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A study of the hysteresis property of the current voltage characteristic in high-temperature superconductors / М. И. Петров [et al.] // Solid State Commun. - 1992. - Vol. 82, Is. 6. - P. 453-456, DOI 10.1016/0038-1098(92)90748-X. - Cited References: 21 . - ISSN 0038-1098

РУБ Physics, Condensed Matter
Рубрики:
HIGH-TC SUPERCONDUCTORS
YBA2CU3O7-X
FILMS
Аннотация: Temperature measurements of current-voltage characteristics (CVC) of the (Y, Lu)1Ba2Cu3O7-delta high-temperature superconductor have been performed. Analysis of the data shows that CVC of HTSC is mainly formed by two mechanisms: the creep of the Abrikosov vortices inside the crystallites and the Andreev reflection of the carriers within the metal character boundary between the crystallites.

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Держатели документа:
Институт физики им. Л.В. Киренского СО РАН

Доп.точки доступа:
Петров, Михаил Иванович; Petrov, M. I.; Krivomazov, S. N.; Khrustalev, B. P.; Хрусталев, Борис Петрович; Aleksandrov, K. S.; Александров, Кирилл Сергеевич
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    Amino-bridged attapulgite@perovskite nanocomposites: The role of bridge linkage to optical property and stability / L. Qiu, M. Guan, W. Wang [et al.] // Inorg. Chem. Front. - 2023. - Vol. 10, Is. 16. - P. 4797-4807, DOI 10.1039/D3QI00863K. - Cited References: 50. - This work was supported by the National Natural Science Foundation of China (Grant Nos. 52072349 and 52172162). Z.D. acknowledges support from the Fundamental Research Funds for the Central Universities, China University of Geosciences (Wuhan) (No. 162301202610), the Natural Science Foundation of Guangdong Province (2022A1515012145), Shenzhen Science and Technology Program (JCYJ20220530162403007), and Key Research and Development Plan of Hubei Province. G.L. acknowledges support from the Natural Science Foundation of Zhejiang Province (LR22E020004). M.S. Molokeev and S.P. Polyutov acknowledge the support by the Ministry of Science and High Education of Russian Federation (Project No. FSRZ2023-0006) . - ISSN 2052-1553
   Перевод заглавия: Аминомостиковые нанокомпозиты аттапульгит@перовскит: роль мостиковой связи в их оптических свойствах и стабильности
Аннотация: Perovskite-based nanocomposites have garnered significant interests due to their potential in interfacial engineering, optical modification, and stability enhancement. However, current understanding of the construction models between perovskites and guest materials is limited, and the design concept of perovskite-based nanocomposites remains unclear. Herein, we thoroughly investigate the effects of amino bridge linkage in attapulgite@perovskite nanocomposites on the crystallization kinetics, optical properties, and stabilities of perovskites by monitoring the difference in structural, compositional, and morphological characteristics. The attapulgite@perovskite nanocomposite with amino bridge linkage exhibited a smaller average size distribution of 23.8 ± 5.8 nm, along with enhanced thermal stability (81% relative PL intensity after a heating-cooling cycle) and photo-stability (84% relative PL intensity after 30 h ultraviolet light irradiation). These improvements can be attributed to the adequate passivation of amino bridge linkages. Our work aims to provide a deeper understanding of perovskite-based nanocomposite construction and inspire new approaches for modifying their optical properties and enhancing their stability.

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Держатели документа:
Faculty of Materials Science and Chemistry, China University of Geosciences, 388 Lumo Road, Wuhan 430074, P. R. China.
Zhejiang Institute, China University of Geosciences, Hangzhou 311305, P. R. China.
Shenzhen Institute, China University of Geosciences, Shenzhen, 518052, P. R. China.
International Research Center of Spectroscopy and Quantum Chemistry — IRC SQC, Siberian Federal University, Krasnoyarsk, 660041, Russia.
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Qiu, Lei; Guan, Mengyu; Wang, Wei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Polyutov, Sergey; Dai, Zhigao; Li, Guogang
}
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    Anomalous mechanical materials squeezing three-dimensional volume compressibility into one dimension / X. Jiang, M. S. Molokeev, L. Dong [et al.] // Nat. Commun. - 2020. - Vol. 11, Is. 1. - Ст. 5593, DOI 10.1038/s41467-020-19219-5. - Cited References: 49. - The authors acknowledge Zhuohong Yin for useful discussions and the experimental time provided by the 4W2 beam line of Beijing Synchrotron Radiation Facility (BSRF). This work was supported by the National Scientific Foundations of China (Grants 51702330, 11974360, 51872297, 51890864, 21975132, and 21991143), the Youth Innovation Promotion Association in CAS (Grant 2017035 for X.J.), Young Elite Scientist Sponsorship Program by CAST (YESS), and Fujian Institute of Innovation (FJCXY18010201) in CAS . - ISSN 2041-1723
   Перевод заглавия: Аномальные механические материалы, преобразующие трехмерную объемную сжимаемость в одномерную
Кл.слова (ненормированные):
high pressure -- mechanical property -- one-dimensional modeling -- precision -- pressure effect -- stress-strain relationship -- three-dimensional modeling
Аннотация: Anomalous mechanical materials, with counterintuitive stress-strain responding behaviors, have emerged as novel type of functional materials with highly enhanced performances. Here we demonstrate that the materials with coexisting negative, zero and positive linear compressibilities can squeeze three-dimensional volume compressibility into one dimension, and provide a general and effective way to precisely stabilize the transmission processes under high pressure. We propose a “corrugated-graphite-like” structural model and discover lithium metaborate (LiBO2) to be the first material with such a mechanical behavior. The capability to keep the flux density stability under pressure in LiBO2 is at least two orders higher than that in conventional materials. Our study opens a way to the design and search of ultrastable transmission materials under extreme conditions.

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Держатели документа:
Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, China
Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Wuhan National Laboratory for Optoelectronics and School of Physics, Huazhong University of Science and Technology, Wuhan, 430074, China
Laboratory of Space Astronomy and Technology, National Astronomical Observatories, Chinese Academy of Sciences, Beijing, 100101, China
University of Chinese Academy of Sciences, Beijing, 100049, China
Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, 100049, China
Institute of Deep-sea Science and Engineering, Chinese Academy of Sciences, Sanya, 572000, China
Institute of Mechanics, Chinese Academy of Sciences, Beijing, 100190, China
School of Materials Science and Engineering; TKL of Metal and Molecule-Based Material Chemistry, Nankai University, Tianjin, 300350, China

Доп.точки доступа:
Jiang, X.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Dong, L.; Dong, Z.; Wang, N.; Kang, L.; Li, X.; Li, Y.; Tian, C.; Peng, S.; Li, W.; Lin, Z.
}
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Chemistry of vinylidene complexes—XXVII—new µ-vinylidene MnPt complexes with platinum-coordinated 1-adamantyl isocyanide ligand: spectroscopic, structural and electrochemical study / V. V. Verpekin, O. S. Chudin, A. A. Kondrasenko [et al.] // Transition Met. Chem. - 2022. - Vol. 47. Is. 7-8. - P. 283-292, DOI 10.1007/s11243-022-00511-w. - Cited References: 46. - This work was conducted within the framework of the budget project 0287–2021-0012 for Institute of Chemistry and Chemical Technology SB RAS . - ISSN 0340-4285
Кл.слова (ненормированные):
Binary alloys -- Cyanides -- Ligands -- Manganese alloys -- Nuclear magnetic resonance spectroscopy -- Platinum compounds -- Redox reactions -- Chemical oxidation -- Electrochemical studies -- Isocyanide ligands -- Redox property -- Spectroscopic studies -- Structural studies -- Vinylidene complexes -- X-ray diffraction studies -- Platinum alloys
Аннотация: New binuclear MnPt µ-vinylidene complexes Cp(CO)2Mn(µ-C=CHPh)Pt(CN–Ad)(L) [L=PPh3 (1a), P(OPri)3 (2a)] bearing a terminal platinum-coordinated 1-adamantyl isocyanide ligand were prepared by the treatment of Cp(CO)2Mn(µ-C=CHPh)Pt(CO)(L) [L=PPh3 (1b), P(OPri)3 (2b)] with CN-Ad. At the same time the reaction between Cp(CO)2Mn(µ-C=CHPh)Pt(L)2 [L=PPh3 (1c), P(OPri)3 (2c)] and CN-Ad did not proceed. The new complexes were characterized by IR and 1H, 13C, 31P NMR spectroscopy. The molecular structure of Cp(CO)2Mn(µ-C=CHPh)Pt(CN–Ad)[P(OPri)3] (2a) was determined by an X-ray diffraction study. The redox properties of the new complexes and their reactions of chemical oxidation were studied. An influence of the platinum-coordinated 1-adamantyl isocyanide ligand on the properties of the synthesized µ-vinylidene compounds 1a and 2a was revealed.

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Держатели документа:
Institute of Chemistry and Chemical Technology SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-24, Krasnoyarsk, 660036, Russian Federation
Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Svobodny Prospect, 79, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Verpekin, V. V.; Chudin, O. S.; Kondrasenko, A. A.; Burmakina, G. V.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Zimonin, D. V.; Rubaylo, A. I.
}
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    Comparative investigations of the crystal structure and photoluminescence property of eulytite-type Ba3Eu(PO4)3 and Sr3Eu(PO4)3 / H. P. Ji [et al.] // Dalton Trans. - 2015. - Vol. 44, Is. 16. - P. 7679-7686, DOI 10.1039/c4dt03887h. - Cited References:65. - This work was supported by the National Natural Science Foundations of China (grant no. 51032007, no. 51002146, no. 51272242), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), Natural Science Foundations of Beijing (2132050), and the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047) and Beijing Youth Excellent Talent Program (YETP0635). VVA is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 1477. - ISSN 1477-9234
   Перевод заглавия: Сравнительный анализ кристаллических структур и люминесцентных свойств Ba3Eu(PO4)3 и Sr3Eu(PO4)3. со структурой эвлитина

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
LIGHT-EMITTING-DIODES
DOPED Sr3Gd(PO4(3 PHOSPHOR
EFFICIENT
Аннотация: In this study, the Ba3Eu(PO4)3 and Sr3Eu(PO4)3 compounds were synthesized and the crystal structures were determined for the first time by Rietveld refinement using powder X-ray diffraction (XRD) patterns. Ba3Eu(PO4)3 crystallizes in cubic space group I3d, with cell parameters of a = 10.47996(9) Å, V = 1151.01(3) Å3 and Z = 4; Ba2+ and Eu3+ occupy the same site with partial occupancies of 3/4 and 1/4, respectively. Besides, in this structure, there exists two distorted kinds of the PO4 polyhedra orientation. Sr3Eu(PO4)3 is isostructural to Ba3Eu(PO4)3 and has much smaller cell parameters of a = 10.1203(2) Å, V = 1036.52(5) Å3. The bandgaps of Ba3Eu(PO4)3 and Sr3Eu(PO4)3 are determined to be 4.091 eV and 3.987 eV, respectively, based on the UV–Vis diffuse reflectance spectra. The photoluminescence measurements reveal that, upon 396 nm n-UV light excitation, Ba3Eu(PO4)3 and Sr3Eu(PO4)3 exhibit orange-red emission with two main peaks at 596 nm and prevailing 613 nm, corresponding to the 5D0 → 7F1 and 5D0 → 7F2 transitions of Eu3+, respectively. The dynamic disordering in the crystal structures contributes to the broadening of the luminescence spectra. The electronic structure of the phosphates was calculated by the first-principles method. The analysis elucidats that the band structures are mainly governed by the orbits of phosphorus, oxygen and europium, and the sharp peaks of the europium f-orbit occur at the top of the valence bands.

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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.
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, 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.
Chinese Acad Sci, Tech Inst Phys & Chem, Beijing Ctr Crystal R&D, Key Lab Funct Crystals & Laser Technol, Beijing 100190, Peoples R China.
Univ Chinese Acad Sci, Beijing 100049, Peoples R China.
Russian Acad Sci, Inst Semicond Phys, SB RAS, Lab Opt Mat & Struct, Novosibirsk 630090, Russia.
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia.
Novosibirsk State Univ, Lab Semicond & Dielect Mat, Novosibirsk 630090, Russia.

Доп.точки доступа:
Ji, Haipeng; Huang, Zhaohui; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Jiang, Xingxing; Lin, Zheshuai; Atuchin, V. V.
}
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    Cyan-emitting LiBaBO3:Eu2+ phosphor: Crystal structure and luminescence property comparison with LiSrBO3:Eu2+ / Z. H. Huang [et al.] // Chem. Phys. Lett. - 2015. - Vol. 628. - P. 21-24, DOI 10.1016/j.cplett.2015.04.004. - Cited References:19. - This work was supported by the National Natural Science Foundations of China (Grant No. 51032007) and the Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20130022110006). . - ISSN 0009. - ISSN 1873-4448
   Перевод заглавия: Голубой люминофор LiBaBO3:Eu2+: сравнение кристаллической структуры и люминесценции с LiSrBO3:Eu2+

РУБ Chemistry, Physical + Physics, Atomic, Molecular & Chemical
Рубрики:
INORGANIC-COMPOUNDS
WHITE-LIGHT
Eu2+
Аннотация: Cyan-emitting LiBaBO3:Eu2+ phosphor was synthesized by solid-state reaction at 800 °C. Structure refinement by Rietveld method reveals that LiBaBO3 crystallizes in a monoclinic cell, space groups P21/c or P21/n. Upon 365 nm excitation, LiBaBO3:Eu2+ shows a symmetric emission band peaking at 496 nm with full-width at half-maximum of 80 nm; when monitoring at 496 nm, a broad excitation band in the UV region (250–420 nm) is observed. The luminescence property of LiBaBO3:Eu2+ is considerably different from LiSrBO3:Eu2+ which holds the same space group. The local structures of the two hosts are compared to explain the different behaviors of Eu2+.

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

Доп.точки доступа:
Huang, Zhaohui; Ji, Haipeng; Fang, Minghao; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Shuyue; Liu, Yan'gai; Wu, Xiaowen
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Degenerate bound states in the continuum in square and triangular open acoustic resonators / A. Sadreev, E. Bulgakov, A. Pilipchuk [et al.] // Phys. Rev. B. - 2022. - Vol. 106, Is. 8. - Ст. 085404, DOI 10.1103/PhysRevB.106.085404. - Cited References: 43 . - ISSN 2469-9950
Кл.слова (ненормированные):
Q factor measurement -- Bound-states -- Eigenstates -- Flow byes -- High Q factor -- Output flow -- Property -- Small perturbations -- Square resonators -- Triangular resonators -- Acoustic resonators
Аннотация: We consider square and equilateral triangular open acoustic resonators with the C4v and C3v symmetries, respectively. There is a unique property of square and triangular resonators of accidental number fourfold degeneracy of eigenstates that gives rise to twofold-degenerate Friedrich-Wintgen (FW) bound states in the continuum (BICs). Compared to usual FW BICs, the degenerate FW BICs maintain high Q factor in wide range of the size of resonators. That removes the fabrication difficulties of the proper choice of resonator. The presence of degenerate BICs in triangular resonators is extremely sensitive to switch output flows by small perturbations with 100% efficiency.

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Держатели документа:
Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
School of Engineering and Information Technology, University of New South Wales Canberra, Northcott Drive, AC2600, Australia

Доп.точки доступа:
Sadreev, A. F.; Садреев, Алмаз Фаттахович; Bulgakov, E. N.; Булгаков, Евгений Николаевич; Pilipchuk, A. S.; Пилипчук, Артем Сергеевич; Miroshnichenko, A.; Huang, L.
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Effect of cobalt impurity ions on the magnetic and electrical properties of iron monosilicide crystals / G. S. Patrin [et al.] // J. Exp. Theor. Phys. - 2011. - Vol. 112, Is. 2. - P. 303-309, DOI 10.1134/S1063776111010146. - Cited References: 23 . - ISSN 1063-7761

РУБ Physics, Multidisciplinary
Рубрики:
GAP FORMATION
FESI
Кл.слова (ненормированные):
Concentration dependence -- Electrical property -- Energy structures -- Experimental data -- Experimental investigations -- Field dependence -- Impurity ions -- Kondo models -- Magnetic and electrical properties -- Si crystals -- Cobalt -- Crystal impurities -- Crystals -- Magnetic susceptibility -- Electric properties
Аннотация: The results of experimental investigations of Fe1 - x Co (x) Si crystals in the impurity limit with x = 0.001, 0.005, and 0.01 are reported. The temperature and field dependences of the magnetic susceptibility have been studied. According to the experimental data, the introduction of cobalt impurity leads to a change in the energy structure, which is most pronounced in a change in the electrical properties. The temperature, field, and concentration dependences of the resistivity have been measured. The results have been interpreted in the framework of the Kondo model.

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Держатели документа:
[Patrin, G. S.
Velikanov, D. A.
Volkov, N. V.
Yurkin, G. Yu.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
[Patrin, G. S.
Beletskii, V. V.] Siberian Fed Univ, Inst Engn Phys & Radio Elect, Krasnoyarsk 660041, Russia
ИФ СО РАН
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk 660036, Russian Federation
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Krasnoyarsk 660041, Russian Federation

Доп.точки доступа:
Patrin, G. S.; Патрин, Геннадий Семёнович; Beletskii, V. V.; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Volkov, N. V.; Волков, Никита Валентинович; Yurkin, G. Yu.
}
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Effect of crystal size on the crystalline structure and magnetic properties of cobalt films obtained via chemical deposition / A. V. Chzhan, S. A. Podorozhnyak, S. A. Gromilov [et al.] // Bull. Russ. Acad. Sci. Phys. - 2022. - Vol. 86, Is. 5. - P. 614-617, DOI 10.3103/S1062873822050045. - Cited References: 18 . - ISSN 1062-8738
Кл.слова (ненормированные):
Anisotropy -- Crystal structure -- Crystals -- Deposition -- Magnetic field effects -- Anisotropic property -- Chemical deposition -- Co-P films -- Cobalt film -- Crystal-size -- Face-centred cubic -- Hexagonal close packed -- Induced anisotropy -- Sizes effect
Аннотация: A study is performed of the relationship between the sizes of cobalt crystallites and the coercive and anisotropic properties of Co–P films obtained via chemical deposition. The emergence of induced anisotropy in films obtained at low pH (7.2–8.7) is due to size effects that transform the cobalt’s crystal lattice from face-centered cubic to hexagonal close-packed as the film grows in a magnetic field.

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Публикация на русском языке Влияние размерных эффектов на кристаллическую структуру и магнитные свойства кобальтовых пленок, полученных химическим осаждением [Текст] / А. В. Чжан, С. А. Подорожняк, С. А. Громилов [и др.] // Изв. РАН. Сер. физич. - 2022. - Т. 86. № 5. - С. 730-734

Держатели документа:
Krasnoyarsk State Agrarian University, Krasnoyarsk, 660049, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation
Kirensky Institute of Physics, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Irkutsk State Transport University, Krasnoyarsk, 660028, Russian Federation

Доп.точки доступа:
Chzhan, A. V.; Podorozhnyak, S. A.; Gromilov, S. A.; Patrin, G. S.; Патрин, Геннадий Семёнович; Moroz, J. M.
}
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10.

    Facile solution-precipitation assisted synthesis and luminescence property of greenish-yellow emitting Ca6Ba(PO4)4O:Eu2+ phosphor / H. Ji [et al.] // Mater. Res. Bull. - 2016. - Vol. 75. - P. 233-238, DOI 10.1016/j.materresbull.2015.11.055. - Cited References: 22. - This work was partly supported by the National Natural Science Foundations of China (grant nos. 51272242, 51472222, 51511130035), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), and the Russian Foundation for Basic Research (grant no. 15-52-53080 GFEN_a). VVA was partly supported by the Ministry of Education and Science of the Russian Federation . - ISSN 0025-5408
   Перевод заглавия: Легкий синтез с помощью осаждения раствора и люминесцентные свойства люминофора Ca6Ba(PO4)4O:Eu2+ излучающего зеленовато-желтый свет.

РУБ Materials Science, Multidisciplinary
Рубрики:
SOLID-SOLUTION PHOSPHORS
   PHOTOLUMINESCENCE PROPERTIES
   VIBRATIONAL PROPERTIES
   ENERGY-TRANSFER
   DIODES
Кл.слова (ненормированные):
Optical materials -- Luminescence -- Optical properties -- Crystal structure -- Phosphors
Аннотация: Greenish-yellow emitting microcrystalline Ca6Ba(PO4)4O:Eu2+ phosphor was successfully prepared by a solution-precipitation assisted high temperature reaction method. Phase structure, morphology and/or luminescence properties of the precursor and the as-prepared phosphors were characterized. The phase-pure Ca6Ba(PO4)4O:Eu2+ phosphors were obtained with smooth grain surface and particle size of 2–8 μm. Ca6Ba(PO4)4O:Eu2+ exhibits bright greenish-yellow color emission with its maximum at 540 nm upon UV-blue light excitation. The maximum position of the broad emission band is independent on the calcination temperature. The emission intensity increases with increasing calcination temperature due to improved crystallinity. Besides, the presence of two Eu2+ emission centers in the Ca6Ba(PO4)4O crystal lattice was confirmed and the coordination effects are considered concerning the roles of isolated O atoms and those from the PO4 tetrahedra.

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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
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, 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
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 Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk, Russian Federation

Доп.точки доступа:
Ji, H.; Huang, Z.; Xia, Z.; Xie, Y; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.
Свободных экз. нет}
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