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Invar effect and solid-state synthesis in Ni/Fe(001)/MgO(001) thin films: structural and magnetic studies / V. G. Myagkov, V. C. Zhigalov, L. E. Bykova, G. N. Bondarenko // Байкальская международная конференция”Магнитные материалы: Новые технологии”, Россия, Иркутск, 2008, С.56

Доп.точки доступа:
Myagkov, V. G.; Мягков, Виктор Григорьевич; Zhigalov, V. S.; Жигалов, Виктор Степанович; Bykova, L. E.; Быкова, Людмила Евгеньевна; Bondarenko, G. N.; Бондаренко, Галина Николаевна
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Synthesis and structure of 4-methyl-3-nitro-1-nitromethyl-1H-1,2,4- triazolium perchlorate [Text] / A. M. Astachov, A. A. Erashov [et al.] // Energetic materials: characterisation, modelling and validation : Proceedings of the 40th International Annual Conference of ICT. - P104

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Доп.точки доступа:
Astachov, A.M.; Erashov, A.A.; Vasiliev, A.D.; Buka, E.S.; "Energetic materials: characterisation, modelling and validation", International Annual Conference of ICT(40 ; 2009 ; June ; 23-26 ; Karlsruhe, Germany)
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Synthesis and magnetic property feature of La0.7Sr0.3MnO3 manganite polycrystalline / Patrin G.S., Polyakova K.P., Patrusheva T.N., Velikanov D.A., Volkov N.V., Balaev D.A., Patrin K.G., Klabukov A.A. // III Байкальская международная конференция, Иркутск, 2008, C. 79

Доп.точки доступа:
Patrin, G. S.; Патрин, Геннадий Семёнович; Polyakova, K. P.; Полякова, Клавдия Павловна; Patrusheva, T. N.; Патрушева, Тамара Николаевна; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Volkov, N. V.; Волков, Никита Валентинович; Balaev, D. A.; Балаев, Дмитрий Александрович; Patrin, K. G.; Патрин, Константин Геннадьевич; Klabukov, A. A.
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Chemical synthesis, crystal structure and electronic parameters of noncentrosymmetric K3WO3F3 [Text] / A. A. Atuchin, V. G. Kesler [et al.] // Proceedings of 4 International forum on strategic technologies (IFOST 2009). - Vol. 3. - P213-215

Доп.точки доступа:
Atuchin, A.A.; Kesler, V.G.; Gavrilova, T.A.; Molokeev, M. S.; Aleksandrov, K. S.; International forum on strategic technologies(4 ; 2009 ; Oct . ; 21-23 ; Ho Chi Minh City, Vietnam)
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Heteronuclear µ-vinylidene complexes containing Re, Cu, Fe, Pt, Pd. Synthesis, structure, IR and NMR spectra [Text] / A. B. Antonova, O. S. Chudin [et al.] // Carbene Chemistry Conference The Ocean Maya. - P. 38

Доп.точки доступа:
Antonova, A.B.; Chudin, O.S.; Rubaylo, A.I.; Pavlenko, N.I.; Sokolenko, W.A.; Verpekin, V.V.; Vasiliev, A.D.; Semeikin, O.V.; Carbene Chemistry Conference The Ocean Maya(2009 ; FEB ; 18-21 ; Playa del Carmen , Mexico)
}
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    Synthesis and properties of the NdSF compound, phase diagram of the NdF3–Nd2S3 system / V. M. Grigorchenko, M. S. Molokeev, A. S. Oreshonkov [et al.] // J. Solid State Chem. - 2024. - Vol. 333. - Ст. 124640, DOI 10.1016/j.jssc.2024.124640. - Cited References: 48. - This research was funded by the Tyumen Oblast Government as part of the West-Siberian Interregional Science and Education Center’s project No. 89-DON (3). - The studies ab initio simulation of electron band structure, analysis of optical properties, XRD analysis was partially supported by "Priority-2030" program for the Siberian Federal University, and the state assignment of Kirensky Institute of Physics . - ISSN 0022-4596. - ISSN 1095-726X
   Перевод заглавия: Синтез и свойства соединения NdSF, фазовая диаграмма системы NdF3–Nd2S3
Кл.слова (ненормированные):
Neodymium fluorosulfide -- Phase diagram -- Optical band gap -- Microhardness
Аннотация: The NdF3–Nd2S3 system attracts attention of researchers due to the possibility of using LnSF compounds (Ln = rare earth element) as possible new p- and n-type materials. The samples of this system were synthesized from NdF3 and Nd2S3. The NdSF compound belongs to the PbFCl structural type, P4/nmm space group, unit cell parameters: a = 3.9331(20) Å, c = 6.9081(38) Å. The experimentally determined direct and indirect NdSF bandgaps are equal to 2.68 eV and 2.24 eV. The electronic band structure was calculated via DFT simulation. The NdSF compound melts congruently at T = 1385 ± 10°С, ΔНm = 40.5 ± 10 kJ/mol, ΔS = 24.4 ± 10 J/mol. The NdSF microhardness is 455 ± 10 HV. Five phase transformations in the NdF3–Nd2S3 system were recorded by DSC; their balance equations were derived. The liquidus of the system calculated from the Redlich–Kister equation is fully consistent with the DSC data.

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Держатели документа:
Tyumen State University, Tyumen, Volodarsky str. 6, 625003, Russia
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Akademgorodok str. 50, Building 38, 660036, Russia
Siberian Federal University, Krasnoyarsk, Svobodnyj av. 79, 660079, Russia
Department of Physical and Applied Chemistry, Kurgan State University, Sovetskaya str. 63/4, Kurgan, 640020, Russia
Institute of Solid State Chemistry, Ural Branch, Russian Academy of Sciences, Yekaterinburg, Pervomaiskaya str. 91, 620990, Russia
Saint-Petersburg State University, 7/9 Universitetskaya Emb., 199034, St. Petersburg, Russia

Доп.точки доступа:
Grigorchenko, V.M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Kertman, A.V.; Abulkhaev, M.U.; Mereshchenko, A.S.; Yurev, I.O.; Shulaev, N.А.; Kamaev, D.N.; Elyshev, A.V.; Andreev, O.V.
}
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    Elucidating elusive quaternary selenide EuCeCuSe3: Synthesis, crystal structure, properties and theoretical studies / M. V. Grigoriev, A. V. Ruseikina, M. S. Molokeev [et al.] // J. Rare Earths. - 2024. - Vol. 42, Is. 1. - P. 163-171, DOI 10.1016/j.jre.2022.11.004. - Cited References: 47 . - ISSN 1002-0721. - ISSN 2509-4963
   Перевод заглавия: Расшифровка труднодоступного четвертичного селенида EuCeCuSe3: синтез, кристаллическая структура, свойства и теоретические исследования
Кл.слова (ненормированные):
Quaternary selenide -- Synthesis -- Crystal structure -- Ab initio calculations -- Magnetic measurements -- Spectroscopy
Аннотация: We report on the novel heterometallic quaternary selenide EuCeCuSe3, the fabrication of which has been a challenge until this work. The structure of the reported selenide was elucidated from the powder X-ray diffraction data, which revealed the formation of EuCeCuSe3 with excellent yield (96.7%) accompanied with a minor fraction of CeSe2 (3.3%), and was best solved in orthorhombic space group Pnma with the BaLaCuS3 structural type. Thus, the crystal structure of the title compound completes the row of the heterometallic quaternary selenides EuRECuSe3 (RE = La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Y), of which the cerium-based derivative exclusively belongs to the BaLaCuS3 structural type. The distortion of the CuSe4 polyhedron was compared for the whole series of EuRECuSe3 compounds using the τ4-descriptor for four coordinated ions, which revealed the highest degree of distortion for the Ce3+-containing selenide, followed by the La3+-based derivative. Furthermore, the crystallographic and geometrical parameters of the reported selenide were discussed in comparison to the Ce3+-based sulfides SrCeCuS3 and EuCeCuS3. Ab initio calculations of the crystal structure, a phonon spectrum and elastic constants for the crystal of EuСeCuSe3 were also performed. The types and wavenumbers of fundamental modes were determined and the involvement of ions participating in the phonon modes was assessed. The experimental IR spectrum of the reported selenide was interpreted and found to be in agreement with the calculated spectrum. The experimental direct band gap of EuCeCuSe3 was measured to be 1.36 eV that is consistent with the concept of its origin due to interband transitions between orbitals emerging mainly from 4f (valence band) and 5d (conduction band) levels of the Eu2+ cation. The dependence of the Young's modulus on the direction demonstrates the anisotropy of the elastic properties, while the Vickers hardness for EuCeCuSe3 was calculated to be 5.2 GPa. Finally, the title compound is paramagnetic above 4 K.

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Держатели документа:
Laboratory of Theory and Optimization of Chemical and Technological Processes, University of Tyumen, Volodarskogo Str. 6, 625003, Tyumen, Russian Federation
Research and Development Department, Kemerovo State University, Krasnaya Str. 6, 650000, Kemerovo, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50 Bld. 38, 660036, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Serysheva Str. 47, 680021, Krasnoyarsk, Russian Federation
Institute of Natural Sciences and Mathematics, Ural Federal University Named After the First President of Russia B.N. Yeltsin, Mira Str. 19, 620002, Ekaterinburg, Russian Federation
Department of Photonics and Laser Technology, Siberian Federal University, Svobodnii Ave. 79, 660079, Krasnoyarsk, Russian Federation
Institute of Physics and Technology, University of Tyumen, Volodarskogo Str. 6, 625003 Tyumen, Russian Federation
Institute for Inorganic Chemistry, University of Stuttgart, Pfaffenwaldring 55, D-70569, Stuttgart, Germany
Advanced Materials for Industry and Biomedicine Laboratory, Kurgan State University, Sovetskaya Str. 63/4, 640020, Kurgan, Russian Federation
Innovation Center for Chemical and Pharmaceutical Technologies, Ural Federal University Named After the First President of Russia B.N. Yeltsin, Mira Str. 19, 620002, Ekaterinburg, Russian Federation
University of Tyumen, Volodarskogo Str. 6, 625003, Tyumen, Russian Federation

Доп.точки доступа:
Grigoriev, Maxim V.; Ruseikina, Anna V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chernyshev, Vladimir А.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Krylova, S. N.; Крылова, Светлана Николаевна; Shestakov, N. P.; Шестаков, Николай Петрович; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Garmonov, Alexander A.; Matigorov, Alexey V.; Ostapchuk, Evgeny A.; Schleid, Thomas; Safin, Damir A.
}
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Synthesis of Ni nanoclusters supported on diamond by plasma technique and their electrochemical properties / N. S. Nikolaev, V. G. Isakova, N. G. Vnukova [et al.] // Diam. Relat. Mater. - 2024. - Vol. 142. - Ст. 110844, DOI 10.1016/j.diamond.2024.110844. - Cited References: 35 . - ISSN 0925-9635. - ISSN 1879-0062
Кл.слова (ненормированные):
High pressure – high temperature (HTHP) diamond -- Nickel plasma -- Cyclic voltammetric -- Electrocatalytic activity -- Methanol -- Paracetamol
Аннотация: In this study, particles of synthetic undoped diamond (DN) obtained via the high pressure – high temperature method were coated with a nickel shell using metallic nickel plasma in a two-jet plasma generator with gas vortex and magnetic flux stabilization. Through the use of scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy, we observed the formation of a nickel diamond composite with a core-shell structure, where DN serves as the core and Ni nanoclusters form the shell (DN@Ni). The results of voltammetric analysis indicated that DN@Ni, when deposited on a graphite electrode, exhibited significant electrocatalytic activity in the oxidation of methanol and paracetamol in an alkaline electrolyte.

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Держатели документа:
Kirensky Institute of Physics, FSBSI "Federal Research Center "Krasnoyarsk Science Center SB RAS", Akademgorodok 50/38, Krasnoyarsk 660036, Russia
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Academician Kirensky str., 28, Krasnoyarsk 660074, Russia
Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences, FSBSI "Federal Research Center "Krasnoyarsk Science Center SB RAS", Akademgorodok 50/24, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Nikolaev, N. S.; Николаев, Никита Сергеевич; Isakova, V. G.; Исакова, Виктория Гавриловна; Vnukova, N. G.; Внукова, Наталья Григорьевна; Elesina, V. I.; Елесина, Виктория Игоревна; Glushenko, G. A.; Глущенко, Гарий Анатольевич; Tomashevich, Y. V.; Томашевич, Евгений Владимирович; Churilov, G. N.; Чурилов, Григорий Николаевич
}
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Microbially mediated synthesis of vivianite by Desulfosporosinus on the way to phosphorus recovery / Yu. V. Knyazev, M. S. Platunov, O. P. Ikkert [et al.] // Environ. Sci.: Adv. - 2024. - Vol. 3, Is. 6. - P. 897-911, DOI 10.1039/D4VA00040D. - Cited References: 120. - This study was supported by the Russian Science Foundation, project no. 22-24-00601 (https://rscf.ru/project/22-24-00601/). The electron microscopy and Mössbauer studies were carried out on the equipment of the Krasnoyarsk Territorial Center for Collective Use, Krasnoyarsk Scientific Center, Siberian Branch of the Russian Academy of Sciences. The research contribution of M. S. P. was partially supported by the Ministry of Science and Higher Education of the Russian Federation within the governmental assignment for Synchrotron radiation facility “SKIF”, Boreskov Institute of Catalysis (project FWUR-2024-0040) . - ISSN 2754-7000
Аннотация: We explored the role of biomineralization in industrial waste sludge formation, using the laboratory cultivation of Desulfovibrio sp. OL sulfate reducing species isolated from the Komsomolsky waste sludge (Russia). The most frequently reported sulfate-reducing bacteria (SRB) biomineralization products are various iron sulfides. Here we present first studies of the products of Desulfosporosinus metallidurans, acidophilic SRB from acid mine drainage. We analyzed the biomineralized sample using X-ray diffraction, electron microscopy, X-ray absorption and Mossbauer spectroscopies, and magnetization measurements via First-Order Reversal Curve (FORC) diagram analysis. Our findings show that the biomineralization occurring under pure culture conditions leads to the formation of greigite (Fe3S4) nanorods, along with larger microbially mediated crystals of vivianite (Fe3(PO4)2·8H2O) and siderite (FeCO3). Energy dispersive X-ray spectroscopy revealed that the crystal sizes of vivianite and siderite were comparatively larger than those of the nanorod-shaped greigite. Transmission electron microscopy and Mossbauer spectroscopy detected ultrafine ferrihydrite (Fe2O3·nH2O) superparamagnetic nanoparticles with an average size of 2.5 nm. FORC analysis showed significant magnetic interactions among these nanoparticles, suggesting their potential for magnetic separation applications. The current study demonstrates that ferrihydrite nanoparticles have a strong magnetic affinity for other crystal phases produced by Desulfosporosinus metallidurans. Therefore, we believe that the investigated bacterial species can be exploited in advanced magnetic separation techniques. This offers a cost-effective and environmentally friendly method for purifying sediments in industrial waste sludge.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia
Department of Plant Physiology, Biotechnology, and Bioinformatics, Tomsk State University, Tomsk, Russia
Synchrotron Radiation Facility SKIF, Boreskov Institute of Catalysis SB RAS, Kol'tsovo, Russia
Budker Institute of Nuclear Physics, Novosibirsk, Russia
Siberian Federal University, Krasnoyarsk, Russia
Institute of Solid State Chemistry and Mechanochemistry, Novosibirsk, Russia

Доп.точки доступа:
Knyazev, Yu. V.; Князев, Юрий Владимирович; Platunov, M. S.; Ikkert, O. P.; Semenov, S. V.; Семёнов, Сергей Васильевич; Bayukov, O. A.; Баюков, Олег Артемьевич; Nikolenko, A. D.; Nazmov, V. P.; Volochaev, M. N.; Волочаев, Михаил Николаевич; Dubrovskiy, A. A.; Дубровский, Андрей Александрович; Molokeev, M. S.; Молокеев, Максим Сергеевич; Smorodina, E. D.; Balaev, D. A.; Балаев, Дмитрий Александрович; Karnachuk, O. V.
}
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10.

    Solid state synthesis, structural, DFT and spectroscopic analysis of EuAl3(BO3)4 / A. S. Oreshonkov, A. S. Aleksandrovsky, O. D. Chimitova [et al.] // Mater. Chem. Phys. - 2024. - Vol. 320. - Ст. 129400, DOI 10.1016/j.matchemphys.2024.129400. - Cited References: 55. - The work was carried out within the state assignment No FWES-2024-0003 of Kirensky Institute of Physics. This work was partially supported by the state order of BINM SB RAS (0273-2021-0008). The samples for this research were synthesized using equipment of the CCU BINM SB RAS. The reflectance spectrum was obtained at the Center for Optical and Laser Materials Research of Research park of St. Petersburg State University. The SEM measurements were performed at Krasnoyarsk Regional Center of Research Equipment of Federal Research Center "Krasnoyarsk Science Center SB RAS" . - ISSN 0254-0584. - ISSN 1879-3312
   Перевод заглавия: Твердофазный синтез, структурный, квантово-химический (DFT) и спектроскопический анализ EuAl3(BO3)4
Кл.слова (ненормированные):
EuAl(BO) -- Huntite -- X-ray diffraction -- SEM -- DFT -- Charge transfer -- Raman -- Infrared -- Luminescence
Аннотация: Huntite-like borates are versatile and promising materials with wide range of applications in frequency conversion, UV light generation, lighting, displays, quantum information storage, and more, demonstrated by their various properties and uses in scientific research. In this work, EuAl3(BO3)4 powder was prepared through multi-stage solid-state reaction method using high-purity starting reagents: Eu2O3, Al2O3 and H3BO3, considering a 20 wt% excess of H3BO3 to compensate for B2O3 volatilization. Obtained samples undergo several treatments at varying temperatures and their phase purity is subsequently verified through powder X-ray diffraction analysis. The scanning electron microscopy reveals that resulting EuAl3(BO3)4 powder consists of granules exhibiting irregular morphologies with dimensions of 0.5–8 μm. The electronic band structure of EuAl3(BO3)4, calculated using the GGA PBE method, reveals f-states of Eu near 4 eV. These states do not produce emphasized peaks on simulated absorbance spectra. Using of DFT + U for the f-states of Eu pushed up f-bands above 6 eV and the charge transfer from p-O to d-Eu was obtained (Egdirect = 5.63 eV, Egindirect = 5.37 eV using Ueff = 4 eV). The variation of Ueff has a weak influence on the position of the bottom of the conduction band. The experimental bandgaps of EuAl3(BO3)4 crystalline powder, both direct and indirect, are found to be 3.96 and 3.67 eV, correspondingly. These values are lower than theoretical values what is associated with limitations of DFT calculations involving f electrons. The Raman spectrum of EuAl3(BO3)4 powder is discussed, detailing the contributions of different ions to specific spectral bands. Investigation of high-resolution luminescence spectra shows the possibility to estimate the content of defects by the testing the violation of the prohibition of ultranarrow 5D0 → 7F0 line that is forbidden in the ideal crystalline structure of trigonal EuAl3(BO3)4.

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Держатели документа:
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
School of Engineering and Construction, Siberian Federal University, Krasnoyarsk, 660041, Russia
Laboratory of Coherent Optics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, Krasnoyarsk, 660041, Russia
Laboratory of Oxide Systems, Baikal Institute of Nature Management, SB RAS, Ulan-Ude, 670047, Russia
Center for Optical and Laser Materials Research, Saint-Petersburg State University, Saint-Petersburg, 199034, Russia
Emanuel Institute of Biochemical Physics of Russian Academy of Sciences, Moscow, 119334, Russia
Plekhanov Russian University of Economics, Moscow, 117997, Russia
Moscow Institute of Physics and Technology, Dolgoprudny, 141700, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
School of Engineering Physics and Radio Electronics, Siberian Federal University, Krasnoyarsk, 660041, Russia
Institute of Automation and Electrometry, Russian Academy of Sciences, Novosibirsk, 630090, Russia
Department of Molecular Electronics, Federal Research Center Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences, Krasnoyarsk, 660036, Russia
Institute of Fundamental Biology and Biotechnology, Siberian Federal University, Krasnoyarsk, 660041, Russia

Доп.точки доступа:
Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Chimitova, O.D.; Pankin, D.V.; Popov, Z.I.; Sukhanova, E.V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Adichtchev, S.V.; Pugachev, A.M.; Nemtsev, I. V.; Немцев, Иван Васильевич
}
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11.

    Soldatenko, A. S.
    N-silylmethyl-2-(1-naphthyl)acetamides: Synthesis, structure and computational screening / A. S. Soldatenko, M. S. Molokeev, N. F. Lazareva // Curr. Org. Chem. - 2024. - Vol. 28, Is. 12. - P. 959-966, DOI 10.2174/0113852728296495240409062733. - Cited References: 75. - This work was supported by the Russian Science Foundation using the analytical equipment of the Baikal Center for Collective Use of the SB RAS and the analytical equipment of the Krasnoyarsk Center for Collective Use of SB RAS. M.S. Molokeev’s work was carried out within the framework of the Strategic Academic Leadership Program "Priority-2030" for the Siberian Federal University . - ISSN 1385-2728. - ISSN 1875-5348
   Перевод заглавия: N-силилметил-2-(1-нафтил)ацетамиды: синтез, структура и вычислительный скрининг
Кл.слова (ненормированные):
N-organyl-2-(1-naphthyl)-N-(silylmethyl)acetamides -- NMR spectroscopy -- X-ray diffraction analysis -- computational screening -- PASS -- ADME
Аннотация: Synthesis of new hybrid organosilicon compounds based on the amides 1- naphthylacetic acid was described. N-Organyl-2-(1-naphthyl)-N-[(triethoxysilyl)methyl]- acetamides were obtained by the reaction of 1-naphthylacetyl chloride with α-silylamines RNHCH2Si(OEt)3 (R = Me, i-Pr and Ph). Their subsequent interaction with N(CH2CH2OH)3 led to the formation of N-organyl-2-(1-naphthyl)-N-(silatranylmethyl)acetamides. The structure of these hybrid compounds was characterized by 1H, 13C, and 29Si NMR spectroscopy. The structure of N-methyl- and N-isopropyl-2-(1-naphthyl)-N-(silatranylmethy)acetamides was confirmed by X-ray diffraction analysis. Results of computational screening showed that these silatranes are bioavailable and have drug-likeness.

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Держатели документа:
Siberian Division of the Russian Academy of Sciences, A.E. Favorsky Irkutsk Institute of Chemistry, 1 Favorsky Street, Irkutsk 664033, Russia
Laboratory of Crystal Physics, Federal Research Center KSC SB RAS, Kirensky Institute of Physics, Krasnoyarsk 660036, Russia
Institute of Engineering Physics and Radio Electronic, Siberian Federal University, Krasnoyarsk 660041, Russia

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Lazareva, N. F.
}
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12.

Synthesis, structure and magnetic properties of monoclinic lanthanum-chromium borate LaCr3(BO3)4 / E. A. Volkova, M. S. Platunov, A. M. Antipin [et al.] // J. Alloys Compd. - 2024. - Vol. 994. - Ст. 174683, DOI 10.1016/j.jallcom.2024.174683. - Cited References: 38. - Single crystal X-ray analysis was carried out within the State assignment NRC "Kurchatov institute" (research contribution of A.M.A.). The research contribution of M.S.P. was partially supported by the Ministry of Science and Higher Education of the Russian Federation within the governmental assignment for Synchrotron radiation facility "SKIF", Boreskov Institute of Catalysis (project FWUR-2024–0040) . - ISSN 0925-8388. - ISSN 1873-4669
Кл.слова (ненормированные):
Borates -- Flux growth -- Crystal structure -- Differential scanning calorimetry -- Powder X-ray diffraction -- IR spectroscopy -- Antiferromagnet
Аннотация: Single crystals of LaCr3(BO3)4 were synthesized through spontaneous nucleation from a K2Mo3O10 flux melt. The crystal structure was determined using single-crystal X-ray diffraction (XRD) at temperatures of 293 K and 85 K. LaCr-borate crystallizes in the monoclinic C2/c space group with unit cell parameters a = 7.47980(5) Å, b = 9.55180(7) Å, c = 11.48330(8) Å, β= 104.0060(6)°, V = 796.04(1) Å3 (for C1, T = 293 K), and a = 7.47380(5) Å, b = 9.55520(7) Å, c = 11.47100(8) Å, β = 103.9330(6)°, V = 795.08(1) Å3 (for C2, T = 85 K), each with Z = 4. The temperature dependence of the unit cell parameters, including the monoclinic angle (β) and the unit cell volume (V), was investigated over the range of 85–293 K. No structural phase transitions were observed in the low-temperature region down to 85 K. Differential scanning calorimetry (DSC) measurements revealed no high-temperature phase transitions between 50 and 1350°C. Infrared (IR) spectroscopy confirmed the monoclinic structure of LaCr3(BO3)4 crystals, revealing characteristic absorption bands, including the lowest frequency mode associated with the translational vibrations of the La3+ ion.

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Держатели документа:
Faculty of Geology, Lomonosov Moscow State University, Moscow, Russian Federation
Synchrotron radiation facility SKIF, Boreskov Institute of Catalysis SB RAS, Kol’tsovo, Russian Federation
Shubnikov Institute of Crystallography, Complex "Crystallography and Photonics", NRC "Kurchatov institute", Moscow, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Krasnoyarsk, Russian Federation
Melnikov Research Institute of Comprehensive Exploitation of Mineral Resources of the Russian Academy of Sciences, Moscow, Russian Federation

Доп.точки доступа:
Volkova, E. A.; Platunov, M. S.; Платунов, Михаил Сергеевич; Antipin, A. M.; Alpanova, R. R.; Dubrovskiy, A. A.; Дубровский, Андрей Александрович; Pyastolova, Yu. V.; Пястолова, Юлия Валентиновна; Podobraznyh, A. D.; Kosorukov, V. L.; Koporulina, E. V.; Maltsev, V. V.
}
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13.

Synthesis and study of superhigh-concentrated organosols of silver nanoparticles / S. A. Vorobyev, M. Yu. Flerko, S. A. Novikova [et al.] // Colloid J. - 2024. - Vol. 86, Is. 2. - P. 208-217, DOI 10.1134/S1061933X23601294. - Cited References: 33. - The work was carried out with the financial support of the basic project FWES-2021-0014 of the Institute of Chemistry and Chemical Technology, Siberian Branch, Russian Academy of Sciences, and the Federal Program "Priority 2030" using the equipment of the Krasnoyarsk regional center for collective use of the Federal Research Center Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences . - ISSN 1061-933X. - ISSN 1608-3067
Кл.слова (ненормированные):
silver nanoparticles (NPs) -- concentrated silver organosols -- phase transfer of nanoparticles -- X-ray photoelectron spectroscopy (XPS) -- transmission electron microscopy (TEM) -- conductive silver films
Аннотация: Due to their unique properties, organosols of silver nanoparticles are widely used in optical and semiconductor devices, to produce electrically and thermally conductive films, as catalysts, antibacterial materials, etc. This work proposes a simple and highly productive method for the preparation of silver organosols, which have a metal concentration as high as 1800 g/L and contain spherical nanoparticles with low polydispersity and a median size of 9.1 nm. The method consists in the initial preparation of silver nanoparticle hydrosols with a concentration of higher than 30 g/L followed by the transfer of the NPs into an organic phase of o-xylene. A set of physical research methods has been employed to study the regularities of the extraction of silver nanoparticles with o-xylene in the presence of cetyltrimethylammonium bromide (CTAB) and ethanol and to determine the optimal process conditions, under which the extraction degree is as high as 62.5%. It has been found that bromine anions contained in CTAB molecules cause the aggregation of some amount of silver nanoparticles with the formation of silver metal sediment in the aqueous phase. According to X-ray photoelectron spectroscopy data, the sediment contains bromide ions (up to 4 at %) on the particle surface. Organosols synthesized under optimal conditions are stable for more than 7 months and withstand repeated cycles of drying and redispersing. Silver organosols have been used to obtain metal films with an electrical conductivity of about 68 500 S/cm, which increases to 412 000 and 509 500 S/cm (87.8% of the electrical conductivity of bulk silver) after thermal treatment at 150 and 250°C, respectively.

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Institute of Chemistry and Chemical Technology, Siberian Branch, Russian Academy of Sciences, 660036, Krasnoyarsk, Russia
Siberian Federal University, 660041, Krasnoyarsk, Russia
Kirenskii Institute of Physics, Siberian Branch, Russian Academy of Sciences, 660036, Krasnoyarsk, Russia
Tomsk National Research State University, 634050, Tomsk, Russia

Доп.точки доступа:
Vorobyev, S. A.; Flerko, M. Yu.; Novikova, S. A.; Mazurova, E. V.; Tomashevich, Ye. V.; Likhatski, M. N.; Saikova, S. V.; Samoilo, A. S.; Zolotovsky, N. A.; Золотовский, Н. А.; Volochaev, M. N.; Волочаев, Михаил Николаевич
}
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14.

    Получение и активация TiO2 фотонно- кристаллических структур для повышения эффективности реакции фотоэлектрохимического разложения воды / Т. А. Кенова, Н. А. Зосько, М. В. Пятнов [и др.] // Журн. СФУ. Химия. - 2024. - Т. 17, № 1. - С. 27-38 ; J. Sib. Fed. Univ. Chem. - Библиогр.: 25. - Исследование выполнено за счет гранта Российского научного фонда и Красноярского краевого фонда поддержки научной и научно-технической деятельности № 22-22-20078, https://rscf.ru/project/22-22-20078/ с использованием оборудования Красноярского регионального центра коллективного пользования ФИЦ КНЦ СО РАН . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Synthesis and activation of TiO2 photonic crystal structures for enhanced photoelectrochemical water splitting
Кл.слова (ненормированные):
фотонно-кристаллические TiO2 наноструктуры -- активация TiO2 фотонных кристаллов -- фотоэлектрохимическая активность -- разложение воды -- photonic-crystal TiO2 nanostructures -- TiO2 photonic crystals activation -- photoelectrochemical activity -- water splitting
Аннотация: Наноструктурированные фотонно-кристаллические пленки TiO2 анодно синтезированы при импульсном и ступенчатом изменениях напряжения. Полученные фотонные структуры активированы методом циклической вольтамперометрии в 0,5M Na2SO4. Фотоэлектрохимическая активность электродов исследована в реакции разложения воды в области длин волн 360–700 нм. Активация приводит к изменению энергии запрещенной зоны, красному сдвигу спектра IPCE и увеличению его значений в исследованном диапазоне длин волн.
TiO2 photonic crystal nanostructure films are anodic synthesized with pulsed and stepwise voltage changes. The obtained photonic structures were activated by cyclic voltammetry in 0.5M Na2SO4. The photoelectrochemical activity of the electrodes was studied in the water splitting reaction in the wavelength range 360–700 nm. Activation leads to a change in the band gap energy, a red shift in the IPCE spectrum and an increase in its values in the studied wavelength range.

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Держатели документа:
Институт химии и химической технологии СО РАН ФИЦ "Красноярский научный центр СО РАН", Российская Федерация, Красноярск
Институт физики им. Л.В. Киренского СО РАН ФИЦ "Красноярский научный центр СО РАН", Российская Федерация, Красноярск
Сибирский федеральный университет, Российская Федерация, Красноярск

Доп.точки доступа:
Кенова, Т. А.; Зосько, Н. А.; Пятнов, Максим Владимирович; Pyatnov, M. V.; Александровский, Александр Сергеевич; Aleksandrovsky, A. S.; Максимов, Н. Г.; Жижаев, А. М.; Таран, О. П.

}
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15.

Features of the melt–solution synthesis of the TbCr3(BO3)4 single crystals / I. A. Gudim, N. V. Mikhashenok, A. D. Vasiliev [et al.] // J. Cryst. Growth. - 2024. - Vol. 637-638. - Ст. 127716, DOI 10.1016/j.jcrysgro.2024.127716. - Cited References: 22. - The authors thank A.V. Zamkov for assistance in preparing the samples for the conoscopic study. The characterization and examination of the samples were performed at the Center for Collective Use, Krasnoyarsk Scientific Center, Siberian Branch of the Russian Academy of Sciences. - This study was supported in part by the Russian Science Foundation and the Krasnoyarsk Territorial Foundation for Support of Scientific and R&D Activity, project no. 22-12-20019 . - ISSN 0022-0248. - ISSN 1873-5002
Кл.слова (ненормированные):
Growth from melt-solution -- Single crystal growth -- Cromium borates -- Rare-earth compounds -- Oxides -- Magnetic materials
Аннотация: The phase formation of terbium chromoborate TbCr3(BO3)4 in the bismuth trimolybdate and lithium tungstate melt–solutions has been studied. The absence of the terbium chromoborate trigonal phase in the bismuth trimolybdate-based system at all component ratios has been shown. The component ratio in the lithium tungstate-based system has been found at which the TbCr3(BO3)4 trigonal crystals are formed at temperatures above 1100 °C; below this temperature, the monoclinic phase dominates. The structural and magnetic properties of the grown crystals have been studied. It has been established that the trigonal and monoclinic TbCr3(BO3)4 crystals synthesized from the lithium tungstate-based solvent exhibit identical magnetic properties. At the same time, a significant difference of the magnetic properties of the single crystals synthesized from the bismuth molybdate melt–solution has been observed. This difference has been attributed to the effect of Bi3+ ions that partially replace Tb3+ ions.

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Держатели документа:
Kirensky Institute of Physics, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk 660036 Russia

Доп.точки доступа:
Gudim, I. A.; Гудим, Ирина Анатольевна; Mikhashenok, N. V.; Михашенок, Наталья Владимировна; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Melnikova, S. V.; Мельникова, Светлана Владимировна; Pavlovskii, M. S.; Павловский, Максим Сергеевич; Skorobogatov, S. A.; Скоробогатов, Станислав Алексеевич; Pankrats, A. I.; Панкрац, Анатолий Иванович
}
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16.

Copper ferrite nanoparticles synthesized using anion-exchange Resin: Influence of synthesis parameters on the cubic phase stability / S. Saikova, A. Pavlikov, D. Karpov [et al.] // Materials. - 2023. - Vol. 16, Is. 6. - Ст. 2318, DOI 10.3390/ma16062318. - Cited References: 67. - The Russian team acknowledges the support of the Russian Science Foundation (Project 22-73-10047) . - ISSN 1996-1944
Кл.слова (ненормированные):
copper ferrite -- magnetic properties -- anion-exchange resin precipitation -- magnetic nanoparticles
Аннотация: Copper ferrite is of great interest to researchers as a material with unique magnetic, optical, catalytic, and structural properties. In particular, the magnetic properties of this material are structurally sensitive and can be tuned by changing the distribution of Cu and Fe cations in octahedral and tetrahedral positions by controlling the synthesis parameters. In this study, we propose a new, simple, and convenient method for the synthesis of copper ferrite nanoparticles using a strongly basic anion-exchange resin in the OH form. The effect and possible mechanism of polysaccharide addition on the elemental composition, yield, and particle size of CuFe2O4 are investigated and discussed. It is shown that anion-exchange resin precipitation leads to a mixture of unstable cubic (c-CuFe2O4) phases at standard temperature and stable tetragonal (t-CuFe2O4) phases. The effect of reaction conditions on the stability of c-CuFe2O4 is studied by temperature-dependent XRD measurements and discussed in terms of cation distribution, cooperative Jahn–Teller distortion, and Cu2+ and oxygen vacancies in the copper ferrite lattice. The observed differences in the values of the saturation magnetization and coercivity of the prepared samples are explained in terms of variations in the particle size and structural properties of copper ferrite.

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Держатели документа:
School of Non-Ferrous Metals and Material Science, Siberian Federal University, 660041 Krasnoyarsk, Russia
Institute of Chemistry and Chemical Technology, Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, Akademgorodok, 660036 Krasnoyarsk, Russia
Kirensky Institute of Physics, Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, Akademgorodok, 660036 Krasnoyarsk, Russia
Department of Physics and Astronomy, Uppsala University, P.O. Box 516, SE-751 20 Uppsala, Sweden

Доп.точки доступа:
Saikova, Svetlana; Pavlikov, Aleksandr; Karpov, Denis; Samoilo, Aleksandr; Kirik, Sergey; Volochaev, M. N.; Волочаев, Михаил Николаевич; Trofimova, Tatyana; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Kuklin, Artem
}
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17.

    Synthesis, structures and magnetic properties of the Eu-based quaternary tellurides EuGdCuTe3 and EuLuCuTe3 / A. V. Ruseikina, M. V. Grigoriev, A. A. Garmonov [et al.] // CrystEngComm. - 2023. - Vol. 25, Is. 12. - P. 1716-1722, DOI 10.1039/D2CE01578A. - Cited References: 41. - This research was funded by the Tyumen Oblast Government, as part of the West-Siberian Interregional Science and Education Center's project No. 89-DON (3) . - ISSN 1466-8033
   Перевод заглавия: Синтез, структура и магнитные свойства четверных теллуридов EuGdCuTe3 и EuLuCuTe3 на основе Eu
Аннотация: Novel heterometallic quaternary tellurides EuGdCuTe3 and EuLuCuTe3 are reported for the first time. Both compounds were obtained from the elements as single crystals using the flux-assisted synthetic approach. The crystal structure of EuGdCuTe3 was solved in orthorhombic space group Pnma with the structural type Eu2CuS3, while the crystal structure of EuLuCuTe3 belongs to orthorhombic space group Cmcm with the structural type KZrCuS3. The 3D crystal structure of EuGdCuTe3 is constructed from EuTe7 capped trigonal prisms, GdTe6 distorted octahedra as well as CuTe4 tetrahedra. The octahedra form 2D layers, further strengthened by 1D polymeric chains (CuTe4)n. These layers are separated by 1D dimeric ribbons, formed by EuTe7 capped trigonal prisms and 1D free channels. The 3D crystal structure of EuLuCuTe3 is constructed from EuTe6 trigonal prisms, LuTe6 distorted octahedra and CuTe4 tetrahedra. The latter two polyhedra also form 2D layers, which are separated by alternating 1D polymeric chains (EuTe6)n and 1D free channels. Both tellurides were found to be paramagnetic with the transition to a ferrimagnetic state at about 8 K for EuGdCuTe3 and to a ferromagnetic state at about 3 K for EuLuCuTe3.

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Держатели документа:
Laboratory of Theory and Optimization of Chemical and Technological Processes, University of Tyumen, Tyumen, Russian Federation
Institute for Inorganic Chemistry, University of Stuttgart, Stuttgart, Germany
Institute of Physics and Technology, University of Tyumen, Tyumen, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Scientific and Educational and Innovation Center for Chemical and Pharmaceutical Technologies, Ural Federal University named after the First President of Russia B.N. Yeltsin, Ekaterinburg, Russian Federation
University of Tyumen, Tyumen, Russian Federation

Доп.точки доступа:
Ruseikina, Anna V.; Grigoriev, Maxim V.; Garmonov, Alexander A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Schleid, Thomas; Safin, Damir A.
}
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18.

Muzalevsky, K. V.
Synthesis of an ultra-wideband pulse by a log-periodic antenna with continuous excitation by harmonic oscillations / K. V. Muzalevsky // Radiophys. Quantum Electron. - 2023. - Vol. 65, Is. 8. - P. 615-623, DOI 10.1007/s11141-023-10242-2. - Cited References: 38. - This work was supported by the Russian Science Foundation and the Krasnoyarsk Regional Science Foundation (project No. 22–17–20042) . - ISSN 0033-8443. - ISSN 1573-9120
Аннотация: We propose a method for synthesizing ultra-wideband pulses using a vector network analyzer and a wideband transceiving log-periodic antenna. The transfer characteristic of the antenna-feeder transmission line of the system is described by the model of a two-port network whose S-matrix elements are calibrated for at least two heights of the antenna above the reflecting surface (metal plate). The proposed method of calibrating the transfer characteristic of a log-periodic antenna allows one to minimize the amplitude- and phase-frequency distortions, which are introduced to the sensing pulse by the antenna. Employing the developed method, we experimentally demonstrate a possibility of synthesizing an ultra-wideband pulse with a duration of 0.46 ns at the level of half amplitude of the envelope (when the pulse contains several field oscillations) using a log-periodic antenna with a passband of 1.36 to 4.88 GHz (at the level −10 dB). This method is specially developed for creating miniature radar systems using portable vector network analyzers and log-periodic antennas for applications to remote sensing of an underlying surface by ultra-wideband pulses from small-size unmanned aerial vehicles.

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Публикация на русском языке Музалевский, Константин Викторович. Синтезирование сверхширокополосного импульса логопериодической антенной с непрерывным возбуждением гармоническими колебаниями [Текст] / К. В. Музалевский // Изв. вузов. Радиофиз. - 2022. - Т. 65 № 8. - С. 677-686

Держатели документа:
L. V. Kirenskii Institute of Physics of Siberian Branch of the Russian Academy of Sciences, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Музалевский, Константин Викторович
}
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19.

Microwave-assisted synthesis of the new solid-solution (V1–xCrx)2GaC (0 ≤ x ≤ 1), a Pauli paramagnet almost matching the Stoner criterion for x = 0.80 / N. Kubitza, R. Xie, I. Tarasov [et al.] // Chem. Mater. - 2023. - Vol. 35, Is. 11. - P. 4427-4434, DOI 10.1021/acs.chemmater.3c00591. - Cited References: 54. - This work has been supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) within CRC/TRR 270, projects B03 and B02, A05 (Project-ID 405553726) . - ISSN 0897-4756. - ISSN 1520-5002
Аннотация: MAX phases that exhibit long-range magnetic order in the bulk are still very hard to synthesize. Chromium and manganese are the cutoff elements when transitioning through the 3dmetals that still form stable full and doped MAX phases, respectively. An iron-based (on the M-site) bulk MAX phase does not exist. Therefore, other strategies to induce long-range magnetic ordering in bulk MAX phases are necessary to open the path to new functional materials. Here, we demonstrate the nonconventional synthesis of a hitherto unknown MAX phase solid-solution (V1–xCrx)2GaC by microwave heating. The full series with 0 ˂ x ˂ 1 (x = 0.20, 0.40, 0.50, 0.60, 0.80) forms almost single phase with minimal differences in their morphology. Their magnetic properties, however, differ rather significantly, with a maximum susceptibility around x = 0.80. Both the experimental and theoretical/ab initio magnetic analysis confirm that the solid-solution (V1–xCrx)2GaC is an itinerant Pauli paramagnet that almost fulfills the Stoner criterion for ferromagnetic order (for compositions with x around 0.80). This is a powerful insight into how chemical composition couples with electronic structure and the resulting bulk magnetic properties because it provides crucial guidelines to produce long-range ordered magnetic MAX phases.

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Department of Chemistry, Technische Universität Darmstadt, 64287 Darmstadt, Germany
Institute of Materials Science, Technische Universität Darmstadt, 64287 Darmstadt, Germany
Faculty of Physics and Center for Nanointegration Duisburg-Essen, University of Duisburg-Essen, 47057 Duisburg, Germany

Доп.точки доступа:
Kubitza, Niels; Xie, Ruiwen; Tarasov, I. A.; Тарасов, Иван Анатольевич; Shen, Chen; Zhang, Hongbin; Wiedwald, Ulf; Birkel, Christina S.
}
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20.

    Structural and spectroscopic effects of Li+ substitution for Na+ in LixNa1–xCaLa0.5Er0.05Yb0.45(MoO4)3 upconversion scheelite-type phosphors / C. S. Lim, A. Aleksandrovsky, M. Molokeev [et al.] // Crystals. - 2023. - Vol. 13, Is. 2. - Ст. 362, DOI 10.3390/cryst13020362. - Cited References: 63. - This study was funded by the Research Program through the Campus Research Foundation funded by Hanseo University in 2022 (2022046) . - ISSN 2073-4352
   Перевод заглавия: Структурные и спектроскопические эффекты замещения Na+ на Li+ в LixNa1-xCaLa0.5Er0.05Yb0.45(MoO4)3 ап-конверсионных люминофорах типа шеелита
Кл.слова (ненормированные):
microwave sol-gel synthesis -- complex molybdate -- scheelite -- crystal structure -- Raman -- frequency up-conversion -- band structure
Аннотация: New triple molybdates LixNa1−xCaLa0.5(MoO4)3:Er3+0.05/Yb3+0.45 (x = 0, 0.05, 0.1, 0.2, 0.3) were manufactured successfully using the microwave-assisted sol-gel-based technique (MAS). Their room-temperature crystal structures were determined in space group I41/a by Rietveld analysis. The compounds were found to have a scheelite-type structure. In Li-substituted samples, the sites of big cations were occupied by a mixture of (Li, Na, La, Er, Yb) ions, which provided a linear cell volume decrease with the Li content increase. The increased upconversion (UC) efficiency and Raman spectroscopic properties of the phosphors were discussed in detail. The mechanism of optimization of upconversion luminescence upon Li content variation was shown to be due to the control of excitation/energy transfer channel, while the control of luminescence channels played a minor role. The UC luminescence maximized at lithium content x = 0.05. The mechanism of UC optimization was shown to be due to the control of excitation/energy transfer channel, while the control of luminescence channels played a minor role. Over the whole spectral range, the Raman spectra of LixNa1−xCaLa0.5(MoO4)3 doped with Er3+ and Yb3+ ions were totally superimposed with the luminescence signal of Er3+ ions, and increasing the Li+ content resulted in the difference of Er3+ multiple intensity. The density functional theory calculations with the account for the structural disorder in the system of Li, Na, Ca, La, Er and Yb ions revealed the bandgap variation from 3.99 to 4.137 eV due to the changing of Li content. It was found that the direct electronic transition energy was close to the indirect one for all compounds. The determined chromaticity points (ICP) of the LiNaCaLa(MoO4)3:Er3+,Yb3+ phosphors were in good relation to the equal-energy point in the standard CIE (Commission Internationale de L’Eclairage) coordinates.

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Department of Aerospace Advanced Materials and Chemical Engineering, Hanseo University, Seosan 31962, Republic of Korea
Laboratory of Coherent Optics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, 660041 Krasnoyarsk, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, 660041 Krasnoyarsk, Russia
Department of Physics, Far Eastern State Transport University, 680021 Khabarovsk, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
School of Engineering and Construction, Siberian Federal University, 660041 Krasnoyarsk, Russia
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, 630090 Novosibirsk, Russia
Research and Development Department, Kemerovo State University, 650000 Kemerovo, Russia
Department of Industrial Machinery Design, Novosibirsk State Technical University, 630073 Novosibirsk, Russia
R&D Center “Advanced Electronic Technologies”, Tomsk State University, 634034 Tomsk, Russia

Доп.точки доступа:
Lim, Chang S.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Atuchin, V.
}
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