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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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Nemtsev, A. V.
Ab initio study of the polarization, electronic, magnetic, and optical properties of perovskite SrMO3 (M = Fe, Mn) crystals and thin films containing magnetic ions / A. V. Nemtsev, V. S. Zhandun, V. I. Zinenko // J. Exp. Theor. Phys. - 2018. - Vol. 126, Is. 4. - P. 497-505, DOI 10.1134/S1063776118030056. - Cited References: 30 . - ISSN 1063-7761
Кл.слова (ненормированные):
Antiferromagnetism -- Density functional theory -- Electronic properties -- Iron compounds -- Manganese compounds -- Optical properties -- Perovskite -- Perovskite solar cells -- Polarization -- Strontium compounds
Аннотация: The magnetic, electronic, and polarization properties of the SrFeO3 and SrMnO3 compounds with a perovskite structure are calculated using the density functional theory in the bulk and thin-film states. A ferroelectric instability is found to be absent in the bulk state, and the polar mode is softened in the thin-film state of SrMnO3 in the presence of tensile stresses in the substrate. As a result, a polar phase with a polarization of 23 μC/cm2 appears, which agrees with experimental data. The study of the magnetic and electronic properties demonstrates the existence of G-type antiferromagnetic ordering in SrMnO3 and the appearance of a dielectric gap of about 1.5 eV in its thin film. A ferromagnetic phase with metallic conduction in both the bulk and thin-film states is detected in SrFeO3.

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Публикация на русском языке Немцев, Андрей В. Исследования ab initio электронных, магнитных и оптических свойств кристаллов и тонких пленок перовскитов SrMeOs (Me = Fe, Mn), содержащих магнитные ионы [Текст] / А. В. Немцев, В. С. Жандун, В. И. Зиненко // Журн. эксперим. и теор. физ. - 2018. - Т. 153 Вып. 4. - С. 605-614

Держатели документа:
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Zhandun, V. S.; Жандун, Вячеслав Сергеевич; Zinenko, V. I.; Зиненко, Виктор Иванович; Немцев, Андрей В.
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Popov, E. A.
Absorption of light by exchange-coupled ions in a 2D antiferromagnet / E. A. Popov, B. V. Beznosikov // Phys. Solid State. - 2003. - Vol. 45, Is. 8. - P. 1475-1478, DOI 10.1134/1.1602882. - Cited References: 9 . - ISSN 1063-7834

РУБ Physics, Condensed Matter
Рубрики:
OPTICAL-ABSORPTION
RB2MNCL4
Аннотация: The optical absorption spectra of Rb2MnxCd1-xCl4 crystals are experimentally studied in the vicinity of a magnon sideband of the exciton band at a manganese content x ranging from 1.0 to 0.4. Additional absorption bands are observed with an increase in the magnetic structural disorder upon replacement of manganese ions by cadmium ions. An analysis of the evolution of the additional absorption bands in a magnetic field during the spin-flop phase transition and the change in the intensity with variations in the manganese content x demonstrates that these bands are associated with the excitation of the exchange-coupled pairs of manganese ions located in different environments in a plane square lattice. The phase boundary between the antiferromagnetic and spin-flop phases is constructed using the results of optical measurements. The manganese content corresponding to the magnetic percolation point is evaluated. (C) 2003 MAIK "Nauka/Interperiodica".

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Держатели документа:
Siberian State Aerosp Univ, Krasnoyarsk 660014, Russia
Russian Acad Sci, LV Kirensky Phys Inst, Sierian Div, Krasnoyarsk 660036, Russia
ИФ СО РАН
Siberian State Aerospace University, Krasnoyarsk 660014, Russian Federation
Kirensky Institute of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Beznosikov, B. V.; Безносиков, Борис Валерьевич
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Krasnov, I. V.
All-optical confinement of ultracold plasma with resonant ions / I. V. Krasnov // Phys. Lett. A. - 2009. - Vol. 373, Is. 26. - P. 2291-2297, DOI 10.1016/j.physleta.2009.04.042. - Cited References: 40 . - ISSN 0375-9601

РУБ Physics, Multidisciplinary
Рубрики:
RADIATION-PRESSURE
   NEUTRAL PLASMAS
   POTENTIAL WELLS
   ATOMIC MOTION
   LIGHT-FIELD
   FORCE
   SUPERLATTICE
   RECTIFICATION
   WAVE
Кл.слова (ненормированные):
Laser cooling and trapping -- Ultracold neutral plasma -- Rectified radiation forces -- Laser cooling and trapping -- Rectified radiation forces -- Ultracold neutral plasma
Аннотация: The solution of the problem of all-optical (nonmagnetic) confinement of ultracold electron-ion neutral plasma based on selective action on plasma ions with quantum transition J = 1 -> J = 0 of so-called rectified radiation forces in a strong nonmonochromatic light field is suggested. The presented scheme of the three-dimensional dissipative optical trap for plasma allows one to obtain long-lived ultracold plasma with controlled characteristics. The lifetime of the ultracold plasma in such a trap may exceed considerably (by orders of magnitude) the time of free plasma expansion and the lifetime in the (earlier proposed) optical molasses for the ultracold plasma. (C) 2009 Elsevier B.V. All rights reserved.

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Держатели документа:
Russian Acad Sci, Inst Computat Modeling, Siberian Div, Krasnoyarsk 660036, Russia
ИВМ СО РАН
Institute of Computational Modeling, Siberian Division, Russian Academy of Sciences, 660036 Krasnoyarsk, Russian Federation
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Analysis of the exchange magnetic structure in Pb3Mn7O15 / E. V. Eremin [et al.] // J. Exp. Theor. Phys. - 2017. - Vol. 124, Is. 5. - P. 792-804, DOI 10.1134/S1063776117040112. - Cited References: 16 . - ISSN 1063-7761
Кл.слова (ненормированные):
Crystallography -- Magnetic properties -- Magnetic structure -- Magnetism -- Manganese -- Indirect couplings -- Manganese ions -- Structural and magnetic properties -- Single crystals
Аннотация: The indirect-coupling model is used to analyze the exchange magnetic structure of Pb3Mn7O15 in the hexagonal setting. The ratios of manganese ions Mn4+/Mn3+ in each nonequivalent position are determined. Pb3(Mn0.95Ge0.05)7O15 and Pb3(Mn0.95Ga0.05)7O15 single crystals are grown by the solution–melt method in order to test the validity of the proposed model. The structural and magnetic properties of the single crystals are studied. The magnetic properties of the grown single crystals are compared with those of nominally pure Pb3Mn7O15. © 2017, Pleiades Publishing, Inc.

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Публикация на русском языке Анализ обменной магнитной структуры Pb3Mn7O15 [Текст] / Е. В. Еремин [и др.] // Журн. эксперим. и теор. физ. : Наука, 2017. - Т. 151 Вып. 5. - С. 930-943

Держатели документа:
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, pr. Akademika Lavrent’eva 3, Novosibirsk, Russian Federation
Novosibirsk State University, ul. Pirogova 2, Novosibirsk, Russian Federation

Доп.точки доступа:
Eremin, E. V.; Еремин, Евгений Владимирович; Volkov, N. V.; Волков, Никита Валентинович; Sablina, K. A.; Саблина, Клара Александровна; Bayukov, O. A.; Баюков, Олег Артемьевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Komarov, V. Y.
}
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Ovchinnikov, S. G.
Anisotropic interactions in magnetic crystals with S-state ions. Nanostructures / S. G. Ovchinnikov, V. V. Rudenko // Phys. Usp. - 2014. - Vol. 57, Is. 12. - P. 1180-1198, DOI 10.3367/UFNe.0184.201412b.1299. - Cited References:97. - We are grateful to L M Rudenko, T V Spirina, and N V Veretennikova for the assistance in the preparation of this review. This study was supported in part by the Program of Federal Support for Leading Scientific Schools of the Russian Federation (project No. NSh 1044.2012.2); by the President's Program of Support for Leading Scientific Schools (project No. NSh-2886.2014.2); and by the Russian Foundation for Basic Research (project No. 13-02-00358). . - ISSN 1063. - ISSN 1468-4780. - ISSN

РУБ Physics, Multidisciplinary
Рубрики:
PARAMAGNETIC-RESONANCE
ANTIFERROMAGNETIC-RESONANCE
EXCHANGE
Аннотация: Anisotropy mechanisms in compounds with S-state ions are discussed, including the 'single-ion' exchange mechanism that was developed theoretically by Nikiforov and coworkers based on the two-ion model and which has only recently received detailed experimental study. Results demonstrating the significant role of the 'single-ion' source are presented. An independent generalized method for quantitatively describing and predicting the anisotropy of magnetically ordered crystals is discussed, and its potential for the investigation of the BiFeO3 multiferroic in the region of the existence of a spin cycloid is examined. The anisotropic interactions responsible for the formation of nanostructures in the form of spin vortices (skyrmions) in MnSi and Cu2OSeO3 are analyzed.

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Публикация на русском языке Овчинников, Сергей Геннадьевич. Анизотропные взаимодействия в магнитных кристаллах с ионами в S-состоянии. Наноструктуры [Текст] / С. Г. Овчинников, В. В. Руденко // Успехи физ. наук : Ред. журн. "Успехи физ. наук", 2014. - Т. 184 № 12. - С. 1299-1318

Доп.точки доступа:
Rudenko, V. V.; Руденко, Валерий Васильевич; Овчинников, Сергей Геннадьевич; Program of Federal Support for Leading Scientific Schools of the Russian Federation [NSh 1044.2012.2]; President's Program of Support for Leading Scientific Schools [NSh-2886.2014.2]; Russian Foundation for Basic Research [13-02-00358]
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Anomalous in-plane electronic scattering in charge ordered Na 0.41CoO 2•0.6H 2O / G. X. Cao [et al.] // Phys. Rev. Lett. - 2012. - Vol. 108, Is. 23. - Ст. 236401, DOI 10.1103/PhysRevLett.108.236401. - Cited References: 41. - We thank H. Habermeier, D. Mandrus, B. C. Sales, I. Eremin, I. I. Mazin, and P. J. Hirschfeld for useful discussions. G. Cao acknowledges support from NSFC (No. 10804068, 10774097). M. M. K. acknowledges support from RFBR (Grant No. 09-02-00127), Presisium of RAS program "Quantum physics of condensed matter" N5.7, Integration Grant of SBRAS-UrBRAS N40, and Russian FCP (GK 16.740.12.0731), and The Dynasty Foundation and ICFPM. Work at ORNL was supported by the Department of Energy, BES, Materials Science and Engineering Division. . - ISSN 0031-9007

РУБ Physics, Multidisciplinary
Рубрики:
SUPERCONDUCTIVITY
   TRIPLET
   FLUCTUATIONS
   IONS
Аннотация: We report electronic transport measurements on high quality floating zone grown NaxCoO2 and Na0.41CoO2·0.6H2O single crystals. We find an in-plane electronic scattering minimum near 11 K and a clear charge ordering at approximately 50 K. The electronic and magnetic properties in hydrated and nonhydrated Na0.41CoO2 samples are similar at higher temperature, but evolve in markedly different ways below ∼50 K, where a strong ferromagnetic tendency is observed in the hydrated sample. Model calculations show the relationship of this tendency to the structure of the Fermi surface. The results, particularly the clear differences between the hydrated and nonhydrated material show a substantially enhanced ferromagnetic tendency upon hydration. Implications for superconductivity are discussed.

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Держатели документа:
[Cao, Guixin
Gao, Yuze
Le Tacon, Mathieu
Lin, Chengtian] Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
[Cao, Guixin] Shanghai Univ, Dept Phys, Shanghai 200444, Peoples R China
[Cao, Guixin] Univ Tennessee, Dept Mat Sci & Engn, Knoxville, TN 37996 USA
[Korshunov, Maxim M.] Univ Florida, Dept Phys, Gainesville, FL 32611 USA
[Korshunov, Maxim M.] Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
[Korshunov, Maxim M.] Siberian Fed Univ, Krasnoyarsk 660041, Russia
[Singh, David J.] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA

Доп.точки доступа:
Cao, G. X.; Korshunov, M. M.; Коршунов, Максим Михайлович; Gao, Y. Z.; Le Tacon, M.; Singh, D. J.; Lin, C. T.
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Antiferromagnetic Resonance and Dielectric Properties of Rare-earth Ferroborates in the Submillimeter Frequency Range / A. M. Kuz'menko [et al.] // J. Exp. Theor. Phys. - 2011. - Vol. 113, Is. 1. - P. 113-120, DOI 10.1134/S106377611105013X. - Cited References: 27. - This work was supported by the Russian Foundation for Basic Research, project no. 10-02-00846. . - ISSN 1063-7761

РУБ Physics, Multidisciplinary
Рубрики:
GDFE3(BO3)(4)
SPECTROSCOPY
CRYSTAL
Кл.слова (ненормированные):
Antiferromagnetic resonance -- Basic parameters -- Effective anisotropy constant -- Ferroborates -- Ferroics -- Ferromagnetic orderings -- Frequency ranges -- Magnetic interactions -- Magnetoresonance -- Millimeter frequency range -- Rare earth ions -- Submillimeters -- Antiferromagnetic materials -- Crystallography -- Erbium -- Europium -- Ferromagnetic resonance -- Ion exchange -- Magnetic anisotropy -- Magnetic devices -- Magnetic structure -- Permittivity -- Resonance -- Antiferromagnetism
Аннотация: The magnetoresonance and dielectric properties of a number of crystals of a new family of multiferroics, namely, rare-earth ferroborates RFe(3)(BO(3))(4) (R = Y, Eu, Pr, Tb, Tb(0.25)Er(0.75)), are studied in the submillimeter frequency range (nu = 3-20 cm(-1)). Ferroborates with R = Y, Tb, and Eu exhibit permittivity jumps at temperatures of 375, 198, and 58 K, respectively, which are caused by the R32 -> P3(1)2(1) phase transition. Antiferromagnetic resonance (AFMR) modes in the subsystem of Fe(3+) ions are detected in the range of antiferromagnetic ordering (T < T(N) = 30-40 K) in all ferroborates that have either an easy-plane (Y, Eu) or easy-axis (Pr, Tb, Tb(0.25)Er(0.75)) magnetic structure. The AFMR frequencies are found to depend strongly on the magnetic anisotropy of a rare-earth ion and its exchange interaction with the Fe subsystem, which determine the type of magnetic structure and the sign and magnitude of an effective anisotropy constant. The basic parameters of the magnetic interactions in these ferroborates are found, and the magnetoelectric contribution to AFMR is analyzed.

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Держатели документа:
[Kuz'menko, A. M.
Mukhin, A. A.
Ivanov, V. Yu.
Lebedev, S. P.] Russian Acad Sci, Inst Gen Phys, Moscow 119991, Russia
[Kadomtseva, A. M.] Moscow MV Lomonosov State Univ, Moscow 119991, Russia
[Bezmaternykh, L. N.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
ИФ СО РАН
Institute of General Physics, Russian Academy of Sciences, ul. Vavilova 38, Moscow, 119991, Russian Federation
Moscow State University, Moscow, 119991, Russian Federation
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Kuz'menko, A. M.; Mukhin, A. A.; Ivanov, V. Y.; Kadomtseva, A. M.; Lebedev, S. P.; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич
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    Arrangement of Rh3+ ions in fac-triamminetrichloridorhodium from powder data and in fac-triamminetrinitratorhodium crystals twinned by merohedry / A. D. Vasiliev [et al.] // Acta Crystallogr. C. - 2013. - Vol. 69, Pt. 12. - P. 1462–1466 ; Spec. is. Interplay of crystallogr., spectrosc. and theor. meth. for solving chem. prob., DOI 10.1107/S010827011303076X . - ISSN 0108-2701
   Перевод заглавия: Расположение ионов Rh3+ в гран-триамминтрихлоридродии из порошковых данных и в мероэдрически двойникованном кристалле гран-триамминтринитрародия
Кл.слова (ненормированные):
crystal structure -- powder diffraction -- merohedral twinning -- fac-triamminetrichloridorhodium -- low solubility -- fac-triamminetrinitratorhodium
Аннотация: The rhodium complexes [RhCl3(NH3)3], (I), and [Rh(NO3)3(NH3)3], (II), are built from octahedral RhX3(NH3)3 units; in (I) they are isolated units, while in (II) the units are stacked in columns with partially filled sites for the Rh atoms. The octahedra of monoclinic crystals of (I) are linked by N-H...Cl hydrogen bonds and the Rh3+ ions are located on the mirror planes. In the trigonal crystals of (II), the discontinuous `columns` along the threefold axis are linked by N-H...O hydrogen bonds. The structure of (I) has been solved using laboratory powder diffraction data, the structure of (II) has been solved by single-crystal methods using data from a merohedrally twinned sample. Both compounds possess low solubility in water.

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Держатели документа:
Kirensky Inst Phys SB RAS, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660041, Russia
Nikolaev Inst Inorgan Chem SB RAS, Novosibirsk 630090, Russia

Доп.точки доступа:
Vasiliev, A. D.; Васильев, Александр Дмитриевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Baidina, I. A.; Belyaev, A. V.; Vorob`eva, S. N.

}
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10.

Avramov, P. V.
Atomic-core dynamics and the electronic structure of some endo- and exohedral complexes of fullerenes with light elements / P. V. Avramov, S. A. Varganov, S. G. Ovchinnikov // Phys. Solid State. - 2000. - Vol. 42, Is. 11. - P. 2168-2175, DOI 10.1134/1.1324059. - Cited References: 39 . - ISSN 1063-7834

РУБ Physics, Condensed Matter
Рубрики:
M-AT-C-60 ENDOHEDRAL COMPLEXES
   MOLECULAR-DYNAMICS
   PHASE-TRANSITION
   AB-INITIO
   SOLID C60
   C-60
   IONS
Аннотация: The atomic and electronic structure of some endo-, exo-, and endo-exohedral complexes of the fullerene C-60 with various guest atoms and molecules (He-n, H-2, and Li-2) are investigated using semiempirical and nonempirical quantum-chemical methods. The atomic core dynamics is studied by the method of molecular dynamics. It is shown that guest atoms and molecules in fullerene polyhedra acquire an orbital angular momentum due to the correlated motion of nuclei above the low-energy barriers of the potential surface within the carbon polyhedron even at low temperatures (from 4 to 78 K). The emergence of orbital angular momenta of nuclei of guest atoms and molecules is attributed to a change in the contribution of the orbital angular momentum of electrons to the potential surface of the complexes. The motion of Li ions in a polyhedron leads to blurring of the top of the valence band and to the emergence of a charge polarization wave in the carbon polyhedron. (C) 2000 MAIK "Nauka/Interperiodica".

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Держатели документа:
Russian Acad Sci, Kirenskii Inst Phys, Siberian Div, Krasnoyarsk 660036, Russia
Krasnoyarsk State Univ, Krasnoyarsk, Russia
Krasnoyarsk State Univ, Krasnoyarsk 660062, Russia
ИФ СО РАН

Доп.точки доступа:
Varganov, S. A.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Аврамов, Павел Вениаминович
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11.

    Blue-shift of Eu2+ emission in (Ba,Sr)3Lu(PO4)3:Eu2+ eulytite solid-solution phosphors resulting from release of neighbouring-cation-induced stress / Z. Y. Wang [et al.] // Dalton Trans. - 2014. - Vol. 43, Is. 44. - P. 16800-16804, DOI 10.1039/c4dt02319f. - Cited References: 16. - The present work was supported by the National Natural Science Foundations of China (grant no. 51002146, no. 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635) and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306). V.V.A. is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 1477-9226. - ISSN 1477-9234
   Перевод заглавия: Синее смещение излучения Eu2+ в твердых растворах (Ba,Sr)3Lu(PO4)3:Eu2 со структурой эулита, вызванное снятием напряжения, индуцированного соседними катионами

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
TUNABLE COLOR TONE
   EXCITED WHITE LEDS
   CRYSTAL-STRUCTURE
   TEMPERATURE
   IONS
Аннотация: A series of iso-structural eulytite-type (Ba,Sr)(3)Lu(PO4)(3):Eu2+ solid-solution phosphors with different Sr/Ba ratios were synthesized by a solid-state reaction. Crystal structures of (Ba,Sr)(3)Lu(PO4)(3):Eu2+ were resolved by the Rietveld method, which shows an eulytite-type cubic Bi-4(SiO4)(3) structure with cations disordered in a single C-3 site while the oxygen atoms were distributed over two partially occupied sites. The emission peaks of Ba(3-x)SrxLu(PO4)(3):Eu2+ (0

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
SB RAS, Inst Semicond Phys, 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:
Wang, Z. Y.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Атучин, Виктор Валерьевич; Liu, Q. L.
}
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12.

Golovnev, N.
Bridging behaviour of the 2-thiobarbiturate anion in its complexes with LiI and NaI / N. Golovnev, M. Molokeev // Acta Crystallographica Section C Crystal Structure Communications. - 2013. - Vol. 69, Pt. 7. - P. 704-708, DOI 10.1107/S0108270113014078 . - ISSN 0108-2701
Кл.слова (ненормированные):
2-thiobarbituric acid -- Coordinated water -- Dihydrates -- Edge sharing -- Hydrogen bonding interactions -- Three-dimensional networks -- Atoms -- Complex networks -- Hydrogen bonds -- Ligands -- Negative ions -- Positive ions -- Three dimensional -- Lithium
Аннотация: The structures of the LiI and NaI salts of 2-thiobarbituric acid (2-sulfanylidene-1-3-diazinane-4,6-dione, H 2TBA) have been studied. μ-Aqua-octaaquabis(μ-2- thiobarbiturato-κ2 O:O′)bis(2-thiobarbiturato-κO) tetralithium(I) dihydrate, [Li4(C4H3N 2O2S)4(H2O)9]·2H 2O, (I), crystallizes with four symmetry-independent four-coordinated LiI cations and four independent HTBA- anions. The structure contains two structurally non-equivalent LiI cations and two non-equivalent HTBA- anions (bridging and terminal). Eight of the coordinated water ligands are terminal and the ninth acts as a bridge between LiI cations. Discrete [Li4(HTBA)4(H2O)9] ·2H2O complexes form two-dimensional layers. Neighbouring layers are connected via hydrogen-bonding interactions, resulting in a three-dimensional network. Poly[μ2-aqua-tetraaqua(μ4-2- thiobarbiturato-κ4 O:O:S:S)(μ2-thiobarbiturato- κ2 O:S)disodium(I)], [Na2(C4H 3N2O2S)2(H2O) 5] n , (II), crystallizes with six-coordinated NaI cations. The octahedra are pairwise connected through edge-sharing by a water O atom and an O atom from the μ4-HTBA- ligand, and these pairs are further top-shared by the S atoms to form continuous chains along the a direction. Two independent HTBA- ligands integrate the chains to give a three-dimensional network. © 2013 International Union of Crystallography.

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Держатели документа:
Siberian State Univ, Krasnoyarsk 660041, Russia
Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич
}
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13.

Brownian dynamic of laser cooling and crystallization of electron-ion plasma / A. P. Gavriliuk [et al.] // Phys. Rev. E. - 2009. - Vol. 80, Is. 5. - Ст. 56404, DOI 10.1103/PhysRevE.80.056404. - Cited References: 29 . - ISSN 1539-3755

РУБ Physics, Fluids & Plasmas + Physics, Mathematical
Рубрики:
ULTRACOLD NEUTRAL PLASMAS
   OPTICAL MOLASSES
   LIQUIDS
   ATOMS
   TRAP
Кл.слова (ненормированные):
Brownian motion -- laser cooling -- plasma collision processes -- plasma light propagation -- plasma nonlinear processes -- plasma simulation -- plasma transport processes -- Brownian Dynamics -- Brownian dynamics simulations -- Electron ion plasma -- Electron subsystem -- Friction force -- Ionic structure -- Nonlinear dependence -- Plasma cooling -- Brownian movement -- Crystallization -- Ions -- Laser cooling -- Lasers -- Cooling
Аннотация: Laser cooling and crystallization of electron-ion plasma is studied using the Brownian dynamics simulation technique and taking into consideration the interaction of ions with the electron subsystem. It has been shown that the nonlinear dependence of laser friction force on the velocity of ions has to be taken into account in order to simulate in an adequate manner the cooling dynamics and obtain a correct estimate for minimum temperatures. It has been found that times required for formation of an ordered ionic structure can be much longer than the typical plasma cooling time.

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Держатели документа:
[Gavriliuk, A. P.
Krasnov, I. V.
Shaparev, N. Ya.] Russian Acad Sci, Inst Computat Modeling, Krasnoyarsk, Russia
[Isaev, I. L.
Karpov, S. V.] Russian Acad Sci, LV Kirensky Phys Inst, Krasnoyarsk, Russia
[Karpov, S. V.] Siberian Fed Univ, Krasnoyarsk, Russia
ИФ СО РАН
Institute of Computational Modeling, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
L.V. Kirenskiy Institute of Physics, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Gavriliuk, A. P.; Isaev, I. L.; Исаев, Иван Леонидович; Karpov, S. V.; Карпов, Сергей Васильевич; Krasnov, I. V.; Shaparev, N. Y.
}
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14.

    Changes of the local magnetic properties of the optically excited Nd3+ ions and their manifestation in the near IR spectra of the Nd0.5Gd0.5Fe3(BO3)4 crystal / A. V. Malakhovskii [et al.] // Opt. Mater. - 2016. - Vol. 52. - P. 126-133, DOI 10.1016/j.optmat.2015.12.029. - Cited References: 29. - The work was supported by the Russian Foundation for Basic Researches Grant 16-02-00273 and by the President of Russia Grant No. Nsh-2886.2014.2. . - ISSN 0925-3467. - ISSN 1873-1252
   Перевод заглавия: Изменения локальных магнитных свойств оптически возбужденных ионов Nd3+ и их проявление в ближних ИК-спектрах кристалла Nd0.5Gd0.5Fe3(BO3)4

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
SINGLE-CRYSTAL
GdFe3(BO3)4
STATES
Кл.слова (ненормированные):
f-f transitions -- Nd3+ ion -- Excited states -- Local magnetic properties
Аннотация: Polarized absorption spectra of f–f transitions 4I9/2 → 4F3/2 and (2H9/2 + 4F5/2) in the Nd3+ ion in the Nd0.5Gd0.5Fe3(BO3)4 single crystal were studied as a function of temperature in the range of 2–40 K and as a function of magnetic field in the range of 0–65 kOe at 2 K. It was found out that the selection rules for f–f electron transitions substantially changed in the magnetically ordered state of the crystal, and they strongly depended on the orientation of the Fe and Nd ions magnetic moments relative to the light polarization. The splitting of the ground and excited states of the Nd3+ ion in the exchange field of the Fe sublattice were determined. It was revealed that the value of the exchange splitting (the exchange interaction) in the excited states did not correlate with the theoretical Landé factors. The Landé factors of the excited states were experimentally found. In general, the local magnetic properties in the vicinity of the excited ion depend substantially on its electron state. In particular: (1) in one of the excited states a weak ferromagnetic moment appears, (2) the changes of type of the local magnetic anisotropy take place in some excited states, and (3) in some excited states the energetically favorable orientation of the Nd3+ ion magnetic moment is opposite to that in the ground state. In some excited states the nonequivalent Nd3+ centers were found out.
Поляризованные спектры поглощения F-е переходов 4I9/2 → 4F3/2 и (2H9/2 + 4F5/2) в иона Nd3+ в Nd0.5Gd0.5Fe3(BO3)4 монокристалл изучались как функции температуры в интервале 2-40 K и в зависимости от магнитного поля в диапазоне 0-65 кЭ при 2 К. Выяснилось, что Правила отбора для F-F электронных переходов существенно изменился в магнитно-упорядоченном состоянии кристалла, и они сильно зависели от ориентации магнитных моментов ионов Fe и Nd по отношению к поляризация света. Расщепление основного и возбужденного состояний иона Nd3+ в обменном поле подрешетки Fe были определены. Было выявлено, что величина обменного расщепления (обменное взаимодействие) в возбужденных состояниях не коррелируют с теоретическими факторами Ланде. Факторы Ланде возбужденных состояний были найдены экспериментально. В целом, локальные магнитные свойства в непосредственной близости от возбужденного иона существенно зависят от его электронного состояния. В частности: (1) в одном из возбужденной состояния появляется слабый ферромагнитный момент, (2) изменения типа локальных магнитной анизотропии происходит в некоторых возбужденных состояниях, и (3) в некоторых возбужденных состояниях энергетически благоприятных ориентация иона Nd3+ магнитного момента противоположны тем, что в основном состоянии. В некоторых возбужденных состояниях были обнаружены неэквивалентные центры Nd3+.

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Держатели документа:
Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia.
Natl Acad Sci Ukraine, B Verkin Inst Low Temp Phys & Engn, UA-61103 Kharkov, Ukraine.

Доп.точки доступа:
Malakhovskii, A. V.; Малаховский, Александр Валентинович; Gnatchenko, S. L.; Kachur, I. S.; Piryatinskaya, V. G.; Temerov, V. L.; Темеров, Владислав Леонидович; Russian Foundation [16-02-00273]; [Nsh-2886.2014.2]
}
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15.

    Chemical unit cosubstitution and tuning of photoluminescence in the Ca2(Al1-xMgx)(Al1-xSi1+x)O7:Eu2+ phosphor / Z. Xia [et al.] // J. Am. Chem. Soc. - 2015. - Vol. 137, Is. 39. - P. 12494-12497, DOI 10.1021/jacs.5b08315. - Cited References: 24. - This work was supported by the National Natural Science Foundations of China (Grant Nos. 51572023 and 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), and the Funds of the State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, CAS (RERU2015022). C.M. acknowledges financial support from National Natural Science Foundation of China (Grant No. 11204393), Natural Science Foundation Project of Chongqing (Grant No. CSTC2014JCYJA50034), and National Training Programs of Innovation and Entrepreneurship for Undergraduates (Grant No. 201410617001). K.R. recognizes that this material is based upon work supported by the National Science Foundation Graduate Research Fellowship Program under Grant No. DGE-1324585. . - ISSN 0002-7863
   Перевод заглавия: Со-замещение химической группы и регулирование фотолюминесценции в люминофоре Ca2(Al1-xMgx)(Al1-xSi1+x)O7:Eu2+

РУБ Chemistry, Multidisciplinary
Рубрики:
LUMINESCENCE PROPERTIES
TRANSITIONS
IONS
Аннотация: The union of structural and spectroscopic modeling can accelerate the discovery and improvement of phosphor materials if guided by an appropriate principle. Herein, we describe the concept of chemical unit cosubstitution as one such potential design scheme. We corroborate this strategy experimentally and computationally by applying it to the Ca2(Al1-xMgx)(Al1-xSi1+x)O7:Eu2+ solid solution phosphor. The cosubstitution is shown to be restricted to tetrahedral sites, which enables the tuning of luminescent properties. The emission peaks shift from 513 to 538 nm with a decreasing Stokes shift, which has been simulated by a crystal-field model. The correlation between the 5d crystal-field splitting of Eu2+ ions and the local geometry structure of the substituted sites is also revealed. Moreover, an energy decrease of the electron-phonon coupling effect is explained on the basis of the configurational coordinate model. © 2015 American Chemical Society.

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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
College of Sciences, Chongqing University of Posts and Telecommunications, Chongqing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Department of Chemistry, Northwestern University, Evanston, IL, United States

Доп.точки доступа:
Xia, Zhiguo; Ma, C.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.; Rickert, K.; Poeppelmeier, K. R.
}
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16.

Coexisting 1D and 3D magnetic interactions in the insulating copper-oxygen compound CuB2O4 / M. . Boehm [et al.] // Physica B. - 2006. - Vol. 378-80: International Conference on Strongly Correlated Electron Systems (SECES 05) (JUL 26-30, 2005, Vienna, AUSTRIA). - P. 1128-1129, DOI 10.1016/j.physb.2006.01.540. - Cited References: 8 . - ISSN 0921-4526

РУБ Physics, Condensed Matter
Рубрики:
SPIN-WAVE SPECTRUM
PHASE 10 K
METABORATE
Кл.слова (ненормированные):
cuprates -- magnetic soliton lattice -- Heisenberg exchange -- low-dimensional excitations -- Cuprates -- Heisenberg exchange -- Low-dimensional excitations -- Magnetic soliton lattice -- Dispersions -- Insulating materials -- Magnetic properties -- Neutron scattering -- Positive ions -- Cuprates -- Heisenberg exchange -- Low-dimensional excitations -- Magnetic soliton lattice -- Copper compounds
Аннотация: We performed inelastic neutron scattering measurements on CuB2O4 with a magnetic field applied in the tetragonal basal plane. The spin dynamics in this cuprate is determined by the interplay of two magnetic Cu2+ subsystems, the magnetic cage with predominant 3d Heisenberg exchange and quasi Id zig-zag chains. The comparison of the dispersion spectra along the chain direction in zero field and under applied field suggests a decoupling of the two magnetic sublattices under field. (c) 2006 Elsevier B.V. All rights reserved.

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Держатели документа:
Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
Paul Scherrer Inst, Neutron Scattering Lab, CH-5232 Villigen, Switzerland
Russian Acad Sci, Inst Phys, SB, Krasnoyarsk 660036, Russia
ИФ СО РАН
Institut Laue Langevin, 6, rue Jules Horowitz, F-38042 Cedex 9, France
Laboratory of Neutron Scattering, Paul Scherrer Institute, CH-5232 Villigen, Switzerland
Institute of Physics, SB RAS, 660036 Krasnoyarsk, Russian Federation

Доп.точки доступа:
Boehm, M.; Roessli, B.; Schefer, J.; Ouladdiaf, B.; Kulda, J.; Petrakovskii, G. A.; Петраковский, Герман Антонович
}
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17.

Sokolov, V. V.
Comparative study of magnetic circular dichroism of f-f transitions in ErAl3(BO3)4 and ErFe3(BO3)4 / V. V. Sokolov, A. V. Malakhovskii, I. A. Gudim // XVII International Feofilov Symposium on spectroscopy of crystals doped with rare earth and transition metal ions (IFS'XVII) : book of abstracts. - 2018. - P. 207-208

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Доп.точки доступа:
Malakhovskii, A. V.; Малаховский, Александр Валентинович; Gudim, I. A.; Гудим, Ирина Анатольевна; Соколов, Валерий Владимирович; International Feofilov Symposium on spectroscopy of crystals doped with rare earth and transition metal ions(17 ; 2018 ; Sept. ; 23-28 ; Ekaterinburg, Russia)
}
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18.

Comparative study of PbTiO3 and SrTiO3 (100) thin films lattice dynamics and ferroelectric properties in a nonempirical model of polarizable ions / V. S. Zhandun, V. I. Zinenko // Ferroelectrics. - 2011. - Т. 412, № 1. - P. 23-31, DOI 10.1080/00150193.2011.542691 . - ISSN 0015-0193. - ISSN 1563-5112

РИНЦ
Держатели документа:
L.V. Kirensky Institute of Physics,Siberian Division,Russian Academy of Sciences

Доп.точки доступа:
Zhandun, V. S.; Жандун, Вячеслав Сергеевич; Zinenko, V. I.; Зиненко, Виктор Иванович
}
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19.

Comparison of the absorption spectra of Nd3+ ions in the NdFe3(BO3)4, Nd0.5Gd0.5Fe3(BO3)4, and Ho0.75Nd0.25Fe3(BO3)4 crystals / A. L. Sukhachev, A. V. Malakhovskii, C. S. Nelson [et al.] // Phys. Solid State. - 2021. - Vol. 63, Is. 1. - P. 113-121, DOI 10.1134/S1063783421010200. - Cited References: 21. - The reported study was funded by Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science, to the research project: number 19-42-240003 “Influence of the local en-vironment on magneto-optical properties of f–f transitions in rare-earth aluminum and iron borates” . - ISSN 1063-7834
Кл.слова (ненормированные):
neodymium -- hantite-structure ferroborates -- f–f electronic transitions -- structural transition
Аннотация: The polarized optical absorption spectra in the region of a series of the f–f transitions of Nd3+ ions in the Ho0.75Nd0.25Fe3(BO3)4, Nd0.5Gd0.5Fe3(BO3)4, and NdFe3(BO3)4 crystals at 90 K have been compared. The spectral features related to the difference in the local environment of Nd3+ ions in these crystals have been established. In the region of the transition 4I9/2 → 4G5/2 + 2G7/2 of Nd3+ ions in the Ho0.75Nd0.25Fe3(BO3)4 crystal, the appearance of some absorption lines at the structural transition R32 → P3121 around ~200 K due to the local symmetry variation has been found. The intensity of these lines smoothly increases with a decrease in temperature from the transition point. The temperature dependence of the lattice parameters of the Ho0.75Nd0.25Fe3(BO3)4 crystal has been measured. It has been found that, at the transition temperature, the lattice parameter a changes stepwise, which is indicative of the occurrence of a first-order phase transition. The lattice parameter c changes smoothly.

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Публикация на русском языке Сравнение спектров поглощения ионов Nd3+ в кристаллах NdFe3(BO3)4, Nd0.5Gd0.5Fe3(BO3)4 и Ho0.75Nd0.25Fe3(BO3)4 [Текст] / А. Л. Сухачев, А. В. Малаховский, C. S. Nelson [и др.] // Физ. тверд. тела. - 2021. - Т. 63 Вып. 1. - С. 111-119

Держатели документа:
Kirensky Institute of Physics, FRC KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, NY 11973, United States

Доп.точки доступа:
Sukhachev, A. L.; Сухачев, Александр Леонидович; Malakhovskii, A. V.; Малаховский, Александр Валентинович; Nelson, C. S.; Gudim, I. A.; Гудим, Ирина Анатольевна; Temerov, V. L.; Темеров, Владислав Леонидович
}
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20.

Conformational changes in DNA aptamers upon binding to Pb ions / R. V. Moryachkov, A. N. Berlina, P. V. Artyushenko [et al.] // The Fifth Asian School-Conference on Physics and Technology of Nanostructured Materials : Proceedings. - VLadivostok : Dalnauka Publishing, 2020. - Ст. VII.31.01p. - P. 193. - The reported study was funded by RFBR, project number 19-32-90266. . - ISBN 978-5-8044-1698-1

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Доп.точки доступа:
Moryachkov, R. V.; Морячков, Роман Владимирович; Berlina, A. N.; Artyushenko, P. V.; Zabluda, V. N.; Заблуда, Владимир Николаевич; Peters, G. S.; Sokolov, A. Е.; Соколов, Алексей Эдуардович; Asian School-Conference on Physics and Technology of Nanostructured Materials(5 ; 2020 ; 30 Jul - 3 Aug ; Vladivostok); Азиатская школа-конференция по физике и технологии наноструктурированных материалов(5 ; 2013 ; 30 июля - 3 авг. ; Владивосток)
}
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