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Effect of cobalt concentration on the magnetic properties of the Co1–xMgxFe2O4 nanocrystals / O. S. Ivanova, I. S. Edelman, S. G. Ovchinnikov [et al.] // JETP Lett. - 2024. - Vol. 119, Is. 2. - P. 104-110, DOI 10.1134/S0021364023603457. - Cited References: 26. - The research was carried out at the expense of the Russian Science Foundation Grant # 23-22-10025, https://rscf.ru/project/23-22-10025/, Krasnoyarsk Regional Science Foundation . - ISSN 0021-3640. - ISSN 1090-6487
Аннотация: Nanoparticles of Co1–xMgxFe2O4 with x equal to 0, 0.2, 0.4, 0.6, 0.8 and 1.0 have been synthesized. For all values of x, they are nanocrystals with a cobalt ferrite structure and an average linear size (56 ± 3) nm. Based on the analysis of the Mossbauer effect spectra, the Co2+ ions were shown to occupy only octahedral positions at all values of x. The experimentally obtained dependence of the nanoparticles magnetization on x corresponds to the dependence calculated using the Mossbauer effect data, except for the sample with x = 1.0. The effective magnetic anisotropy constant estimated for 0 K from the analysis of the coercive force temperature dependences decreases from 5.27 × 106 at x = 0 to 1.29 × 106 erg/cm3 at x = 0.8 and drops sharply to 4 × 104 erg/cm3 at x = 1.0

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Публикация на русском языке Влияние концентрации кобальта на магнитные свойства нанокристаллов семейства Co1–xMgxFe2O4 [Текст] / О. С. Иванова, И. С. Эдельман, С. Г. Овчинников [и др.]. - 7 с. // Письма в ЖЭТФ. - 2024. - Т. 119 Вып. 2. - С. 111-117

Держатели документа:
Kirensky Institute of Physics, Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, 660036, Krasnoyarsk, Russia
Siberian Federal University, 660041, Krasnoyarsk, Russia
Amity University Haryana, 122413, Gurugram, Haryana, India

Доп.точки доступа:
Ivanova, O. S.; Иванова, Оксана Станиславовна; Edelman, I. S.; Эдельман, Ирина Самсоновна; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Thakur, A.; Thakur, P.; Sukhachev, A. L.; Сухачев, Александр Леонидович; Knyazev, Yu. V.; Князев, Юрий Владимирович; Ivantsov, R. D.; Иванцов, Руслан Дмитриевич; Molokeev, M. S.; Молокеев, Максим Сергеевич
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Characteristics of nanocomplexes with iron Fe3+ in Glass Ionomer Cement powder by ESR method / V. V. Shapovalov, V. A. Shapovalov, Yu. A. Sluzhbin [et al.] // Phys. Solid State. - 2023. - Vol. 65, Is. 2. - P. 296-298, DOI 10.21883/PSS.2023.02.55415.489. - Cited References: 13 . - ISSN 1063-7834. - ISSN 1090-6460
Кл.слова (ненормированные):
Electronic Spin Resonance (ESR) -- nanocrystals -- crystal field potential -- intensity of ESR lines
Аннотация: The study is part of nanomedical biotechnology and is carried out by probing these systems using the Electronic Spin Resonance (ESR) method. The paper investigates Glass Ionomer Cement powder widely used in dental practice Glass Ionomer Cement C-Plus Triplekit-TM. To assess the quality of Glass Ionomer Cement and use ESR radiospectroscopy in the range from low (T=4.2 K) to room (T=300 K) temperatures. A new characteristic of compounds with nanocomplexes of magnetic iron ions Fe3+ is applied.

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Публикация на русском языке Характеристика нанокомплексов c железом Fe3+ в порошке стеклоиномерного цемента методом ЭПР [Текст] / V. V. Shapovalov, В. А. Шаповалов, Ю. А. Службин [и др.] // Физ. тверд. тела. - 2023. - Т. 65 Вып. 2. - С. 302-304

Держатели документа:
Organization “Math for America”, New York, USA
Galkin Donetsk Institute for Physics and Enginireeng, Donetsk, Russia
Kirensky Institute of Physics, Federal Research Center KSC SB, Russian Academy of Sciences, Krasnoyarsk, Russia

Доп.точки доступа:
Shapovalov, V. V.; Shapovalov, V. A.; Sluzhbin, Yu. A.; Drokina, T. V.; Дрокина, Тамара Васильевна; Vorotynov, A. M.; Воротынов, Александр Михайлович; Valkov, V. I.
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    Coordination units of Mn2+ modulation toward tunable emission in zero-dimensional bromides for white light-emitting diodes / G. J. Zhou, J. L. Ding, X. X. Jiang [et al.] // J. Mater. Chem. C. - 2022. - Vol. 10, Is. 6. - P. 2095-2102, DOI 10.1039/d1tc05680h. - Cited References: 57. - The present work was supported by the Natural Science Foundation of China (21871167), the 1331 Project of Shanxi Province and the Postgraduate Innovation Project of Shanxi Normal University (2019XBY018), the Beijing Natural Science Foundation (No. 2214068) and funded by RFBR according to the research project no. 19-52-80003 . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Модуляция координационных блоков с Mn2+ для управляемой люминесценции в нульмерных бромидах для белых светодиодов

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
HALIDE PEROVSKITE NANOCRYSTALS
RECENT PROGRESS
DOPING MN2+
Аннотация: Organic–inorganic metal halides have become a multifunctional platform for manipulating photoluminescence due to highly efficient and tunable emissions, especially for lead-free Mn2+-based halides. Herein, the zero-dimensional (0D) bromides of (C5H14N3)2MnBr4 and (CH6N3)2MnBr4 with different coordination environments were designed and synthesized by a solvent evaporation method. They exhibit green and red broadband emission peaks at 528 nm and 627 nm with high photoluminescence quantum yields of 86.83% and 61.91%, respectively, which are attributed to the d–d transition (4T1(G) → 6A1(S)) of [MnBr4]2− tetrahedral and [Mn3Br12]6− octahedral units. The cases emphasize the effect of organic ligands on the intrinsic emissions of Mn2+ ions, thereby revealing the luminescence mechanism of Mn2+ ions in 0D isolated structures through the Tanabe–Sugano (TS) energy diagram. Thanks to their bright and stable emissions, the fabricated white light-emitting diode (LED) based on (C5H14N3)2MnBr4 and (CH6N3)2MnBr4 provides an outstanding color rendering index (Ra) of 90.8 at a correlated color temperature (CCT) of 3709 K, along with the CIE chromaticity coordinates of (0.3985, 0.3979) and a luminous efficacy of 51.2 lm W−1. This work aims at clarifying the relationship between the coordination units of Mn2+ and tunable emissions, and in particular, proposes a new strategy to explore phosphors excited by blue light for white LEDs.

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Держатели документа:
Shanxi Normal Univ, Sch Chem & Mat Sci, Key Lab Magnet Mol & Magnet Informat Mat, Minist Educ, Taiyuan 030006, Peoples R China.
Chinese Acad Sci, China Tech Inst Phys & Chem, Beijing 100190, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
Beijng Technol & Business Univ, Dept Phys, Beijing 100048, Peoples R China.
Taiyuan Univ Technol, Coll Chem & Chem Engn, Key Lab Interface Sci & Engn Adv Mat, Minist Educ, Taiyuan 030024, Shanxi, Peoples R China.

Доп.точки доступа:
Zhou, Guojun; Ding, Jialiang; Jiang, Xingxing; Zhang, Jian; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ren, Qiqiong; Zhou, Jun; Li, Shili; Zhang, Xian-Ming
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    Магнетизм бериллиевой керамики со структурой перовскита BeTiO3 / А. В. Павлов, Л. И. Квеглис, А. В. Джес [и др.] // Фундамент. пробл. совр. материаловед. - 2022. - Т. 19, № 1. - С. 115-124 ; Basic Probl. Mater. Sci., DOI 10.25712/ASTU.1811-1416.2022.01.013. - Библиогр.: 24 . - ISSN 1811-1416
   Перевод заглавия: Magnetism of beryllium ceramics with the perovskite structure BeTiO3
Кл.слова (ненормированные):
бериллиевая керамика -- магнитный гистерезис -- электронная структура -- икосаэдрические кластеры -- martensitic transformations -- orientation relations -- Pitch deformation -- polar decomposition of the tensor -- martensite nanocrystals
Аннотация: Известно, что введение в ВеО-керамику добавки TiO2 после термообработки в восстановительной атмосфере сопровождается значительным увеличением электропроводности и способностью поглощать электромагнитное излучение в широком диапазоне частот. До сих пор механизм этого влияния до конца не установлен. С использованием методов Лоренцевой электронной микроскопии в сканирующем электронном микроскопе, а также вибрационного магнитометра, установлено проявление ферромагнетизма. Такая особенность бериллиевой керамики способствует поглощению электромагнитной энергии в объемных образцах, содержащих наночастицы TiO2. Установлено, что присутствие наночастиц способствует формированию структуры перовскита в зонах спекания BeO + TiO2. В структуре перовскита возможна поляризация молекул за счет формирования поляронов, что приводят к деформации решетки и смещению атомов. В результате такого смещения происходит изменение ближнего порядка в структуре перовскита и к образованию икосаэдрической фазы из исходной фазы со структурой кубоктаэдра. Малый размер атома бериллия позволяет организоваться тетраэдрической плотной упаковке в форме икосаэдра из атомов кислорода вокруг центрального атома бериллия. В результате повышается атомная плотность и плотность электронных состояний на уровне Ферми. Предлагаются модели для объяснения причины появления ферромагнетизма и электропроводности, которые обнаружены в бериллиевой керамике. С помощью метода спин-поляризованных электронов проведены расчеты электронной структуры нанокластеров с различным ближним порядком.
It is known that the introduction of TiO2 additives into BeO ceramics after heat treatment in a reducing atmosphere is accompanied by a significant increase in electrical conductivity and the ability to absorb electromagnetic radiation in a wide frequency range. Until now, the mechanism of this influence has not been fully established. Using the methods of Lorentzian electron microscopy in a scanning electron microscope, as well as a vibration magnetometer, the manifestation of ferromagnetism was established. This feature of beryllium ceramics promotes the absorption of electromagnetic energy in bulk samples containing TiO2 nanoparticles. It was found that the presence of nanoparticles promotes the formation of the perovskite structure in the BeO + TiO2 sintering zones. In the structure of perovskite, polarization of molecules is possible due to the formation of polarons, which leads to deformation of the lattice and displacement of atoms. As a result of this displacement, a change in the short-range order in the perovskite structure occurs and to the formation of an icosahedral phase from the initial phase with a cuboctahedral structure. The small size of the beryllium atom makes it possible to organize a tetrahedral close packing in the form of an icosahedron of oxygen atoms around the central beryllium atom. As a result, the atomic density and the density of electronic states at the Fermi level increase. Models are proposed to explain the reasons for the appearance of ferromagnetism and electrical conductivity found in beryllium ceramics. Using the spin-polarized electron method, the electronic structure of nanoclusters with different short-range orders has been calculated.

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Держатели документа:
Сибирский федеральный университет, пр. Свободный, 79, 660041, Красноярск, Россия
Восточно-Казахстанский университет им. С. Аманжолова, ул. 30-ой Гвардейской дивизии, 34, 070002, Усть-Каменогорск, Республика Казахстан
Восточно-Казахстанский технический университет им. Д. Серикбаева, ул. Протозанова, 69, 070004, Усть-Каменогорск, Республика Казахстан
Национальный исследовательский Томский государственный университет, пр. Ленина, 36, 634050, Томск, Россия
Институт физики им. Л.В. Киренского, Академгородок, 50, стр. 38, 660036, Красноярск, Россия

Доп.точки доступа:
Павлов, А. В.; Квеглис, Людмила Иосифовна; Kveglis L. I.; Джес, А. В.; Сапрыкин, Д. Н.; Насибуллин, Р. Т.; Великанов, Дмитрий Анатольевич; Velikanov, D. A.; Немцев, Иван Васильевич; Nemtsev, I. V.; Шалаев, П. О.

}
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Solvatochromic Photoluminescent Effects in All-Inorganic Manganese(II)-Based Perovskites by Highly Selective Solvent-Induced Crystal-to-Crystal Phase Transformations / H. Xiao, P. P. Dang, X. H. Yun [et al.] // Angew. Chem. Int. Edit. - 2021. - Vol. 60, Is. 7. - P. 3699-3707, DOI 10.1002/anie.202012383. - Cited References: 85. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018) . - ISSN 1433-7851. - ISSN 1521-3773

РУБ Chemistry, Multidisciplinary
Рубрики:
LEAD-FREE
   HALIDE PEROVSKITE
   NANOCRYSTALS
   MN2+
   LUMINESCENCE
Кл.слова (ненормированные):
lead-free materials -- low-dimensional perovskites -- luminescence -- manganese -- phase transitions
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, 5625 Renmin St, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Hefei 230026, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, Wuhan 430074, Peoples R China.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr,KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Xiao, Hui; Dang, Peipei; Yun, Xiaohan; Li, Guogang; Wei, Y.i.; Xiao, Xiao; Zhao, Yajie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cheng, Ziyong; Lin, Jun
}
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Square plate shaped magnetite nanocrystals / S. V. Komogortsev, S. V. Stolyar, L. A. Chekanova [et al.] // J. Magn. Magn. Mater. - 2021. - Vol. 527. - Ст. 167730, DOI 10.1016/j.jmmm.2021.167730. - Cited References: 42. - This work was supported by Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Region Science and Technology Support Fund to the research projects No. 20-42-240001 and 20-42-242902 and by the Council of the President of the Russian Federation for State Support of Young Scientists and Leading Scientific Schools (project no. MK-1263.2020.3). We are grateful to the Center of collective use of FRC KSC SB RAS for the provided equipment . - ISSN 0304-8853
Кл.слова (ненормированные):
Magnetite -- Nanoparticles -- Magnetic anisotropy
Аннотация: Square plate shaped magnetite nanocrystals have been synthesized by chemical precipitation from solution using arabinogalactan. A high crystal quality was observed in the plate plane while, across the plate, there is some stratification. The magnetic hysteresis in such particles is determined by the bulk magnetocrystalline anisotropy, plate shape anisotropy, and surface magnetic anisotropy. It is shown using the micromagnetic simulation that the ferromagnetic square nanoplates exhibit the extraordinary magnetization switching anisotropy, which should be taken into account for understanding the hysteretic properties of the particles.

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Держатели документа:
Krasnoyarsk Scientific Center, 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

Доп.точки доступа:
Komogortsev, S. V.; Комогорцев, Сергей Викторович; Stolyar, S. V.; Столяр, Сергей Викторович; Chekanova, L. A.; Чеканова, Лидия Александровна; Yaroslavtsev, R. N.; Ярославцев, Роман Николаевич; Bayukov, O. A.; Баюков, Олег Артемьевич; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Volochaev, M. N.; Волочаев, Михаил Николаевич; Eroshenko, P. E.; Ерошенко, П. Е.; Iskhakov, R. S.; Исхаков, Рауф Садыкович
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    Liu, Ying.
    Lattice doping of lanthanide ions in Cs2AgInCl6 nanocrystals enabling tunable photoluminescence / Y. Liu, M. S. Molokeev, Zh. Xia // Energy Mater. Adv. - 2021. - Vol. 2021. - Ст. 2585274, DOI 10.34133/2021/2585274. - Cited References: 42. - This work was supported by the National Natural Science Foundation of China (grant numbers 51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (grant number FRFTP-18-002C1), the Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (grant number 2017BT01X137). This work was also funded by RFBR according to the research project no. 19-52-80003 . - ISSN 2692-7640
   Перевод заглавия: Решеточное легирование ионами лантаноидов в нанокристаллах Cs2AgInCl6, обеспечивающее перестраиваемую фотолюминесценцию
Аннотация: Lead-free halide double perovskite Cs2AgInCl6 has become the research hotspot in the optoelectronic fields. It is a challenge to utilize the lattice doping by different lanthanide ions with rich and unique photoluminescence (PL) emissions for emerging photonic applications. Here, we successfully incorporated Dy3+, Sm3+, and Tb3+ ions into Cs2AgInCl6 nanocrystals (NCs) by the hot-injection method, bringing diverse PL emissions of yellowish, orange, and green light in Cs2AgInCl6:Ln3+ (Ln3+ = Dy3+, Sm3+, Tb3+). Moreover, benefiting from the energy transfer process, Sm3+ and Tb3+ ion-codoped Cs2AgInCl6 NCs achieved tunable emission from green to yellow orange and a fluorescent pattern from the as-prepared NC-hexane inks by spray coating was made to show its potential application in fluorescent signs and anticounterfeiting technology. This work indicates that lanthanide ions could endow Cs2AgInCl6 NCs the unique and tunable PL properties and stimulate the development of lead-free halide perovskite materials for new optoelectronic applications.

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The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RASs, Russia
Department of Engineering Physics and Radioelectronics, Siberian Federal University, Russia
Department of Physics, Far Eastern State Transport University, Russia
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Engineering, South China University of Technology, China

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo
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Incorporating rare-earth terbium(III) ions into Cs2AgInCl6:Bi nanocrystals toward tunable photoluminescence / Y. Liu, X. M. Rong, M. Z. Li [et al.] // Angew. Chem. - 2020. - Vol. 132, Is. 28. - P. 11731-11737, DOI 10.1002/ange.202004562. - Cited References: 43 . - ISSN 1521-3757

РУБ Chemistry, Multidisciplinary
Рубрики:
HALIDE DOUBLE PEROVSKITE
   LEAD-FREE
   LANTHANIDE
   STABILITY
   EMISSION
Кл.слова (ненормированные):
doping -- energy transfer -- perovskite nanocrystals -- photoluminescence -- terbium
Аннотация: The incorporation of impurity ions or doping is a promising method for controlling the electronic and optical properties and the structural stability of halide perovskite nanocrystals (NCs). Herein, we establish relationships between rare‐earth ions doping and intrinsic emission of lead‐free double perovskite Cs2AgInCl6 NCs to impart and tune the optical performances in the visible light region. Tb3+ ions were incorporated into Cs2AgInCl6 NCs and occupied In3+ sites as verified by both crystallographic analyses and first‐principles calculations. Trace amounts of Bi doping endowed the characteristic emission (5D4→7F6‐3) of Tb3+ ions with a new excitation peak at 368 nm rather than the single characteristic excitation at 290 nm of Tb3+. By controlling Tb3+ ions concentration, the emission colors of Bi‐doped Cs2Ag(In1−xTbx)Cl6 NCs could be continuously tuned from green to orange, through the efficient energy‐transfer channel from self‐trapped excitons to Tb3+ ions. Our study provides the salient features of the material design of lead‐free perovskite NCs and to expand their luminescence applications.

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Держатели документа:
Univ Sci, Sch Materials Sciences, Beijing Municipal Key Lab New Energy Materials, Technology Beijing,Technologies,Engn, Beijing, P. R. China.
Shenzhen Univ, Coll Materials Sci, Guangdong Res Ctr Interfacial Engn Functional Mat, Shenzhen Key Lab Special Functional Materials, Shenzhen, P. R. China.
Kirensky Inst Phys, Fed Res Ctr KSC SB RASs, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys, Radioelectronics, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
S China Univ Technology, Sch Materials Sci, State Key Lab Luminescent Materials, Guangdong Prov Key Lab Fiber Laser Materials, Guangzhou, P. R. China.

Доп.точки доступа:
Liu, Ying; Rong, Ximing; Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Xia, Zhiguo
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Microstructure and magnetic properties of Co58Ni10Fe5B16Si11 and Co58Ni10Fe5B16Si11-Al2O3 bulk amorphous coatings prepared by plasma spraying / E. A. Denisova, I. V. Nemtsev, S. V. Telegin [et al.] // J. Phys.: Conf. Ser. - 2020. - Vol. 1582, Is. 1. - Ст. 012078DOI 10.1088/1742-6596/1582/1/012078. - Cited References: 18. - This work was funded by the Russian Foundation for Basic Research, the Government of the Krasnoyarsk Territory, the Krasnoyarsk Regional Fund for the Support of Scientific and Technical Activities (project no. 18-42-240006 Nanomaterials with magnetic properties determined by the topological features of the nanostructure). The authors thank the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” for the provided equipment
Кл.слова (ненормированные):
Alumina -- Aluminum oxide -- Cobalt alloys -- Composite coatings -- Deposits -- Glass -- Heat treatment -- Industrial research -- Iron alloys -- Magnetic properties -- Magnetism -- Microstructure -- Nanocrystalline materials -- Nanocrystals -- Plasma jets -- Plasma spraying -- Silicon -- Silicon alloys
Аннотация: The bulk soft magnetic glassy Co58Ni10Fe5B16Si11 alloy specimens have been prepared by plasma spray deposition. In order to increase resistivity of the material, the bulk Co58Ni10Fe5B16Si11-Al2O3 composite materials were fabricated. The investigations of structure and magnetic properties of the bulk samples were carried out by X-ray diffraction, electron microscopy and magnetic measurements. The relation of the structural features and magnetic characteristics of the bulk coating to the main parameters of the deposition regimes was determined. Optimized plasma spray deposition parameters allowed obtaining bulk glassy samples with magnetic parameters that are not inferior to the characteristics of a thermally treated rapidly quenched ribbon with the same composition. It was found that the bulk amorphous coatings can be characterized as a heterophase system. The relaxation annealing of the Co58Ni10Fe5B16Si11 bulk coating leads to a phase transition in this alloy in the precrystallization temperature range. The magnetic properties of the both kinds of coatings are correlated with changes in the microstructure. The appearance of nanocrystalline phase with TC640 K during relaxation heat treatment leads to a decrease of the coercivity and to an increase of the permeability. A comparison between the magnetic properties of the CoNiFe-BSi coating and (CoNiFe-BSi)-Al2O3, composite coating is carried out.

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Держатели документа:
Kirensky Institute of Physics, Sb Russian Academy of Sciences, 50/38, Akademgorodok str., Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, 73 Svobodny ave., Krasnoyarsk, 660041, Russian Federation
Scientific Center, Federal Research Center Ksc Sb Ras, 50 Akademgorodok str., Krasnoyarsk, 660036, Russian Federation
Reshetnev Siberian State University of Science and Technology, 31 Krasnoyarsky Rabochy ave., Krasnoyarsk, 660037, Russian Federation
Krasnoyarsk Institute of Railways Transport, Novaja Zarja str., Krasnoyarsk, Russian Federation

Доп.точки доступа:
Denisova, E. A.; Денисова, Елена Александровна; Nemtsev, I. V.; Telegin, S. V.; Iskhakov, R. S.; Исхаков, Рауф Садыкович; Kuzovnikova, L. A.; Shepeta, N. A.; International Conference on High-Tech and Innovations in Research and Manufacturing(2020 ; 28 Feb. ; Krasnoyarsk)
}
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10.

Tailoring the preferable orientation relationship and shape of α-FeSi2nanocrystals on Si(001): The impact of gold and the Si/Fe flux ratio, and the origin of α/Si boundaries / I. A. Tarasov, T. E. Smolyarova, I. V. Nemtsev [et al.] // CrystEngComm. - 2020. - Vol. 22, Is. 23. - P. 3943-3955, DOI 10.1039/d0ce00399a. - Cited References: 52. - The experimental part of the reported study was funded by the Russian Science Foundation, project no. 16-13-00060-Π. Theoretical analysis of the ORs of the α-FeSi2 nanocrystals grown was supported by the Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science via research project No. 18-42-243013. We also acknowledge the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” for support with carrying out the microscopic investigations. I. A. Tarasov personally thanks M. A. Visotin for continuous fruitful discussion about the energetics of the formation of the α-FeSi2 nanocrystals . - ISSN 1466-8033
Кл.слова (ненормированные):
Gold -- Morphology -- Nanocrystals -- Silicides
Аннотация: The growth of α-FeSi2 nanocrystal ensembles on gold-activated and gold-free Si(001) surfaces at different Si/Fe flux ratios via molecular beam epitaxy is reported. The study reveals that the utilisation of gold as a catalyst regulates the preferable orientation relationship (OR) of the nanocrystals to silicon and their morphology at a given Si/Fe flux ratio. α-FeSi2 free-standing crystals with continuously tuned sizes from 30 nm up to several micrometres can be grown with an α(001)//Si(001) basic OR under gold-assisted conditions and an α(111)//Si(001) OR under gold-free growth conditions on a Si(001) surface. The preferred morphology of nanocrystals with a particular OR can be altered through changes to the Si/Fe flux ratio. Herein, the microstructure and basic OR between the silicide nanocrystals and the silicon substrate, and the formation of nanocrystal facets were analysed in detail with the help of microscopic techniques and simulation methods based on the analysis of near coincidence site (NCS) distributions at silicide/silicon interfaces. On the basis of the simulations used, we managed to reveal the nature of the interfaces observed for the main types of α-FeSi2 nanocrystals grown. Three types of interfaces typical for nanoplates with an α(001)//Si(001) basic OR, which are (i) stepped, (ii) stressed, and (iii) flat, are explained based on the tendency for the NCS density to increase at the interface. The results presented reveal the potential for the bottom-up fabrication of α-FeSi2 nanocrystals with tuned physical properties as potentially important contact materials and as building blocks for future nanoelectronic devices.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center, KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, 660037, Russian Federation
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Tarasov, I. A.; Тарасов, Иван Анатольевич; Smolyarova, T. E.; Смолярова, Татьяна Евгеньевна; Nemtsev, I. V.; Немцев, Иван Васильевич; Yakovlev, I. A.; Яковлев, Иван Александрович; Volochaev, M. N.; Волочаев, Михаил Николаевич; Solovyov, L. A.; Varnakov, S. N.; Варнаков, Сергей Николаевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
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