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1.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Bondarenko G. V., Ovchinnikov S. G., Rudenko V. V., Sosnin V. M., Tugarinov V. I., Vorotynov A. M.
Заглавие : The generalized method of quantitative description of the uniaxial anisotropy in weak ferromagnet rhombohedral calcite type structure crystals with S-state ions
Место публикации : J. Magn. Magn. Mater. - 2013. - Vol. 335. - P.90-96. - ISSN 0304-8853, DOI 10.1016/j.jmmm.2013.01.037
Примечания : Cited References: 35
Ключевые слова (''Своб.индексиров.''): weak ferromagnetism--magnetic anisotropy--impurity
Аннотация: The method for investigation of the uniaxial and hexagonal anisotropies in weakly ferromagnetic rhombohedral FeBO3 crystals with the Fe2þ magnetic impurity with the use of the single-ion and pair approximation has been developed. In the framework of this method, a quantitative discrepancy between theoretical and experimental data on a uniaxial field has been eliminated. The energy contributions to the hexagonal anisotropy that are caused by the Dzyaloshinsky–Moriya interaction, the crystal field of Fe3þ ions and the temperature dependence of this anisotropy were analytically treated. The experimental temperature dependence of the hexagonal anisotropy of FeBO3 crystals is explained. It is shown that the compensation point and the typical temperature dependence of the hexagonal anisotropy result from the competition of the contributions of Fe3þ and Fe2þ ions. It is shown that respective considerable contributions to the anisotropy of Fe3þ and Fe2þ ions are made by the cubic symmetry and the uniaxial symmetry of the exchange ‘‘single-ion’’ type. The anisotropy constants for FeBO3 crystal was obtained by using the described results. It was shown, that for the calcite type structure crystals (iron borate and manganese carbonate) with S-state ions, the single ion and pair models (which previously raised doubts in their validity and accuracy) describe the experimental data good enough.
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2.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Atuchin V. V., Molokeev M. S., Yurkin G. Yu., Gavrilova T. A., Kesler V. G., Laptash N. M., Flerov I. N., Patrin G. S.
Заглавие : Synthesis, structural, magnetic, and electronic properties of cubic CsMnMoO3F3 oxyfluoride
Место публикации : J. Phys. Chem. C: American Chemical Society, 2012. - Vol. 116, Is. 18. - P.10162-10170. - ISSN 1932-7447, DOI 10.1021/jp302020f
Примечания : Cited References: 64. - We thank Dr. A.M. Ziatdinov for the electron paramagnetic resonance measurements. This study was partly supported by SB RAS (Grant 28).
Предметные рубрики: RAY PHOTOELECTRON-SPECTROSCOPY
PHASE-TRANSITIONS
CORE LEVELS
SURFACE CHARACTERIZATION
CRYSTAL-STRUCTURE
CLEAVED SURFACE
MIXED-VALENCE
OXIDES
MN
MOLYBDENUM
Chemical bondings
Cubic phase
Energy differences
Heat capacity measurements
Oxyfluorides
Powder samples
Solid-state synthesis
Space Groups
Temperature range
Valence electron
Binding energy
Chemical bonds
Electronic structure
Fluorine compounds
Magnetic properties
Metal ions
Photoelectrons
Rietveld method
X ray photoelectron spectroscopy
Electronic properties
Аннотация: A powder sample of CsMnMoO3F3 oxyfluoride has been prepared by solid state synthesis. The pyrochlore-related crystal structure of CsMnMoO3F3 has been refined by the Rietveld method at T = 298 K (space group Fd-3m, a = 10.59141(4) angstrom, V = 1188.123(8) angstrom(3); R-B = 3.44%). The stability of the cubic phase has been obtained over the temperature range T = 110-293 K by heat capacity measurements. Magnetic properties have been measured over the range of T = 2-300 K. The electronic structure of CsMnMoO3F3 has been evaluated by X-ray photoelectron spectroscopy. Chemical bonding effects have been discussed for all metal ions using binding energy difference parameters and wide comparison with related oxides and fluorides. The competition between O-2(-) and F- ions for metal valence electrons has been found.
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3.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Cao G. X., Korshunov M. M., Gao Y. Z., Le Tacon M., Singh D. J., Lin C. T.
Заглавие : Anomalous in-plane electronic scattering in charge ordered Na 0.41CoO 2•0.6H 2O
Место публикации : Phys. Rev. Lett.: American Physical Society, 2012. - Vol. 108, Is. 23. - Ст.236401. - ISSN 0031-9007, DOI 10.1103/PhysRevLett.108.236401
Примечания : 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.
Предметные 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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4.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Dudnikov V. A., Ovchinnikov S. G., Orlov Yu.S., Kazak N. V., Michel C. R., Patrin G. S., Yurkin G.Yu.
Заглавие : Contribution of Co3+ ions to the high-temperature magnetic and electrical properties of GdCoO3
Место публикации : J. Exp. Theor. Phys.: MAIK Nauka-Interperiodica / Springer, 2012. - Vol. 114, Is. 5. - P.841-849. - ISSN 1063-7761, DOI 10.1134/S106377611203003X
Примечания : Cited References: 28. - This work was supported by the Ural Branch of the Russian Academy of Sciences and Siberian Branch of the Russian Academy of Sciences (project no. 40), the Russian Foundation for Basic Research (project nos. 09-02-00171-a, 10-02-00251), program 2.3 of the Department of Physical Sciences of Russian Academy of Sciences, and Nonprofit Dinastiya Foundation.
Предметные рубрики: SPIN-STATE
RCOO3 R
TRANSITIONS
COBALTITES
LACOO3
OXIDES
SM
EU
ND
Аннотация: The temperature dependence of the static magnetization of polycrystalline rare-earth cobaltite GdCoO3 is measured in the temperature range 2-800 K. The magnetic behaviors of GdCoO3 and Gd3+ are found to be different at temperatures above room temperature, which is caused by the appearance of a contribution from Co3+ ions at high temperatures. The temperature dependence of the magnetic susceptibility of GdCoO3 is determined by the magnetization of rare-earth gadolinium ions and the additional paramagnetic contribution induced by the thermally excited magnetic terms of Co3+ ions. The LDA + GTB method is used to calculate the electronic structure of GdCoO3 in the temperature range 0-300 K with allowance for strong electron correlations. The energy spectrum of GdCoO3 is found to have intragap states that decrease the dielectric gap width with increasing temperature.
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5.

Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Malakhovskii A. V., Gnatchenko S. L., Kachur I. S., Piryatinskaya V. G., Sukhachev A. L., Sokolov A. E., Temerov V. L., Gudim, I. A.
Заглавие : Influence of f-f electron transitions on the local properties in vicinity of the excited ions in trigonal alumo- and ferroborates
Коллективы : International Feofilov symposium on spectroscopy of crystals doped with rare earth and transition metal ions (15; 2013 ; Sept. ; 16-20; Казань)
Место публикации : XV Int. Feofilov symp. on spectroscopy of crystals doped with rare earth and transition metal ions. - Kazan, 2013. - Ст.PI_4. - P.112
Аннотация: Представлены результаты изучения спектров поглощения кристаллов TbFe3(BO3)4, TmAl3(BO3)4, YbAl3(BO3)4, DyFe3(BO3)4 и Nd0.5Gd0.5Fe3(BO3)4. Показано, что геометрия локального окружения и локальные магнитные свойства могут меняться в процессе f-f электронных переходов.
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6.

Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Sukhachev A. L., Malakhovskii A. V., Kutsak T. V., Strokova A. Yu., Sokolov A. E., Temerov V. L., Gudim, I. A.
Заглавие : Magneto-optical activity of f-f transitions in trigonal alumo- and ferroborates
Коллективы : International Feofilov symposium on spectroscopy of crystals doped with rare earth and transition metal ions
Место публикации : XV Int. Feofilov symp. on spectroscopy of crystals doped with rare earth and transition metal ions. - Kazan, 2013. - P.113
Аннотация: Представлены результаты изучения спектров поглощения и магнитного кругового дихроизма и магнитооптической активности (МОА) f-f переходов в кристаллах DyFe3(BO3)4, Nd0.5Gd0.5Fe3(BO3)4, ErAl3(BO3)4, TmAl3(BO3)4, YbAl3(BO3)4. Обнаружено, что МОА большинства переходов не следует закону Кюри-Вейсса. Это явление объяснено теоретически.
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7.

Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Gnatchenko S. L., Kachur I. S., Piryatinskaya V. G., Malakhovskii A. V., Sukhachev A. L., Gudim, I. A.
Заглавие : Low temperature behavior of f-f transitions in Nd0.5Gd0.5Fe3(BO3)4 multiferroic crystal
Коллективы : International Feofilov symposium on spectroscopy of crystals doped with rare earth and transition metal ions
Место публикации : XV Int. Feofilov symp. on spectroscopy of crystals doped with rare earth and transition metal ions. - Kazan, 2013. - Ст.PI_7. - P.115
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8.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Vasiliev A. D., Molokeev M. S., Baidina I. A., Belyaev A. V., Vorob`eva S. N.
Заглавие : Arrangement of Rh3+ ions in fac-triamminetri­chlorido­rhodium from powder data and in fac-triammine­trinitratorhodium crystals twinned by merohedry
Место публикации : Acta Crystallogr. C. - 2013. - Vol. 69, Pt. 12. - P.1462–1466. - ISSN 0108-2701, DOI 10.1107/S010827011303076X; Spec. is. Interplay of crystallogr., spectrosc. and theor. meth. for solving chem. prob.
Ключевые слова (''Своб.индексиров.''): 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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9.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Malakhovskii A. V., Kutsak T. V., Sukhachev A. L., Aleksandrovsky A. S., Krylov A. S., Gudim, Irina A., Molokeev M. S.
Заглавие : Spectroscopic properties of ErAl3(BO3)4 single crystal
Место публикации : Chem. Phys.: Elsevier Science, 2014. - Vol. 428. - P.137–143. - ISSN 0301-0104, DOI 10.1016/j.chemphys.2013.11.008. - ISSN 1873-4421
Примечания : Cited References: 43. - The work was supported by the Russian Foundation for Basic Researches grant 12-02-00026, by the Russian President Grants SS-1044.2012.2 and 4828.2012.2, by project No 3.9.5 PSB RAS, and by the Ministry of Education and Science of Russian Federation grant 8365
Предметные рубрики: RARE-EARTH IONS
GREEN UP-CONVERSION
ER3+ IONS
MICROCHIP LASER
ABSORPTION INTENSITIES
YAL3(BO3)4 CRYSTAL
OPTICAL-ABSORPTION
FIELD ANALYSIS
GROWTH
LUMINESCENCE
Ключевые слова (''Своб.индексиров.''): rare earth compounds--er3+--spectroscopic properties--judd-ofelt analysis--luminescence
Аннотация: Single crystal of ErAl3(BO3)4 was grown and its structure was studied. Polarized absorption spectra of ErAl3(BO3)4 single crystal were measured in the spectral range 1670–330 nm (6000–30000 cm−1). The Judd–Ofelt spectroscopic parameters have been determined: Ω2 = 4.87 × 10−20 cm2, Ω4 = 2.49 × 10−20 cm2, Ω6 = 2.72 × 10−20 cm2. These parameters have been used to calculate the radiative transition probabilities, the multiplet luminescence branching ratios and the fluorescence life times of the manifolds. The luminescence spectra due to transitions 2H11/2 → 4I15/2 (526 nm), 4S3/2 → 4I15/2 (548 nm), 4F9/2 → 4I15/2 (662 nm), 2H11/2 → 4I13/2 + 4I9/2 → 4I15/2 (800 nm) and 4S3/2 → 4I13/2 (855 nm) were recorded in α, σ and π polarizations. The most intensive luminescence belonged to 4S3/2 → 4I15/2 transition (548 nm).Поляризованные спектры поглощения ErAl3 (BO3) 4 монокристалла были измерены в спектральном диапазоне 1670-330 нм (6000-30000 см-1). Спектроскопические параметры Джадда-Офельта были определены как: Ω2 = 4,87 • 10-20 см2, Ω4 = 2.49 • 10-20 см2, Ω6 = 2,72 • 10-20 см2. Параметры были использованы для расчета вероятностей излучающих переходов, мультиплетные отношения люминесценции раскола и времена жизни мультиплетов. Спектры люминесценции за счет переходов 2П11 / 2 → 4I15 / 2 (526 нм), 4S3 / 2 → 4I15 / 2 (548 нм), 4F9 / 2 → 4I15 / 2 (662 нм), 2П11 / 2 → 4I13 / 2 + 4I9 / 2 → 4I15 / 2 (800 нм) и 4S3 / 2 → 4I13 / 2 (855 нм) были записаны в α, σ и π поляризации. Наиболее интенсивное свечение принадлежало переходу 4S3 / 2 → 4I15 / 2 (548 нм).
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10.

Вид документа : Статья из сборника (выпуск продолж. издания)
Шифр издания :
Автор(ы) : Edelman I. S., Ivanova O. S., Ivantsov R. D., Velikanov D. A., Petrakovskaja E. A., Artemenko A., Curely J., Kliava J., Zaikovskiy V. I., Stepanov S.
Заглавие : Magnetic properties and morphology of manganese ferrite nanoparticles in glasses
Коллективы : Baltic Conference on Silicate Materials
Место публикации : IOP Conf. Ser.: Mater. Sci. Eng. - 2011. - Vol. 25, Is. 1. - Ст.012017. - , DOI 10.1088/1757-899X/25/1/012017
Ключевые слова (''Своб.индексиров.''): average diameter--borate glass--co-doped--electron magnetic resonance--magnetic and magneto-optical properties--magnetic behaviour--magnetic circular dichroisms--magnetic nanoparticles--magnetically ordered material--manganese ferrite nanoparticles--manganese ferrites--morphological characteristic--paramagnetic ions--resonance field--size and shape--static magnetization--temperature dependence--temperature dependent--variable temperature--visible and near infrared--alumina--dichroism--ferrite--glass--iron oxides--magnetic properties--magnetic resonance--magnetocrystalline anisotropy--manganese--manganese oxide--nanoparticles--paramagnetism--silicates--spectroscopy--nanomagnetics
Аннотация: Static magnetization (SM), magnetic circular dichroism (MCD) and electron magnetic resonance (EMR) studies are reported of borate glasses 22.5 K 2O-22.5 Al 2O 3-55 B 2O 3 co-doped with iron and manganese oxides. In as-prepared glasses the paramagnetic ions usually are in diluted state; however, if the ratio of the iron and manganese oxides in the charge is 3/2, magnetic nanoparticles are found already in as-prepared glass. After additional thermal treatment all glasses show magnetic behaviour, MCD and EMR due to the presence of magnetic nanoparticles with characteristics close to those of manganese ferrite. By computer simulating the EMR spectra at variable temperatures, their morphological characteristics are deduced: relatively broad size and shape distribution with average diameter of ca. 3-4 nm. The characteristic temperature-dependent shift of the apparent resonance field is explained by a strong temperature dependence of the magnetocrystalline anisotropy in the nanoparticles. The potassium-alumina-borate glasses containing magnetic nanoparticles represent a novel class of materials: "transparent magnets". Indeed, they remain transparent in a part of visible and near infrared spectral range while showing magnetic and magneto-optical properties characteristic of magnetically ordered materials.
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