scholarly journals SPECTROSCOPIC PROPERTIES OF SOLIDIFIED MELTS OF THE EuF3-CeF3-NaCl-KCl SYSTEM

2020 ◽  
Vol 86 (10) ◽  
pp. 120-128
Author(s):  
Viktor Zinchenko ◽  
Oleg Ieriomin ◽  
Valerii Antonovich ◽  
Nataliia Chivireva ◽  
Iryna Stoianova ◽  
...  

The nature of the interaction in the EuF3-CeF3 system in the process of high-temperature (1050 °C) oxidation - reduction reaction was established by the methods of IR transmission spectroscopy, diffuse reflection spectroscopy and fluorescence spectroscopy. Here is a significant bathochromic shift to 480-485 nm band of blue luminescence of Eu(II) - containing phases, due to the 5d–4f electronic transitions, as well as the manifestation of orange-red luminescence of Eu(III) - containing phases due to 4f–4f electronic transitions in the range of 590–690 nm. There is a bathochromic shift of the IR bandwidth in the spectrum of the solidified salt melt as a result of dissolution of the fluoride system. Diffuse reflection spectra reveal changes in the composition of the phases that dissolve in the salt melt due to exchange reactions. The wide absorption band in the UV range gives way to a negative absorption band consisting of two peaks due to luminescence. The almost complete disappearance of the band of 4f–4f transitions in Eu(III) in the near-IR range of the spectrum is evidence of its entire reduction in the chloride melt to Eu(II). The character of the luminescence spectra of solidified salt melts also changes in comparison with the initial sample of the EuF3-CeF3 system, namely, the luminescence band of Ce3+ ions disappears, and the luminescence band of Eu2+ ions at 430–440 nm becomes narrow and highly intensive. The luminescence band of Eu3+ ions in the orange-red region of the spectrum disappears completely. Thus, Eu2+ ions become dominant in the formation of the spectral picture of the solidified salt melt, which is evidence of the completion of the redox process in the system.

2015 ◽  
Vol 16 (1) ◽  
pp. 74-78 ◽  
Author(s):  
O. M. Bordun ◽  
I. Y. Kukharskyy ◽  
B. O. Bordun

Photoexcitation spectra and luminescence of thin films of ZnGa2O4 under photo-, cathode and X-ray excitation were investigated. Luminescence spectra were factorized on ultimate constituents using Alentsev-Fock method. Emission bands with maximums at 3.35, 2.85, 2.50 and 2.38 eV were referred to the luminescence at the expense of electronic transitions between 4Т2, 4Т1, 2Е and 4А2 terms in octahedral complexes (GaO6)9–. It was proposed an energy level diagram with corresponding electronic transitions in such structure. Luminescence band with maximum at 1.75 eV is attributed to oxygen vacancies.


2021 ◽  
Vol 26 (1(77)) ◽  
pp. 26-36
Author(s):  
V. F. Zinchenko ◽  
O. G. Ieriomin ◽  
I. V. Stoianova ◽  
G. V. Volchak ◽  
N. O. Chivireva ◽  
...  

Redox interactions between the components of the SmF3-CeF3 and SmF3-CeF3-NaCl-KCl systems have been established by IR transmission spectroscopy, diffuse reflectance electron spectroscopy and luminescence spectroscopy. A significant decrease in the transparency in the IR range of the spectrum was found when passing from the first of the systems to the second, which is explained by an increase in scattering by ultramicrodispersed particles of fluorides in the salt melt. In both systems, the formation of a significant amount of Sm (II) and a decrease in the content of Sm (III) are observed. The change in the valence state of Samarium both during solid-phase heat treatment (1100 °C) and during holding in a salt melt at 700 °C is manifested in the disappearance of some absorption bands, the appearance of new bands, and a gypsochromic shift of the remaining bands. The luminescence spectra exhibit high-intensity emission bands in the 640–740 nm range, which correspond to 5d‑4f electronic transitions in Sm2+ ions. At the same time, the highest intensity is observed in the band corresponding to intracenter 5d‑4f electronic transitions in Ce3+ ions. Apparently, the Ce(IV) compound, formed as a result of the exchange reaction of complex fluoride with a salt melt, volatilizes with subsequent decomposition and does not affect the character of luminescence. On the whole, the luminescence intensity after treatment in the molten salt increases by several tens of times, which indicates a significant change in the radiation mechanism. The mechanism of redox reactions in the solid-phase state, as well as exchange processes in the salt melt and after its crystallization, is discussed. A significant role of solvation shells around particles of lanthanide fluorides in luminescence processes is assumed.


2015 ◽  
Vol 87 (17) ◽  
pp. 8740-8747 ◽  
Author(s):  
Stephanie A. DeJong ◽  
Zhenyu Lu ◽  
Brianna M. Cassidy ◽  
Wayne L. O’Brien ◽  
Stephen L. Morgan ◽  
...  

Catalysts ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 123 ◽  
Author(s):  
Andrea Bellmann ◽  
Christine Rautenberg ◽  
Ursula Bentrup ◽  
Angelika Brückner

UV–Vis spectroscopy as well as in situ FTIR spectroscopy of pyridine and CO adsorption were applied to determine the nature of Co species in microporous, mesoporous, and mixed oxide materials like Co–ZSM-5, Co/Na–ZSM-5, Co/Al–SBA-15, and Co/Al2O3–SiO2. Because all sample types show comparable UV–Vis spectra with a characteristic band triplet, the former described UV–Vis band deconvolution method for determination and quantification of individual cationic sites in the zeolite appears doubtful. This is also confirmed by results of pyridine and CO adsorption revealing that all Co–zeolite samples contain two types of Co2+ species located at exchange positions as well as in oxide-like clusters independent of the Co content, while in Co/Al–SBA-15 and Co/Al2O3–SiO2 only Co2+ species in oxide-like clusters occur. Consequently, the measured UV–Vis spectra represent not exclusively isolated Co2+ species, and the characteristic triplet band is not only related to γ-, β-, and α-type Co2+ sites in the zeolite but also to those dispersed on the surface of different oxide supports. The study demonstrates that for proper characterization of the formed Co species, the use of complementary methods is required.


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