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1.


   
    Exchange interaction between excited states of magnetic ions / S. G. Ovchinnikov, V. A. Gavrichkov, S. I. Polukeev, A. V. Malakhovskii // Euro-asian symposium "Trends in magnetism" (EASTMAG-2019) : Book of abstracts / чл. конс. ком.: S. G. Ovchinnikov, N. V. Volkov [et al.] ; чл. прогр. ком. D. M. Dzebisashvili [et al.]. - 2019. - Vol. 2. - Ст. H.I1. - P. 36-37. - Cited References: 8. - Support by RSF grant 18-12-00022 is acknowledged . - ISBN 978-5-9500855-7-4

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia

Доп.точки доступа:
Ovchinnikov, S. G. \чл. конс. ком.\; Овчинников, Сергей Геннадьевич; Volkov, N. V. \чл. конс. ком.\; Волков, Никита Валентинович; Dzebisashvili, D. M. \чл. прогр. ком.\; Дзебисашвили, Дмитрий Михайлович; Ovchinnikov, S. G.; Gavrichkov, V. A.; Гавричков, Владимир Александрович; Polukeev, S. I.; Полукеев, Семен Игоревич; Malakhovskii, A. V.; Малаховский, Александр Валентинович; Российская академия наук; Уральское отделение РАН; Институт физики металлов им. М. Н. Михеева Уральского отделения РАН; Уральский федеральный университет им. первого Президента России Б.Н. Ельцина; Российский фонд фундаментальных исследований; Euro-Asian Symposium "Trends in MAGnetism"(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg); "Trends in MAGnetism", Euro-Asian Symposium(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg)
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2.


   
    Multiple substitution strategies toward tunable luminescence in Lu2MgAl4SiO12:Eu2+ phosphors / Z. Ming, J. Qiao, M. S. Molokeev [et al.] // Inorg. Chem. - 2020. - Vol. 59, Is. 2. - P. 1405-1413, DOI 10.1021/acs.inorgchem.9b03142. - Cited References: 31. - This research is supported by the National Natural Science Foundation of China (Grants 51972118, 51722202, and 51572023), Natural Science Foundations of Beijing (Grant 2172036), and Fundamental Research Funds for the Central Universities (Grant FRF-TP-18-002C1) . - ISSN 0020-1669. - ISSN 1520-510X
   Перевод заглавия: Стратегии множественного замещения для перестраиваемой люминесценции в люминофорах Lu2MgAl4SiO12:Eu2+
Рубрики:
Physical and chemical processes
   Phosphors

   Luminescence

   Cations

   Ions

Аннотация: The equivalent or heterovalent substitution strategy is an efficient way to stimulate photoluminescence tuning or to optimize the luminescence performances of phosphor materials. Garnet-type compounds receive much attention as phosphor hosts because of their flexible structural frameworks. Herein, a garnet-type Lu2MgAl4SiO12:Eu2+ phosphor with broad-band blue-green emission is first explored with two-site occupation by varying the Eu2+ content. Two host-substitution approaches to controlling the luminescence behavior of Lu2MgAl4SiO12:Eu2+ phosphor are implemented. The cation substitution strategy of Ca2+ for Mg2+ achieves tunable emission from 463 to 503 nm together with broadening emission bands in Lu2Mg1–yCayAl4SiO12:Eu2+ phosphors. Moreover, chemical unit cosubstitution of [Ca2+–Ge4+] replacing [Lu3+–Al3+] results in Lu2–zCazMgAl4–zGezSiO12:Eu2+ phosphors, which induce a red shift of the emission peak of about 60 nm and a broadening in the emission spectra with increasing Ca2+ and Ge4+ concentrations. The possible photoluminescence tuning mechanism is ascribed to the coordination sphere variation in the EuO8 polyhedron depending on the changing neighboring cations. The proposed approaches on equivalent or heterovalent substitution can contribute to the development of Eu2+-activated garnet-type phosphors with regulation of the luminescence performance and further initiate research discovering new phosphors for white-light-emitting diodes.

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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing 100083, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Siberian Federal University, Krasnoyarsk, 660041, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russia
Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, 9300, South Africa
State Key Laboratory of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641, China

Доп.точки доступа:
Ming, Zhiqiang; Qiao, Jianwei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Swart, Hendrik C.; Xia, Zhiguo
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3.


   
    Pressure-Induced Structural Transition to the Polar Phase in GdFe3(BO3)4 / I. S. Lyubutin [et al.] // Cryst. Growth Des. - 2019. - Vol. 19, Is. 12. - P. 6935-6944, DOI 10.1021/acs.cgd.9b00609. - Cited References: 39. - The authors express their deep gratitude to Prof. S. G. Ovchinnikov for initiating this work and fruitful discussions. These studies were performed with the support of the Ministry of Science and Higher Education within the State assignment FSRC "Crystallography and Photonics" RAS in part for the synchrotron Mössbauer measurements. Support from RFBR Grant No. 17-02-00766 in part for the Raman spectroscopy measurements and from No. 18-02-00696 in part for the theoretical calculations is also acknowledged. For preparation and tests of high-pressure cells, (39) the facilities of Center for Collective Use “Accelerator Center for Neutron Research of the Structure of Substance and Nuclear Medicine” of the INR RAS were used. . - ISSN 1528-7483
   Перевод заглавия: Индуцированный давлением структурный переход в полярную фазу в GdFe3(BO3)4
Кл.слова (ненормированные):
Boron -- Crystal lattices -- Ferroelectricity -- Ions -- Iron compounds
Аннотация: The GdFe3(BO3)4 crystal has attracted great interest as a magnetic-field-induced multiferroic. In this paper, we show that the multiferroic properties in this crystal can be induced by high pressure. At high pressures up to 50 GPa, created in diamond anvil cells, the structural and vibrational (phonon) properties of the GdFe3(BO3)4 crystal were studied. The structural phase transition was detected at about 23–25 GPa by Raman and synchrotron Mössbauer (NFS) spectroscopy. First-principle calculations of the crystal lattice dynamics at pressures below and above the structural transition were carried out. It was established that at pressures above the structural transition, the space group R32 of GdFe3(BO3)4 is changed to the polar space group R3, and the crystal becomes a ferroelectric. At the R32 → R3 transition, the displacement of the boron ion B(2) and oxygen O results in the formation of boron–oxygen B(2)O4 tetrahedrons instead of the plane BO3 triangles. Meanwhile, the triangle oxygen environment of boron in the site B(1) remains unchanged. The nearest environment of the gadolinium ion also changes significantly. Instead of six oxygen ions in the R32 phase, the nearest surroundings of Gd in the R3 phase consist of nine oxygen ions forming a complex polyhedron. A large hysteresis of the transition indicates that this crystal remains a ferroelectric with a decrease in pressure to about ambient pressure.

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Держатели документа:
Shubnikov Institute of Crystallography of FSRC Crystallography and Photonics RAS, Moscow, 119333, Russian Federation
Institute for Nuclear Research, Russian Academy of Sciences, Troitsk, Moscow, 108840, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
REC Functional Nanomaterials, Immanuel Kant Baltic Federal University, Kaliningrad, 236041, Russian Federation

Доп.точки доступа:
Lyubutin, I. S.; Gavriliuk, A. G.; Andryushin, N. D.; Андрюшин, Никита Дмитриевич; Pavlovskiy, M. S.; Павловский, Максим Сергеевич; Zinenko, V. I.; Зиненко, Виктор Иванович; Lyubutina, M. V.; Troyan, I. A.; Smirnova, E. S.
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4.


   
    High-resolution optical spectroscopy and modeling of spectral and magnetic properties of multiferroic ErFe3(BO3)4 / M. N. Popova, E. P. Chukalina, D. S. Erofeev [et al.] // Phys. Rev. B. - 2020. - Vol. 101, Is. 20. - Ст. 205108, DOI 10.1103/PhysRevB.101.205108. - Cited References: 38. - Financial support of the Russian Science Foundation under Grant No. 19-12-00413 is acknowledged. . - ISSN 2469-9950. - ISSN 2469-9969
РУБ Materials Science, Multidisciplinary + Physics, Applied + Physics, Condensed Matter
Рубрики:
F-F TRANSITIONS
   ENERGY-LEVELS

   ER3+ IONS

   GROWTH

Аннотация: We carried out the high-resolution broadband temperature-dependent polarized optical spectroscopy and theoretical studies of ErFe3(BO3)4 single crystals in the paramagnetic and antiferromagnetic (T˂TN=39K) phases. On the basis of the experimentally determined 45 crystal-field (CF) levels of Er3+ ions at sites with the C2 point symmetry, CF calculations were performed, a set of physically grounded CF parameters was obtained and used to model the temperature dependences of the Er magnetic moments measured in neutron-scattering experiments, as well as the magnetic susceptibility and magnetization of the compound; the contributions of the quasi-one-dimensional iron magnetic subsystem were calculated in the frame of the previously developed self-consistent four-particle cluster model. The modeling strongly supports an easy-plane collinear structure of iron magnetic moments and excludes earlier proposed additional magnetic phase.

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Держатели документа:
Russian Acad Sci, Inst Spect, Moscow 108840, Russia.
Natl Res Univ, Moscow Inst Phys & Technol, Dolgoprudnyi 141701, Moscow Region, Russia.
LV Kirenskii Inst Phys, Siberian Branch RAS, Krasnoyarsk 660036, Russia.
Kazan Fed Univ, Kazan 420008, Russia.

Доп.точки доступа:
Popova, M. N.; Chukalina, E. P.; Erofeev, D. S.; Jablunovskis, A.; Gudim, I. A.; Гудим, Ирина Анатольевна; Malkin, B. Z.; Russian Science FoundationRussian Science Foundation (RSF) [19-12-00413]
}
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5.


   
    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. - Int. Edit. - 2020. - Vol. 59, Is. 28. - P. 11634-11640, DOI 10.1002/anie.202004562. - Cited References: 43. - This work is supported by the National Natural Science Foundation of China (51961145101, 51972118 and 51722202), Fundamental Research Funds for the Central Universities (FRFTP-18-002C1), Guangdong Provincial Science & Technology Project (2018A050506004) and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003. . - ISSN 1433-7851. - ISSN 1521-3773
   Перевод заглавия: Включение редкоземельного тербия (III) в нанокристаллы Cs2AgInCl6: Bi для перестраиваемой фотолюминесценции
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−x Tbx )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 & Technol Beijing, Beijing Municipal Key Lab New Energy Mat & Techno, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
Shenzhen Univ, Shenzhen Key Lab Special Funct Mat, Shenzhen Engn Lab Adv Technol Ceram, Guangdong Res Ctr Interfacial Engn Funct Mat,Coll, Shenzhen 518060, Peoples R China.
Fed Res Ctr KSC SB RASs, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Technol, Guangzhou 510641, Peoples 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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6.


    Orlov, Yu. S.
    Magnetic properties and spin crossover in transition metal oxides with d5 Ions at high pressures / Y. S. Orlov, S. V. Nikolaev, S. G. Ovchinnikov // J. Exp. Theor. Phys. - 2019. - Vol. 129, Is. 6. - P. 1062-1069, DOI 10.1134/S1063776119120185. - Cited References: 33. - This study was supported by the Russian Science Foundation (project no. 18-12-00022) . - ISSN 1063-7761
Кл.слова (ненормированные):
Antiferromagnetic materials -- Antiferromagnetism -- Chemical bonds -- Elasticity -- Electronic states -- Ferromagnetic materials -- Ferromagnetism -- Magnetic properties -- Paramagnetism -- Phase diagrams -- Transition metals
Аннотация: We analyze the influence of cooperative effects on the magnetic properties and spin crossover between the high-spin (HS) term S = 5/2 and low-spin (LS) term S = 1/2 in Mott–Hubbard dielectrics with 3d5 ions under high pressures. Two cooperation mechanisms (superexchange interaction and effective interaction via the elastic system) are considered. The sign of the exchange interaction changes because of the crossover from the antiferromagnetic in the HS state to the ferromagnetic in the LS state. In view of the large difference between the ionic radii of the HS and LS states, the systems with spin crossover acquire an additional strong coupling via the elastic system. Using the Hubbard operator representation and considering the electronic states of the two terms simultaneously, we obtain the effective Hamiltonian with allowance for the cooperative effects. The magnetic phase diagram and the spin crossover are investigated in the mean field approximation. It is shown that the inclusion of cooperative effects at low temperatures leads to a first-order phase transition between the antiferromagnetic HS state and the ferromagnetic LS state. At higher temperatures, more complicated sequences of phase transitions are possible upon an increase in pressure, including the HS paramagnet–HS antiferromagnet–LS paramagnet and HS antiferromagnet–LS paramagnet–LS ferromagnet transitions.

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Публикация на русском языке Орлов, Юрий Сергеевич. Магнитные свойства и спиновый кроссовер при высоких давлениях в окислах переходных металлов с d5-ионами [Текст] / Ю. С. Орлов, С. В. Николаев, С. Г. Овчинников // Журн. эксперим. и теор. физ. - 2019. - Т. 156 Вып. 6. - С. 1165-1174

Исправлено Orlov Yu. S. Erratum to: Magnetic properties and spin crossover in transition metal oxides with d5 ions at high pressures [Текст] / Y. S. Orlov, S. V. Nikolaev, S. G. Ovchinnikov // J. Exp. Theor. Phys. - 2020. - Vol. 131 Is. 2.- P.374-374

Держатели документа:
Kirensky Institute of Physics, Federal Research Center “Krasnoyarsk Science Center,” Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Nikolaev, S. V.; Николаев, Сергей Викторович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Орлов, Юрий Сергеевич
}
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7.


   
    Spin state of iron ions in Bi2(Sn1−xFex)2O7 / L. V. Udod [et al.] // VII Euro-Asian Symposium "Trends in MAGnetism" (EASTMAG-2019) : Book of abstracts. - 2019. - Vol. 2. - Ст. K.P19. - P. 352-353. - References:

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, Russia
Siberian Federal University, Krasnoyarsk, Russia

Доп.точки доступа:
Udod, L. V.; Удод, Любовь Викторовна; Aplesnin, S. S.; Аплеснин, Сергей Степанович; Romanova, O. B.; Романова, Оксана Борисовна; Bayukov, O. A.; Баюков, Олег Артемьевич; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Euro-Asian Symposium "Trends in MAGnetism"(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg); "Trends in MAGnetism", Euro-Asian Symposium(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg); Российская академия наук; Уральское отделение РАН; Институт физики металлов им. М. Н. Михеева Уральского отделения РАН; Уральский федеральный университет им. первого Президента России Б.Н. Ельцина; Российский фонд фундаментальных исследований
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8.


   
    Investigation of the Magnetic Properties of Ludwigites / R. M. Eremina [et al.] // Bull. Russ. Acad. Sci. Phys. - 2019. - Vol. 83, Is. 7. - P. 912-914, DOI 10.3103/S1062873819070141. - Cited References: 6. - This work was supported by the Russian Foundation for Basic Research, project no. 17-02-00953. . - ISSN 1062-8738
Кл.слова (ненормированные):
Aluminum compounds -- Copper compounds -- Gallium compounds -- Magnetic susceptibility -- Metal ions -- Single crystals -- Temperature distribution -- X ray powder diffraction
Аннотация: Single crystals of Cu2AlBO5 and Cu2GaBO5 copper oxyborates are synthesized via solution-melt crystallization and subjected to X-ray diffraction analysis. Parameters of the crystal lattice and the positions of atoms in a unit cell are determined. Copper ions form a structural chain along axis а in Cu2AlBO5 and Cu2GaBO5. Temperature dependences of the magnetic susceptibility are measured. The obtained curves feature kinks at Т = 2.4 (Cu2AlBO5) and 4.1 K (Cu2GaBO5). © 2019, Allerton Press, Inc.

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Публикация на русском языке Исследование магнитных свойств людвигитов [Текст] / Р. М. Еремина [и др.] // Изв. РАН. Сер. физич. - 2019. - Т. 83 № 7. - С. 999-1002

Держатели документа:
Zavoisky Physical-Technical Institute, Kazan Scientific Center, Russian Academy of Sciences, Kazan, 420029, Russian Federation
Kazan Federal University, Kazan, 420008, Russian Federation
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, 660037, Russian Federation

Доп.точки доступа:
Eremina, R. M.; Moshkina, E. M.; Мошкина, Евгения Михайловна; Gavrilova, T. P.; Gilmutdinov, I. F.; Sofronova, S. N.; Софронова, Светлана Николаевна; Kiiamov, A. G.
}
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9.


   
    Influence of cation substitution on dielectric and electric properties of bismuth stannates Bi2Sn1.9Meo.1O7 (Me=Cr, Mn) / S. S. Aplesnin [et al.] // IOP Conf. Ser.: Mater. Sci. Eng. : IOP, 2019. - Vol. 467: 21st International Scientific Conference Reshetnev Readings 2017 (8 November 2018 through 8 November 2018) Conference code: 144163, Is. 1, DOI 10.1088/1757-899X/467/1/012014. - Cited References: 9. - This study was supported by the Russian Foundation for Basic Research project N 17-32-50080, the state order № 3.5743.2017/6.7.
Кл.слова (ненормированные):
Activation energy -- Capacitance -- Chromium -- Current voltage characteristics -- Dielectric losses -- Ions -- Manganese
Аннотация: The article studies effect of nonstoichiometric substitution of the tin ions by chromium and manganese ions on the dielectric and electrical properties of bismuth pyrostannate. The research performs measurements of the current-voltage characteristics, capacitance and tangent of the dielectric loss angle in the temperature range from 300 to 800 K; it finds a qualitative difference in the temperature behavior of the permittivity of bismuth pyrostannate with chromium and manganese ions. A change in the type of conductivity from hopping to tunneling emission is established. The change in the activation energy as a function of the ion radius is found.

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Держатели документа:
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, 660037, Russian Federation
Federal Research Center Krasnoyarsk Science Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Aplesnin, S. S.; Аплеснин, Сергей Степанович; Udod, L. V.; Удод, Любовь Викторовна; Loginov, Y. Y.; Kretinin, V. V.; Masyugin, A. N.; International Scientific Conference Reshetnev Readings 2017(21st ; 8 November 2018 ; Krasnoyarsk, Russian Federation)
}
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10.


   
    Exchange Interaction between the Excited States of Magnetic Ions / S. G. Ovchinnikov [et al.] // Phys. Metals Metallogr. - 2019. - Vol. 120, Is. 13. - P. 91-94, DOI 10.1134/S0031918X19130210. - Cited References: 11. - This work was supported by the Russian Science Foundation, project no. 18-12-00022. . - ISSN 0031-918X. - ISSN 1555-6190
   Перевод заглавия: Обменное взаимодействие между магнитными ионами в возбужденном состоянии
Кл.слова (ненормированные):
exchange interaction -- spin crossover -- exchange in an excited state
Аннотация: Within the framework of the LDA + GTB multi-electron approach to the electron structure of Mott–Hubbard insulators a scheme is developed for constructing the effective low-energy Hamiltonian that includes not only the ground state of the magnetic cation, but also the excited terms. The mathematical apparatus of the theory are Hubbard operators built on the many-electron states of the cation in the dn configuration. The occupation of the excited term under optical pumping can change the sign of the exchange interaction of the excited cation with the neighboring cation in the ground state. Another variant of the occupation of the excited states is connected with a spin crossover when the excited and the ground terms change over, for example, at high pressure. Examples are given for such crystals as FeBO3, Nd0.5Gd0.5Fe3(BO3)4 and NiO.

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Держатели документа:
L.V. Kirensky Institute of Physics of SB of RAS, Krasnoyarsk, 660036 Russia

Доп.точки доступа:
Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Gavrichkov, V. A.; Гавричков, Владимир Александрович; Polukeev, S. I.; Полукеев, Семен Игоревич; Malakhovskii, A. V.; Малаховский, Александр Валентинович
}
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