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Cerenkov nonlinear diffraction of femtosecond pulses in random nonlinear photonic crystal / A. M. Vyunishev [et al.] // Third Russia-Taiwan School-Seminar on Nonlinear Optics and Photonics : Program and Book of Abstracts. - 2013. - Ст. S1-11-O30. - P. 20

Доп.точки доступа:
Vyunishev, A. M.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Zaitsev, A. I.; Зайцев, Александр Иванович; Slabko, V. V.; Слабко, Виталий Васильевич; Russia-Taiwan School-Seminar on Nonlinear Optics and Photonics (3 ; 2013 ; Jun. ; 14-18 ; Владимир / Суздаль)
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    X-ray structure of S,S¢-dimethyl-N-nitroimidodithiocarbamate / F. M. Astachov [et al.] // Proc. 17th Semi. on New Trends in Res. of Energetic Mater. - 2014. - P. 533-537. - Poster see: Abctracts, P. 512 . - ISBN 978-80-7395-770-4
   Перевод заглавия: Рентгеновская структура S,S¢-диметил-N-нитроимидодитиокарбамата
Аннотация: The molecule of S,S’-dimethyl-N-nitroimidodithiocarbonate (I) is highly planar(except H-atoms of methyl groups). In contrast to derivatives of nitroguanidine bond lengths of nitrimine fragment C=N-NO2 of (I) have normal distances in compliance with traditional valence formula. The molecule of (I)is characterized by the presense of the shortened intramolecular S...O contact. This conformation is stabilized via electrostatic attraction forces involving oppositely charged oxygen and sulphur atoms. The feature of the crystal structure of (I) is a low energy of crystal lattice.

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Доп.точки доступа:
Astachov, F. M.; Vasil'ev, A. D.; Васильев, Александр Дмитриевич; Antishin, D. V.; Buka, E. S.; "New trends in research of energetic materials", international seminar (17 ; 2014 ; апр. ; 9-11 ; Pardubice, Czech Republic)
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    Low-temperature synthesis and structural properties of ferroelectric K 3WO3F3 elpasolite / V. V. Atuchin [et al.] // Chem. Phys. Lett. - 2010. - Vol. 493, Is. 1-3. - P. 83-86, DOI 10.1016/j.cplett.2010.05.023. - Cited References: 37 . - ISSN 0009-2614
Рубрики:
PEROVSKITE-LIKE OXYFLUORIDES
   CORE-LEVEL SPECTROSCOPY
   PHASE-TRANSITIONS
   SOLID-STATE
   ELECTRON-DIFFRACTION
   DIFFUSE-SCATTERING
   RHEED ANALYSIS
   POLAR
   BEHAVIOR
   (NH4)(3)TIOF5
Кл.слова (ненормированные):
Chemical synthesis -- Elpasolite -- Ferroelectric phase transition -- Fluorine atoms -- Low temperature synthesis -- Low temperatures -- Oxyfluorides -- Partial ordering -- Room temperature -- SEM -- Space Groups -- Structure parameter -- XRD -- Chemical properties -- Ferroelectric materials -- Ferroelectricity -- Fluorine -- Oxygen -- Phase transitions -- Rietveld method -- Single crystals -- Synthesis (chemical) -- X ray photoelectron spectroscopy -- X ray powder diffraction -- Scanning electron microscopy
Аннотация: Low-temperature ferroelectric G2 polymorph of K3WO 3F3 has been prepared by chemical synthesis. Structural and chemical properties of the final product have been evaluated with X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Structure parameters of G2-K 3WO3F3 are refined by the Rietveld method from XRD data measured at room temperature (space group Cm, Z = 2, a = 8.7350(3), b = 8.6808(5), c = 6.1581(3), ? = 135.124(3), V = 329.46(3) 3; RB = 2.47%). Partial ordering of oxygen and fluorine atoms has been found over anion positions. Mechanism of ferroelectric phase transition in A2BMO3F3 oxyfluorides is discussed. В© 2010 Elsevier B.V. All rights reserved.

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Держатели документа:
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russian Federation
Laboratory of Nanolithography and Nanodiagnostics, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russian Federation
Laboratory of Physical Principles for Integrated Microelectronics, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russian Federation
Laboratory of Crystal Physics, Institute of Physics, SB RAS, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Atuchin, V. V.; Gavrilova, T. A.; Kesler, V. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrov, K. S.; Александров, Кирилл Сергеевич
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Hierarchical structure investigations of biogenic ferrihydrite samples / M. Balasoiu [et al.] // Rom. J. Phys. - 2010. - Vol. 55, Is. 7-8. - P. 782-789. - Cited References: 21. - The work was accomplished with the financial support of Grant 224/11.04.2008 of Romanian Governmental Plenipotentiary at JINR. . - ISSN 1221-146X

РУБ Physics, Multidisciplinary
Рубрики:
ELECTRON NANODIFFRACTION
   6-LINE FERRIHYDRITE
   SYNTHETIC 2-LINE
   FERROFLUIDS
Кл.слова (ненормированные):
ferrihydrite nanoparticles -- Klebsiella oxytoca bacteria -- optical microscopy -- SEM -- SAXS
Аннотация: Results of observation and preliminary analysis on morphology and structure of ferrihydrite particles produced in vivo by Klebsiella oxytoca bacteria are presented. In particular, optical microscopy, scanning electron microscopy and small angle X-ray scattering in accordance with one another point out the fractal structure of the biomineral particle surface. The effect of the bacteria age (the duration of growth) on the fractal dimension is established and characterized.

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Держатели документа:
[Balasoiu, M.] Horia Hulubei Natl Inst Phys & Nucl Engn, Bucharest, Romania
[Stolyar, S. V.
Iskhakov, R. S.
Ishchenko, L. A.] Siberian Fed Univ, Krasnoyarsk 660041, Russia
[Raikher, Yu. L.] RAS, Ural Branch, Inst Continuum Media Mech, Perm 614013, Russia
[Balasoiu, M.
Kuklin, A. I.
Orelovich, O. L.
Kovalev, Yu. S.
Arzumanian, G. M.] Joint Inst Nucl Res, Dubna 141980, Russia
[Kurkin, T. S.] RAS, Inst Synthet Polymer Mat, Moscow 117393, Russia
[Stolyar, S. V.
Iskhakov, R. S.] RAS, Siberian Branch, Inst Phys, Krasnoyarsk 660036, Russia
ИФ СО РАН

Доп.точки доступа:
Balasoiu, M.; Stolyar, S. V.; Столяр, Сергей Викторович; Iskhakov, R. S.; Исхаков, Рауф Садыкович; Ishchenko, L. A.; Raikher, Y. L.; Kuklin, A. I.; Orelovich, O. L.; Kovalev, Y. S.; Kurkin, T. S.; Arzumanian, G. M.
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    Structural and spectroscopic properties of self-activated monoclinic molybdate BaSm2(MoO4)4 / V. V. Atuchin [et al.] // J. Alloys Compd. - 2017. - Vol. 729. - P. 843-849, DOI 10.1016/j.jallcom.2017.07.259. - Cited References: 60. - This work was supported by the National Natural Science Foundation of China (U1632146). The reported study was funded by RFBR according to the research projects 16-52-48010, 16-32-00351, 17-02-00920 and 17-52-53031. Also, the work was supported by (Act 211) the Government of the Russian Federation, contract 02.A03.21.0011, by Project № 0356-2015-0412 of SB RAS Program№II. 2P, and by the Ministry of Education and Science of the Russian Federation (4.1346.2017/PP). . - ISSN 0925-8388
   Перевод заглавия: Структурные и спектроскопические свойства самоактивируемого моноклинного молибдата BaSm2(MoO4)4
Кл.слова (ненормированные):
Coordination -- Crystal structure -- Luminescence -- Raman -- SEM -- Synthesis
Аннотация: The crystal structure of new monoclinic molybdate BaSm2(MoO4)4 is refined in monoclinic unit cell C2/m with cell parameters a = 5.29448 Å, b = 12.7232 Å, c = 19.3907 Å, β = 91.2812°, V = 1305.89 Å3. The crystal structure consists of the SmO8 square antiprism joined with each other by the edges forming a 2D layer perpendicular to the c-axis. MoO4 tetrahedra join SmO8 by nodes and also participate in layer formation, and Ba ions are located between these layers. The lattice dynamics is theoretically calculated on the base of the crystal structure data. The Raman spectra are recorded and analyzed in comparison with theoretical calculations. The discrepancy between the experimental and calculated Raman frequencies does not exceed 2 cm−1 for the most of Raman lines. The luminescence spectra of Sm3+ ions, which are positioned in the lowest local symmetry site C1, strongly differ from those detected for another molybdate crystal, β-RbSm(MoO4)2, with the C2 local symmetry. The 4G5/2 → 6H9/2 band is dominating in the BaSm2(MoO4)4 luminescence.

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Держатели документа:
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, Russian Federation
Functional Electronics Laboratory, Tomsk State University, Tomsk, Russian Federation
Laboratory of Single Crystal Growth, South Ural State University, Chelyabinsk, Russian Federation
Laboratory of Coherent Optics, Kirensky Institute of Physics, Federal Research Center KSC, SB RAS, Krasnoyarsk, Russian Federation
Laboratory for Nonlinear Optics and Spectroscopy, Siberian Federal University, Krasnoyarsk, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center, KSC SB RAS, Krasnoyarsk, Russian Federation
Department of Photonics and Laser Technologies, Siberian Federal University, Krasnoyarsk, Russian Federation
Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education & International Center for Dielectric Research, Xi'an Jiaotong University, Xi'an, Shaanxi, China
Materials Science and Engineering, University of Sheffield, Sheffield, United Kingdom

Доп.точки доступа:
Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Zhou, D.
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The Raman spectroscopy, XRD, SEM, and AFM study of arabinogalactan sulfates obtained using sulfamic acid / B. N. Kuznetsov [et al.] // Russ. J. Bioorgan. Chem. - 2017. - Vol. 43, No. 7. - P. 32-36, DOI 10.1134/S106816201707010X. - Cited References: 9. - The work was financially supported by the Russian Foundation for Basic Research and the Government of the Krasnoyarsk krai (project no. 16-43-242083). . - ISSN 1068-1620
Кл.слова (ненормированные):
physicochemical investigation -- sulfated arabinogalactan -- «green» synthesis -- sulfamic acid -- urea
Аннотация: The structure of sodium salts of sulfated arabinogalactan (AG), obtained by sulfation of larch wood AG with sulfamic acid – urea mixture in the medium of 1,4-dioxane was investigated with the use of Raman spectroscopy, X-ray diffraction (XRD), scaning electron microscopy (SEM) and aromatic force microscopy (AFM) methods. The introduction of sulfate groups into the structure of AG was confirmed by appearance in Raman spectra new absorption bands characteristic for the deformation vibrations of d (SO3) at 420 cm-1 and d (O=S=O) at 588 cm-1, stretching vibrations n (C–O–S) at 822 cm-1, symmetric stretching vibrations ns (O=S=O) at 1076 cm-1, asymmetric stretching vibrations nas (О=S=O) at 1269 cm-1. According to XRD data the amorphization of arabinogalactan structure take place during it`s sulfation. The difference in the morphology of initial and sulfated arabinogalactans was established by SEM method. Initial arabinigalactan consists of particles of globular shape with size of 10–90 µm, but sulfates of AG – from particles of different shapes and sizes of 1–8 µm. According to AFM data the surface of film of arabinogalactan sulfates is formed by the rather homogeneous spherical particles with sizes near 70 nm. The mean-square value of the surface rounghness is equal to 33 nm.

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Публикация на русском языке Исследование методами КР, РФА, РЭМ и АСМ сульфатов арабиногалактана, полученных с использованием сульфаминовой кислоты [Текст] / Б. Н. Кузнецов [и др.] // Хим. растит. сырья. - 2016. - № 4. - С. 43-48

Держатели документа:
Институт химии и химической технологии СО РАН
Сибирский федеральный университет
Институт физики им. Л. В. Киренского СО РАН

Доп.точки доступа:
Kuznetsov, B. N.; Vasil'eva, N. Yu.; Levdansky, A. V.; Karacharov, A. A.; Krylov, A. S.; Крылов, Александр Сергеевич; Mazurova, E. V.; Bondarenko, G. N.; Levdansky, V. A.; Kazachenko, A. S.
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    Состав, структура и реакционная способность при восстановлении водородом композиционных материалов системы α-Fe2O3–CaFe2O4 / В. В. Юмашев [и др.] // Журнал СФУ. Химия. - 2019. - Т. 12, Вып. 1. - С. 54-72 ; J. Sib. Fed. Univ. Chem., DOI 10.17516/1998-2836-0108. - Библиогр.: 37 . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Composition, Structure and Reduction Reactivity of Composite Materials of the α-Fe2O3-CaFe2O4 System by Hydrogen

РУБ Chemistry, Multidisciplinary
Рубрики:
CHEMICAL LOOPING GASIFICATION
OXYGEN CARRIER
PARTIAL OXIDATION
Кл.слова (ненормированные):
твердофазный синтез -- феррит кальция -- РФА -- СЭМ-ЭДС -- термопрограммируемое восстановление водородом -- solid-phase synthesis -- calcium ferrite -- XRD -- SEM-EDS -- temperature-programmed reduction by hydrogen
Аннотация: В работе изучены композиционные материалы системы α-Fe2O3-CaFe2O4, полученные методом высокотемпературного твердофазного синтеза из оксидов Са и Fe(III) с вариацией мольного отношения СаО/Fe2O3 от 0.15 до 1.00. Материалы охарактеризованы методами рентгеновской дифракции (РФА), сканирующей электронной микроскопии с системой энергодисперсионного микроанализа (СЭМ-ЭДС) и синхронного термического анализа (СТА) в режиме термопрограммируемого восстановления водородом (H2-ТПВ). СЭМ-ЭДС - исследование образцов выявило формирование сложной микроструктуры материала по типу «ядро-оболочка» с фазой гематита в качестве «ядра». H2-ТПВ образцов позволило установить, что с увеличением содержания фазы CaFe2O4 (от 33.4 до 97.5 мас. %) наблюдается снижение вклада низкотемпературных форм решеточного кислорода в областях 350-510 °С (до 2.6 раза) и 510-650 °С (до 1.7 раза) и рост вклада высокотемпературной формы кислорода в интервале 650-900 °С (до 2 раз). На основе оценки подвижности решеточного кислорода высказано предположение о перспективности использования полученных композиционных материалов с содержанием фазы CaFe2O4 более 55.2 мас. % в качестве носителей кислорода в химических циклических процессах получения синтез-газа.
In this paper, α-Fe2O3–CaFe2O4 composite materials obtained by high-temperature solid-phase synthesis from Ca and Fe (III) oxides with varying molar ratio CaO/Fe2O3 in the range 0.15-1.00 were investigated. The materials are characterized by Х-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray microanalysis (SEM-EDS) and simultaneous thermal analysis (STA) in the hydrogen temperature-programmed reduction mode (H2-TPR). SEM-EDS studies of the specimens were revealed a formation of the “core-shell” type complex microstructure of material with the hematite phase as the “core”. H2-TPR of the specimens allowed to establish a decrease of the contribution of low-temperature forms of lattice oxygen in areas of 350-510 °С (up to 2.6 times) and 510-650 °С (up to 1.7 times), and the growth of the contribution of the high-temperature oxygen form in the range of 650-900 °С (up to 2 times) with an increase in the content of the phase CaFe2O4 from 33.4 to 97.5 wt. %. Relying on the assessment of lattice oxygen mobility, it was suggested, that the samples with content of CaFe2O4 phase more than 55.4 wt. % are promising for use as oxygen carriers in chemical looping processes of syngas production.

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Держатели документа:
FRC Krasnoyarsk Sci Ctr SB RAS, Inst Chem & Chem Technol SB RAS, 50-24 Akademgorodok, Krasnoyarsk 660036, Russia.
FRC Krasnoyarsk Sci Ctr SB RAS, Kirensky Inst Phys SB RAS, 50-38 Akademgorodok, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Юмашев, Владимир Витальевич; Yumashev, Vladimir V.; Кирик, Надежда Павловна; Kirik N. P.; Шишкина, Нина Николаевна; Shishkina, Nina N.; Князев, Юрий Владимирович; Knyazev, Yu. V.; Жижаев, Анатолий Михайлович; Zhyzhaev, A. M.; Соловьев, Леонид Александрович; Solov'ev, L. A.

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    Reactivity and Chemical Sintering of Carey Lea Silver Nanoparticles / S. Vorobyev [et al.] // Nanomaterials. - 2019. - Vol. 9, Is. 11. - Ст. 1525, DOI 10.3390/nano9111525. - Cited References: 46. - This research was funded by Russian Science Foundation, grant number 18-73-00142. . - ISSN 2079-4991
   Перевод заглавия: Реакционная способность и химическое спекание наночастиц серебра “Carey Lea”
Кл.слова (ненормированные):
silver nanoparticles -- Carey Lea colloid -- citrate-derived capping -- X-ray photoelectron spectroscopy -- SEM -- oxidation -- sulfidation -- sintering
Аннотация: Carey Lea silver hydrosol is a rare example of very concentrated colloidal solutions produced with citrate as only protective ligands, and prospective for a wide range of applications, whose properties have been insufficiently studied up to now. Herein, the reactivity of the immobilized silver nanoparticles toward oxidation, sulfidation, and sintering upon their interaction with hydrogen peroxide, sulfide ions, and chlorocomplexes of Au(III), Pd(II), and Pt(IV) was investigated using SEM and X-ray photoelectron spectroscopy (XPS). The reactions decreased the number of carboxylic groups of the citrate-derived capping and promoted coalescence of 7 nm Ag NPs into about 40 nm ones, excluding the interaction with hydrogen peroxide. The increased nanoparticles form loose submicrometer aggregates in the case of sulfide treatment, raspberry-like micrometer porous particles in the media containing Pd(II) chloride, and densely sintered particles in the reaction with inert H2PtCl6 complexes, probably via the formation of surface Ag-Pt alloys. The exposure of Ag NPs to HAuCl4 solution produced compact Ag films along with nanocrystals of Au metal and minor Ag and AgCl. The results are promising for chemical ambient temperature sintering and rendering silver-based nanomaterials, for example, for flexible electronics, catalysis, and other applications.

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Federal Research Center Krasnoyarsk Scientific Center, Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia
Department of Chemistry and The Smalley-Curl Institute, Rice University, 6100 Main Street, Houston, TX 77005, USA
Federal Research Center Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences, Akademgorodok 50, 660036 Krasnoyarsk, Russia

Доп.точки доступа:
Vorobyev, S.; Vishnyakova, E.; Likhatski, M.; Romanchenko, A.; Nemtsev, I. V.; Немцев, Иван Васильевич; Mikhlin, Yu.
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    Synthesis, structural and spectroscopic properties of orthorhombic compounds BaLnCuS3 (Ln = Pr, Sm) / N. O. Azarapin [et al.] // J. Alloys Compd. - 2020. - Vol. 832. - Ст. 153134, DOI 10.1016/j.jallcom.2019.153134. - Cited References: 68. - This study was supported by the Russian Science Foundation (19-42-02003). Also, this study was supported by RFBR (18-32-20011, 18-03-00750, in part of Raman analysis). This work was partially supported by DST-RSF project under the India-Russia Programme of Cooperation in Science and Technology (No. DST/INT/RUS/RSF/P-20 dated May 16, 2019). Shaibal Mukherjee would like to thank the Ministry of Electronics and Information Technology (MeitY) for the Young Faculty Research Fellowship (YFRF) under Visvesvaraya Ph.D. Scheme for Electronics and IT. This publication is an outcome of the R&D work undertaken in the project under the Visvesvaraya Ph.D. Scheme of MeitY being implemented by Digital India Corporation (formerly Media Lab Asia). SEM investigations were carried out using the equipment of CKP “Nanostructures”, Novosibirsk, Russia. . - ISSN 0925-8388. - ISSN 1873-4669
   Перевод заглавия: Синтез, структурные и спектроскопические свойства ромбических кристаллов BaLnCuS3 (Ln = Pr, Sm)
Кл.слова (ненормированные):
Complex sulfides -- Crystal structure -- SEM -- Raman
Аннотация: Ternary sulfides BaPrCuS3 and BaSmCuS3 are first synthesized by the sulphidation reaction of a mixture of related oxides and metal Cu in a flow of (CS2, H2S) at 1170 K. The crystal structures of BaPrCuS3 and BaSmCuS3 are obtained by Rietveld method. BaPrCuS3 crystallizes in space group Pnma with unit cell parameters a = 10.56074(6), b = 4.11305(2) and c = 13.42845(7) Å, V = 583.289 (5) Å3, Z = 2 (structure type Eu2CuS3). BaSmCuS3 crystallizes in space group Cmcm with unit cell parameters a = 4.07269(4), b = 13.4499(1) and c = 10.3704(1) Å, V = 568.06 (1) Å3, Z = 2 (structure type KZrCuS3). The structural model is proposed for the Cmcm→Pnma transition in ABCX3 (X = S, Se) compounds for the sequence Sm-Pm-Nd-Pr. The dimensionless tolerance factor t = IR(A) × IR(C)/IR(B)2 is suggested to control the boundary between the Cmcm and Pnma structures. The micromorphological, thermal and spectroscopic properties are evaluated for BaPrCuS3. The compound melts incongruently at Tmelt = 1580.9 K. In BaPrCuS3, the band gap is estimated to be 2.1 eV. The vibrational parameters of BaPrCuS3 and BaSmCuS3 are comparatively observed by Raman spectroscopy.

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Держатели документа:
Institute of Chemistry, Tyumen State University, Tyumen, 625003, Russia
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Department of Photonics and Laser Technologies, Siberian Federal University, Krasnoyarsk, 660041, Russia
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russia
Functional Electronics Laboratory, Tomsk State University, Tomsk, 634050, Russia
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russia
Laboratory of Nanodiagnostics and Nanolithography, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russia
Siberian Federal University, Krasnoyarsk, 660079, Russia
Hybrid Nanodevice Research Group (HNRG), Electrical Engineering, Indian Institute of Technology Indore, Madhya Pradesh, 453552, India

Доп.точки доступа:
Azarapin, N. O.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Atuchin, V. V.; Gavrilova, T. A.; Krylov, A. S.; Крылов, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Mukherjee, S.; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Andreev, O. V.; Андреев О. В.
}
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10.

    Shabanova, O. V.
    Development of SEM method for analysis of organ-containing objects using inverse opals / O. V. Shabanova, I. V. Nemtsev, A. V. Shabanov // Sib. J. Sci. Technol. - 2020. - Vol. 21, Is. 4. - P. 565-573 ; Сибирский журнал науки и технологий, DOI 10.31772/2587-6066-2020-21-4-565-573. - Cited References: 25 . - ISSN 2587-6066
   Перевод заглавия: Разработка электронно-микроскопического метода анализа органсодержащих объектов с использованием инверсных опалов
Кл.слова (ненормированные):
scanning electron microscopy -- mesoporous structure -- inverse opal -- lactic acid bacteria -- erythrocyte -- сканирующая электронная микроскопия -- мезопористая структура -- инверсный опал -- молочнокислая бактерия -- эритроцит
Аннотация: The purpose of this study is to test the possibility of using inorganic macroporous structures of inverse opal in sample preparation for scanning electron microscopy of biological objects. As an absorbent substrate we used silica inverse opals prepared by a sol-gel method to study the biological objects.The process of manufacturing the inverse opal involves a complex multi-stage technological process. First, we synthesized submicron spherical particles from polymethylmethacrylate by the method of emulsifier-free emulsion polymerization of methylmethacrylate in an aqueous medium in the presence of a diazoinitiator. This method can be used to obtain an ensemble of particles with high monodispersity, the average size of which can vary in the range from 100 to 500 nm. Then, by self-assembly technique, we deposited the beads of polymethylmethacrylate into ordered matrices (templates), mainly with a face-centered cubic lattice. The resulting mesoporous structures, called artificial opals or colloidal crystals, had lateral dimensions of about 10 × 10 × 2 mm. Then we heat-treated the opals to 120 °C to harden the template before being impregnated with the precursor. Further, we impregnated the opals with silica sol with a particle size distribution from 1 to 5 nm, obtained by hydrolysis of tetraethoxysilane in the presence of hydrochloric acid, and then, after curing and drying the impregnating composition in air at room temperature, we multi-stage fired them up to 550 °C at normal pressure in the air atmosphere to remove all organic components. As a result, the macroporous metamaterial (the so-called inverse opals) with an open system of pores up to 400 nm in size, occupying about 80 % of the volume, were obtained. We studied lactic acid bacteria of cucumber brine and human red blood cells with TM4000 Plus, SU3500 and S-5500 scanning electron microscopes. Auxiliary substance for the sample preparation was ionic liquid VetexQ EM (Interlab LLC). We showed that it is possible to use the inverse opal as an absorbent substrate for sample preparation and rapid analysis in scanning electron microscopy without pre-drying, chemical treatment, or temperature exposure. To improve imaging in the electron microscope, we used sputter coater to cover the inverse opal surface with a thin film of platinum. The use of ionic liquid in combination with the absorbent porous medium allows preserving an original shape of the biological structures. Using the human red blood cells and lactic acid bacteria, we showed that it is possible to carry out of the morphological analysis of the cells using various scanning electron microscopes. We found that on the basis of the inverse opal, there is a fundamental possibility of creating the absorbent substrate suitable for repeated use in the study of the biological objects. At the same time, trace remnants of previous samples remaining after annealing the plate do not introduce significant distortions when conducting new series of observations. In this study, we obtained high-quality electronic micrographs of the biological objects with high resolution and contrast. At the same time, due to the use of the inverse opals as the absorbent substrate, time and financial costs for researchare reduced.
Целью данного исследования является апробация возможности применения неорганических макропористых структур инверсного опала при пробоподготовке для сканирующей электронной микроскопии биообъектов. Изготовленные золь-гель способом инверсные опалы на основе кремнезёма применялись в качестве впитывающей подложки для изучения биологических образцов. Изготовление инверсного опала представляет собой сложный многоступенчатый технологический процесс. Сначала методом безэмульгаторной эмульсионной полимеризации метилметакрилата в водной среде в присутствии диазоинициатора были синтезированы субмикронные сферические частицы из полиметилметакрилата. Таким способом можно получать ансамбль частиц с высокой монодисперсностью, средний размер которых может варьироваться в диапазоне от 100 до 500 нм. Затем методом самосборки субмикросферы полиметилметакрилата осаждались в упорядоченные матрицы (шаблоны) преимущественно с гранецентрированной кубической решёткой. Полученные мезопористые структуры, называемые искусственными опалами или коллоидными кристаллами, имели размеры порядка 10 ×10 × 2 мм. Затем опалы подвергались термической обработке до 120 °С для упрочнения шаблона перед пропиткой прекурсором. Далее опалы пропитывались золем кремнезёма с размером частиц от 1 до 5 нм, полученным путём гидролиза тетраэтоксисилана в присутствии соляной кислоты и затем, после отверждения и сушки пропитывающего состава на воздухе при комнатной температуре, подвергались многоступенчатому обжигу до 550 °С при нормальном давлении в воздушной атмосфере для удаления всех органических компонентов. В результате получались образцы макропористых метаматериалов (так называемые, инверсные или инвертированные опалы) с открытой системой пор размером до 400 нм, занимающих около 80 % объёма. В сканирующих электронных микроскопах TM4000 Plus, SU3500 и S-5500 с использованием макропористых структур были исследованы молочнокислые бактерии и красные кровяные тельца. Для улучшения визуализации использовались системы напыления металлов для покрытия поверхности инверсного опала тонкой плёнкой платины. Вспомогательным веществом в пробоподготовке выступала ионная жидкость VetexQ EM (Interlab LLC). Показано, что инверсный опал можно использовать как впитывающую подложку для пробоподготовки и экспресс-анализа в сканирующей электронной микроскопии без предварительной сушки, химической обработки или температурного воздействия биообъектов. Использование ионной жидкости в сочетании с впитывающей пористой средой позволяет сохранить первоначальную форму биологических структур. Показана возможность изучения морфологических особенностей биоструктур на примере эритроцитов человека и молочнокислых бактерий. Экспериментально установлено, что впитывающую подложку на основе инверсного опала можно использовать многократно при исследовании биологических объектов. Следовые остатки предыдущих проб, оставшиеся после отжига пластины, не вносят существенных искажений при проведении новых серий наблюдений. В нашем исследовании были получены высококачественные электронные микрофотографии биообъектов с высоким разрешением и контрастом. При этом за счёт использования инверсных опалов в качестве впитывающей подложки обеспечивается сокращение временных и финансовых затрат на исследования.

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Держатели документа:
Special Designing and Technological Bureau “Nauka” KSC SB RAS, 50, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Federal Research Center Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences, 50, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
L.V. Kirensky Institute of Physics SB RAS, 50, building 38, Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Nemtsev, I. V.; Немцев, Иван Васильевич; Shabanov, A. V.; Шабанов, Александр Васильевич

}
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11.

    Synthesis, structure, melting and optical properties of three complex orthorhombic sulfides BaDyCuS3, BaHoCuS3 and BaYbCuS3 / N. O. Azarapin, V. V. Atuchin, N. G. Maximov [et al.] // Mater. Res. Bull. - 2021. - Vol. 140. - Ст. 111314, DOI 10.1016/j.materresbull.2021.111314. - Cited References: 60. - This study was supported by the Russian Science Foundation (19-42-02003). The authors would like to thank Alexey A. Lubin for his studies on SEM. The studies were carried out on the basis of laboratory of electron and probe microscopy in REC ‘Nanotechnologies’. This work was partially supported by the DST-RSF project under the India-Russia Programme of Cooperation in Science and Technology (No. DST/ INT/RUS/RSF/P-20 dated May 16, 2019). Shaibal Mukherjee would like to thank MeitY for the YFRF under the Visvesvaraya Ph.D. Scheme for Electronics and IT. This publication is an outcome of the R&D work undertaken in the project under the Visvesvaraya Ph.D. Scheme of MeitY being implemented by Digital India Corporation (formerly Media Lab Asia). We are grateful to the Krasnoyarsk Regional Center of Research Equipment of the Federal Research Center «Krasnoyarsk Science Center SB RAS» for the provided equipment . - ISSN 0025-5408
   Перевод заглавия: Синтез, строение, плавление и оптические свойства трех сложных орторомбических сульфидов BaDyCuS3, BaHoCuS3 и BaYbCuS3
Кл.слова (ненормированные):
Complex sulfides -- Crystal structure -- SEM -- Raman -- Melting point
Аннотация: Complex sulfides BaDyCuS3, BaHoCuS3 and BaYbCuS3 were synthesized in a flow of sulfiding gases (CS2, H2S) at 900°C from standard solutions of lanthanide and copper nitrates, as well as from the same standard Ba(OH)2 solution. The crystal structures of BaDyCuS3, BaHoCuS3 and BaYbCuS3 were obtained by the Rietveld refinement method. All three compounds crystallize in the Cmcm space group (KZrCuS3 structural type) as predicted by the tolerance factor analysis. Their micromorphological, thermal and spectroscopic properties are evaluated. BaDyCuS3 and BaHoCuS3 melt congruently at 1376.5 °C and 1363.8 °C. BaYbCuS3 melts incongruently at 1353.3 °C. The optical band gap is 2.45 eV for BaDyCuS3, 2.37 eV for BaHoCuS3 and 1.82 eV for BaYbCuS3. The low bandgap of BaYbCuS3 is explained by the charge transfer band of Yb at the bottom of conduction band. The vibrational parameters of BaDyCuS3, BaHoCuS3 and BaYbCuS3 crystals were determined with the use of Raman and Infrared spectroscopies.

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Держатели документа:
Institute of Chemistry, Tyumen State University, Tyumen, 625003, Russian Federation
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Krasnoyarsk, 660049, Russian Federation
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Hybrid Nanodevice Research Group (HNRG), Electrical Engineering and Centre for Advanced Electronics (CAE), Indian Institute of Technology IndoreMadhya Pradesh 453552, India
Laboratory of the Chemistry of Rare Earth Compounds, Institute of Solid State Chemistry, UB RAS, Ekaterinburg, 620137, Russian Federation

Доп.точки доступа:
Azarapin, N. O.; Atuchin, V. V.; Maximov, N. G.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Shestakov, N. P.; Шестаков, Николай Петрович; Krylov, A. S.; Крылов, Александр Сергеевич; Burkhanova, T. M.; Mukherjee, S.; Andreev, O. V.
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12.

    Nemtsev, I. V.
    Manufacturing of opals from polymethylmethacrylate particles in dispersion media with different viscosities / I. V. Nemtsev, O. V. Shabanova // J. Sib. Fed. Univ. Math. Phys. - 2021. - Vol. 14, Is. 2. - P. 176-183 ; Журн. СФУ. Матем. и физика, DOI 10.17516/1997-1397-2021-14-2-176-183. - Cited References: 42. - The study was carried out with the support of the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center "Krasnoyarsk Science Center SB RAS". The work was supported by the framework of the state assignment of the Ministry of Science and Higher Education of the Russian Federation (topic no. AAAA-A18-118041990041-8) . - ISSN 1997-1397. - ISSN 2313-6022
   Перевод заглавия: Синтез опалов из частиц полиметилметакрилата в дисперсионных средах с различной вязкостью
Кл.слова (ненормированные):
Emulsion-free polymerization -- Viscosity of dispersion medium -- PMMA beads -- Submicrosphere -- Self-assembly -- 2D and 3D colloidal crystals -- Photonic crystal -- Metamaterial -- SEM micrographs -- IR spectroscopy -- безэмульсионная полимеризация -- вязкость дисперсионной среды -- гранулы ПММА -- субмикросфера -- амосборка -- 2D и 3D коллоидные кристаллы -- фотонный кристалл -- метаматериал -- СЭМ-микрофотографии -- ИК-спектроскопия
Аннотация: The article was prepared based on the materials of the report at the first All-Russian scientific conference with international participation "YENISEI PHOTONICS – 2020". Photonic crystals are structures that have a spatial architecture with a periodically changing complex dielectric function at scales comparable to the wavelengths of light in the visible frequency range. The purpose of this study is to obtain three-dimensional photonic crystals by self-assembly from submicron spherical monodisperse particles of polymethylmethacrylate in dispersion media with different viscosities.
Фотонные кристаллы — это структуры, которые имеют пространственную архитектуру с периодически изменяющейся сложной диэлектрической функцией в масштабах, сопоставимых с длинами волн света в видимом диапазоне частот. Целью данной работы является получение трёхмерных фотонных кристаллов путём самосборки из субмикронных сферических монодисперсных частиц полиметилметакрилата в дисперсных средах с различной вязкостью.

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Federal Research Center, KSC SB RAS, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Special Designing and Technological Bureau "Nauka", Krasnoyarsk, Russian Federation

Доп.точки доступа:
Shabanova, O. V.; Немцев, Иван Васильевич

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13.

Laser processing of polymer films fabricated from phas differing in their monomer composition / T. G. Volova, A. I. Golubev, I. V. Nemtsev [et al.] // Polymers. - 2021. - Vol. 13, Is. 10. - Ст. 1553, DOI 10.3390/polym13101553. - Cited References: 87. - This work was supported by the Russian Foundation for Basic Research/Regional State Autonomous Institution “Krasnoyarsk Regional Fund for the Support of Scientific and Scientific-Technical Activities” foundations under Grant number 19-43-240012 (laser treatment and films properties) and by the State Assignment of the Ministry of Science and Higher Education of the Russian Federation No. FSRZ-2020-0006 (polymer synthesis) . - ISSN 2073-4360
Кл.слова (ненормированные):
P(3HB) -- copolymers -- films -- CO2 laser -- SEM -- AFM -- water contact angles -- MTT assay -- NIH 3T3 fibroblasts
Аннотация: The study reports results of using a CO2-laser in continuous wave (3 W; 2 m/s) and quasi-pulsed (13.5 W; 1 m/s) modes to treat films prepared by solvent casting technique from four types of polyhydroxyalkanoates (PHAs), namely poly-3-hydroxybutyrate and three copolymers of 3-hydroxybutyrate: with 4-hydroxybutyrate, 3-hydroxyvalerate, and 3-hydroxyhexanoate (each second monomer constituting about 30 mol.%). The PHAs differed in their thermal and molecular weight properties and degree of crystallinity. Pristine films differed in porosity, hydrophilicity, and roughness parameters. The two modes of laser treatment altered these parameters and biocompatibility in diverse ways. Films of P(3HB) had water contact angle and surface energy of 92° and 30.8 mN/m, respectively, and average roughness of 144 nm. The water contact angle of copolymer films decreased to 80–56° and surface energy and roughness increased to 41–57 mN/m and 172–290 nm, respectively. Treatment in either mode resulted in different modifications of the films, depending on their composition and irradiation mode. Laser-treated P(3HB) films exhibited a decrease in water contact angle, which was more considerable after the treatment in the quasi-pulsed mode. Roughness parameters were changed by the treatment in both modes. Continuous wave line-by-line irradiation caused formation of sintered grooves on the film surface, which exhibited some change in water contact angle (76–80°) and reduced roughness parameters (to 40–45 mN/m) for most films. Treatment in the quasi-pulsed raster mode resulted in the formation of pits with no pronounced sintered regions on the film surface, a more considerably decreased water contact angle (to 67–76°), and increased roughness of most specimens. Colorimetric assay for assessing cell metabolic activity (MTT) in NIH 3T3 mouse fibroblast culture showed that the number of fibroblasts on the films treated in the continuous wave mode was somewhat lower; treatment in quasi-pulsed radiation mode caused an increase in the number of viable cells by a factor of 1.26 to 1.76, depending on PHA composition. This is an important result, offering an opportunity of targeted surface modification of PHA products aimed at preventing or facilitating cell attachment.

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Держатели документа:
Basic Department of Biotechnology, School of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodnyi Av, Krasnoyarsk, 660041, Russian Federation
Institute of Biophysics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, 50/50 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
L.V. Kirensky Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, 50/38 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Special Design and Technological Bureau ‘Nauka’ Federal Research Center “Krasnoyarsk Science Center SB RAS”, 50/45 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, 50 Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Volova, T. G.; Golubev, A. I.; Голубев Алексей И.; Nemtsev, I. V.; Немцев, Иван Васильевич; Lukyanenko, A. V.; Лукьяненко, Анна Витальевна; Dudaev, A. E.; Shishatskaya, E. I.
}
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14.

Antiferromagnetic resonance and magnetic anisotropy in PrxY1−xFe3(BO3)4 crystals in the region of the magnetic structure transformation “easy axis – easy plane” / A. I. Pankrats, S. M. Zharkov, G. M. Zeer, I. A. Gudim // J. Alloys Compd. - 2022. - Vol. 909. - Ст. 164821, DOI 10.1016/j.jallcom.2022.164821. - Cited References: 37. - The authors acknowledge the assistance of R. Mironov in some resonance measurements. The SEM and EDS investigations were conducted in the SFU Joint Scientific Center supported by the State assignment (#FSRZ-2020–0011) of the Ministry of Science and Higher Education of the Russian Federation . - ISSN 0925-8388
Кл.слова (ненормированные):
Magnetically ordered materials -- Rare earth alloys and compounds -- Spin dynamics -- Anisotropy -- Magnetic measurements -- Scanning electron microscopy, SEM
Аннотация: The spin dynamics, magnetic structures and magnetic anisotropy of single crystals PrxY1−xFe3(BO3)4 have been studied using antiferromagnetic resonance (AFMR) in a wide range of frequencies, magnetic fields, and temperatures. The frequency-field dependences of AFMR for the crystals with x = 0.25 and 0.45 are characteristic of antiferromagnets with the easy plane (EP) anisotropy. The crystals with x = 0.75 and 1.0 exhibit frequency-field dependences that are typical for antiferromagnets with the easy axis (EA) anisotropy. In these crystals, a significant decrease in the effective anisotropy fields of praseodymium upon the transition to the spin-flop state has been found. It is shown that this is the main reason for the large lability intervals, within which the regions of coexistence of the collinear and spin-flop states overlap. In the crystal with x = 0.67, the magnetic field applied along the trigonal axis of the crystal leads to the spin reorientation transition from the EA to the EP state. A magnetic phase diagram of the states on the plane "magnetic field - temperature" is built. In this crystal, the effective anisotropy field of praseodymium also decreases upon the transition to the field-induced EP state. Diamagnetic dilution of the praseodymium subsystem leads to the contribution of this subsystem to the total anisotropy field depending almost linearly on the praseodymium concentration.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 79 Svobodny st., Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Pankrats, A. I.; Панкрац, Анатолий Иванович; Zharkov, S. M.; Жарков, Сергей Михайлович; Zeer, G. M.; Gudim, I. A.; Гудим, Ирина Анатольевна
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15.

    Valleriite-containing ore from Kingash deposit (Siberia, Russia): Mossbauer and X-ray photoelectron spectroscopy characterization, thermal and interfacial properties / Y. L. Mikhlin, M. N. Likhatski, A. S. Romanchenko [et al.] // J. Sib. Fed. Univ. Chem. - 2022. - Vol. 15, Is. 3. - P. 303-317 ; Журн. СФУ. Химия, DOI 10.17516/1998-2836-0294. - Cited References: 25. - This research was funded by the Russian Foundation for Basic Research, Krasnoyarsk Territory Science Foundation and Krasnoyarsk Territory Administration, grant number 20-43-242903. Facilities of the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center «Krasnoyarsk Science Center SB RAS» were employed in the work . - ISSN 1998-2836
   Перевод заглавия: Валлериитсодержащая руда Кингашского месторождения (Сибирь, Россия): Мессбауэровская и рентгенофотоэлектронная спектроскопия, термические и межфазные свойства
Кл.слова (ненормированные):
valleriite -- ore -- two-dimensional sulfide-hydroxide composite -- SEM -- EDX -- XPS -- Mossbauer spectroscopy -- thermal analysis -- zeta potential -- валлериит -- руда -- двумерный сульфидно-гидроксидный композит -- СЭМ -- ЭРМ -- РФЭС -- мессбауэровская спектроскопия -- термический анализ -- дзета-потенциал
Аннотация: Valleriite, (Cu,Fe)S2×n(Mg,Al,Fe)(OH)2, and related layered minerals are of interest due to their unusual two-dimensional structure, formation mechanisms, physical and chemical properties, and potential involvement into mineral processing and materials science applications. Here, we have studied Kingash Cu-Ni ore samples containing 10-25% of valleriite in association with serpentines (lizardite and chrysotile) and magnetite using scanning electron microscopy and electron microprobe analysis, Mössbauer spectroscopy, X-ray photoelectron spectroscopy (XPS), thermal analysis and zeta potential measurement. The data are compared with those for Al-doped valleriite synthesized via a hydrothermal route. It was found that the Kingash valleriite contains excessive iron relative to CuFeS2 stoichiometry, which mainly occurs, leaving aside magnetite, as Fe3+-OH species in hydroxide layers of valleriite and minor Fe centers in serpentines. Thermal dehydroxylation of hydroxide layers of valleriites occurs near 500oC in inert atmosphere; in air, sulfide sheets oxidize with an exothermal peak at 447oC, and sulfur oxides don't volatilize but react with hydroxide groups of valleriite rather than serpentines. Zeta potential measurements of coarse ore particles using the flow potential technique suggested that the surface of valleriite is negatively charged in a wide pH range while the positive values at low pHs for fine particles are inflicted by serpentine. The findings demonstrate close resemblance of the natural and synthetic Al-doped valleriites, and the key role of valleriite, despite its moderate content, for the interfacial characteristics of the valleriite-bearing ores.
Валлериит, (Cu, Fe)S2×n(Mg, Al, Fe)(OH)2 и родственные ему слоистые минералы представляют интерес в связи с их необычной двумерной структурой, механизмами образования, физическими и химическими свойствами и возможностью применения в процессах переработки полезных ископаемых и материаловедения. В настоящей работе с помощью сканирующей электронной микроскопии и электронного микрозондового анализа, мессбауэровской спектроскопии, рентгеновской фотоэлектронной спектроскопии (РФЭС), термического анализа и измерения дзета-потенциала нами были изучены образцы медно-никелевых руд Кингашского месторождения, содержащие 10–25 % валлериита в ассоциации с серпентинами (лизардит и хризотил) и магнетитом. Было проведено сравнение полученных данных с результатами измерений легированного алюминием валлериита, синтезированного гидротермальным способом. Установлено, что валлериит Кингашского месторождения содержит избыточное железо по отношению к стехиометрии CuFeS2, которое представлено в основном, не считая магнетита, в виде центров Fe3+-OH, расположенных в гидроксидных слоях валлериита и небольшого числа примесей Fe в серпентинах. Термическое дигидроксилирование гидроксидных слоев валлериитов происходит около 500 °C в инертной атмосфере; на воздухе сульфидные слои окисляются с экзотермическим пиком при 447 °C, а оксиды серы не улетучиваются, а реагируют скорее с гидроксидными группами валлериита, чем с серпентинами. Измерения дзета-потенциала крупных частиц руды с использованием метода потенциала протекания показали, что поверхность валлериита отрицательно заряжена в широком диапазоне рН, в то время как положительные показатели при низких значениях рН для более мелких частиц обусловлены присутствием серпентина. Полученные данные демонстрируют близкое сходство природного и синтетического валлериитов, легированного алюминием, и его ключевую роль для межфазных характеристик валлериитсодержащих руд, даже при его умеренном содержании.

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Держатели документа:
Institute of Chemistry and Chemical Technology, Krasnoyarsk Science Center of the Siberian Branch, The Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Krasnoyarsk Science Center of the Siberian Branch, The Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Krasnoyarsk Science Center of the Siberian Branch, The Russian Academy of Sciences, Krasnoyarsk, Russian Federation

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Mikhlin, Y. L.; Likhatski, M. N.; Romanchenko, A. S.; Vorobyev, S. A.; Tomashevich, Y. V.; Fetisova, O. Yu.; Bayukov, O. A.; Баюков, Олег Артемьевич; Knyazev, Yu. V.; Князев, Юрий Владимирович; Nemtsev, I. V.; Karasev, S. V.; Karacharov, A. A.; Borisov, R. V.

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16.

    Modification of polyhydroxyalkanoates polymer films surface of various compositions by laser processing / E. I. Shishatskaya, N. O. Zhila, A. E. Dudaev [et al.] // Polymers. - 2023. - Vol. 15, Is. 3. - Ст. 531, DOI 10.3390/polym15030531. - Cited References: 91. - The study was funded by the State Assignment of the Ministry of Science and Higher Education of the Russian Federation (Project No. 0287-2021-0025) . - ISSN 2073-4360
   Перевод заглавия: Модификация поверхности полимерных пленок полигидроксиалканоатов различного состава методом лазерной обработки
Кл.слова (ненормированные):
PHAs -- polymer films -- CO2 laser -- laser processing -- SEM -- AFM -- water contact angles -- fibroblast NIH 3T3 -- MTT test
Аннотация: The results of surface modification of solvent casting films made from polyhydroxyalkanoates (PHAs) of various compositions are presented: homopolymer poly-3-hydroxybutyrate P(3HB) and copolymers comprising various combinations of 3-hydroxybutyrate (3HB), 3-hydroxyvalerate (3HV), 4-hydroxybutyrate(4HB), and 3-hydroxyhexanoate (3HHx) monomers treated with a CO2 laser in continuous and quasi-pulsed radiation modes. The effects of PHAs film surface modification, depending on the composition and ratio of monomers according to the results of the study of SEM and AFM, contact angles of wetting with water, adhesion and growth of fibroblasts have been revealed for the laser radiation regime used. Under continuous irradiation with vector lines, melted regions in the form of grooves are formed on the surface of the films, in which most of the samples have increased values of the contact angle and a decrease in roughness. The quasi-pulse mode by the raster method causes the formation of holes without pronounced melted zones, the total area of which is lower by 20% compared to the area of melted grooves. The number of viable fibroblasts NIH 3T3 on the films after the quasi-pulse mode is 1.5–2.0 times higher compared to the continuous mode, and depends to a greater extent on the laser treatment mode than on the PHAs’ composition. The use of various modes of laser modification on the surface of PHAs with different compositions makes it possible to influence the morphology and properties of polymer films in a targeted manner. The results that have been obtained contribute to solving the critical issue of functional biodegradable polymeric materials.

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Department of Medical Biology, School of Fundamental Biology and Biotechnology, Siberian Federal University, Svobodnyi Av., 79, 660041 Krasnoyarsk, Russia
Institute of Biophysics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, 50/50 Akademgorodok, 660036 Krasnoyarsk, Russia
Chemistry Engineering Centre, ITMO University, Kronverkskiy Prospekt, 49A, 197101 Saint Petersburg, Russia
Basic Department of Biotechnology, School of Fundamental Biology and Biotechnology, Siberian Federal University, Svobodnyi Av., 79, 660041 Krasnoyarsk, Russia
L.V. Kirensky Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, 660036 Krasnoyarsk, Russia
Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, 660036 Krasnoyarsk, Russia
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, 660041 Krasnoyarsk, Russia

Доп.точки доступа:
Shishatskaya, Ekaterina I.; Zhila, Natalia O.; Dudaev, Alexey E.; Nemtsev, I. V.; Немцев, Иван Васильевич; Lukyanenko, A. V.; Лукьяненко, Анна Витальевна; Volova, Tatiana G.
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17.

Structural and magnetic transitions in the Bi2Fe4O9/BiFeO3 composite / L. V. Udod, S. S. Aplesnin, M. N. Sitnikov [et al.] // J. Alloys Compd. - 2023. - Vol. 958. - Ст. 170445, DOI 10.1016/j.jallcom.2023.170445. - Cited References: 51 . - ISSN 0925-8388. - ISSN 1873-4669
Кл.слова (ненормированные):
Сomposite materials -- Magnetisation -- Optical properties -- Scanning electron microscopy (SEM) -- Ultrasonics -- Phase transitions
Аннотация: A Bi2Fe4O9/BiFeO3 composite with a percentage ratio of 67/33 has been synthesized, its morphological analysis has been carried out. The average crystallite sizes for each phase have been determined. The magnetization hysteresis has been established and the temperature of its disappearance has been found. Using the infrared absorption spectra, temperatures of the magnetic phase transitions in each phase have been determined from the magnetic susceptibility, magnetostriction constant, ultrasound damping coefficient, and phonon mode softening. The change of magnetostriction constant sign observed in the vicinity of the spin reorientation transition and antiferromagnetic transition in mullite has been attributed to the change of the sign of the magnetoelastic constants. The interaction between the phases in the composite and the correlation of its structural and magnetic properties have been established.

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Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Reshetnev Siberian State University of Science and Technology, 660037 Krasnoyarsk, Russia
Siberian Federal University, 660041 Krasnoyarsk, Russia

Доп.точки доступа:
Udod, L. V.; Удод, Любовь Викторовна; Aplesnin, S. S.; Аплеснин, Сергей Степанович; Sitnikov, M. N.; Eremin, E. V.; Еремин, Евгений Владимирович; Molokeev, M. S.; Молокеев, Максим Сергеевич; Shabanov, A. V.; Шабанов, Александр Васильевич; Romanova, O. B.; Романова, Оксана Борисовна; Kharkov, A. M.
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18.

    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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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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