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    2-Thiobarbiturate complexes of Ca(II): synthesis, crystal structure and thermal properties / N. N. Golovnev [et al.] // 3 Int. Conf. on the Advancement of Mater. and Nanotechn. (ICAMN 2013) : Programme and abstracts book. - 2013. - P. 157
   Перевод заглавия: 2-тиобарбитуровые комплексы Ca(II): синтез, кристаллическая структура и термические свойства
Кл.слова (ненормированные):
calcium -- 2-thiobarbituric acid -- crystal structure -- thermal decomposition -- IR spectroscopy

Доп.точки доступа:
Golovnev, N. N.; Головнёв, Николай Николаевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Vereschagin, S. N.; Верещагин, С. Н.; Atuchin, V. V.; Атучин, Виктор Валерьевич; International Conference on the Advancement of Materials and Nanotechnology (3 ; 2013 ; Nov. ; 19-22 ; Penang, Malaysia)
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    A novel single-phase white light emitting phosphor Ca9La(PO4)5(SiO4)F2:Dy3+: Synthesis, crystal structure and luminescence properties / H. Liu [et al.] // RSC Adv. - 2016. - Vol. 6, Is. 29. - P. 24577-24583, DOI 10.1039/c5ra23348h. - Cited References: 33. - We gratefully acknowledge the financial support by the National Natural Science Foundations of China (Grant no. 41172053), the Fundamental Research Funds for the Central Universities (Grant no. 2652013043), and Science and Technology Innovation Fund of the China University of Geosciences (Beijing). . - ISSN 2046-2069
   Перевод заглавия: Новый однофазный люминофор Ca9La(PO4)5(SiO4)F2:Dy3+, излучающий белый свет: синтез, кристаллическая структура и люминесцентные свойства

РУБ Chemistry, Multidisciplinary
Рубрики:
Energy-transfer
   Diodes
   LEDs
   Emission
   Ions
   Excitation
   Ce3+
   Eu2+
   Ln
Аннотация: A novel single-phase white light emitting phosphor Ca9La(PO4)5(SiO4)F2:Dy3+ was prepared through traditional high-temperature solid state technology. The crystal structures of Ca9La(PO4)5(SiO4)F2 with or without Dy3+ ions were refined by the Rietveld method. The diffuse reflection spectra, excitation spectra, emission spectra, and decay times were characterized to investigate the photoluminescence properties for application in white light-emitting diodes. The results showed that the Ca9La(PO4)5(SiO4)F2:Dy3+ phosphor could efficiently assimilate n-UV light and emit blue (∼485 nm) and yellow light (∼580 nm), originating from the f-f transitions of Dy3+. The critical Dy3+ quenching concentration (QC) was determined to be about 15 mol%, and the corresponding QC mechanism was verified to be the dipole-dipole interaction. Additionally, the emission colors of all samples were located close to the ideal white light region, and the optimal chromaticity coordinates and correlated color temperature (CCT) were determined to be (x = 0.338, y = 0.336) and 5262 K. All the above results indicate that the as-prepared Ca9La(PO4)5(SiO4)F2:Dy3+ phosphor could serve as a promising candidate for white-light n-UV-LEDs. © The Royal Society of Chemistry 2016.

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Держатели документа:
Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing, China
Laboratory of Crystal Physics, Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation

Доп.точки доступа:
Liu, H.; Liao, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Guo, Q.; Zhang, Y.; Mei, L.
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    Anisotropic thermal expansion and electronic structure of LiInSe2 / V. V. Atuchin, L. I. Isaenko, S. I. Lobanov [et al.] // Molecules. - 2022. - Vol. 27, Is. 16. - Ст. 5078, DOI 10.3390/molecules27165078. - Cited References: 65. - This work was partly supported by the Ministry of Education and Science of the Russian Federation (grant FSUS-2020-0036), state assignment of IGM SB RAS (preliminary crystal charge composition analysis), Russian Science Foundation (grants #19-12-00085-P, crystal growth, and 21-19-00046, conceptualization), National Scientific Foundations of China (Grants 51702330, 11974360 and 51872297), the Young Elite Scientist Sponsorship Program by CAST (YESS), and the CAS Project for Young Scientists in Basic Research (Grants YSBR-024) and the Government of the Russian Federation (075-15-2022-1132). The XPS measurements were carried out at the Surface Analysis Laboratory of the University of New South Wales, Sydney, Australia . - ISSN 1420-3049
   Перевод заглавия: Тепловое расширение и электронная структура LiInSe2
Кл.слова (ненормированные):
LiInSe2 -- crystal growth -- thermal expansion -- band structure -- XPS -- DFT
Аннотация: Optical quality cm-sized LiInSe2 crystals were grown using the Bridgman–Stockbarger method, starting from pure element reagents, under the conditions of a low temperature gradient of 5–6 degrees/cm and a slight melt overheating. The phase purity of the grown crystal was verified by the powder XRD analysis. The thermophysical characteristics of LiInSe2 were determined by the XRD measurements in the temperature range of 303–703 K and strong anisotropy of the thermal expansion coefficients was established. The following values of thermal expansion coefficients were determined in LiInSe2: αa = 8.1 (1), αb = 16.1 (2) and αc = 5.64 (6) MK−1. The electronic structure of LiInSe2 was measured by X-ray photoelectron spectroscopy. The band structure of LiInSe2 was calculated by ab initio methods.

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Держатели документа:
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russian Federation
Department of Applied Physics, Novosibirsk State University, Novosibirsk, 630090, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation
Department of Industrial Machinery Design, Novosibirsk State Technical University, Novosibirsk, 630073, Russian Federation
R&D Center "Advanced Electronic Technologies", Tomsk State University, Tomsk, 634034, Russian Federation
Laboratory of Crystal Growth, Sobolev Institute of Geology and Mineralogy, SB RAS, Novosibirsk, 630090, Russian Federation
Laboratory of Functional Materials, Novosibirsk State University, Novosibirsk, 630090, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Physics and Radioelectronic, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport UniversityKhabarovsk 680021, Russian Federation
Australian Science and Technology Organisation (ANSTO), Lucas Heights, Australia
Functional Crystals Laboratory, Technical Institute of Physics and Chemistry, Chinese Academy of SciencesBeijing 100190, China
University of the Chinese Academy of SciencesBeijing 100049, China

Доп.точки доступа:
Atuchin, V. V.; Isaenko, L. I.; Lobanov, S. I.; Goloshumova, A. A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhang, Z.; Zhang, X.; Jiang, X.; Lin, Z.
}
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    Astakhov, A. M.
    Crystal and molecular structure of a co-crystal of 5-nitrimino-1,4H-1,2,4-triazole with dimethyl sulfoxide / A. M. Astakhov, A. D. Vasiliev // Crystallogr. Rep. - 2022. - Vol. 67, Is. 7. - P. 1146-1151, DOI 10.1134/S1063774522070409. - Cited References: 16 . - ISSN 1063-7745. - ISSN 1562-689X
   Перевод заглавия: Кристаллическая и молекулярная структура ко-кристалла 5-нитримино-1,4H-1,2,4-триазола с диметил сульфоксидом
Аннотация: The structure of the labile co-crystal of 5-nitrimino-1,4Н-1,2,4-triazole with dimethyl sulfoxide was determined by X-ray diffraction. It was established that the molecule, previously known as 3(5)-nitra-mino-1,2,4-triazole, has a nitrimine structure. The geometric parameters of the molecules are similar to those of other nitrimino-1,2,4-triazoles. Intermolecular interactions in the co-crystal are considered. An explanation is provided for the lability of the co-crystal.

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Держатели документа:
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, 660049 Russia
Kirensky Institute of Physics, Siberian Branch of the Russian Academy of Sciences, Krasnoyarsk, 660036 Russia
Siberian Federal University, Krasnoyarsk, 660041 Russia

Доп.точки доступа:
Vasiliev, A. D.; Васильев, Александр Дмитриевич
}
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    Astakhov, A. M.
    X-Ray structure of the complex of 5-nitrimino-1,4H-1,2,4-triazole and DMSO / A. M. Astakhov, A. D. Vasiliev // New Trends in Res. of Energetic Mater. : Proceedings. - 2013. - P. 466-473
   Перевод заглавия: Структура комплекса 5-нитримино-1,4Н-1,2,4-триазола и DMSO

Доп.точки доступа:
Vasiliev, A. D.; Васильев, Александр Дмитриевич; Seminar on New Trends in Research of Energetic Materials (16 ; 2013 ; Apr. ; 10-12 ; Pardubice, Czech Republic)
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    Bis(μ3-barbiturato−O,O,O′)-(μ2-aqua)- aqua-barium(II): crystal structure, spectroscopic and thermal properties / L. A. Solovyov [et al.] // J. Coord. Chem. - 2017. - Vol. 70, Is. 12. - P. 1984-1993, DOI 10.1080/00958972.2017.1319943. - Cited References: 21 . - ISSN 0095-8972
   Перевод заглавия: Бис(μ3-барбитурат-O,O,O')-(μ2-аква)-аква-бария(II): Кристаллическая структура, спектроскопические и термические свойства
Кл.слова (ненормированные):
Barbituric acid -- barium -- coordination compound -- X-ray diffraction -- infrared spectroscopy -- thermal analysis
Аннотация: A polymeric coordination compound, [Ba(H2O) 2(Hba)2] (1) (H2ba – barbituric acid, C4H4N2O3), was obtained. The structure of 1 was solved using powder X-ray diffraction methods. The Ba2+ ion in 1 formed a three-capped trigonal prism. The BaO9 polyhedra, connected with each other by the edges and faces, formed a chain. Several 4- and 12-membered cycles due to the bridging μ2-H2O and bridging μ3-Hba– also formed implementing a 3-D polymer structure. The structures of 1 and other thiobarbiturate complexes were compared. The replacement of a S atom by an O atom in the heterocyclic ligand Htba− (thiobarbiturate ion) of the compound Ba(H2O)2(Htba)2 resulted in changes of the coordination number Ba(II) and supramolecular structure. The intermolecular hydrogen bonds O–H⋯O and N–H⋯O formed a 3-D net where pronounced 2-D layers of Hba– ions could be found. A new topological net in 1 was observed. The IR and thermal stability were investigated.

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Institute of Chemistry and Chemical Technology, SB RAS, FRC “Krasnoyarsk Science Center SB RAS”, Krasnoyarsk, Russian Federation
Department of Chemistry, 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

Доп.точки доступа:
Solovyov, L. A.; Golovnev, N. N.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lesnikov, M. K.
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    Borodina, A. O.
    Highly anisotropic phases in the cOpT films: synthesis, magnetic properties / A. O. Borodina, V. S. Zhigalov, T. V. Strekaleva // Молодежь. Общество. Современная наука, техника и инновации. - 2017. - № 16. - P. 271-274
   Перевод заглавия: Высокоанизотропные фазы в системе пленок cOpT: синтез, магнитные свойства
Кл.слова (ненормированные):
solid-phase synthesis -- Film samples -- Perpendicular anisotropy -- magnetic properties -- crystal structure -- твердофазный синтез -- плёночные образцы -- перпендикулярная анизотропия -- магнитные свойства -- кристаллическая структура
Аннотация: The original Co(001)/Pt(111) film structure has been obtained by consequent thermal deposition of Co layer with a cubic crystal lattice and Pt(111) from the target sprayed using a magnetron sputtering technique on a single crystal substrate of MgO(001) in the vacuum of 10 -6 Torr. In the experiments we have used thesamples with the atomic ratio: 1Сo:3Pt and1Сo:1Pt; totalthickness is about300 nm. The X-ray diffraction analysis has shown that in two-layer structures with the atomic ratio of reagents 1/3, at temperatures of annealing T = 500 and 850 ?С in the interlayer chemical interaction, phases of epitaxial cubic compounds CoPt 3 (L1 2 ) are formed. The annealingof the samestructures with1/1 ratio leads to the formationof the second phaseCoPt(L1 0 )withtetragonal distortion. The newly formedL1 0 CoPtphasegrowsepitaxiallyon the base of the pre-synthesized L1 2 CoPt 3 phasewith the sameorientation relationship. The peculiarity of the films withatomic ratio Co / Pt = 1/1at T =850°Cis the presence of“perpendicular” anisotropy due tothe exchange interactionof twoformed ordered phasesCoPt (111) and CoPt 3 (111).
Исходные плёночные структуры получены последовательным термическим осаждением слоя Со с кубической кристаллической решеткой и Pt(111) из мишени, распыляемой с использованием методики магнетронного распыления на монокристаллическую подложку MgO(001) в вакууме 10 -6 торр. В экспериментах использовались образцы с 1Со:3Pt и 1Со:1Pt атомным отношением общей толщиной порядка 300 нм. Рентгеноструктурные исследования показали, что в двухслойных структурах с атомным соотношением реагентов 1/3, при температурах отжига при Т = 500 и 850 о С в результате межслойного химического взаимодействия формируются фазы эпитаксиального кубического соединения CoPt 3 (L1 2 ). Отжиги этих же структур с соотношением 1/1 приводят к формированию второй фазы СoPt (L1 0 ) с тетрагональным искажением. Вновь сформированная L1 0 CoPt фаза растет эпитаксиально на базе предварительно синтезированной L1 2 CoPt 3 фазе с тем же ориентационном соотношением. Особенностями пленки с атомным соотношением Co/Pt = 1/1 при Т = 850 о С является наличие «перпендикулярной» анизотропии, обусловленной обменным взаимодействием двух сформированных упорядоченных фаз CoPt(111) и CoPt 3 (111).

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Держатели документа:
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences
Reshetnev Siberian State Aerospace University

Доп.точки доступа:
Zhigalov, V. S.; Жигалов, Виктор Степанович; Strekaleva, T. V.; Стрекалева Т.В.; Бородина А. О.
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    Ca/Sr ratio dependent structure and up-conversion luminescence of (Ca1-xSrx)In2O4 : Yb3+/Ho3+ phosphors / M. Guan [et al.] // RSC Adv. - 2015. - Vol. 5, Is. 73. - P. 59403-59407, DOI 10.1039/c5ra08467a. - Cited References:25. - This present work was supported by the National Natural Science Foundations of China (Grant no. 51202226), the Fundamental Research Funds for the Central Universities (Grant no. 2652014125, 2652013128, 2652013043), and the Research Fund for the Doctoral Program of Higher Education of China (Grant no. 20130022110006). . - ISSN 2046-2069
   Перевод заглавия: Структура зависящая от Ca/Sr соотношения и люминесценция с апконверсией в люминофоре (Ca1-xSrx)In2O4: Yb3+/Ho3+

РУБ Chemistry, Multidisciplinary
Рубрики:
CO-DOPED CAIN2O4
   ENERGY-TRANSFER
   PHOTOLUMINESCENCE
   EMISSION
   SRIN2O4
Аннотация: Up-conversion (UC) phosphors of (Ca1-xSrx)In2O4 : Yb3+/Ho3+ (x = 0, 0.1, 0.3, 0.5, 0.7, 0.9, 1.0) were prepared. Based on the crystal structure evolution of these series solid solution samples, which were characterized by Rietveld refinement, the variation of UC luminescent properties was discussed in detail. Sr and Ca occupied one position and Yb/Ho dissolved in the In ion site in the (Ca1-xSrx)In2O4 lattice. With increasing Sr substituting Ca atoms, the cell parameters and cell volumes of these samples increased linearly, and distortions of (Ca/Sr)O-8 polyhedron were formed. The distortions on crystal structures showed a negative relation with UC luminescent intensities in these series phosphors.

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Держатели документа:
China Univ Geosci, Natl Lab Mineral Mat, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Sch Mat Sci & Technol, Beijing 100083, Peoples R China.
SB RAS, LV Kirensky Phys Inst, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Univ Auckland, Dept Chem & Mat Engn, Auckland 1142, New Zealand.

Доп.точки доступа:
Guan, Ming; Zheng, Hong; Huang, Zhaohui; Ma, Bin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Huang, Saifang; Mei, Lefu
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    Co-substitution in Ca1−xYxAl12−xMgxO19 phosphors: local structure evolution, photoluminescence tuning and application for plant growth LEDs / Y. Zheng [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 15. - P. 4217-4224, DOI 10.1039/c8tc00165k. - Cited References: 47. - The present work was supported by the National Natural Science Foundation of China (Grant No. 21671070), the Project for Construction of High-level University in Guangdong Province, and the Teamwork Projects funded by the Guangdong Natural Science Foundation (Grant No. S2013030012842), and the Guangzhou Science & Technology Projects (No. 201704030086, 201605030005), and the reported study was funded by the RFBR according to the research project 17-52-53031. Special Funds for the Cultivation of Guangdong College Students’ Scientific and Technological Innovation (‘‘Climbing Program’’ Special Funds) were granted for Dr Yinjian Zheng. . - ISSN 2050-7534
   Перевод заглавия: Созамещение в Ca1−xYxAl12−xMgxO19 люминофорах: локальная структура, настройка фотолюминесценции и применение светодиодов для роста растений
Кл.слова (ненормированные):
CO substitution -- Crystal structure transformation -- High temperature solid-state reaction -- Lighting systems -- Local structure -- Luminescence measurements -- Structural refinement -- Tunable luminescences
Аннотация: Herein, Mn4+-activated Ca1-xYxAl12-xMgxO19 (x = 0-0.50) solid solutions were prepared using a conventional high-temperature solid-state reaction. Crystal structure transformation via chemical co-substitution of Y3+/Mg2+ for Ca2+/Al3+ was investigated in detail. The optical properties of Ca1-xYxAl12-xMgxO19 (x = 0-0.50) have been reported for the first time using a combination of techniques including structural refinement and luminescence measurements. Co-doping of Mg and Y cations within the CaAl12O19 host in a controlled manner resulted in the as-prepared samples with red/far-red ratio-tunable luminescence properties. The emission bands well-matched with the absorption band of phytochrome. Interestingly, enhanced Mn4+ luminescence can be obtained upon the addition of Mg2+ and Y3+. Unexpectedly, the quantum yields exhibit a slight change when x is in the range from 0.05 to 0.40; this indicates that these solid solutions have significant potential as lighting systems for plant growth.

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Guangdong Provincial Engineering Technology Research Center for Optical Agricultural, College of Materials and Energy, South China Agricultural University, Guangzhou, China
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
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

Доп.точки доступа:
Zheng, Y.; Zhang, H.; Xia, Z.; Liu, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lei, B.
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10.

    Complex of Ca(II) with ceftriaxone: Synthesis, structure, spectral and antibacterial properties / G. V. Novikova, D. I. Tsyplenkova, A. A. Kuzubov [и др.] // J. Sib. Fed. Univ. Chem. - 2021. - Vol. 14, Is. 3. - P. 290-301 ; Журн. СФУ. Химия, DOI 10.17516/1998-2836-0238. - Cited References: 39. - The research was funded by RFBR, Krasnoyarsk Territory and Krasnoyarsk Regional Fund of Science, project number 20-43-240007 . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Комплекс Ca(II) с цефтриаксоном: синтез, структура, спектральные и антибактериальные свойства

РУБ Chemistry, Multidisciplinary
Рубрики:
BASIS-SETS
   ALGORITHM
   1ST-ROW
   CALCIUM
Кл.слова (ненормированные):
ceftriaxone -- calcium -- DFT -- IR spectroscopy -- luminescence properties -- antibacterial screening -- цефтриаксон -- кальций -- теория функционала плотности -- ИК-спектроскопия -- люминесцентные свойства -- антибактериальный скрининг
Аннотация: The calcium complex of ceftriaxone was synthesized and characterized by elemental, atomic-emission analysis, TGA, IR spectroscopy and density functional theory calculations. The luminescence and antibacterial properties of the ceftriaxone disodium and calcium complex wcrc investigated. Ca(II) complex was obtained in a crystalline form, cell parameters of the compound were determined. Ceftriaxone was coordinated to the calcium ion by the oxygen of the triazine cycle in the 6th position, the nitrogen of the amine group of the thiazole ring, and the oxygens of the lactam carbonyl and carboxylate groups. The complex of Ca(II) with ceftriaxone was screened for antibacterial activity against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, and the results were compared with the activity of ceftriaxone disodium salt.
Кальциевый комплекс цефтриаксона был синтезирован и охарактеризован с помощью элементного, атомно-эмиссионного анализа, ТГА, ИК‑спектроскопии и расчетов теории функционала плотности. Исследованы люминесцентные и антибактериальные свойства динатриевой соли цефтриаксона и комплекса цефтриаксона с кальцием. Комплекс Ca(II) получен в кристаллическом виде, определены параметры кристаллической решетки соединения. Цефтриаксон координировался к иону кальция через атом кислорода триазинового цикла в 6-м положении, атом азота аминогруппы тиазольного кольца и атомами кислорода карбонильной и карбоксилатной групп. Комплекс Са(II) с цефтриаксоном обладает антибактериальной активностью против Staphylococcus aureus, Escherichia coli и Pseudomonas aeruginosa, полученные результаты сравнивали с активностью динатриевой соли цефтриаксона.

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Держатели документа:
Siberian Fed Univ, Sch Nonferrous Met & Mat Sci, Krasnoyarsk, Russia.
FRC Krasnoyarsk Sci Ctr SB RAS, LV Kirensky Inst Phys SB RAS, Krasnoyarsk, Russia.
FRC Krasnoyarsk Sci Ctr SB RAS, Sci Res Inst Med Problems North, Krasnoyarsk, Russia.
FRC Krasnoyarsk Sci Ctr SB RAS, Inst Chem & Chem Technol SB RAS, Krasnoyarsk, Russia.

Доп.точки доступа:
Novikova, Galina, V; Tsyplenkova, Darya, I; Kuzubov, A. A.; Кузубов, Александр Александрович; Kolenchukova, Oksana A.; Samoilo, Alexander S.; Vorobyev, Sergey A.; RFBR, Krasnoyarsk Territory; Krasnoyarsk Regional Fund of Science [20-43-240007]

}
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11.

    Complex of ceftriaxone with Mg(II): Synthesis, structure, spectral and antibacterial properties / G. V. Novikova, D. I. Tsyplenkova, A. A. Kuzubov [et al.] // J. Sib. Fed. Univ. Chem. - 2023. - Vol. 16, Is. 1. - P. 5-15 ; Журн. СФУ. Химия. - Cited References: 28. - The research was funded by RFBR, Krasnoyarsk Territory and Krasnoyarsk Regional Fund of Science, project number 20–43–240007 . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Комплекс цефтриаксона с Mg(II): синтез, структура, спектральные и антибактериальные свойства
Кл.слова (ненормированные):
cephalosporin antibiotic -- ceftriaxone -- magnesium -- density functional theory -- molecular spectroscopy -- antibacterial screening -- цефалоспориновые антибиотики -- цефтриаксон -- магний -- теория функционала плотности -- молекулярная спектроскопия -- антибактериальный скрининг
Аннотация: Magnesium complex of ceftriaxone was obtained and characterized by atomic-emission and elemental analysis, TGA, FTIR and Raman spectroscopy, X-ray diffraction and density functional theory calculations. Ceftriaxone was coordinated to the magnesium ion by the oxygen of the triazine cycle in the 6th position, the nitrogen of the amine group of the thiazole ring, and oxygen atoms of the lactam carbonyl and carboxylate groups. The disodium salt of ceftriaxone and magnesium complex were screened for antibacterial activity against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa.
Получен и охарактеризован магниевый комплекс цефтриаксона методами атомно-эмиссионного и элементного анализов, ТГА, ИК- и КР‑спектроскопии, РФА и расчетов теории функционала плотности. Цефтриаксон координируется к иону магния через кислород триазинового цикла в шестом положении, азот аминогруппы тиазольного цикла и атомы кислорода карбоксильной и лактамной групп. Динатриевая соль цефтриаксона и комплекс магния были исследованы на антибактериальную активность в отношении Staphylococcus aureus, Escherichia coli и Pseudomonas aeruginosa.

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Держатели документа:
Siberian Federal University, Krasnoyarsk, Russian Federation
L.V. Kirensky Institute of Physics SB RAS Federal Research Center "Krasnoyarsk Science Center SB RAS", Krasnoyarsk, Russian Federation
Scientific Research Institute of Medical Problems of the North Federal Research Center “Krasnoyarsk Scientific Center of the SB RAS”, Krasnoyarsk, Russian Federation
Institute of Chemistry and Chemical Technology SB RAS Federal Research Center "Krasnoyarsk Scientific Center of the SB RAS", Krasnoyarsk, Russian Federation

Доп.точки доступа:
Novikova, G. V.; Tsyplenkova, D. I.; Kuzubov, A. A.; Кузубов, Александр Александрович; Kolenchukova, O. A.; Samoilo, A. S.; Vorobyev, S. A.

}
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12.

    Crystal and electronic structure, thermochemical and photophysical properties of europium-silver sulfate monohydrate AgEu(SO4)2·H2O / Y. G. Denisenko, A. E. Sedykh, M. S. Molokeev [et al.] // J. Solid State Chem. - 2021. - Vol. 294. - Ст. 121898, DOI 10.1016/j.jssc.2020.121898. - Cited References: 54. - This work was partially supported by the Russian Foundation for Basic Research (Grant 19-33-90258∖19 ). Use of equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center « Krasnoyarsk Science Center SB RAS» is acknowledged . - ISSN 0022-4596
   Перевод заглавия: Кристаллическая и электронная структура, термохимические и фотофизические свойства моногидрата сульфата европия-серебра AgEu(SO4)2·H2O
Кл.слова (ненормированные):
Structure -- Thermochemistry -- Luminescence -- Sulfates -- Europium
Аннотация: In order to synthesize single crystals of europium-silver double sulfate monohydrate, a hydrothermal reaction route was used. It was found that the crystallization cannot be performed under standard conditions. The compound AgEu(SO4)2·H2O crystallizes in the trigonal crystal system, space group P3221 (a = 6.917(1), c = 12.996(2) Å, V = 538.53(17) Å3). The structure consists of triple-capped trigonal prisms [EuO9], in which one oxygen atom belongs to crystalline water, silver octahedra [AgO6], and sulfate tetrahedra [SO4]. The hydrogen bonds in the system additionally stabilize the structure. The electronic band structure wasstudied by density functional theory calculations which show that AgEu(SO4)2·H2O is an indirect band gap dielectric. Temperature dependent photoluminescence spectroscopy shows emission bands of transitions from the 5D0 state to the spin-orbit components of the 7FJmultiplet (J = 0–6).The ultranarrow transition 5D0 - 7F0 shows a red shift with respect to other europium-containing water-free sulfates that is ascribed to the presence of OH group in the crystal structure in the close vicinity of the Eu3+ ion. An effect of abnormal sensitivity of the Ω4 intensity factor to minor distortions of the local environment is detected for the observed low local symmetry of C2.

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Держатели документа:
Institute of Chemistry, Tyumen State University, Tyumen, 625003, Russian Federation
Institute of Inorganic and Analytical Chemistry, Justus-Liebig-University of Giessen, Giessen35392, Germany
Department of General and Special Chemistry, Industrial University of Tyumen, Tyumen, 625000, Russian Federation
Center for Materials Research (LaMa), Justus-Liebig-University of Giessen, Giessen35392, Germany
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
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
Komissarov Department of General Chemistry, Northen Trans-Ural Agricultural University, Tyumen, 625003, Russian Federation
Laboratory of the Chemistry of Rare Earth Compounds, Institute of Solid State Chemistry, UB RAS, Ekaterinburg, 620137, Russian Federation

Доп.точки доступа:
Denisenko, Y. G.; Sedykh, A. E.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Khritokhin, N. A.; Sal'nikova, E. I.; Andreev, O. V.; Muller-Buschbaum, K.
}
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13.

    Crystal and local atomic structure of MgFeBO4,Mg0.5Co0.5FeBO4, and CoFeBO4: effects of Co substitution / N. V. Kazak [et al.] // Phys. Status Solidi B. - 2015. - Vol. 252, Is. 10. - P. 2245-2258, DOI 10.1002/pssb.201552143. - Cited References: 46. - This work has been financed by the MECOM Project MAT11/23791, and DGA IMANA project E-34, Council for Grants of the President of the Russian Federation (project nos. NSh-2886.2014.2, SP-938.2015.5), and Russian Foundation for Basic Research (project nos. 13-02-00958-a, 13-02-00358-a, 14-02-31051-mol-a). The work of one of the coauthors (M.S.P.) was supported by the program of Foundation for promoting the development of small enterprises in scientific and technical sphere ("UMNIK" program). . - ISSN 0370. - ISSN 1521-3951
   Перевод заглавия: Кристаллическая и локальная атомная структура MgFeBO4, Mg0.5Co0.5FeBO4 and CoFeBO4: эффект замещения Со

РУБ Physics, Condensed Matter
Рубрики:
SPIN-GLASS BEHAVIOR
   MAGNETIC WARWICKITES
   SINGLE-CRYSTALS
   PHASE-RELATIONS
   OXYBORATE
   SYSTEM
   SPECTROSCOPY
   ANISOTROPY
   MN2OBO3
   FE2OBO3
Кл.слова (ненормированные):
crystal structure -- XANES -- EXAFS -- magnetic semiconductor -- oxyborate
Аннотация: Single-crystalline MgFeBO4, Mg0.5Co0.5FeBO4, and CoFeBO4 have been grown by the ﬂux method. The samples have been characterized by X-ray spectral analysis, X-ray diffraction, and X-ray absorption spectroscopy. The X-ray absorption near-edge structure (XANES) and extended X-ray absorption ﬁne structure (EXAFS) spectra have been measured at the Fe and Co K-edges over a wide temperature range (6.5– 300 K). The composition, the charge state, and local environ- ment of both Fe and Co atoms have been determined. The effects of Co substitution for Mg on the local structural distortions have been revealed experimentally and the M–O bond anisotropy has been found.
Монокристаллические образцы CoFeBO4 были выращены раствор-расплавным методом. Образцы были охарактеризованы с помощью рентгеноспектрального анализа, рентгеновской дифракции и спектроскопии поглощения рентгеновских лучей. Спектры вблизи K-края поглощения рентгеновского излучения структуры (XANES) и далее рентгеновского поглощения тонкой структуры (EXAFS) были измерены для Fe и Co в широком диапазоне температур (6.5- 300К). Состав, состояние заряда, и локальная положение и Fe и Co атомов были определены. Эффекты замещения Co магнием Mg на местные структурные искажения были выявлены экспериментально и анизотропия связи М-О была найдена.

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Держатели документа:
Kirensky Institute of Physics, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
National Research Center Kurchatov Institute, Moscow, Russian Federation
Servicio de Medidas Fi, sicas, Universidad de Zaragoza, Zaragoza, Spain
Departamento de Fisica de la Materia Condensada, Instituto de Ciencia de Materiales de Aragon, CSIC, Universidad de Zaragoza, Zaragoza, Spain
O. O. Galkin Institute for Physics and Engineering, National Academy of Sciences of Ukraine, Donetsk, Ukraine

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Platunov, M. S.; Платунов, Михаил Сергеевич; Knyazev, Yu. V.; Князев, Юрий Владимирович; Ivanova, N. B.; Иванова, Наталья Борисовна; Zubavichus, Y. V.; Veligzhanin, A. A.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Bayukov, O. A.; Баюков, Олег Артемьевич; Arauzo, A.; Bartolome, J.; Lamonova, K. V.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
}
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14.

    Crystal structure and luminescence properties of green-emitting Sr1−xAl12O19:xEu2+ phosphors / B. Ma [et al.] // Ceram. Int. - 2016. - Vol. 42, Is. 5. - P. 5995-5999, DOI 10.1016/j.ceramint.2015.12.149. - Cited References: 30. - This work was supported by the National Natural Science Foundation of China (Grant nos. 51032007 and 51372232) and the Fundamental Research Funds for the Central Universities (Grant no. 2652015024). . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Кристаллическая структура и люминесцентные свойства зеленого люминофора Sr1-xAl12O19:xEu2+

РУБ Materials Science, Ceramics
Рубрики:
COLOR-TUNABLE PHOSPHOR
   ENERGY-TRANSFER
   Dy3+ PHOSPHORS
   NEAR-UV
   Eu2+
   DIODES
   PHASE
   STATE
   Ce3+
Кл.слова (ненормированные):
Crystal structure -- Magnetoplumbite -- Phosphor
Аннотация: In this paper, a series of novel luminescent Sr1−xAl12O19:xEu2+ phosphors were synthesized by a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, as well as the decay curves were investigated. The quenching concentration of Eu2+ in SrAl12O19 was about 0.15 (mol). Upon excitation at 378 nm, the composition-optimized Sr0.85Al12O19:0.15Eu2+ exhibited strong broad-band green emission at 530 nm with the CIE chromaticity (0.2917, 0.5736). The results indicate that Sr1−xAl12O19:xEu2+ phosphors have potential applications as green-emitting phosphors for UV-pumped white-light LEDs.

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Beijing 100083, Peoples R China.
SB RAS, Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Ma, Bin; Guo, Q. F.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lv, Zhenfei; Yao, Jun; Mei, Lefu; Huang, Zhaohui
}
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15.

    Crystal structure and luminescence properties of novel Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphor with apatite structure / Q. F. Guo [et al.] // Ceram. Int. - 2016. - Vol. 42, Is. 10. - P. 11687-11691, DOI 10.1016/j.ceramint.2016.04.086. - Cited References:26. - This present work is supported by the National Natural Science Foundation of China (Grant no. 41172053). . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Кристаллическая структура и люминесцентные свойства нового люминофора Sr10-x(SiO4)3(SO4)3O:xEu2+ со структурой апатита

РУБ Materials Science, Ceramics
Рубрики:
Light-Emitting-Diodes
   Energy-transfer
   Tunable phosphor
   LEDs
   Eu-2+
   Ions
   Ce3+
Кл.слова (ненормированные):
Crystal structure -- Apatite -- Phosphor
Аннотация: In this paper, a series of novel luminescent Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphors with apatite structure were synthesized by a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, as well as the PL thermal stability were investigated. Sr9.92(SiO4)3(SO4)3O:0.08Eu2+ phosphor exhibits better thermal quenching resistance, retaining the luminance of 66.55% at 150 °C compared with that at 25 °C. The quenching concentration of Eu2+ in Sr10(SiO4)3(SO4)3O was about 0.08 (mol) with the dipole–quadrupole interaction. The Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphors exhibited a broad-band green emission at 538 nm upon excitation at 396 nm. The results indicate that Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs.

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Beijing 100083, Peoples R China.
SB RAS, Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Guo, Q. F.; Ma, B.; Liao, L. B.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Mei, L. F.; Liu, H. K.
}
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16.

    Crystal structure and magnetic properties of Mn substituted ludwigite Co3O2BO3 / Yu. V. Knyazev [et al.] // J. Magn. Magn. Mater. - 2012. - Vol. 324, Is. 6. - P. 923-927, DOI 10.1016/j.jmmm.2011.07.044. - Cited References: 15. - The study was supported by the Russian Foundation for Basic Research (Project no. 09-02-00171-a), the Federal Agency for Science and Innovation (Rosnauka) (Project no. MK-5632.2010.2), the Physical Division of the Russian Academy of Science, the program "Strongly Correlated Electrons", Project 2.3.1. . - ISSN 0304-8853
   Перевод заглавия: Кристаллическая структура и магнитные свойства Mn-замещенного людвигита Co3O2BO3

РУБ Materials Science, Multidisciplinary + Physics, Condensed Matter
Рубрики:
BOND VALENT SUMS
   COORDINATION CHEMISTRY
   OXIDATION -STATE
   O BONDS
   COMPLEXES
   MANGANESE
   COBALT
Кл.слова (ненормированные):
Transition metal oxyborate -- Distinct crystallographic position -- Spin glass magnetic ordering
Аннотация: The needle shape single crystals Co3−x MnxO2BO3 with ludwigite structure have been prepared. According to the X-ray diffraction data the preferable character of distinct crystallographic positions occupation by Mn ions is established. Magnetization field and temperature dependencies are measured. Paramagnetic Curie temperature value Θ=−100 K points out the predominance of antiferromagnetic interactions. Spin-glass magnetic ordering takes the onset at TN=41 K. The crystallographic and magnetic properties of Co3O2BO3:Mn are compared with the same for the isostructural analogs Co3O2BO3 and CoO2BO3:Fe.

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Доп.точки доступа:
Knyazev, Yu.V.; Князев, Юрий Владимирович; Ivanova, N. B.; Иванова, Наталья Борисовна; Kazak, N. V.; Казак, Наталья Валерьевна; Platunov, M. S.; Платунов, Михаил Сергеевич; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Yurkin, G. Yu.; Юркин, Глеб Юрьевич
}
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17.

    Crystal structure and magnetism OF Co2-xNixB2O5 pyroborate / M. S. Platunov [et al.] // Moscow Int. Symp. on Magnet. (MISM-2011) : Book of abstracts. - 2011. - Ст. 22PO-I-59 . - P. 158
   Перевод заглавия: Кристаллическая структура и магнетизм пиробората Co2-xNixB2O5
Аннотация: The crystal structure and magnetic properties of Co3B2O6 single crystals are studied. Orthorhombic symmetry with space group Pnnm is detected at room temperature. The measurements of static magnetization and dynamic magnetic susceptibility reveal two magnetic anomalies at T 1 = 33 K and T 2 = 10 K and an easy-axis magnetic anisotropy. The effective magnetic moment indicates a high-spin state of the Co2+ ion. A spin-flop transition is found at low temperatures and H sf = 23 kOe. EXAFS spectra of the K-edge absorption of Co are recorded at various temperatures, the temperature-induced changes in the parameters of the local environment of cobalt are analyzed, and the effective Co-Co and Co-O distances are determined. The magnetic interactions in the crystal are analyzed in terms of an indirect coupling model.

Материалы конференции

Доп.точки доступа:
Platunov, M. S.; Платунов, Михаил Сергеевич; Ivanova, N. B.; Иванова, Наталья Борисовна; Kazak, N. V.; Казак, Наталья Валерьевна; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Vasil'ev, A. D.; Васильев, Александр Дмитриевич; Eremin, E. V.; Еремин, Евгений Владимирович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Moscow International Symposium on Magnetism(5 ; 2011 ; Aug. ; 21-25 ; Moscow)
}
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18.

    Crystal structure and phase transitions of a layered perovskite-like CsScF4 crystal / A. S. Krylov [et al.] // CrystEngComm. - 2016. - Vol. 18, Is. 43. - P. 8472-8486, DOI 10.1039/c6ce01144f. - Cited References:47. - The authors are grateful to Prof. I. N. Flerov for valuable support and useful discussions. This work was partly supported by the Russian Foundation for Basic Research, Project 16-02-00102. The research is partially conducted within the framework of the state task of the Ministry of Education and Science of the Russian Federation for Siberian Federal University on R&D performance in 2014 (Task 3.2534.2014/K). X-ray data from powders, Raman NMR, and IR spectra were obtained with use the analytical equipment of Krasnoyarsk Center of collective use SB RAS. . - ISSN 1466-8033
   Перевод заглавия: Кристаллическая структура и фазовые переходы в слоистом перовскитоподобном кристалле CsScF4

РУБ Chemistry, Multidisciplinary + Crystallography
Рубрики:
NEGATIVE THERMAL-EXPANSION
RAMAN-SCATTERING
LATTICE-DYNAMICS
Аннотация: This work is devoted to the complex research on temperature phase transitions in a CsScF4 crystal. The crystal structure was solved and refined at different temperatures by using the Rietveld method. Structural phase transitions were investigated by using the following spectroscopic methods, some of them for the first time: Brillouin spectroscopy, Raman spectroscopy, IR absorption spectroscopy and NMR. The symmetry analysis of the Brillouin zone center of all phases is presented. The vibrational spectra of the crystal in three phases have been calculated. The structural phase transition mechanism was determined. The transitions at T-1 = 475 K and T-2 = 317.5 K are of displacement type. The Raman soft modes have been associated with rotations of the ScF6 octahedral group.

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Держатели документа:
SB RAS, LV Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
SB RAS, Inst Automat & Electrometry, Novosibirsk 630090, Russia.

Доп.точки доступа:
Krylov, A. S.; Крылов, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Misyul, S. V.; Krylova, S. N.; Крылова, Светлана Николаевна; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Ivanenko, A. A.; Иваненко, Александр Анатольевич; Zykova, V. A.; Ivanov, Y. N.; Иванов, Юрий Николаевич; Sukhovsky, A. A.; Суховский, Андрей Андреевич; Voronov, V. N.; Воронов, Владимир Николаевич; Safonov, I. N.; Vtyurin, A. N.; Втюрин, Александр Николаевич; Russian Foundation for Basic Research [16-02-00102]
}
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19.

    Crystal structure and photoluminescence evolution of La5(Si2+xB1–x)(O13–xNx):Ce3+ solid solution phosphors / Z. G. Xia [et al.] // J. Phys. Chem. C. - 2015. - Vol. 119, Is. 17. - P. 9488-9495, DOI 10.1021/acs.jpcc.5b01211. - Cited References:25. - The present work was supported by the National Natural Science Foundations of China (Grants 51002146 and 51272242), Natural Science Foundations of Beijing (Grant 2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306) and Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1). . - ISSN 1932-7447
   Перевод заглавия: Кристаллическая структура и постепенное изменение фотолюминесценции в твердых растворах La5(Si2+xB1-x)(O13-xNx):Ce3+

РУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
ENERGY-TRANSFER PROPERTIES
LUMINESCENCE PROPERTIES
TUNABLE
Аннотация: A series of iso-structural La-5(Si2+xB1-x)(O13-xNx):Ce3+ phosphors with apatite structure have been prepared. A combination of powder X-ray diffraction and neutron scattering technique was employed to explore the crystal structural evolution and the rigid nature from oxy- to oxynitride-based apatites, and some local structures were also characterized by HRTEM and Si-29 NMR data, respectively. The new La-5(Si2+xB1-x)(O13-xNx):Ce3+ solid solution phosphors gave continuously controlled emission from 421 nm [La5Si2BO13:Ce3+, end-member (x = 0)] to 463 nm (La(5)Si3O12N:Ce3+, end-member (x = 1)). Substitution of B3+ and O-2 by Si4+ and N-3 in La-5(Si2+xB1-x)(O13-xNx):Ce3+ phosphors produced more covalency into the crystal field environment around the Ce3+ ions inducing the red-shifted emission, further improving the thermal stability of the oxynitride-based apatite phosphors. The proposed approach from oxy- to oxynitride based iso-structural phases could significantly contribute to future research in designing complex solid solution phosphors.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
RAS, SB, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
Far Eastern State Transport Univ, Khabarovsk 680021, Russia
Chonnam Natl Univ, Sch Mat Sci & Engn, Kwangju 500757, South Korea

Доп.точки доступа:
Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Im, Won Bin; Unithrattil, Sanjith; Liu, Quanlin
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20.

    Crystal structure characterization and up-conversion luminescent properties of BaIn2O4 phosphor / S. Chen [et al.] // J. Lumin. - 2017. - Vol. 192. - P. 218-223, DOI 10.1016/j.jlumin.2017.06.034. - Cited References: 29. - This present work was supported by the National Natural Science Foundations of China (Grant No. 51202226), the Fundamental Research Funds for the Central Universities (Grant nos. 2652016051, 2652016037), and Science and Technology Innovation Fund of the China University of Geosciences (Beijing) (Grant no. 201511415021). . - ISSN 0022-2313
   Перевод заглавия: Кристаллическая структура и апконверсионные люминесцентные свойства BaIn2O4
Кл.слова (ненормированные):
Crystal structure -- Up-conversion -- BaIn2O4
Аннотация: Er3+ / Yb3+ doped BaIn2O4 up-conversion (UC) phosphors are synthesized and their UC luminescent properties are characterized. BaIn2O4 has P21/c space group but Rietveld refinement suggests it has twice smaller cell parameter (a = 10.3975 Å, b = 5.8295 Å, c = 14.4457 Å) and volume than previous reported structure. Refinement also reveals Er3+/Yb3+ replaces In3+ ions in lattice because of the existence of InO6 octahedra. In these BaIn2O4 phosphors, co-doping with Yb3+ ions changes the predominant UC emission from green ( 2H11/2, 4S3/2 → 4I15/2 of Er3+) to red (about 665 nm, 4F9/2 → 4I15/2 of Er3+). By controlling of Er3+/Yb3+ concentrations, the BaIn2O4 phosphors have the potential of generating various UC spectra and color tunability. The pumping powers study shows two-photon process in these phosphors.

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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation

Доп.точки доступа:
Chen, S.; Wang, W.; Wang, K.; Guan, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Mei, L.; Huang, Z.
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