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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Myagkov V. G., Zhigalov V. S., Bykova L. E., Bondarenko G. N.
Заглавие : Invar effect and solid-state synthesis in Ni/Fe(001)/MgO(001) thin films: structural and magnetic studies
Место публикации : Байкальская международная конференция”Магнитные материалы: Новые технологии”, Россия, Иркутск, 2008, С.56
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Вид документа : Статья из сборника (однотомник)
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Автор(ы) : Astachov A.M., Erashov A.A., Vasiliev A.D., Buka E.S.
Заглавие : Synthesis and structure of 4-methyl-3-nitro-1-nitromethyl-1H-1,2,4- triazolium perchlorate
Коллективы : "Energetic materials: characterisation, modelling and validation", International Annual Conference of ICT
Место публикации : Energetic materials: characterisation, modelling and validation: Proceedings of the 40th International Annual Conference of ICT. - С. 104
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Вид документа : Статья из сборника (однотомник)
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Автор(ы) : Patrin G. S., Polyakova K. P., Patrusheva T. N., Velikanov D. A., Volkov N. V., Balaev D. A., Patrin K. G., Klabukov A. A.
Заглавие : Synthesis and magnetic property feature of La0.7Sr0.3MnO3 manganite polycrystalline
Место публикации : III Байкальская международная конференция, Иркутск, 2008, C. 79
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Atuchin A.A., Kesler V.G., Gavrilova T.A., Molokeev M. S., Aleksandrov K. S.
Заглавие : Chemical synthesis, crystal structure and electronic parameters of noncentrosymmetric K3WO3F3
Коллективы : International forum on strategic technologies
Место публикации : Proceedings of 4 International forum on strategic technologies (IFOST 2009). - Vol. 3. - С. 213-215
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Antonova A.B., Chudin O.S., Rubaylo A.I., Pavlenko N.I., Sokolenko W.A., Verpekin V.V., Vasiliev A.D., Semeikin O.V.
Заглавие : Heteronuclear µ-vinylidene complexes containing Re, Cu, Fe, Pt, Pd. Synthesis, structure, IR and NMR spectra
Коллективы : Carbene Chemistry Conference The Ocean Maya
Место публикации : Carbene Chemistry Conference The Ocean Maya. - P.38
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Grigorchenko V.M., Molokeev M. S., Oreshonkov A. S., Aleksandrovsky A. S., Kertman A.V., Abulkhaev M.U., Mereshchenko A.S., Yurev I.O., Shulaev N.А., Kamaev D.N., Elyshev A.V., Andreev O.V.
Заглавие : Synthesis and properties of the NdSF compound, phase diagram of the NdF3–Nd2S3 system
Колич.характеристики :9 с
Место публикации : J. Solid State Chem. - 2024. - Vol. 333. - Ст.124640. - ISSN 00224596 (ISSN), DOI 10.1016/j.jssc.2024.124640. - ISSN 1095726X (eISSN)
Примечания : 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
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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Grigoriev, Maxim V., Ruseikina, Anna V., Molokeev M. S., Chernyshev, Vladimir А., Aleksandrovsky A. S., Krylov A. S., Krylova S. N., Shestakov N. P., Velikanov D. A., Garmonov, Alexander A., Matigorov, Alexey V., Ostapchuk, Evgeny A., Schleid, Thomas, Safin, Damir A.
Заглавие : Elucidating elusive quaternary selenide EuCeCuSe3: Synthesis, crystal structure, properties and theoretical studies
Колич.характеристики :9 с
Место публикации : J. Rare Earths. - 2024. - Vol. 42, Is. 1. - P.163-171. - ISSN 10020721 (ISSN), DOI 10.1016/j.jre.2022.11.004. - ISSN 25094963 (eISSN)
Примечания : Cited References: 47
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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Nikolaev N. S., Isakova V. G., Vnukova N. G., Elesina V. I., Glushenko G. A., Tomashevich Y. V., Churilov G. N.
Заглавие : Synthesis of Ni nanoclusters supported on diamond by plasma technique and their electrochemical properties
Колич.характеристики :6 с
Место публикации : Diam. Relat. Mater. - 2024. - Vol. 142. - Ст.110844. - ISSN 09259635 (ISSN), DOI 10.1016/j.diamond.2024.110844. - ISSN 18790062 (eISSN)
Примечания : Cited References: 35
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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Knyazev Yu. V., Platunov M. S., Ikkert O. P., Semenov S. V., Bayukov O. A., Nikolenko A. D., Nazmov V. P., Volochaev M. N., Dubrovskiy A. A., Molokeev M. S., Smorodina E. D., Balaev D. A., Karnachuk O. V.
Заглавие : Microbially mediated synthesis of vivianite by Desulfosporosinus on the way to phosphorus recovery
Колич.характеристики :15 с
Место публикации : Environ. Sci.: Adv. - 2024. - Vol. 3, Is. 6. - P.897-911. - ISSN 27547000 (eISSN), DOI 10.1039/D4VA00040D
Примечания : 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)
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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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Oreshonkov A. S., Aleksandrovsky A. S., Chimitova O.D., Pankin D.V., Popov Z.I., Sukhanova E.V., Molokeev M. S., Adichtchev S.V., Pugachev A.M., Nemtsev I. V.
Заглавие : Solid state synthesis, structural, DFT and spectroscopic analysis of EuAl3(BO3)4
Колич.характеристики :10 с
Место публикации : Mater. Chem. Phys. - 2024. - Vol. 320. - Ст.129400. - ISSN 02540584 (ISSN), DOI 10.1016/j.matchemphys.2024.129400. - ISSN 18793312 (eISSN)
Примечания : 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"
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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11.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Soldatenko A. S., Molokeev M. S., Lazareva N. F.
Заглавие : N-silylmethyl-2-(1-naphthyl)acetamides: Synthesis, structure and computational screening
Колич.характеристики :8 с
Место публикации : Curr. Org. Chem. - 2024. - Vol. 28, Is. 12. - P.959-966. - ISSN 13852728 (ISSN), DOI 10.2174/0113852728296495240409062733. - ISSN 18755348 (eISSN)
Примечания : 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
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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12.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Volkova E. A., Platunov M. S., Antipin A. M., Alpanova R. R., Dubrovskiy A. A., Pyastolova Yu. V., Podobraznyh A. D., Kosorukov V. L., Koporulina E. V., Maltsev V. V.
Заглавие : Synthesis, structure and magnetic properties of monoclinic lanthanum-chromium borate LaCr3(BO3)4
Колич.характеристики :9 с
Место публикации : J. Alloys Compd. - 2024. - Vol. 994. - Ст.174683. - ISSN 0925-8388, DOI 10.1016/j.jallcom.2024.174683. - ISSN 1873-4669
Примечания : 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)
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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13.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : 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., Volochaev M. N.
Заглавие : Synthesis and study of superhigh-concentrated organosols of silver nanoparticles
Колич.характеристики :10 с
Место публикации : Colloid J. - 2024. - Vol. 86, Is. 2. - P.208-217. - ISSN 1061933X (ISSN), DOI 10.1134/S1061933X23601294. - ISSN 16083067 (eISSN)
Примечания : 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
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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14.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Кенова Т. А., Зосько Н. А., Пятнов, Максим Владимирович, Александровский, Александр Сергеевич, Максимов Н. Г., Жижаев А. М., Таран О. П.
Заглавие : Получение и активация TiO2 фотонно- кристаллических структур для повышения эффективности реакции фотоэлектрохимического разложения воды
Колич.характеристики :12 с
Место публикации : Журн. СФУ. Химия. - 2024. - Т. 17, № 1. - С. 27-38. - ISSN 19982836 (ISSN); J. Sib. Fed. Univ. Chem. - ISSN 23136049 (eISSN)
Примечания : 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
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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15.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Gudim I. A., Mikhashenok N. V., Vasiliev A. D., Melnikova S. V., Pavlovskii M. S., Skorobogatov S. A., Pankrats A. I.
Заглавие : Features of the melt–solution synthesis of the TbCr3(BO3)4 single crystals
Колич.характеристики :6 с
Место публикации : J. Cryst. Growth. - 2024. - Vol. 637-638. - Ст.127716. - ISSN 00220248 (ISSN), DOI 10.1016/j.jcrysgro.2024.127716. - ISSN 18735002 (eISSN)
Примечания : 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 SciencesThis 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
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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16.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Saikova, Svetlana, Pavlikov, Aleksandr, Karpov, Denis, Samoilo, Aleksandr, Kirik, Sergey, Volochaev M. N., Trofimova, Tatyana, Velikanov D. A., Kuklin, Artem
Заглавие : Copper ferrite nanoparticles synthesized using anion-exchange Resin: Influence of synthesis parameters on the cubic phase stability
Место публикации : Materials. - 2023. - Vol. 16, Is. 6. - Ст.2318. - ISSN 19961944 (eISSN), DOI 10.3390/ma16062318
Примечания : Cited References: 67. - The Russian team acknowledges the support of the Russian Science Foundation (Project 22-73-10047)
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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17.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ruseikina, Anna V., Grigoriev, Maxim V., Garmonov, Alexander A., Molokeev M. S., Schleid, Thomas, Safin, Damir A.
Заглавие : Synthesis, structures and magnetic properties of the Eu-based quaternary tellurides EuGdCuTe3 and EuLuCuTe3
Место публикации : CrystEngComm. - 2023. - Vol. 25, Is. 12. - P.1716-1722. - ISSN 14668033 (eISSN), DOI 10.1039/D2CE01578A
Примечания : 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)
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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18.

Вид документа : Статья из журнала
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Автор(ы) : Muzalevsky K. V.
Заглавие : Synthesis of an ultra-wideband pulse by a log-periodic antenna with continuous excitation by harmonic oscillations
Место публикации : Radiophys. Quantum Electron. - 2023. - Vol. 65, Is. 8. - P.615-623. - ISSN 00338443 (ISSN), DOI 10.1007/s11141-023-10242-2. - ISSN 15739120 (eISSN)
Примечания : Cited References: 38. - This work was supported by the Russian Science Foundation and the Krasnoyarsk Regional Science Foundation (project No. 22–17–20042)
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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19.

Вид документа : Статья из журнала
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Автор(ы) : Kubitza, Niels, Xie, Ruiwen, Tarasov I. A., Shen, Chen, Zhang, Hongbin, Wiedwald, Ulf, Birkel, Christina S.
Заглавие : 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
Место публикации : Chem. Mater. - 2023. - Vol. 35, Is. 11. - P.4427-4434. - ISSN 08974756 (ISSN), DOI 10.1021/acs.chemmater.3c00591. - ISSN 15205002 (eISSN)
Примечания : 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)
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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20.

Вид документа : Статья из журнала
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Автор(ы) : Lim, Chang S., Aleksandrovsky A. S., Molokeev M. S., Oreshonkov A. S., Atuchin V.
Заглавие : Structural and spectroscopic effects of Li+ substitution for Na+ in LixNa1–xCaLa0.5Er0.05Yb0.45(MoO4)3 upconversion scheelite-type phosphors
Место публикации : Crystals. - 2023. - Vol. 13, Is. 2. - Ст.362. - ISSN 20734352 (eISSN), DOI 10.3390/cryst13020362
Примечания : Cited References: 63. - This study was funded by the Research Program through the Campus Research Foundation funded by Hanseo University in 2022 (2022046)
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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