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    Tuning of photoluminescence and local structures of substituted cations in xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7:Eu2+ phosphors / M. Chen [et al.] // Chem. Mater. - 2017. - Vol. 29, Is. 3. - P. 1430-1438, DOI 10.1021/acs.chemmater.7b00006. - Cited References: 37. - The present work was supported by the National Natural Science Foundation of China (Grants 91622125 and 51572023), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-15-003A2). . - ISSN 0897-4756
   Перевод заглавия: Управляемая люминесценция и локальная структура замещаемых катионов в люминофоре xSr2Ca(PO4)2-(1-x)Ca10Li(PO4)7:Eu2+
Кл.слова (ненормированные):
Calcium -- Energy transfer -- Europium -- Light emission -- Lithium -- Luminescence -- Phosphors -- Photoionization -- Photoluminescence -- Single crystals -- Composition ranges -- Crystal-field splitting -- Luminescence measurements -- Non-linear variation -- Photoionization process -- Polyhedra distortion -- Rare earth doped solids -- Temperature dependent -- Solid solutions
Аннотация: Local structure modification in solid solution is an essential part of photoluminescence tuning of rare earth doped solid state phosphors. Herein we report a new solid solution phosphor of Eu2+-doped xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7 (0 ≤ x ≤ 1), which share the same β-Ca3(PO4)2 type structure in the full composition range. Depending on the x parameter variation in xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7:Eu2+, the vacancies generated in the M(4) site enable the nonlinear variation of cell parameters and volume, and this increases the magnitude of M(4)O6 polyhedra distortion. The local structure modulation around the Eu2+ ions causes different luminescent behaviors of the two-peak emission and induces the photoluminescence tuning. The shift of the emission peaks in the solid solution phosphors with different compositions has been discussed. It remains invariable at x ≤ 0.5, but the red-shift is observed at x > 0.5 which is attributed to combined effect of the crystal field splitting, Stokes shift, and energy transfer between Eu2+ ions. The temperature-dependent luminescence measurements are also performed, and it is shown that the photoionization process is responsible for the quenching effect.

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Держатели документа:
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, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
State Key Laboratory of Tribology, Tsinghua University, Beijing, China

Доп.точки доступа:
Chen, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wang, T.; Liu, Q.
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Terahertz spectroscopy of multiferroic EuFe3(BO3)4 / K. N. Boldyrev [et al.] // Phys. Lett. A. - 2012. - Vol. 376, Is. 37. - P. 2562-2564, DOI 10.1016/j.physleta.2012.06.028. - Cited References: 19. - This work was partially supported by the Russian Foundation for Basic Research under Grants No. 10-02-01071-a and No. 09-02-00171-a, by the Ministry of Education and Science under Grant HIII-4828.2012.2, and by the Russian Academy of Sciences under the programs for basic research. . - ISSN 0375-9601

РУБ Physics, Multidisciplinary
Рубрики:
SINGLE-CRYSTAL
GDFE3(BO3)4
Кл.слова (ненормированные):
Terahertz spectroscopy -- Multiferroics -- Europium iron borate
Аннотация: The terahertz spectra of a rare-earth iron borate with the huntite structure are obtained for the first time. We study the low-temperature (4.0–90 K) α-polarized transmittance spectra of the EuFe3(BO3)4 single crystal in the region 0.9–6.0 THz. Pronounced shifts of phonon frequencies and appearance of new phonon modes at the temperature T S = 58 K of the R 32 → P 3 1 21 structural phase transition are observed. Additional shifts of phonon frequencies occur at the temperature T N = 34 K of the magnetic ordering of the Fe subsystem, thus evidencing the spin–phonon coupling in this multiferroic material.

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Держатели документа:
[Boldyrev, K. N.
Klimin, S. A.
Popova, M. N.] RAS, Inst Spect, Troitsk 142190, Moscow Region, Russia
[Stanislavchuk, T. N.] New Jersey Inst Technol, Dept Phys, Newark, NJ 07102 USA
[Bezmaternykh, L. N.] RAS, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Boldyrev, K. N.; Stanislavchuk, T. N.; Klimin, S. A.; Popova, M. N.; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич
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    Temperature and Eu2+-doping induced phase selection in NaAlSiO4 polymorphs and the controlled yellow/blue emission / M. Zhao [et al.] // Chem. Mater. - 2017. - Vol. 29, Is. 15. - P. 6552-6559, DOI 10.1021/acs.chemmater.7b02548. - Cited References: 48. - The present work was supported by the National Natural Science Foundation of China (Grants 91622125 and 51572023 and 11574003), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-16-002A3). L.N. acknowledges the support from the Special and Excellent Research Fund of Anhui Normal University. . - ISSN 0897-4756
   Перевод заглавия: Фазовый переход индуцированный температурой и допированием Eu2+ в NaAlSiO4, и контролируемое излучение желтого/голубого света
Кл.слова (ненормированные):
Chemical modification -- Coordination reactions -- Europium -- Light emitting diodes -- Photoluminescence -- Functional properties -- High color rendering index -- Local coordination structures -- Near ultraviolet excitations -- Structural transformation -- Synthesis temperatures -- Temperature dependent -- White light emitting diodes -- Density functional theory
Аннотация: The union of temperature-dependent phase transition and relating structural transformation via modification of chemical compositions is of fundamental importance for the discovery of new materials or their functional properties optimization. Herein, the synthesis temperature and Eu2+-doping content induced phase selection and variations of the local structures in nepheline, low-carnegieite and high-carnegieite types of NaAlSiO4 polymorphs were studied in detail. The luminescence of Eu2+ in low-carnegieite and nepheline phases shows blue (460 nm) and yellow (540 nm) broad-band emissions, respectively, under near-ultraviolet excitation. The photoluminescence evolution can be triggered by the different synthesis temperatures in relation to the Eu2+-doping concentration, as corroborated by density functional theory calculations on the local coordination structures and corresponding mechanical stabilities in terms of the Debye temperature. The fabricated white light-emitting diode device with high color rendering index demonstrates that the multicolor phosphors from one system provides a new gateway for the photoluminescence tuning. © 2017 American Chemical Society.

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Держатели документа:
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, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Anhui Key Laboratory of Optoelectronic Materials Science and Technology, Department of Physics, Anhui Normal University, Wuhu, Anhui, China

Доп.точки доступа:
Zhao, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ning, L.; Liu, Q.
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Synthesis, structure, and thermophysical properties of EuGaGe2O7 / L. T. Denisova, M. S. Molokeev, L. A. Irtyugo [et al.] // Inorg. Mater. - 2020. - Vol. 56, Is. 8. - P. 854-858, DOI 10.1134/S002016852008004X. - Cited References: 18 . - ISSN 0020-1685. - ISSN 1608-3172

РУБ Materials Science, Multidisciplinary
Рубрики:
TEMPERATURE HEAT-CAPACITY
THERMODYNAMIC PROPERTIES
CRYSTAL-STRUCTURE
Кл.слова (ненормированные):
europium gallium germanate -- solid-state synthesis -- differential scanning calorimetry -- heat capacity -- structure -- thermodynamic properties
Аннотация: The europium gallium germanate EuGaGe2O7 has been prepared by solid-state reaction in air in the temperature range 1273–1473 K using a stoichiometric mixture of Eu2O3, Ga2O3, and GeO2. Its crystal structure has been determined by X-ray diffraction (sp. gr. P21/c, a = 7.1693(7) Å, b = 6.57008(6) Å, c = 12.7699(1) Å, β = 117.4522(5)°, V = 533.768(8) Å3). The heat capacity of polycrystalline samples has been determined by differential scanning calorimetry in the temperature range 350–1053 K and the experimental data have been used to calculate the thermodynamic properties (enthalpy increment, entropy change, and reduced Gibbs energy change) of EuGaGe2O7.

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Публикация на русском языке Синтез, структура и теплофизические свойства EuGaGe2O7 [Текст] / Л. Т. Денисова, М. С. Молокеев, Л. А. Иртюго [и др.] // Неорган. матер. - 2020. - Т. 56 № 8. - С. 901-905

Держатели документа:
Siberian Fed Univ, Inst Nonferrous Met & Mat Sci, Svobodnyi Pr 79, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Siberian Branch, Fed Res Ctr, Kirensky Inst Phys,Krasnoyarsk Sci Ctr, Akademgorodok 50-38, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Engn Phys & Radio Elect, Ul Akad Kirenskogo 28-12 B, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Baikov Inst Met & Mat Sci, Leninskii Pr 49, Moscow 119991, Russia.

Доп.точки доступа:
Denisova, L. T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Irtyugo, L. A.; Beletskii, V. V.; Kargin, Yu. F.; Denisov, V. M.
}
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Synthesis, crystall structure, thermochemical and luminescent-spectral properties of europium sulphates / Yu. G. Denisenko [et al.] // XXI Mendeleev Congress on General and Applied Chemistry : Book of abstracts : in 6 vols. - 2019. - Vol. 2b. - P. 90. - Cited References: 2

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Держатели документа:
Idustrial University of Tyumen
Institute of Semiconductor Physics, SB RAS
L.V. Kirensky Institute of Physics, SB RAS
Tyumen State Uneversity

Доп.точки доступа:
Denisenko, Yu. G.; Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Andreev, O. V.; Mendeleev Congress on General and Applied Chemistry(21 ; 2019 ; Sept. ; 9-13 ; Petersburg, Russia); Менделеевский съезд по общей и прикладной химии(21 ; 2019 ; сент. ; 9-13 ; Санкт-Петербург); Российская академия наук; Российское химическое общество им. Д.И. Менделеева; Российский фонд фундаментальных исследований; Санкт-Петербургский государственный университет; Санкт-Петербургский горный университет; Российский союз химиков; Институт физической химии и электрохимии имени А.Н. Фрумкина РАН
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    Synthesis and spectroscopic properties of monoclinic α-Eu2(MoO4)3 / V. V. Atuchin [et al.] // J. Phys. Chem. C. - 2014. - Vol. 118, Is. 28. - P. 15404-15411, DOI 10.1021/jp5040739. - Cited References: 63. - This study is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 1932-7447
   Перевод заглавия: Синтез и спектроскопические свойства моноклинного а-Eu2(MoO4)3

РУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
RARE-EARTH MOLYBDATES
   VIBRATIONAL PROPERTIES
   LUMINESCENCE PROPERTIES
   CRYSTAL-STRUCTURE
   PHASE-TRANSITIONS
   TRIPLE MOLYBDATE
   SINGLE-CRYSTAL
   X-RAY
   PHOSPHORS
   EUROPIUM
Аннотация: The microcrystals of monoclinic europium molybdate, alpha-Eu-2(MoO4)(3), have been fabricated by solid-state synthesis at T = 753-1273 K for 300 h. The crystal structure of alpha-Eu-2(MoO4)(3) has been refined by the Rietveld method and was found to belong to the space group C2/c with unit cell parameters a = 7.5576(1), b = 11.4709(2), c = 11.5158(2) angstrom, and beta = 109.278(1)degrees (R-B = 3.39%). About 40 narrow Raman lines have been observed in the Raman spectrum of the alpha-Eu-2(MoO4)(3) powder sample. The luminescence spectra of alpha-Eu-2(MoO4)(3) under excitation at 355 and 457.9 nm reveal domination of induced electric dipole transition D-5(0) - F-7(2) and the presence of ultranarrow lines at D-5(0) - F-7(0) and D-5(1) - F-7(0) transitions.

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Держатели документа:
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
SB RAS, Lab Coherent Opt, Kirensky Inst Phys, Krasnoyarsk 660036, Russia
SB RAS, Lab Oxide Syst, Baikal Inst Nat Management, Ulan Ude 670047, Russia
SB RAS, Inst Semicond Phys, Lab Nanodiagnost & Nanolithog, Novosibirsk 630090, Russia
SB RAS, Kirensky Inst Phys, Lab Mol Spect, Krasnoyarsk 660036, Russia
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Chimitova, O. D.; Gavrilova, T. A.; Krylov, A. S.; Крылов, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Bazarov, B. G.; Bazarova, J. G.; Ministry of Education and Science of the Russian Federation
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Relaxation of low-temperature magnetoresistance and magnetization of polycrystalline (La0.5Eu0.5)(0.7)Pb0.3MnO3 / K. A. Shaykhutdinov [et al.] // J. Phys. D. - 2011. - Vol. 44, Is. 25. - Ст. 255001, DOI 10.1088/0022-3727/44/25/255001. - Cited References: 34. - This work was partially supported by the Lavrentyev Competition of the Young Scientist's Projects of the Siberian Branch of the Russian Academy of Sciences, Project No 12. The authors are grateful to A D Balaev and V M Sosnin for useful discussions on the results. . - ISSN 0022-3727

РУБ Physics, Applied
Рубрики:
INSULATOR-METAL TRANSITION
   GRANULAR FILMS
   NANOPARTICLES
   PR0.7CA0.3MNO3
   PERCOLATION
   MANGANITES
Кл.слова (ненормированные):
Antiferromagnetic boundaries -- Characteristic value -- Ferromagnetic domains -- Ferromagnetic metal -- Lanthanum manganites -- Logarithmic law -- Low temperatures -- Magneto-resistive effect -- Polycrystalline -- Relative orientation -- Relaxation of magnetization -- Temperature fluctuation -- Time evolutions -- Time interval -- Tunnel magnetoresistance -- Antiferromagnetism -- Electric resistance -- Europium -- Ferromagnetic materials -- Ferromagnetism -- Grain boundaries -- Grain size and shape -- Lanthanum compounds -- Lead -- Magnetic domains -- Magnetic moments -- Magnetoelectronics -- Magnetoresistance -- Manganese oxide -- Magnetization
Аннотация: Hysteresis and relaxation of magnetoresistance and magnetization of substituted (La0.5Eu0.5)(0.7)Pb0.3MnO3 lanthanum manganite in a low-temperature region (< 40 K) are investigated. It is shown that at these temperature features of the magnetoresistive effect are determined mainly by spin-dependent tunnelling of carriers via insulating grain boundaries. As was demonstrated previously, the grain boundaries may be antiferromagnetically ordered. Therefore, relaxation of magnetization and resistance is determined by the processes of relative orientation of the magnetic moments of ferromagnetic domains neighbouring the antiferromagnetic boundary of ferromagnetic domains under the action of temperature fluctuations. It is shown that relaxation follows the logarithmic law within the time interval t similar to 10(2)-3x10(3) s. A comparison between time evolutions of the magnetic moment and resistance shows that magnetoresistance and magnetization are related as delta R = delta M-n, where n = 2.5. The obtained value n is close to the characteristic value n = 2 for tunnel magnetoresistance of granular ferromagnetic metal/insulator systems.

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Держатели документа:
[Shaykhutdinov, K. A.
Balaev, D. A.
Semenov, S. V.
Popkov, S. I.
Dubrovskiy, A. A.
Sapronova, N. V.
Volkov, N. V.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
ИФ СО РАН
Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Shaykhutdinov, K. A.; Шайхутдинов, Кирилл Александрович; Balaev, D. A.; Балаев, Дмитрий Александрович; Semenov, S. V.; Семенов, Сергей Васильевич; Popkov, S. I.; Попков, Сергей Иванович; Dubrovskiy, A. A.; Дубровский, Андрей Александрович; Sapronova, N. V.; Volkov, N. V.; Волков, Никита Валентинович
}
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Pulsed laser deposition of europium borate glass films and their optical and magneto-optical properties / A. S. Aleksandrovsky [et al.] // Laser-Assisted Micro- and Nanotechnologies. Proceedings of SPIE : [11-15 May 2005]. - 2006. - P. 61610A

РИНЦ
Держатели документа:
L. V. Kirensky Institute of Physics, Akademgorodok, Krasnoyarsk 660036

Доп.точки доступа:
Konov, V. I. \ed.\; Panchenko, V. Y. \ed.\; Sugioka, K. \ed.\; Veiko, V. P. \ed.\; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Potseluyko, A. M.; Potseluyko; Seredkin, V. A.; Середкин, Виталий Александрович; Zaitsev, A. I.; Зайцев, Александр Иванович; Zamkov, A. V.; Замков, Анатолий Васильевич; International Conference on Lasers, Applications, and Technologies(2005 ; May ; St. Peterburg, Russia)
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    Probing Eu2+ luminescence from different crystallographic sites in Ca10M(PO4)7:Eu2+ (M = Li, Na, and K) with β-Ca3(PO4)2-type structure / M. Chen [et al.] // Chem. Mater. - 2017. - Vol. 29, Is. 17. - P. 7563-7570, DOI 10.1021/acs.chemmater.7b02724. - Cited References: 34. - The present work was supported by the National Natural Science Foundation of China (Grants 51722202, 91622125, and 51572023), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-16-002A3). C.C.L. and C.C.S. acknowledge the financial support from the Ministry of Science and Technology of Taiwan (Contract No. MOST 104-2113-M-027-007-MY3), and M. Molokeev acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 0897-4756
   Перевод заглавия: Исследование люминесценции Eu2+ в разных кристаллографических положениях в Ca10M(PO4)7:Eu2+ (M = Li, Na and K) со структурой типа beta-Ca3(PO4)2
Кл.слова (ненормированные):
Calcium -- Doping (additives) -- Excited states -- Light emission -- Lithium -- Luminescence -- Phosphors -- Photoluminescence -- Positive ions -- Rietveld refinement -- Single crystals -- Color tuning -- Crystallographic sites -- Different distributions -- Emission bands -- Local environments -- Long wavelength bands -- Luminescent centers -- Power diffraction data -- Europium
Аннотация: Eu2+ local environments in various crystallographic sites enable the different distributions of the emission and excitation energies and then realize the photoluminescence tuning of the Eu2+ doped solid state phosphors. Herein we report the Eu2+-doped Ca10M(PO4)7 (M = Li, Na, and K) phosphors with β-Ca3(PO4)2-type structure, in which there are five cation crystallographic sites, and the phosphors show a color tuning from bluish-violet to blue and yellow with the variation of M ions. The difference in decay rate monitored at selected wavelengths is related to multiple luminescent centers in Ca10M(PO4)7:Eu2+, and the occupied rates of Eu2+ in Ca(1), Ca(2), Ca(3), Na(4), and Ca(5) sites from Rietveld refinements using synchrotron power diffraction data confirm that Eu2+ enters into four cation sites except for Ca(5). Since the average bond lengths d(Ca-O) remain invariable in the Ca10M(PO4)7:Eu2+, the drastic changes of bond lengths d(M-O) and Eu2+ emission depending on the variation from Li to Na and K can provide insight into the distribution of Eu2+ ions. It is found that the emission band at 410 nm is ascribed to the occupation of Eu2+ in the Ca(1), Ca(2), and Ca(3) sites with similar local environments, while the long-wavelength band (466 or 511 nm) is attributed to Eu2+ at the M(4) site (M = Na and K). We show that the crystal-site engineering approach discussed herein can be applied to probe the luminescence of the dopants and provide a new method for photoluminescence tuning.

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Держатели документа:
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, Federal Research Center, KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Institute of Organic and Polymeric Materials, National Taipei University of Technology, Taipei, Taiwan
National Synchrotron Radiation Research Center, Hsinchu, Taiwan

Доп.точки доступа:
Chen, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lin, C. C.; Su, C.; Chuang, Y. -C.; Liu, Q.
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10.

Origin of color centers in the flux-grown europium gallium garnet / A. S. Aleksandrovsky [et al.] // J. Appl. Phys. - 2008. - Vol. 103, Is. 8. - Ст. 83102, DOI 10.1063/1.2902365. - Cited References: 7 . - ISSN 0021-8979

РУБ Physics, Applied
Рубрики:
SPECTRA
IONS
Кл.слова (ненормированные):
Absorption -- Europium alloys -- Garnets -- Ultraviolet radiation -- Calcium-free flux -- Flux-grown europium gallium garnet -- Color centers
Аннотация: Europium gallium garnet (EuGG) single crystals were grown from fluxes with various contents. Optical absorption spectra of EuGG grown from a flux containing calcium show an additional band in the ultraviolet and blue regions of the spectra as compared to the case of a calcium-free flux. Mossbauer spectra of the samples grown from the fluxes with different additives show no signs of other valence states of the europium ions except for 3+. However, they indicate changes in the crystal field due to the entrance of additive ions. The nature of the additional absorption must be the same as that for calcium-doped gadolinium gallium garnet, i.e., anion vacancies. Mossbauer isotope shifts and quadrupole splitting for EuGG are determined. (C) 2008 American Institute of Physics.

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Держатели документа:
[Aleksandrovsky, A. S.
Arkhipkin, V. G.
Bezmaternykh, L. N.
Gudim, I. A.
Krylov, A. S.] LV Kirenskii Inst Phys, Krasnoyarsk 660036, Russia
[Aleksandrovsky, A. S.
Arkhipkin, V. G.
Bezmaternykh, L. N.
Gudim, I. A.
Krylov, A. S.] Siberian Fed Univ, Krasnoyarsk 660079, Russia
[Vagizov, F.] Texas A&M Univ, Dept Phys, College Stn, TX 77840 USA
ИФ СО РАН
L. V. Kirensky Institute of Physics, Siberian Federal University, Akademgorodok, Krasnoyarsk 660036, Russian Federation
Department of Physics, Texas A and M University, College Station, TX 77840, United States

Доп.точки доступа:
Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Arkhipkin, V. G.; Архипкин, Василий Григорьевич; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Gudim, I. A.; Гудим, Ирина Анатольевна; Krylov, A. S.; Крылов, Александр Сергеевич; Vagizov, F.
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