ◽  
Vol 40 (5) ◽  
pp. 503-507 ◽  
Author(s):  
R. Braun ◽  
R. Otto ◽  
W. Wischert ◽  
S. Kemmler-Sack

By activation of the host lattices Sr3La2W2O12 and Ca2La0,5Na0,5WO6 with the trivalent rare earth ions Ln3+ = Pr, Sm, Eu, Tb, Dy, Ho, Er a cathodoluminescence in the visible region is obtained. The influence of the electronic structure and concentration of the activator on the relative emission efficiency as well as the host lattice participation in the energy transfer processes are discussed.


2017 ◽  
Vol 14 (2) ◽  
pp. 140-145 ◽  
Author(s):  
K. Goud ◽  
Ch. Ramesh ◽  
B. Appa Rao

To develop efficient upconversion laser materials in the visible region an active lead borate glasses doped with Er3+/Yb3+ rare earth ions (GEY) has been studied extensively. In this investigation characterization techniques like Optical absorption, FTIR and photoluminescence were recorded and the data was analyzed. To evaluate the values of Ω2, Ω4 and Ω6 Judd-Ofelt theory has been applied to the f ↔ f transitions. Based on Judd–Ofelt theory branching ratio (βr) oscillator strength and the radiative life time (τR) values were determined. The upconversion spectra exhibited three emission bands at around 525 nm (2H11/2 ® 4I15/2), 545 nm (4S3/2 ® 4I15/2) and 660 nm (4F9/2 ® 4I15/2). The energy transfer mechanism between Yb3+ and Er3+ was discussed very clearly. Comparing the data obtained in other Er3+/Yb3+ doped materials, the lead bismuth gallium borate glasses doped with 0.6 mol% of Er2O3­/0.2 mol% of Yb2O3 ions are suitable materials for developing red upconversion lasers in the visible region.


2007 ◽  
Vol 1035 ◽  
Author(s):  
Wojciech M. Jadwisienczak ◽  
Ajay S. Vemuru ◽  
Saima Khan ◽  
Aurangzeb Khan ◽  
Marty E. Kordesch

AbstractWe report on the luminescence of rare earth (RE) (Sm, Er, Tm) ions doped ZnO films grown by the rf-magnetron sputtering technique. Samples were insitu doped with Sm ion or with Sm, Er, and Tm ions simultaneously without any intentional co-dopants and deposited on c-Si or quartz substrates at low temperatures. Selected ZnO:RE samples were thermally annealed in 200ºC-1000ºC temperature range in oxygen or argon gas at ambient pressure. As-grown and annealed samples were amorphous (a-ZnO) as was confirmed by the X-ray analysis. Furthermore, a-ZnO:RE samples were investigated by energy diffraction, photoluminescence and cathodoluminescence. In general, CL spectra of as-grown RE-doped a-ZnO films show characteristic emission lines due to 4f-shell transitions of RE3+ ions. Optical excitation of as-grown a-ZnO doped with RE ions using above the bandgap excitation resulted in strong host emission overlapped with weak RE3+ emission bands. It was observed that a thermal annealing process promotes changes of RE ions' environments resulting in significant 4f-shell transition luminescence intensity quenching.


1994 ◽  
Vol 358 ◽  
Author(s):  
A.J. Kenyon ◽  
P.F. Trwoga ◽  
M. Federighi ◽  
C.W. Pitt

ABSTRACTWe report the fabrication of rare-earth doped silicon-rich silica thin films by PECVD. The films exhibit absorption edges in the visible region of the optical spectrum consistent with the presence of silicon microclusters. Weak visible photoluminescence due to silicon microclusters is observed. In addition, strong luminescence from the rare-earth ion is obtained even when excited away from characteristic absorption bands; indeed, the luminescence intensity is largely independent of excitation wavelength below 514 nm. We ascribe this to excitation of silicon microclusters followed by an efficient transfer of energy to the rare-earth ions.The very broad absorption of this material opens up the possibility for flashlamp-pumped optoelectronic devices. In addition, we report the fabrication of silicon-rich silica films by PECVD. We show that the optical properties of these films are consistent with the presence of silicon microclusters and show absorption spectra similar to those of the rare-earth doped silicon-rich silica samples. This supports the hypothesis that the principal absorbing species in the rare-earth doped films is microclustered silicon


1986 ◽  
Vol 41 (10) ◽  
pp. 1228-1232 ◽  
Author(s):  
R. Otto ◽  
S. Kemmler-Sack

By activation of the host Gd3Te2Li3O12 with the trivalent rare earth ions Ln3+ = Pr, Sm, Eu, Tb-Tm and of Y3Te2Li3O12 with Ln3+ = Pr, Eu, Tb a cathodoluminescence in the visible region is obtained. The influence of the electronic structure and concentration of the activator on the relative emission efficiency as well as the host lattice participation in the energy transfer processes are discussed.


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.


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