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Каталог книг и брошюр библиотеки ИФ СО РАН

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Труды сотрудников ИФ СО РАН

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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Atuchin V. V., Gavrilova T. A., Kesler V. G., Molokeev M. S., Aleksandrov K. S.
Заглавие : Structural and electronic parameters of ferroelectric K3WO3F3
Коллективы :
Место публикации : Solid State Commun. - 2010. - Vol. 150, Is. 43-44. - P.2085-2088. - ISSN 0038-1098, DOI 10.1016/j.ssc.2010.09.023
Примечания : Cited References: 34. - This study was partly supported by RFBR (Grant 09-02-00062) and SB RAS (Grant 34).
Предметные рубрики: CORE-LEVEL SPECTROSCOPY
PHASE-TRANSITIONS
RHEED ANALYSIS
SURFACE
OXYFLUORIDE
ELPASOLITE
(NH4)(2)KWO3F3
SUBSTITUTION
TEMPERATURE
DIFFRACTION
Ключевые слова (''Своб.индексиров.''): ferroelectrics--chemical synthesis--electronic structure--photoelectron spectroscopies
Аннотация: The low-temperature ferroelectric G2 polymorph of K3WO3F3 oxyfluoride is formed by chemical synthesis. The electronic parameters of G2-K3WO3F3 have been measured by X-ray photoelectron spectroscopy under excitation with Al K alpha radiation (1486.6 eV). Detailed spectra have been recorded for all element core levels and Auger lines. The chemical bonding effects in the WO3 F-3 and WO6 octahedrons are considered by using the binding energy difference Delta BE(O-W) = BE(O 1s) BE(W 4f(7/2)). (C) 2010 Elsevier Ltd. All rights reserved.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Aplesnin S. S., Udod L. V., Sitnikov M. N., Shestakov N. P.
Заглавие : Bi2(Sn0.95Cr0.05)2O7: Structure, IR spectra, and dielectric properties
Место публикации : Ceram. Int.: Elsevier, 2016. - Vol. 42, Is. 4. - P.5177-5183. - ISSN 02728842 (ISSN), DOI 10.1016/j.ceramint.2015.12.040
Примечания : Cited References: 45. - This work was supported by the Russian Foundation for Basic Research Projects no. 15-42-04099 r_siberia_a, Siberian Branch of Science and NAS of Belarus “Electronic and magnetic phase transitions in materials with magnetoelectric affect” and government work no. 114090470016.
Предметные рубрики: BISMUTH PYROSTANNATE
PYROCHLORE STRUCTURE
MAGNETIC-PROPERTIES
PARTIAL OXIDATION
HIGH-TEMPERATURE
X-RAY
Bi2Sn2O7
SUBSTITUTION
CATALYSTS
DIFFRACTION
Ключевые слова (''Своб.индексиров.''): bismuth pyrostannate--infrared absorption spectra--structural transition--permittivity--debye model
Аннотация: Infrared absorption spectra of the bismuth pyrostannate Bi2(Sn0.95Cr0.05)2O7 were investigated in the frequency range 350-1100 cm-1 at temperatures of 110-525 K. Four frequency regions with split absorption lines are distinguished. Softening of frequencies at the structural transitions was observed. The maxima of permittivity measured in the frequency range 1-200 kHz at temperatures 100-400 K were determined. It was found that the magnetic susceptibility changes its sign in the low-temperature region. The correlation between anomalies in the magnetic susceptibility, permittivity, and absorption line intensity was established. Softening of frequencies is explained by the variation in the coefficient of thermal expansion of the lattice. The temperature behavior of permittivity is described using the Debye model. © 2015 Elsevier Ltd and Techna Group S.r.l.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xia Z., Miao S., Molokeev M. S., Chen M., Liu Q.
Заглавие : Structure and luminescence properties of Eu2+ doped LuxSr2-xSiNxO4-x phosphors evolved from chemical unit cosubstitution
Место публикации : J. Mater. Chem. C: Royal Society of Chemistry, 2016. - Vol. 4, Is. 6. - P.1336-1344. - ISSN 20507534 (ISSN), DOI 10.1039/c5tc04222d
Примечания : Cited References: 32. - This work was supported by the National Natural Science Foundation of China (Grant No. 51572023 and 51272242), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), the Funds of the State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, CAS (RERU2015022), and Fundamental Research Funds for the Central Universities (FRF-TP-15-003A2).
Предметные рубрики: SOLID-SOLUTION PHOSPHORS
WHITE-LIGHT
PHOTOLUMINESCENCE
SUBSTITUTION
DISCOVERY
TRANSITIONLEDS
EVOLUTION
HOST
LEDS
Аннотация: The design scheme of the chemical unit cosubstitution of [Lu3+-N3-] for [Sr2+-O2-] in Sr2SiO4:Eu2+ has been put into practice to discover the new phosphor systems with tunable luminescence properties, and the structures and photoluminescence tuning of yellow-emitting LuxSr2-xSiNxO4-x:Eu2+ phosphors have been investigated. Crystal structures of LuxSr2-x-ySiNxO4-x:yEu2+ samples were resolved using the Rietveld method, suggesting that the as-prepared Sr2SiO4 belonged to monoclinic symmetry (P21/n) of β-phase Sr2SiO4, while Sr1.97Eu0.03SiO4 and Sr1.965Eu0.03Lu0.005SiO3.995N0.005 belonged to orthorhombic symmetry (Pnma) of α-Sr2SiO4. The emission peaks of LuxSr1.97-xSiNxO4-x:0.03Eu2+ phosphors were red-shifted from 563 to 583 nm upon increasing the [Lu3+-N3-] substitution content from x = 0 to x = 0.005, furthermore, the PL emission peaks of Lu0.005Sr1.965-ySiN0.005O3.995:yEu2+ also showed a red-shift from 583 nm to 595 nm with increasing Eu2+ concentration (y = 0.03, 0.07, 0.10 and 0.15), and their corresponding red-shift mechanism has been discussed. The temperature dependent luminescence results further verified that the introduction of [Lu3+-N3-] for [Sr2+-O2-] in Sr2SiO4:Eu2+ can improve the thermal stability of the photoluminescence, which indicated that the LuxSr2-x-ySiNxO4-x:yEu2+ phosphors have potential applications in white light-emitting diodes (wLEDs). © 2016 The Royal Society of Chemistry.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ji H., Wang L., Molokeev M. S., Hirosaki N., Huang Z., Xia Z., Ten Kate O. M., Liu L., Xie R.
Заглавие : New garnet structure phosphors, Lu3-xYxMgAl3SiO12:Ce3+ (x = 0-3), developed by solid solution design
Место публикации : J. Mater. Chem. C: Royal Society of Chemistry, 2016. - Vol. 4, Is. 12. - P.2359-2366. - ISSN 20507534 (ISSN), DOI 10.1039/c6tc00089d
Примечания : Cited References: 33. - This work was partly supported by the National Natural Science Foundation of China (Grant No. 51511130035, 51272259, 61575182, 51572232 and 51561135015) and the Russian Foundation for Basic Research (Grant No. 15-52-53080). H. J. thanks the China Scholarship Council (CSC) for providing a scholarship to support his study in NIMS.
Предметные рубрики: Particle-diagnosis approach
Luminescence
Photoluminescence
Ce3+
Substitution
Discovery
Oxygen
Аннотация: New garnet phosphors, Lu3−xYxMgAl3SiO12:Ce3+ (x = 0–3), which can be efficiently excited by blue light and emit the yellow-orange light, were developed using the solid solution design strategy combining the chemical unit substitution and the cation substitution. Crystal structures of the four compounds were reported for the first time via the Rietveld refinement of their powder XRD patterns. All phosphors show the general cubic garnet structure with the space group Iad. The specific occupancy of Lu/Y, Al/Mg, Al/Si and O atoms in different positions was identified. The evolution of cell parameters and Y/Lu/Ce–O bond lengths were identified. Photoluminescence properties were evaluated on aspects of emission/excitation spectra, internal/external quantum efficiency and thermal emission stability. Under the 450 nm blue light excitation, the phosphors exhibit bright yellow color emission, peaking in the 575–597 nm spectral range. The internal and external quantum efficiency can reach 83% and 58%, respectively. The emission red-shift in response to the Y/Lu ratio variation was discussed in relation to the local structure evolution. The phosphors are relatively promising to act as wavelength converter of blue light in white light emitting diodes.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Flerov I. N., Kartashev A. V., Grankina V. A.
Заглавие : Heat capacity and phase transitions in NH4LiSO4, Cs-x(NH4)(1-x) LiSO4, and RbLiSO4
Разночтения заглавия :авие SCOPUS: Heat capacity and phase transitions in NH4LiSO4, Csx(NH4)1-xLiSO4, and RbLiSO 4
Место публикации : Phys. Solid State: AMER INST PHYSICS, 2005. - Vol. 47, Is. 4. - P720-728. - ISSN 1063-7834, DOI 10.1134/1.1913987
Примечания : Cited References: 29
Предметные рубрики: ROOM-TEMPERATURE
MONTE-CARLO
LINH4SO4
SUBSTITUTION
CRYSTALS
SULFATE
CSLISO4
Аннотация: The heat capacity of NH4LiSO4, RbLiSO4, and Cs-x(NH4)(1 - x) LiSO4 crystals and its behavior over a broad temperature range including the phase transition regions were studied. The entropy changes corresponding to structural transformations in these crystals were found not to be characteristic of straightforward ordering of structural blocks. The results obtained are discussed in terms of phenomenological theory and model concepts. (C) 2005 Pleiades Publishing, Inc.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ovchinnikov S. G.
Заглавие : Role of zinc and nickel impurities in high-temperature superconductors
Место публикации : Phys. Solid State: AMER INST PHYSICS, 1999. - Vol. 41, Is. 4. - P534-538. - ISSN 1063-7834, DOI 10.1134/1.1130819
Примечания : Cited References: 32
Предметные рубрики: PR2-XCEXCUO4+DELTA SINGLE-CRYSTALS
SR-CU-O
COPPER OXIDES
MAGNETIC-PROPERTIES
NI
MODEL
ZN
SUBSTITUTION
SCATTERING
SPECTRUM
Аннотация: The local changes produced in the electronic structure and their effect on the physical properties of the superconducting and normal phases when zinc and nickel are substituted for copper are examined on the basis of a multiband p-d model. It is shown that strong electronic correlations suppress the S = 1 configuration of Ni2+ and cause the superposition of the S = 1/2 and S = 0 states of nickel. The change in the density of states in p- and n-type systems is studied, and the peculiarity of Zn impurity for p- type systems and Ni impurity for n-type systems is shown. The universal dependence of the T-c on the residual resistance in lightly doped superconductors and deviations from it in optimally doped systems are discussed. (C) 1999 American Institute of Physics. [S1063-7834(99)00704-2].
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Petrakovskii G. A., Vorotynov A. M., Sablina K. A., Pankrats A. I., Velikanov D. A.
Заглавие : Effect of Li+ and Ga3+ ion diamagnetic dilution on magnetic and resonance properties of CuGeO3
Место публикации : Fiz. Tverd. Tela: MEZHDUNARODNAYA KNIGA, 1996. - Vol. 38, Is. 11. - P3430-3438. - ISSN 0367-3294
Примечания : Cited References: 9
Предметные рубрики: DOPED CUGEO3
NEEL STATE
SUBSTITUTION
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ji H., Wang L., Molokeev M. S., Hirosaki N., Xie R., Huang Z., Xia Z., Ten Kate O. M., Liu L., Atuchin V. V.
Заглавие : Structure evolution and photoluminescence of Lu3(Al,Mg)2(Al,Si)3O12:Ce3+ phosphors: New yellow-color converters for blue LED-driven solid state lighting
Место публикации : J. Mater. Chem. C: Royal Society of Chemistry, 2016. - Vol. 4, Is. 28. - P.6855-6863. - ISSN 20507534 (ISSN), DOI 10.1039/c6tc00966b
Примечания : Cited References: 44. - This work was partially supported by the National Natural Science Foundations of China (Grant No. 51511130035, 51272259, 61575182, 51561135015, and 51572232) and the Russian Foundation for Basic Research (Grant No. 15-52-53080). We are also grateful to financial support from the JSPS KAKENHI (No. 15K06448). H. J. thanks the China Scholarship Council (CSC) for scholarship support. V. V. A. was partially supported by the Ministry of Education and Science of the Russian Federation.
Предметные рубрики: WHITE LEDS
LUMINESCENCE PROPERTIES
EMITTING-DIODES
GARNET PHOSPHORS
SUBSTITUTION
Ce3+
PHASE
Ca
Аннотация: This paper reports the development of new phosphors using the chemical unit cosubstituting solid solution design strategy. Starting from Lu3Al5O12, the Al3+-Al3+ couple in respective octahedral and tetrahedral coordination was simultaneously substituted by a Mg2+-Si4+ pair forming the Lu3(Al2-xMgx)(Al3-xSix)O12:Ce3+ (x = 0.5-2.0) series; as a result, the CeO8 polyhedrons were compressed and the emission got red-shifted from green to yellow together with the broadening. The evolution of, the unit cell, the local structural geometry as well as the optical properties of Ce3+ in these garnet creations, in response to the gradual Mg-Si substitution for Al-Al, were studied by combined techniques of structural refinement and luminescence measurements. The new composition Lu2.97Ce0.03Mg0.5Al4Si0.5O12 was comprehensively evaluated regarding its potential application in blue LED-driven solid state white lighting: the maximum emission is at 550 nm under ?ex = 450 nm; the internal and external quantum efficiencies can reach 85% and 49%, respectively; a 1-phosphor-converted wLED lamp fabricated using the as-prepared phosphor exhibits the luminous efficacy of 105 lm W-1, the correlated color temperature of 6164 K and the color rendering index (Ra) of 75.6. The new solid solution composition series is open for further optimization to enhance the competence for commercial consideration. © 2016 The Royal Society of Chemistry.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Yang, Zhiyu, Zhao, Yifei, Zhou, Yayun, Qiao, Jianwei, Chuang, Yu-Chun, Molokeev M. S., Xia, Zhiguo
Заглавие : Giant red-shifted emission in (Sr,Ba)Y2O4:Eu2+ phosphor toward broadband near-infrared luminescence
Коллективы : International Cooperation Project of National Key Research and Development Program of China [2021YFE0105700]; National Natural Science Foundations of ChinaNational Natural Science Foundation of China (NSFC) [51972118, 51961145101]; Guangzhou Science & Technology Project [202007020005]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01X137]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]
Место публикации : Adv. Funct. Mater. - 2022. - Vol. 32, Is. 1. - Ст.2103927. - ISSN 1616-301X, DOI 10.1002/adfm.202103927. - ISSN 1616-3028(eISSN)
Примечания : Cited References: 60. - This research was supported by the International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), National Natural Science Foundations of China (Grant No. 51972118 and 51961145101), Guangzhou Science & Technology Project (202007020005), 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
Предметные рубрики: LIGHT-SOURCES
PHOTOLUMINESCENCE
TRANSITION
CE3+
BLUE
SUBSTITUTION
Аннотация: Near-infrared (NIR) light-emitting diodes (LEDs) light sources are desirable in photonic, optoelectronic, and biological applications. However, developing broadband red and NIR-emitting phosphors with good thermal stability is always a challenge. Herein, the synthesis of Eu2+-activated SrY2O4 red phosphor with high photoluminescence quantum efficiency and broad emission band ranging from 540 to 770 nm and peaking at 620 nm under 450 nm excitation is designed. Sr/Ba substitution in SrY2O4:Eu2+ has been further utilized to achieve tunable emission by modifying the local environment, which facilitates the giant red-shifted emission from 620 to 773 nm while maintaining the outstanding thermal stability of SrY2O4:Eu2+. The NIR emission is attributed to the enhanced Stokes shift and crystal field strength originated from the local structural distortions of [Y1/Eu1O6] and [Y2/Eu2O6]. The investigation in charge distribution around Y/Eu provides additional insight into increasing covalency to tune the emission toward the NIR region. As-fabricated NIR phosphor-converted LEDs demonstration shows its potential in night-vision technologies. This study reveals the NIR luminescence mechanism of Eu2+ in oxide-based hosts and provides a design principle for exploiting Eu2+-doped NIR phosphors with good thermal stability.
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