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1.


   
    Biodegradable polyhydroxyalkanoates with a different set of valerate monomers: Chemical structure and physicochemical properties / T. G. Volova, N. O. Zhila, E. G. Kiselev [et al.] // Int. J. Mol. Sci. - 2023. - Vol. 24, Is. 18. - Ст. 14082, DOI 10.3390/ijms241814082. - Cited References: 99. - The study was funded by the Russian Science Foundation (project no. 23-64-10007) . - ISSN 1661-6596. - ISSN 1422-0067
Кл.слова (ненормированные):
copolymers -- P(3HB-co-3HV-co-4HV) -- P(3HB-co-3HV-co-3H4MV) -- physicochemical properties -- thermal behavior -- isothermal crystallization -- spherulites formation rate -- morphology
Аннотация: The properties, features of thermal behavior and crystallization of copolymers containing various types of valerate monomers were studied depending on the set and ratio of monomers. We synthesized and studied the properties of three-component copolymers containing unusual monomers 4-hydroxyvalerate (4HV) and 3-hydroxy-4-methylvalerate (3H4MV), in addition to the usual 3-hydroxybutyrate (3HB) and 3-hydroxyvalerate (3HV) monomers. The results showed that P(3HB-co-3HV-co-4HV) and P(3HB-co-3HV-co-3H4MV) terpolymers tended to increase thermal stability, especially for methylated samples, including an increase in the gap between melting point (Tmelt) and thermal degradation temperature (Tdegr), an increase in the melting point and glass transition temperature, as well as a lower degree of crystallinity (40–46%) compared with P(3HB-co-3HV) (58–66%). The copolymer crystallization kinetics depended on the set and ratio of monomers. For terpolymers during exothermic crystallization, higher rates of spherulite formation (Gmax) were registered, reaching, depending on the ratio of monomers, 1.6–2.0 µm/min, which was several times higher than the Gmax index (0.52 µm/min) for the P(3HB-co-3HV) copolymer. The revealed differences in the thermal properties and crystallization kinetics of terpolymers indicate that they are promising polymers for processing into high quality products from melts.

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Держатели документа:
Institute of Biophysics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, 50/50 Akademgorodok, Krasnoyarsk 660036, Russia
Basic Department of Biotechnology, School of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodnyi Av., Krasnoyarsk 660041, Russia
L.V. Kirensky Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, 50/38 Akademgorodok, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Volova, Tatiana G.; Zhila, Natalia O.; Kiselev, Evgeniy G.; Sukovatyi, Aleksey G.; Lukyanenko, A. V.; Лукьяненко, Анна Витальевна; Shishatskaya, Ekaterina I.
}
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2.


   
    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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3.


   
    Controlled hydrothermal crystallization of anhydrous Ln2(OH)4SO4 (Ln = Eu-Lu, Y) as a new family of layered rare earth metal hydroxides / X. J. Wang [et al.] // Chem. - A Eur. J. - 2017. - Vol. 23, Is. 63. - P. 16034-16043, DOI 10.1002/chem.201703282. - Cited References:54. - This work is supported in part by the National Natural Science Foundation of China (Grants Nos. 51702020, and 51672039), Doctoral Research Fund of Liaoning Province (Grant No. 20170520103) and the Russian Foundation for Basic Research (17-52-53031). X.W. acknowledges the financial support from the China Scholarship Council for her overseas Ph.D. study (Contract No. 201406080035). . - ISSN 0947-6539. - ISSN 1521-3765
   Перевод заглавия: Контролируемая гидротермальная кристаллизация безводного Ln2(OH)4SO4 в качестве нового семейства слоистых редкоземельных гидроксидов
РУБ Chemistry, Multidisciplinary
Рубрики:
ANION-EXCHANGE MATERIALS
   BOND-VALENCE PARAMETERS

   X-RAY-DIFFRACTION

Кл.слова (ненормированные):
hydrothermal synthesis -- layered compounds -- luminescence -- oxide sulfates -- rare earths
Аннотация: Anhydrous hydroxide sulfates Ln2(OH)4SO4 (Ln=Eu–Lu, Y) were hydrothermally synthesized as a new family of layered rare earth metal hydroxides (LRHs). They crystallize in the monoclinic system (space group C2/m) with structures built up by alternate stacking of interlayer SO42− and the two-dimensional host layer composed of tricapped [LnO9] trigonal prisms along the a axis. In distinct contrast to the recently discovered hydrated LRHs Ln2(OH)4SO4⋅2 H2O, which only exist for Ln=La–Dy, the host layers of the anhydrous phase are linked together by sharing edges instead of an O node of the SO42− tetrahedron. Rietveld refinement showed that the cell dimension tends to decrease for smaller Ln3+, while the axis angle (β=98.78–100.31°) behaves oppositely. Comparative thermogravimetric/differential thermal analysis in air revealed that the dehydroxylation and desulfurization temperatures become gradually higher and lower, respectively, for smaller Ln3+, and thus the temperature range of Ln2O2SO4 existence is narrowed. The newly discovered Ln2(OH)4SO4, together with their hydrated counterparts, allow for the first time green synthesis of Ln2O2SO4 with water as the only exhaust for the full spectrum of lanthanides. Calcining Ln2(OH)4SO4 in H2 yielded phase-pure Ln2O2S for Eu and Gd and a mixture of Ln2O2S and Ln2O3 for the other Ln. The effects of the lanthanide contraction were clearly revealed, and photoluminescence was found for the anhydrous LRHs of Eu and Tb.

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Держатели документа:
Bohai Univ, Coll New Energy, Jinzhou 121013, Liaoning, Peoples R China.
Natl Inst Mat Sci, Res Ctr Funct Mat, Tsukuba, Ibaraki 3050044, Japan.
Northeastern Univ, Minist Educ, Key Lab Anisotropy & Texture Mat, Shenyang 110819, Liaoning, Peoples R China.
Northeastern Univ, Inst Ceram & Powder Met, Sch Mat Sci & Engn, Shenyang 110819, Liaoning, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Wang, Xuejiao; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhu, Q.i.; Li, Ji-Guang
}
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4.


   
    Crystallization and studies of A+B3+F4 compounds [Text] / Voronov V.N., Nikolayeva T.V. // Advanced inorganic fluorides : the Third International Siberian workshop Intersibfluorine - 2008, September 01-06, 2008, Vladivostok, Russia : proceedings of ISIF-2008. - Vladivostok, 2008. - p. 200-203 . - ISBN 978-5-98128-036-8


Доп.точки доступа:
Voronov, V. N.; Воронов, Владимир, Николаевич; Nikolayeva, T. V.; "Advanced inorganic fluorides", International Siberian workshop(3 ; 2008 ; SEP. ; Vladivostok)
}
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5.


   
    Crystallization of trigonal (Tb,Er)(Fe,Ga)(3)(BO3)(4) phases with hantite structure in bismuth trimolybdate-based fluxes / L. N. Bezmaternykh [et al.] // Crystallogr. Rep. - 2005. - Vol. 50. - P. S97-S99, DOI 10.1134/1.2133981. - Cited Reference Count: 8 . - ISSN 1063-7745
Рубрики:

Аннотация: The stability regions of the trigonal (Tb,Er)(Fe,Ga)(3)(BO3)(4) phases are established in (Bi2Mo3O12)-based fluxes. The specific features of heterogeneous nucleation and the subsequent phase transformations during transition to the equilibrium are studied in the vicinity of the boundaries. The temperature modes of single crystal growth on seeds are suggested with due regard for the "nonequilibrium effect." (C) 2005 Pleiades Publishing, Inc.

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Доп.точки доступа:
Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Temerov, V. L.; Темеров, Владислав Леонидович; Gudim, I. A.; Гудим, Ирина Анатольевна; Stolbovaya, N.A.
}
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6.


   
    Dielectric properties of a mixed-valence Pb3Mn7O15 manganese oxide / N. V. Volkov [et al.] // J. Phys.: Condens. Matter. - 2010. - Vol. 22, Is. 37. - Ст. 375901, DOI 10.1088/0953-8984/22/37/375901. - Cited References: 14. - This study was supported by the Russian Foundation for Basic Research 'Siberia', project No. 09-02-98003, and the Siberian Branch of the Russian Academy of Sciences, integration project No. 101. . - ISSN 0953-8984
РУБ Physics, Condensed Matter

Кл.слова (ненормированные):
cation -- lead -- manganese derivative -- oxide -- article -- chemical model -- chemistry -- crystallization -- electric conductivity -- electronics -- methodology -- temperature -- Cations -- Crystallization -- Electric Conductivity -- Electronics -- Lead -- Manganese Compounds -- Models, Chemical -- Oxides -- Temperature -- AC electric field -- Analysis of resistivity -- Carrier hopping -- Charge ordering -- Complex dielectric constant -- Crystal site -- Debye models -- Dielectric constants -- Dielectric spectra -- Frequency windows -- Lattice sites -- Low frequency -- Manganese ions -- Mixed valence -- Mixed valence state -- Relaxation behaviors -- Temperature range -- Electric fields -- Manganese -- Manganese oxide -- Permittivity -- Single crystals -- Crystal symmetry
Аннотация: We investigated the low-frequency dielectric properties of a Pb3Mn7O15 single crystal with manganese ions in the mixed-valence state (Mn3+/Mn4+). Dielectric relaxation was found in the frequency window from 20 to 100 kHz in the temperature range 110-180 K. The dielectric spectra of the crystal were analyzed using a Debye model. Estimations made within the model and analysis of resistivity data suggest that the relaxation behavior of the dielectric constant is related to polaronic charge carrier hopping. Around 250 K, charge ordering occurs in the crystal when the Mn3+ and Mn4+ ions are arranged in a specific order among the crystal sites. With a decrease in temperature, an ac electric field can induce a charge hop between the equivalent lattice sites available, related to crystal symmetry. This hopping is equivalent to the reorientation of an electric dipole that yields Debye-type behavior of the complex dielectric constant. The observed anisotropy in the behavior of the dielectric properties and resistivity can be attributed to a pronounced two-dimensional character of the crystal structure.

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Держатели документа:
[Volkov, N. V.
Eremin, E. V.
Sablina, K. A.
Sapronova, N. V.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
ИФ СО РАН
L V Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk, Russia.
L V Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Volkov, N. V.; Волков, Никита Валентинович; Eremin, E. V.; Еремин, Евгений Владимирович; Sablina, K. A.; Саблина, Клара Александровна; Sapronova, N. V.
}
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7.


   
    Directional crystallization and self-assembling initiated by mechanical shock or electron beam in nanocrystalline Co-C and Fe-C films / L. I. Kveglis, V. S. Zhigalov // Surface Science. - 2007. - Т. 601, № 13. - С. 2873-2875, DOI 10.1016/j.susc.2006.12.044 . - ISSN 0039-6028
ГРНТИ


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Держатели документа:
L.V. Kirensky Institute of Physics,Siberian Division,Russian Academy of Science, Akademgorodok
Доп.точки доступа:
Kveglis, L. I.; Квеглис, Людмила Иосифовна; Zhigalov, V. S.; Жигалов Виктор Степанович
}
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8.


    Edelman, I.
    Oxide glasses with magnetic nanoparticles: transparent magnets (Faraday rotation and electron magnetic resonance studies) / I. . Edelman, J. . Kliava // Phys. Status Solidi B. - 2009. - Vol. 246, Is. 10. - P. 2216-2231, DOI 10.1002/pssb.200945169. - Cited References: 87. - This work is supported in part by RFBR-CNRS joint project, grant No 07-02-92174. We are grateful to E. Petrakovskaja and O. Ivanova for measuring and discussing, respectively, the EMR spectra in thermally treated samples and the FR spectral and magnetic field dependences. . - ISSN 0370-1972
РУБ Physics, Condensed Matter
Рубрики:
SPIN-HAMILTONIAN PARAMETERS
   SINGLE-DOMAIN PARTICLES

   SUPERPARAMAGNETIC RESONANCE

   CRYSTALLIZATION BEHAVIOR

   FERRIMAGNETIC RESONANCE

   PARAMAGNETIC-RESONANCE

   TEMPERATURE-DEPENDENCE

   COMPUTER-SIMULATIONS

   FINE PARTICLES

   BORATE GLASSES

Аннотация: In the first part of this paper we outline the state of the art in the field of magnetic nanoparticles in oxide glasses. We describe the theoretical background of two complementary techniques used for the studies of the state of paramagnetic ions, clusters and magnetic particles in a diamagnetic matrix, viz., magnetooptical Faraday rotation (FR) and electron magnetic resonance (EMIR) and we overview previous results obtained with these techniques for several glass systems. In the second part, we highlight the case of potassium-alumina-borate glasses - a glassy system where doping with paramagnetic oxides results in formation of magnetic particles at very low contents of paramagnetic additions: Fe(2)O(3) and MnO. In the special case when the ratio of the iron and manganese oxides in the charge is 3/2, magnetic nanoparticles with characteristics close to those of manganese ferrite are formed already at the first stage of the glass preparation. After thermal treatment all glasses show FR and EMR spectra attesting to the presence of superparamagnetic nanoparticles, characterized by relatively broad size and shape distributions. The formation of magnetic nanoparticles confers to these glasses magnetic and magnetooptical properties typical of magnetically ordered substances. At the same time, the glasses remain transparent in a part of the visible and near infrared spectral range and display a high FR value. Such properties make them particularly interesting for use as new media for various magneto-optical devices. (C) 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

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Держатели документа:
[Edelman, Irina] Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
[Kliava, Janis] Univ Bordeaux 1, Ctr Phys Mol Opt & Hertzienne, CNRS, UMR 5798, F-33405 Talence, France
ИФ СО РАН
L.V. Kirensky Institute of Physics, Siberian Branch of the Russian Academy of Sciences, Akademgorodok 38, 660036 Krasnoyarsk, Russian Federation
Centre de Physique Moleculaire Optique et Hertzienne, Universite Bordeaux1-CNRS, UMR 5798, 351 cours de la Liberation, 33405 Talence cedex, France

Доп.точки доступа:
Kliava, J.; RFBR-CNRS [07-02-92174]
}
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9.


   
    Effect of monomers of 3-hydroxyhexanoate on properties of copolymers poly(3-hydroxybutyrate-co 3-hydroxyhexanoate) / T. G. Volova, M. V. Uspenskaya, E. G. Kiselev [et al.] // Polymers. - 2023. - Vol. 15, Is. 13. - Ст. 2890, DOI 10.3390/polym15132890. - Cited References: 99. - The study was funded by the Russian Science Foundation (project No 23-64-10007) . - ISSN 2073-4360
Кл.слова (ненормированные):
P(3HB-co-3HHx) copolymers -- P(3HB) homopolymer -- various synthesis conditions -- molecular weight -- crystallinity -- thermal properties -- isothermal crystallization -- spherulites
Аннотация: The properties of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) P(3HB-co-3HHx) copolymers with different ratios of monomers synthesized by the wild-type strain Cupriavidus necator B-10646 on sugars, and an industrial sample from Kaneka synthesized by the recombinant strain C. necator NSDG-ΔfadB1 on soybean oil, were studied in a comparative aspect and in relation to poly(3-hydroxybutyrate) P(3HB). The copolymer samples, regardless of the synthesis conditions or the ratio of monomers, had reduced values of crystallinity degree (50–60%) and weight average molecular weight (415–520 kDa), and increased values of polydispersity (2.8–4.3) compared to P(3HB) (70–76%, 720 kDa, and 2.2). The industrial sample had differences in its thermal behavior, including a lower glass transition temperature (−2.4 °C), two peaks in its crystallization and melting regions, a lower melting point (Tmelt) (112/141 °C), and a more pronounced gap between Tmelt and the temperature of thermal degradation (Tdegr). The process, shape, and size of the spherulites formed during the isothermal crystallization of P(3HB) and P(3HB-co-3HHx) were generally similar, but differed in the maximum growth rate of the spherulites during exothermic crystallization, which was 3.5–3.7 μm/min for P(3HB), and 0.06–1.25 for the P(3HB-co-3HHx) samples. The results from studying the thermal properties and the crystallization mechanism of P(3HB-co-3HHx) copolymers are important for improving the technologies for processing polymer products from melts.

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Держатели документа:
Institute of Biophysics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok 50/50, 660036 Krasnoyarsk, Russia
School of Fundamental Biology and Biotechnology, Siberian Federal University, Svobodnyi Av. 79, 660041 Krasnoyarsk, Russia
Chemical Engineering Center, Research Institute «Bioengineering» ITMO University, Kronverksky Pr. 49, 197101 Saint Petersburg, Russia
L. V. Kirensky Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok 50/38, 660036 Krasnoyarsk, Russia
Basic Department of Solid State Physics and Nanotechnology, School of Engineering Physics and Radio Electronics, Siberian Federal University, Kirensky St. 26, 660074 Krasnoyarsk, Russia

Доп.точки доступа:
Volova, Tatiana G.; Uspenskaya, Mayya V.; Kiselev, Evgeniy G.; Sukovatyi, Aleksey G.; Zhila, Natalia O.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Shishatskaya, Ekaterina I.
}
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10.


   
    Formation of noble metal phases (Pt, Pd, Rh, Ru, Ir, Au, Ag) in the process of fractional crystallization of the CuFeS2 melt / E. F. Sinyakova, I. G. Vasilyeva, A. S. Oreshonkov [et al.] // Minerals. - 2022. - Vol. 12, Is. 9. - Ст. 1136, DOI 10.3390/min12091136. - Cited References: 61. - This work was supported by the Russian Federation state assignment of Sobolev Institute of Geology and Mineralogy of SB RAS, Nikolaev Institute of Inorganic Chemistry SB RAS, and Kirensky Institute of Physics of Federal Research Center KSC SB RAS. The grant number is projects II.1.64. and 40330-2016-0001 . - ISSN 2075-163X
Кл.слова (ненормированные):
Cu-Fe-S system -- noble metals -- directional crystallization -- intermediate solid solution -- fine inclusions
Аннотация: The quasi-equilibrium directional crystallization of the melt composition (at. %): Cu 24.998, Fe 25.001, S 49.983, with Ag 0.002, Pd 0.003, Ru 0.004, Rh 0.006, and Au, Pt, Ir (each as 0.001) was carried out. The crystallized cylindrical ingot consisted of two primary zones and three secondary zones with different chemical and phase compositions. The compositions of the primary zones corresponded to high-temperature intermediate solid solution (zone I) and liquid enriched in sulfur (zone II). The compositions of the secondary zones corresponded to low-temperature intermediate solid solution and chalcopyrite (zone Ia), the same intermediate solid solution with chalcopyrite and bornite (zone Ib), and again with bornite, chalcocite, and idaite (zone II). We plotted the distribution curves of Fe, Cu, and S along the ingot, calculated the distribution coefficients of the components during directional crystallization, and clearly showed that, from the initial stoichiometric composition CuFeS2, the intermediate solid solution enriched in Fe and depleted in S is crystallized. Based on the data of directional crystallization and thermal analysis, a cross section was constructed in the intermediate solid solution-sulfide melt region of the Cu-Fe-S system. With solubility in the solid Cu-Fe sulfides lying below detection limit of scanning electron microscopy/energy-dispersive X-ray spectrometry (SEM/EDS), noble elements occurred as individual phases of a size more often <10 µm. They were identified as Ag, RuS2, PdS, Au* (an Au based alloy), (Rh, Ir, Ru)3S8, (Rh, Ir)3S8, Rh3S8, and (Cu, Fe)~2(Pt, Rh)1S~5 phases by electron microprobe. Based on ab initio calculations of crystal structure, electronic band structure, and lattice dynamics of idealized laurite RuS2 phase and the idealized Ir3S8, Rh3S8, and Ru3S8 phases, the interpretation of Raman spectrum of the cation-mixed (Ru, Rh, Ir)S2 sulfide was presented for the first time.

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Держатели документа:
V.S. Sobolev Institute of Geology and Mineralogy, Siberian Branch of the Russian Academy of Sciences, pr. Akademika Koptyuga 3, Novosibirsk, 630090, Russian Federation
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Ac. Lavrentieva ave. 3, Novosibirsk, 630090, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
School of Engineering and Construction, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Sinyakova, E. F.; Vasilyeva, I. G.; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Goryainov, S. V.; Karmanov, N. S.
}
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11.


   
    Glass crystallization making red phosphor for high-power warm white lighting / T. Hu, L. Ning, Y. Gao [et al.] // Light Sci. Appl. - 2021. - Vol. 10, Is. 1. - Ст. 56, DOI 10.1038/s41377-021-00498-6. - Cited References: 50. - The present work was supported by the National Natural Science Foundations of China (Grant Nos. 51972118, 51961145101, 51722202 and 11974022), the Guangzhou Science & Technology Project (202007020005), the Fundamental Research Funds for the Central Universities (D2190980), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137) . - ISSN 2095-5545
   Перевод заглавия: Кристаллизация стекла с синтезом красного люминофора для мощного теплого белого освещения
Кл.слова (ненормированные):
Aluminosilicate glass -- First-principles calculation -- Glass crystallization -- Luminous efficiency -- Preparation method -- Solid state lighting -- Solid-state lighting technology -- Stable luminescence -- Light emission
Аннотация: Rapid development of solid-state lighting technology requires new materials with highly efficient and stable luminescence, and especially relies on blue light pumped red phosphors for improved light quality. Herein, we discovered an unprecedented red-emitting Mg2Al4Si5O18:Eu2+ composite phosphor (λex = 450 nm, λem = 620 nm) via the crystallization of MgO–Al2O3–SiO2 aluminosilicate glass. Combined experimental measurement and first-principles calculations verify that Eu2+ dopants insert at the vacant channel of Mg2Al4Si5O18 crystal with six-fold coordination responsible for the peculiar red emission. Importantly, the resulting phosphor exhibits high internal/external quantum efficiency of 94.5/70.6%, and stable emission against thermal quenching, which reaches industry production. The maximum luminous flux and luminous efficiency of the constructed laser driven red emitting device reaches as high as 274 lm and 54 lm W−1, respectively. The combinations of extraordinary optical properties coupled with economically favorable and innovative preparation method indicate, that the Mg2Al4Si5O18:Eu2+ composite phosphor will provide a significant step towards the development of high-power solid-state lighting.

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Держатели документа:
School of Physics and Optoelectronics, State Key Laboratory of Luminescent Materials and Devices and Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, South China University of Technology, Guangzhou, Guangdong, China
Anhui Key Laboratory of Optoelectric Materials Science and Technology, Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Normal University, Wuhu, Anhui, China
School of Applied Physic and Materials, Wuyi University, Jiangmen, Guangdong, China
Ministry of Education Key Laboratory of Bioinorganic and Synthetic Chemistry, State Key Laboratory of Optoelectronic Materials and Technologies, KLGHEI of Environment and Energy Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou, Guangdong, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, Russian Federation
Institute of Microstructure and Property of Advanced Materials, Beijing University of Technology Beijing, Beijing, China

Доп.точки доступа:
Hu, T.; Ning, L.; Gao, Y.; Qiao, J.; Song, E.; Chen, Z.; Zhou, Y.; Wang, J.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ke, X.; Xia, Z.; Zhang, Q.
}
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12.


   
    Hydrothermal crystallization of a Ln2(OH)4SO4·nH2O layered compound for a wide range of Ln (Ln = La-Dy), thermolysis, and facile transformation into oxysulfate and oxysulfide phosphors / X. Wang [et al.] // RSC Adv. - 2017. - Vol. 7, Is. 22. - P. 13331-13339, DOI 10.1039/c7ra00645d. - Cited References: 54. - This work was partly supported by the National Natural Science Foundation of China (Grants No. 51672039, 51172038, and 51302032), the Fundamental Research Fund for the Central Universities (Grant No. N140204002), the Grants-in-Aid for Scientific Research (KAKENHI No. 26420686), and the Russian Foundation for Basic Research (15-52-53080). Xuejiao Wang acknowledges the financial support received from the China Scholarship Council for her overseas Ph. D. study at the National Institute of Materials Science (Contract No. 201406080035). . - ISSN 2046-2069
   Перевод заглавия: Гидротермальная кристаллизация слоистых соединений Ln2(OH)4SO4·nH2O с широким диапазоном Ln (Ln = La-Dy), термолиз и плавный переход в оксисульфатные и оксисульфидные люминофоры
Кл.слова (ненормированные):
Dysprosium -- Hydrothermal synthesis -- Light emission -- Phase structure -- Phosphors -- Rare earth elements -- Acceleration voltages -- Chemical compositions -- Electron beam irradiation -- Hydrothermal conditions -- Hydrothermal crystallization -- Lanthanide contraction -- Photoluminescence properties -- Structure refinements -- Dysprosium compounds
Аннотация: The synthesis of a layered Ln2(OH)4SO4·nH2O material (Ln-241) with a smaller lanthanide ion (Dy3+) was successfully achieved through the optimization of the hydrothermal conditions, and the effect of lanthanide contraction on the chemical composition, phase structure, and crystallite/particle morphology of the products was investigated and discussed. Structure refinement showed that the lattice parameters (a, b, and c), cell volume, and axis angle across the series (Ln = La-Dy) monotonously decrease as the size of Ln3+ decreases. Comparative TG/DTA analysis in air indicated that the dehydroxylation temperature of Ln-241 tends to increase, whereas the dehydration and desulfurization temperatures decrease as the size of Ln3+ decreases, thus narrowing the stable temperature range for Ln2O2SO4. Taking advantage of the fact that Ln-241 has exactly the same Ln/S molar ratio as Ln2O2SO4 and Ln2O2S, the latter two groups of important compounds (excluding Ce) were facilely transformed from the former via the removal of water by calcination. The photoluminescence properties of Eu3+ and Tb3+, in terms of excitation, emission, fluorescence decay, quantum yield, and emission color, were investigated and compared for the two hosts Gd2O2S and Gd2O2SO4, and the (Gd0.99Tb0.01)2O2S phosphor was shown to be stable under electron beam irradiation in the studied range and exhibited an increasingly higher emission brightness as the acceleration voltage (up to 7 kV) or beam current (up to 50 μA) increased.

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Держатели документа:
Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang, Liaoning, China
Institute of Ceramics and Powder Metallurgy, School of Materials Science and Engineering, Northeastern University, Shenyang, Liaoning, China
Research Centre for Functional Materials, National Institute for Materials Science, Tsukuba, Ibaraki, Japan
College of New Energy, Bohai University, Jinzhou, Liaoning, 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
School of Physics and Electronic Engineering, Jiangsu Normal University, Xuzhou, Jiangsu, China
World Premier International Centre for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Tsukuba, Ibaraki, Japan

Доп.точки доступа:
Wang, X.; Li, J. -G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, W.; Zhu, Q.; Tanaka, H.; Suzuta, K.; Kim, B. -N.; Sakka, Y.
}
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13.


    Kveglis, L. I.
    Scale invariance of the structure upon explosive crystallization of amorphous films / L. I. Kveglis, V. A. Seredkin, A. V. Kuzovnikov // JETP Letters. - 2005. - Vol. 82, Is. 1. - P. 22-25, DOI 10.1134/1.2045332. - Cited References: 19 . - ISSN 0021-3640
РУБ Physics, Multidisciplinary

Аннотация: Experimental results that are obtained in the process of the explosive crystallization of x-ray amorphous films Fe2Tb and CoPd with magnetic anisotropy perpendicular to the film plane are reported. The internal bending of thus obtained "single crystals" reaches 100 deg/mu m. An explanation of the mechanism and kinetics of explosive crystallization in the Fe2Tb and CoPd films is proposed in the framework of the shear transformation zone theory. (C) 2005 Pleiades Publishing, Inc.

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Держатели документа:
Russian Acad Sci, Siberian Div, Kirenski Inst Phys, Krasnoyarsk 660036, Russia
ИФ СО РАН
Kirenski Institute of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Seredkin, V. A.; Середкин, Виталий Александрович; Kuzovnikov, A. V.
}
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14.


    Kveglis, L. I.
    The self-organization of tetrahedrally close-packed structures in magnetic nanocrystalline Tb-Fe and Co-Pd films / L. I. Kveglis, A. V. Kuzovnikov, I. V. Timofeev ; ed.: BM Darinskii, , BM Darinsk // Mechanical spectroscopy III: Mechanical spectroscopy and relaxation phenomena IN SOLIDS. Ser. Solid state phenomena : Trans tech publications LTD, 2006. - Vol. 115. - P. 267-273. - Cited References: 19 . - ISBN 1012-0394. - ISBN 3-908451-24-8
РУБ Materials Science, Multidisciplinary + Physics, Applied + Physics, Condensed Matter + Spectroscopy
Рубрики:
AMORPHOUS FILMS
Кл.слова (ненормированные):
dissipative structures -- explosive crystallization -- thermal conductivity -- Tb-Fe films -- Co-Pd films
Аннотация: The self-organization of an atomic structure in Tb30Fe70 and Co50Pd50 films possessing of high values of the perpendicular magnetic anisotropy (PMA) constant (K perpendicular to similar to 10(6) erg/cm(3)) is investigated by transmission electron microscopy. The crystallization of the films is realized in an explosive way with formation of different dissipative structures from the initial nanocrystalline state. In present work the structural model of a thin film in mezzo-scale and the correlation of a structure with magnetic properties are discussed.

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Доп.точки доступа:
Kuzovnikov, A. V.; Timofeev, I. V.; Тимофеев, Иван Владимирович; Darinskii, B. M. \ed.\; International Conference on Mechanical Spectroscopy and Relaxation Phenomena in Solids (3 ; 2006 ; Cracow, Poland)
}
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15.


   
    Layered hydroxyl sulfate: Controlled crystallization, structure analysis, and green derivation of multi-color luminescent (La,RE)2O2SO4 and (La,RE)2O2S phosphors (RE = Pr, Sm, Eu, Tb, and Dy) / X. Wang [et al.] // Chem. Eng. J. - 2016. - Vol. 302. - P. 577-586, DOI 10.1016/j.cej.2016.05.089. - Cited References: 50. - This work is supported in part by the National Natural Science Foundation of China (Grants Nos. 51172038, 51302032, and U1302272), the Fundamental Research Fund for the Central Universities (Grant No. N140204002), Grants-in-Aid for Scientific Research (KAKENHI No. 26420686), and the Russian Foundation for Basic Research (15-52-53080). X.J. Wang acknowledges financial support from the China Scholarship Council for her overseas Ph.D. study (Contract No. 201406080035) and the assistance of Q. Q. Zhu (University of Science and Technology of China) for his help with calcination. . - ISSN 1385-8947
   Перевод заглавия: Слоистые гидроксил сульфаты: контролируемая кристаллизация, структурный анализ, и зеленый синтез мультицветных люминофоров (La,RE)2O2SO4 и (La,RE)2O2S (RE=Pr, Sm, Eu, Tb, and Dy)
РУБ Engineering, Environmental + Engineering, Chemical
Рубрики:
PHOTOLUMINESCENCE PROPERTIES
   OXYSULFATE/OXYSULFIDE SYSTEMS

   CRYSTAL-STRUCTURE

   OXYGEN-STORAGE

   Ln

   NANOCOMPOSITES

   EMISSION

   CAPACITY

   FAMILY

   FABRICATION

Кл.слова (ненормированные):
Sulfate type layered rare earth hydroxide -- Luminescence -- Oxysulfate -- Oxysulfide
Аннотация: The two important groups of Ln2O2SO4 and Ln2O2S compounds are traditionally synthesized with the involvements of environmentally harmful sulfur-containing reagents. We developed in this work a unique green approach for their synthesis, using Ln2(OH)4SO4·2H2O layered hydroxyl sulfate as the precursor (Ln-241 phase). Phase selective crystallization of La-241 under both atmospheric pressure and hydrothermal conditions was firstly optimized, followed by transformation into La2O2S and La2O2SO4 by controlled calcination. Rietveld structure refinement was performed for La-241, La(OH)SO4, La2O2SO4, and La2O2S, and the crystal structure and cell parameters of La-241 were originally reported. The photoluminescence performances of several important activators (Pr3+, Sm3+, Eu3+, Tb3+, and Dy3+) in the two hosts, in terms of excitation, emission, quantum yield, and color coordinates of emission, were thoroughly investigated, and multi-color luminescence including bright red, green, orange red, and yellow was obtained under ultraviolet excitation. Detailed investigations of Tb3+ photoluminescence revealed that the lack of 5D3 emission in La2O2S and the gradual quenching of 5D3 blue emission at a higher Tb3+ content (hence decreasing I488/I545 ratio and changing color coordinates) in La2O2SO4 were suggested to be due to thermal activation of the 5D3 electrons into the conduction band and cross relaxation between adjacent Tb3+, respectively. The synthesis approach developed in this work for La2O2SO4 and La2O2S, with water vapor as the only exhaust gas, is environmentally benign and holds great potential in the facile synthesis of analogous compounds of other lanthanides. © 2016 Elsevier B.V.

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Держатели документа:
Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), School of Materials Science and Engineering, Northeastern University, Shenyang, Liaoning, China
Advanced Materials Processing Unit, National Institute for Materials Science, Tsukuba, Ibaraki, Japan
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation

Доп.точки доступа:
Wang, X.; Li, J. -G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhu, Q.; Li, X.; Sun, X.
}
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16.


   
    Low-temperature structural and magnetic phase transitions in multiferroic GdFe3(BO3)4 / K. V. Frolov [et al.] // J. Alloys Compd. - 2016. - Vol. 671. - P. 545-551, DOI 10.1016/j.jallcom.2016.02.083. - Cited References:36. - We thank Dr. A.P. Dudka for help in the low temperature XRD measurements. This study was supported in part by the Russian Foundation for Basic Research (projects # 14-02-00483a and 13-02-12442), and the Council on Grants from the President of the Russian Federation for Support of Leading Scientific Schools (grant # NSh-1130.2014.5 and # NSh-924.2014.2). This work was performed using the equipment of the Shared Research Center IC RAS and was supported by the Russian Ministry of Education and Science (project RFMEFI62114X0005). . - ISSN 0925-8388. - ISSN 1873-4669
   Перевод заглавия: Низкотемпературные структурные и магнитные фазовые переходы в мультиферроике GdFe3(BO3)4
РУБ Chemistry, Physical + Materials Science, Multidisciplinary + Metallurgy & Metallurgical Engineering
Рубрики:
IRON BORATE GDFE3(BO3)4
   BIFEO3 THIN-FILMS

   MAGNETOELASTIC PROPERTIES

   RM3(BO3)4 CRYSTALS

   TRIGONAL GDFE3(BO3)4

   ENHANCED POLARIZATION

   HIGH-PRESSURES

   CRYSTALLIZATION

   BEHAVIOR

   GROWTH

Кл.слова (ненормированные):
Multiferroics -- Rare earth compounds -- X-ray diffraction -- Mossbauer -- spectroscopy -- Crystal structure -- Spin dynamics
Аннотация: X-ray analysis revealed that at temperature decreasing from room temperature to Tstr = 155 K the crystal unit cell GdFe3(BO3)4 is reduced only along the c axis (at 0.01 Å), while the a and b axes are unchanged within the error limits. The volume of the crystal decreases uniformly in the direction of all three axes at 155–80 K. At 80–30 K the crystal volume is decreased only by reduction of the parameters a and b, while the parameter c increases conversely. In the paramagnetic region Mössbauer spectra do not distinguish between the two structural positions of iron ions Fe1 and Fe2, appearing at T < Tstr. Below the temperature of the magnetic phase transition at TN = 38.0(1) K the Mössbauer data indicate quasi-one-dimensional magnetic ordering of iron moments in the sublattice Fe2 and a two-dimensional one in the iron sublattice Fe1. The dynamics of spin reorientation in sublattices Fe1 and Fe2 is studied in detail.
Рентгеновский анализ показал, что при уменьшении температуры от комнатной до Tstr = 155 K изменение параметра элементарной ячейки кристалла GdFe3(BO3)4 происходит лишь вдоль оси с (при 0,01 Å), в то время как а и b оси остаются неизменными в пределах погрешности измерений. Объем кристалла уменьшается равномерно в направлении всех трех осей при 155-80 K. При 80-30 K объем кристалла уменьшается только уменьшением параметров a и b, в то время как параметр с наоборот увеличивается. В парамагнитной области Мессбауэровские спектры не различают двух структурных позиций ионов железа Fe1 и Fe2, появляющиеся при Т˂Tstr. Ниже температуры магнитного фазового перехода при TN = 38,0(1) К Мёссбауэрские данные указывают на квази-одномерный магнитное упорядочение моментов железа в подрешетке Fe2 и двумерное в железной подрешетке Fe1. Динамика спиновой переориентации в подрешетках Fe1 и Fe2 подробно изучается.

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Держатели документа:
Russian Acad Sci, AV Shubnikov Crystallog Inst, Moscow 119333, Russia.
Carnegie Inst Sci, Geophys Lab, Washington, DC 20015 USA.
Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Frolov, K. V.; Lyubutin, I. S.; Smirnova, E. S.; Alekseeva, O. A.; Verin, I. A.; Artemov, V. V.; Kharlamova, S. A.; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Gudim, I. A.; Гудим, Ирина Анатольевна; Russian Foundation for Basic Research [14-02-00483a, 13-02-12442]; Council on Grants from the President of the Russian Federation for Support of Leading Scientific Schools [NSh-1130.2014.5, NSh-924.2014.2]; Russian Ministry of Education and Science [RFMEFI62114X0005]
}
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17.


   
    Magnetic nanoparticles in borate glasses: Identification and sizing / I. S. Edelman [et al.] // International Conference on Optimization of Electrical and Electronic Equipment (OPTIM 2014) : IEEE Computer Society, 2014. - P. 95-104, DOI 10.1109/OPTIM.2014.6850939. - Cited References: 60 . - ISBN 978-1-4799-5183-3
Рубрики:
Engineering, Electrical and Electronic
Кл.слова (ненормированные):
SUPERPARAMAGNETIC RESONANCE -- FERROMAGNETIC-RESONANCE -- FERRITE NANOPARTICLES -- OXIDE NANOPARTICLES -- FARADAY-ROTATION -- CERAMICS -- IRON -- CRYSTALLIZATION -- ANISOTROPY -- PARTICLES
Аннотация: Heat treatment of borate glasses co-doped with low contents of iron and larger radius elements: Dy, Tb, Gd, Ho, Er, Y and Bi results in formation of magnetic nanoparticles, radically changing their physical properties. Transmission electron microscopy and synchrotron radiation-based techniques: XRD, EXAFS, XANES and SAXS, show a broad distribution of nanoparticle sizes with characteristic depending on the treatment regime; a crystalline structure of these nanoparticles is detected in heat treated samples. Magnetic circular dichroism (MCD) studies of samples subjected to heat treatment as well as of maghemite, magnetite and iron garnet allow to unambiguously assigning the nanoparticle structure to maghemite. Different features observed in the MCD spectra are related to different electron transitions in Fe3+ ions gathered in the nanoparticles. Variable-temperature electron magnetic resonance (EMR) studies confirm the formation of magnetic nanoparticles and the identification of their nature. Computer simulations of the EMR spectra corroborate the broad distribution of nanoparticle sizes found by 'direct' techniques. © 2014 IEEE.

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Доп.точки доступа:
Edelman, I. S.; Эдельман, Ирина Самсоновна; Ivanova, O. S.; Иванова, Оксана Станиславовна; Zubavichus, Y.; Trofimova, N. N.; Zaikovskiy, V. I.; Artemenko, A.; Curely, J.; Kliava, J.; Russian Foundation for Basic Research; Russian Foundation for Basic Research; International Conference on Optimization of Electrical and Electronic Equipmen (22 May - 24 May 2014 ; Bran, Romania)
}
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18.


   
    Magnetic properties and the metal-insulator transition in GdXMn1-XS solid solutions / O. B. Romanova [et al.] // Solid State Commun. - 2010. - Vol. 150, Is. 13-14. - P. 602-604, DOI 10.1016/j.ssc.2009.12.042. - Cited References: 13. - This study was supported by the Russian Foundation for Basic Research project No. 09-02-00554_a; No. 09-02-92001-NNS_a; No. 08-02-90031 Bel_a and Belarus Foundation for Basic Research project No. F04-182; ADTF "Development of scientific potential of the higher school" No. 2.1.1/401. . - ISSN 0038-1098
РУБ Physics, Condensed Matter

Кл.слова (ненормированные):
Insulator -- Metals -- Crystal growth -- Phase transitions -- Insulator -- Metals -- Crystal growth -- Phase transitions -- Insulator -- Metals -- Antiferromagnetic semiconductors -- Crystal growth -- Cubic lattice -- Metal-insulator phase transition -- Orders of magnitude -- P-type -- Temperature range -- Thermoelectric properties -- Thermopowers -- Antiferromagnetic materials -- Antiferromagnetism -- Crystal growth -- Crystallization -- Electric properties -- Gadolinium -- Grain boundaries -- Magnetic fields -- Magnetic properties -- Manganese -- Manganese compounds -- Metal insulator boundaries -- Metals -- Semiconductor growth -- Semiconductor insulator boundaries -- Sodium chloride -- Solid solutions -- Solidification -- Metal insulator transition
Аннотация: The structural, magnetic, electrical, and thermoelectric properties of GdXMn1-XS (0.01 <= X <= 0.3) solid solutions synthesized for the first time on the basis of alpha-MnS have been studied experimentally in the temperature range 77-1000 K in magnetic fields up to 10 kOe. The synthesized samples are antiferromagnetic semiconductors with an NaCl-type cubic lattice typical of a-MnS. Both concentration (X-c = 0.3) and temperature (T-c = 450 K) metal-insulator phase transitions have been observed. The concentration metal-insulator transition is accompanied by a decrease in resistivity and thermopower by twelve and two orders of magnitude, respectively, with the change in conductivity from p-type to n-type. (C) 2010 Elsevier Ltd. All rights reserved.

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Держатели документа:
[Romanova, O. B.
Ryabinkina, L. I.
Velikanov, D. A.
Balaev, D. A.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
[Sokolov, V. V.
Pichugin, A. Yu.] Russian Acad Sci, Inst Inorgan Chem, Siberian Branch, Novosibirsk 630090, Russia
[Galyas, A. I.
Demidenko, O. F.
Makovetskii, G. I.
Yanushkevich, K. I.] Natl Acad Sci Belarus, GO NPTs Mat Sci Ctr, Minsk 220072, Byelarus
ИФ СО РАН
Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, 660036 Krasnoyarsk, Russian Federation
Institute of Inorganic Chemistry, Russian Academy of Sciences, Siberian Branch, 630090 Novosibirsk, Russian Federation
GO NPTs Materials Science Center, National Academy of Sciences of Belarus, 220072 Minsk, Belarus

Доп.точки доступа:
Romanova, O. B.; Романова, Оксана Борисовна; Ryabinkina, L. I.; Рябинкина, Людмила Ивановна; Sokolov, V. V.; Pichugin, A. Y.; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Balaev, D. A.; Балаев, Дмитрий Александрович; Galyas, A. I.; Demidenko, O. F.; Makovetskii, G. I.; Yanushkevich, K. I.
}
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19.


   
    Mossbauer magnetization and resistivity studies of Fe1.91V0.09BO4 / N. V. Kazak [et al.] // Physica B. - 2005. - Vol. 359: International Conference on Strongly Correlated Electron Systems (SCES 04) (JUL 26-30, 2004, Karlsruhe, GERMANY). - P. 1324-1326, DOI 10.1016/j.physb.2005.01.396. - Cited References: 8 . - ISSN 0921-4526
РУБ Physics, Condensed Matter
Рубрики:
FE2OBO3
Кл.слова (ненормированные):
Mott-hubbard system -- magnetism -- new materials -- Magnetism -- Mott-hubbard system -- New materials -- Crystallization -- Crystallography -- Fermi level -- Ferrimagnetism -- Magnetism -- Magnetization -- Mossbauer spectroscopy -- Phase transitions -- Single crystals -- X ray diffraction analysis -- Charge ordering -- Electron-electron interactions -- Mott-hubbard system -- New materials -- Iron compounds
Аннотация: Single crystals of Fe1.91V0.09BO4 were prepared by spontaneous crystallization using a solution melt technology for the first time and its structure, electronic and magnetic properties were investigated by X-ray diffraction, Mossbauer spectroscopy, magnetization and electrical measurements. Room-temperature Mossbauer measurements indicate that "localized" (Fe2+, Fe3+) and "delocalized" (Fe2.5+) states in ratio 0.31:0.345:0.345 distributed over two crystallographically non-equivalent positions exist. The results of magnetic measurements show that warwickite is a P-type ferrimagnet below T = 130 K. Resistivity measurements show a variable-range-hopping when electron-electron interactions cause a soft Coulomb gap in the density of states at the Fermi energy. (c) 2005 Elsevier B.V. All rights reserved.

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Держатели документа:
Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
Krasnoyarsk State Tech Univ, Krasnoyarsk 660074, Russia
ИФ СО РАН
LV Kirensky Institute of Physics, Siberian Branch of RAS, 660036 Krasnoyarsk, Russian Federation
Krasnoyarsk State Tech. University, 660074 Krasnoyarsk, Russian Federation

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Balaev, A. D.; Балаев, Александр Дмитриевич; Ivanova, N. B.; Иванова, Наталья Борисовна; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
}
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20.


    Myagkov, V. G.
    Multiple self-propagating high-temperature synthesis and solid-phase reactions in thin films / V. G. Myagkov, L. E. Bykova, G. N. Bondarenko // J. Exp. Theor. Phys. - 1999. - Vol. 88, Is. 5. - P. 963-967, DOI 10.1134/1.558878. - Cited References: 28 . - ISSN 1063-7761
РУБ Physics, Multidisciplinary
Рубрики:
DENSE BRANCHING MORPHOLOGY
   SINGLE-CRYSTAL GROWTH

   PATTERN-FORMATION

   AL-GE

   CHEMICAL-REACTIONS

   CRYSTALLIZATION

   SEPARATION

   HEAT

Аннотация: A variety of self-propagating high-temperature synthesis in thin films has been found and investigated. This modification, called multiple self-propagating high-temperature synthesis, occurs in the solid phase and is a reversible phase transition. Multiple self-propagating high-temperature synthesis is similar in many respects to a metal-insulator phase transition. It is shown that for eutectic systems it is equivalent to a repeated transition through the eutectic temperature of bulk samples. It is inferred that multiple self-propagating high-temperature synthesis in bilayer films is governed by phase separation mechanisms that take place during eutectic solidification and eutectoid decomposition. (C) 1999 American Institute of Physics. [S1063-7761(99)01705-9].

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Держатели документа:
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
Russian Acad Sci, Inst Chem & Chem Technol, Siberian Branch, Krasnoyarsk 660036, Russia
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Доп.точки доступа:
Bykova, L. E.; Быкова, Людмила Евгеньевна; Bondarenko, G. N.; Бондаренко, Галина Николаевна; Мягков, Виктор Григорьевич
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