scholarly journals Transition Metals (Cr3+) and Lanthanides (Eu3+) in Inorganic Glasses with Extremely Different Glass-Formers B2O3 and GeO2

Materials ◽  
2021 ◽  
Vol 14 (23) ◽  
pp. 7156
Author(s):  
Karolina Kowalska ◽  
Marta Kuwik ◽  
Justyna Polak ◽  
Joanna Pisarska ◽  
Wojciech A. Pisarski

Glasses containing two different network-forming components and doped with optically active ions exhibit interesting properties. In this work, glass systems based on germanium dioxide and boron trioxide singly doped with lanthanides (Eu3+) and transition metals (Cr3+) ions are research subjects. Optical spectroscopy was the major research tool used to record excitation and emission spectra in a wide spectral range for studied systems. The emitted radiation of glasses doped with Cr3+ ions is dominated by broadband luminescence centered at 770 nm and 1050 nm (4T2 → 4A2). Interestingly, the increase of concentration of one of the oxides contributed to the detectable changes of the R-line (2E → 4A2) of Cr3+ ions. Moreover, EPR spectroscopy confirmed the paramagnetic properties of the obtained glasses. The influence of molar ratio GeO2:B2O3 on spectroscopic properties for Eu3+ ions is discussed. The intensity of luminescence bands due to transitions of trivalent europium ions as well as the ratio R/O decrease with the increase of B2O3. On the other hand, the increase in concentration B2O3 influences the increasing tendency of luminescence lifetimes for the 5D0 state of Eu3+ ions. The results will contribute to a better understanding of the role of the glass host and thus the prospects for new optical materials.

Nanomaterials ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 27
Author(s):  
Sara Targonska ◽  
Rafal J. Wiglusz

In this paper, a series of structurally modified silicate-substituted apatite co-doped with Sr2+ and Eu3+ ions were synthesized by a microwave-assisted hydrothermal method. The concentration of Sr2+ ions was set at 2 mol% and Eu3+ ions were established in the range of 0.5–2 mol% in a molar ratio of calcium ion amount. The XRD (X-ray powder diffraction) technique and infrared (FT-IR) spectroscopy were used to characterize the obtained materials. The Kröger–Vink notation was used to explain the possible charge compensation mechanism. Moreover, the study of the spectroscopic properties (emission, emission excitation and emission kinetics) of the obtained materials as a function of optically active ions and annealing temperature was carried out. The luminescence behavior of Eu3+ ions in the apatite matrix was verified by the Judd–Ofelt (J-O) theory and discussed in detail. The temperature-dependent emission spectra were recorded for the representative materials. Furthermore, the International Commission on Illumination (CIE) chromaticity coordinates and correlated color temperature were determined by the obtained results.


2020 ◽  
Vol 981 ◽  
pp. 73-77
Author(s):  
Nurul Ainaa Najihah Busra ◽  
Ramli Arifin ◽  
Sib Krishna Ghoshal ◽  
Rodziah Nazlan

Enhancing the optical performance of rare earth doped binary inorganic glasses is an ever-demanding quest. Samarium (Sm3+) doped zinc tellurite glasses containing Manganese (Mn) nanoparticles (NPs) with composition (59-x)TeO2-20ZnCl2-10ZnO-10Li2O-1Sm2O3-(x)Mn3O4, where x = 0 to 0.06 mol% are prepared by melt quenching technique. The role played by Mn NPs in enhancing the optical behaviors are analyzed and discussed. The XRD patterns confirm the amorphous nature of the glass. The UV-Vis-NIR spectra reveal seven prominent absorption bands of Sm3+ ions. The photoluminescence spectra display four peaks corresponding to 4G5/2→6H5/2, 4G5/2 →6H7/2, 4G5/2→6H9/2 and 4G5/2 →6H11/2 transitions. An enhancement in the luminescence intensity is observed up to 0.05 mol% concentration of NPs and the intensity quenches beyond it. The enhancement is attributed to local electric field effect of NPs in the proximity of Sm3+ ion. Our results on improved optical response via precise control of NPs contents may be useful for the development of solid state lasers and amplifiers.


2017 ◽  
Vol 91 (1) ◽  
pp. 92-107 ◽  
Author(s):  
M. V. Sambasiva Rao ◽  
A. Suneel Kumar ◽  
G. Chinna Ram ◽  
Ch. Tirupataiah ◽  
D. Krishna Rao

2016 ◽  
Vol 242 ◽  
pp. 29-37 ◽  
Author(s):  
Abhishek Kumar Gupta ◽  
Yogendra Lal Verma ◽  
Manish Pratap Singh ◽  
Rajendra Kumar Singh
Keyword(s):  

1984 ◽  
Vol 23 (19) ◽  
pp. 3010-3017 ◽  
Author(s):  
David E. Morris ◽  
Yasuhiko Ohsawa ◽  
Donald P. Segers ◽  
M. Keith DeArmond ◽  
Kenneth W. Hanck

1988 ◽  
Vol 66 (9) ◽  
pp. 2219-2228 ◽  
Author(s):  
John M. Goodings ◽  
Quang Tran ◽  
Nicholas S. Karellas

The same fuel-rich, premixed, conical, methane–oxygen flame at 2200 K and atmospheric pressure used for studies of Fe, Co, Ni, Cu, and Zn in Part I (1) is doped with the same concentration (~1 ppm) of Sc, Ti, V, Cr, and Mn to complete the first row of ten transition metals. Metallic ions of these metals and their compounds formed by chemical ionization reactions with H3O+ are observed by sampling the flame through a nozzle into a quadrupole mass spectrometer. Concentration profiles of individual and total cations are measured as a function of distance along the flame axis, and also mass spectra at a fixed point in the burnt gas. If A is the metal atom, the observed ions can be represented by four hydrate series including (a) A+•nH2O, (b) AOH+•nH2O, (c) AO+•nH2O, and (d) AO2H+•nH2O with n = 0–3 or 4, giving a maximum of four ligands around the metal atom. However, alternative isomeric structures are possible for each of the four basic series (e.g. AO+•2H2O ~ A(OH)2+•H2O ~ A(OH)3H+). The ions observed with Cr and Mn, in common with those of Fe, Co, Ni, and Cu, strongly favour series (a). On the other hand, Sc is completely different; the ions of series (c) are dominant. All four series are observed with each of Ti and V. Series (b) dominates for Ti and series (c) for V; ions from series (d) were observed for the first time. The ion chemistry of these metals is discussed in detail with emphasis on the probable chemical ionization reactions responsible for metallic ion formation. The pre-eminent role of proton transfer processes is apparent.


Holzforschung ◽  
2014 ◽  
Vol 68 (4) ◽  
pp. 477-486 ◽  
Author(s):  
Myung Jae Lee ◽  
Sedric Pankras ◽  
Paul Cooper

Abstract Canadian refractory wood species treated with micronized copper (MCu) wood preservative become mottled and streaky in appearance. To overcome this issue, the MCu system was modified by adding small amounts of monoethanolamine (Mea). The modified systems were evaluated to clarify the role of Mea in terms of leaching, corrosion, and mold resistance of MCu systems. The mottled and streaky surface on treated spruce was prevented at Mea/Cu molar ratios between 0.7 and 1.5. Copper leaching remained modest and was only slightly higher than that of MCu alone up to a Mea/Cu molar ratio of 1.2. However, adding even a small amount of Mea to the MCu formulation increased fastener corrosion compared with MCu. Protonated Mea increased as more Mea was added and was identified as the main corrosion-causing electrolyte in the system.


2011 ◽  
Vol 335-336 ◽  
pp. 1035-1038
Author(s):  
Qi Sang ◽  
Shao Jun Wang ◽  
Xue Rong Wang ◽  
Jing Wen Lu

A series of the Yb3+ -doped phosphate laser glass have been prepared under high temperature and different doping content and the fluorescence and absorption spectrum is observed, respectively. The influences of the Yb3+ -doped content on the spectral properties of the glass are analyzed and the optimal mole fraction is 4 %. The emission cross-section and fluorescent lifetime is calculated with McCumber theory. Furthermore, the integrated absorption cross-section, the full width at half maximum of the emission spectra and the laser performance parameters such as least particle count, saturation pump intensity and lowest pump intensity of Yb3+ -doped laser glass is calculated.


2018 ◽  
Vol 45 (2) ◽  
pp. 150 ◽  
Author(s):  
Vitaly A. Sineshchekov ◽  
Larissa A. Koppel ◽  
Cordelia Bolle

Phytochrome A (phyA) mediates different photoresponses what may be connected with the existence of its two types, phyAʹ and phyAʹʹ, differing by spectroscopic, photochemical and functional properties. We investigated a role of phyA phosphorylation in their formation turning to transgenic Arabidopsis thaliana (L. Heynh.) phyA or phyAphyB mutants overexpressing rice wild-type phyA (phyA WT) or mutant phyA (phyA SA) with the first 10 serines substituted by alanines. This prevents phyA phosphorylation at these sites and modifies photoresponses. Etiolated seedlings were employed and phyA parameters were evaluated with the use of low temperature fluorescence spectroscopy and photochemistry. Germination of seeds was induced by white light (WL) pre-treatment for 15 min or 3 h. Emission spectra of rice phyA WT and phyA SA were similar and their total content was comparable. However, the phyAʹ/phyAʹʹ proportion in phyA WT was high and varied with the duration of the WL pre-treatment, whereas in phyA SA it was substantially shifted towards phyAʹʹ and did not depend on the pre-illumination. This suggests that phyA SA comprises primarily or exclusively the phyAʹʹ pool and supports the notion that the two phyA types differ by the state of serine phosphorylation. phyAʹʹ was also found to be much more effective in the germination induction than phyAʹ.


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