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1.
Linear structural evolution
induced tunable photoluminescence in clinopyroxene solid-solution
phosphors
/ Zhiguo Xia [и др.]> // Scientific Rep. - 2013. -
Vol. 3
. - Ст. 3310. - P. 1-7,
DOI
10.1038/srep03310. - This research was supported by the National Natural Science Foundations of China (Grant No.51002146, No. 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University ofMinistry of Education of China (NCET-12-0950), Fundamental Research Funds for the Central Universities (2011YYL131), and this study was also partially supported by SB RAS, Grant 28.12. Zhiguo Xia was supported by Beijing Nova Program (Z131103000413047) . - ISSN 2045-2322
Перевод заглавия:
Линейная структурная эволюция индуцированной перестраиваемой фотолюминесценции в твердых растворах клинопироксеновых люминофоров
Аннотация:
Clinopyroxenes along the Jervisite (NaScSi2O6) – Diopside (CaMgSi2O6) join have been studied, and a solid-solution of the type (N[[d]]1-x[[/d]]Ca[[d]]x[[/d]])(Sc[[d]]1-x[[/d]]Mg[[d]]x[[/d]])Si2O6 has been identified in the full range of 0 ≤ x ≤ 1. The powder X-ray patterns of all the phases indicate a structural similarity to the end compounds and show smooth variation of structural parameters with composition. The linear structural evolution of iso-structural (Na[[d]]1-x[[/d]]Ca[[d]]x[[/d]])(Sc[[d]]1-x[[/d]]Mg[[d]]x[[/d]])Si2O6 solid-solutions obeying Vegard’s rule has also been examined and verified by high resolution transmission electron microscopy (HRTEM). The continuous solid-solutions show the same structural type, therefore the photoluminescence spectra of Eu[[p]]2+[[/p]] doped samples possess the superposition of spectral features from blue-emitting component (CaMgSi2O6:Eu[[p]]2+[[/p]]) and yellow-emitting one (NaScSi2O6:Eu[[p]]2+[[/p]]). This indicates that the spectroscopic properties of (Na[[d]]1-x[[/d]]Ca[[d]]x[[/d]])(Sc[[d]]1-x[[/d]]Mg[[d]]x[[/d]])Si2O6 clinopyroxene solid-solutions are in direct relations with structural parameters, and it is helpful for designing color-tunable photoluminescence with predetermined parameters.
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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
SB RAS, Lab Crystal Phys, Inst Phys, Krasnoyarsk 660036, Russia
SB RAS, Inst Semicond Phys, Lab Opt Mat & Struct, Novosibirsk 630090, Russia
Доп.точки доступа:
Xia, Zhiguo; Zhang, Yuanyuan; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Luo, Yi
}
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2.
Structural and luminescence
properties of yellow-emitting NaScSi 2O6:Eu2+
phosphors
: Eu2+ Site preference analysis and generation of red emission by codoping Mn2+ for white-light-emitting diode applications / Z. Xia [et al.]> // J. Phys. Chem. C. - 2013. -
Vol. 117
,
Is. 40
. - P. 20847-20854
DOI
10.1021/jp4062225. - Cover image: Artwork representing main idea of this article
Аннотация:
The structural properties of clinopyroxene NaScSi2O6 have been investigated using the X-ray powder diffraction refinement, and the luminescence properties of Eu2+ and Eu2+/Mn 2+-activated NaScSi2O6 have been studied to explore the new materials for phosphor-converted white light ultraviolet light-emitting diodes (UV-LEDs). Eu2+ was introduced into the NaScSi2O6 host in the reducing atmosphere, and the preferred crystallographic positions of the Eu2+ ions were determined based on the different structural models of the NaScSi2O6 host. The as-obtained NaScSi2O6:Eu2+ phosphor shows greenish yellow emission with the broad-band peak at 533 nm, and efficient energy transfer (ET) takes place between Eu2+ and Mn2+ in NaScSi2O6, leading to a series of color-tunable
phosphors
emitting at 533 and 654 nm for the designed NaScSi2O 6:Eu2+,Mn2+
phosphors
under excitation at 365 nm. The ET mechanism of Eu2+ and Mn2+ has also been evaluated. We have demonstrated that NaScSi2O6:Eu 2+ and NaScSi2O6:Eu2+,Mn 2+ materials exhibit great potential to act as the effective
phosphors
for UV-LEDs. В© 2013 American Chemical Society.
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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
SB RAS, Inst Semicond Phys, Lab Opt Mat & Struct, Novosibirsk 630090, Russia
Доп.точки доступа:
Xia, Zhiguo; Zhang, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.
}
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3.
Cation substitution dependent
bimodal photoluminescence in whitlockite structural Ca3-xSrx(PO4)2:Eu2+ (0 ≤ x ≤ 2) solid solution
phosphors
/ H. P. Ji [et al.]> // Inorg. Chem. - 2014. -
Vol. 53
,
Is. 20
. - P. 11119-11124,
DOI
10.1021/ic501679f. - Cited References: 37. - This work was supported by the National Natural Science Foundations of China (Grant Nos. 51032007, 51002146, 51272242), the Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20130022110006), the Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), and Beijing Youth Excellent Talent Program (YETP0635). V.V.A. acknowledges the Ministry of Education and Science of the Russian Federation for financial support. . - ISSN 0020-1669. - ISSN 1520-510X
Перевод заглавия:
Катион зависимая бимодальная люминесценция в твердом растворе Ca3-xSrx(PO4)2:Eu2+ (0 ˂ x ˂ 2) со структурой витлокита
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
LIGHT-EMITTING-DIODES
EFFICIENT ENERGY-TRANSFER
EMISSION-TUNABLE PHOSPHOR
EXCITED WHITE LEDS
CRYSTAL-STRUCTURE
LUMINESCENCE PROPERTIES
Mn2+ PHOSPHOR
COLOR TONE
PHASE
Eu2+
Аннотация:
Cation substitution dependent tunable bimodal photoluminescence behavior was observed in the Ca3-xSrx(PO4)2:Eu2+ (0 ≤ x ≤ 2) solid solution
phosphors
. The Rietveld refinements verified the phase purity and whitlockite type crystal structure of the solid solutions. The tunable photoluminescence evolution was studied as a function of strontium content, over the composition range 0.1 ≤ x ≤ 2. In addition to the emission band peak at 416 nm in Ca3(PO4)2:Eu2+, the substitution of Ca2+ by Sr2+ induced the emerging broad-band peak at 493-532 nm. A dramatic red shift of the emission peak located in the green-yellow region was observed on an increase of x in the samples with 0.75 ≤ x ≤ 2.00. The two emission bands could be related to the EuOn-Ca9 and EuOn-Ca9-xSrx emitting blocks, respectively. The values for the two kinds of emitting blocks in the solid solutions can be fitted well with the observed intensity evolution of the two emission peaks.
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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
SB RAS, LV Kirensky Phys Inst, Lab Crystal Phys, Krasnoyarsk 660036, Russia
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
Univ Auckland, Dept Chem & Mat Engn, Auckland 1142, New Zealand
Доп.точки доступа:
Ji, H. P.; Huang, Z. H.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Атучин, Виктор Валерьевич; Huang, S. F.
}
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4.
Blue-shift of Eu2+
emission in (Ba,Sr)3Lu(PO4)3:Eu2+ eulytite solid-solution
phosphors
resulting from release of neighbouring-cation-induced stress / Z. Y. Wang [et al.]> // Dalton Trans. - 2014. -
Vol. 43
,
Is. 44
. - P. 16800-16804,
DOI
10.1039/c4dt02319f. - Cited References: 16. - The present work was supported by the National Natural Science Foundations of China (grant no. 51002146, no. 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635) and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306). V.V.A. is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 1477-9226. - ISSN 1477-9234
Перевод заглавия:
Синее смещение излучения Eu2+ в твердых растворах (Ba,Sr)3Lu(PO4)3:Eu2 со структурой эулита, вызванное снятием напряжения, индуцированного соседними катионами
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
TUNABLE COLOR TONE
EXCITED WHITE LEDS
CRYSTAL-STRUCTURE
TEMPERATURE
IONS
Аннотация:
A series of iso-structural eulytite-type (Ba,Sr)(3)Lu(PO4)(3):Eu2+ solid-solution
phosphors
with different Sr/Ba ratios were synthesized by a solid-state reaction. Crystal structures of (Ba,Sr)(3)Lu(PO4)(3):Eu2+ were resolved by the Rietveld method, which shows an eulytite-type cubic Bi-4(SiO4)(3) structure with cations disordered in a single C-3 site while the oxygen atoms were distributed over two partially occupied sites. The emission peaks of Ba(3-x)SrxLu(PO4)(3):Eu2+ (0
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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
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
Доп.точки доступа:
Wang, Z. Y.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Атучин, Виктор Валерьевич; Liu, Q. L.
}
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5.
Microwave-Modified Sol-Gel Preparation
of CaLa2(MoO4)4:Er3+/Yb3+ Upconversion
Phosphors
and The Crystal Structure Refinement / V. V. Atuchin [и др.]> // The 8th Conference on Multi-functional Materials and Applications (ICMMA 2014). - 2014 . - Ст. Poster 04-P. - P84-86
Материалы конференции
Доп.точки доступа:
Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ji Myung Jang; Yong Woo Yoon; Dong Min Won; Lei Zhu; Chang Sung Lim ; Conference on Multi-functional Materials and Applications, (8 ; 2014 ; Nov. ; 27-29 ; Chungnam, Korea)
}
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6.
Photoluminescence tuning via
cation substitution in oxonitridosilicate
phosphors
: DFT calculations, different site occupations, and luminescence mechanisms / G. Li [et al.]> // Chem. Mater. - 2014. -
Vol. 26
,
Is. 9
. - P. 2991-3001,
DOI
10.1021/cm500844v. - Cited References: 62. - The authors would like to thank the Ministry of Science and Technology of Taiwan (Contract No. MOST 101-2113-M-002-014-MY3), the National Synchrotron Radiation Research Center, Taiwan, the National Natural Science Foundation of China (Grant No. NSFC 21301162), and the Fundamental Research Funds for the Central Universities (Grant No. CUG 130402) for financially supporting this research. Victor V. Atuchin gratefully acknowledges the Ministry of Education and Science of the Russian Federation for the financial support. . - ISSN 0897-4756. - ISSN 1520-5002
Перевод заглавия:
Управление фотолюминесценцией посредством замещения катионов в оксонитридосиликатных люминофорах: ТФП вычисления, заселения различных позиций и механизмы люминесценции
РУБ
Chemistry, Physical + Materials Science, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
HIGH-TEMPERATURE SYNTHESIS
LED CONVERSION
PHOSPHORS
CRYSTAL X-RAY
WHITE-LIGHT
ORDERED DISTRIBUTION
GREEN PHOSPHOR
LAYERED OXONITRIDOSILICATE
REAL STRUCTURE
AB-INITIO
Аннотация:
Tuning and optimizing luminescent properties of oxonitridosilicates
phosphors
are important for white light-emitting diode (WLED) applications. To improve the color rendering index, correlated color temperature and thermal stability of layer-structured MSi2O2N2:Eu (M = Sr, Ba)
phosphors
, cation substitutions have been used to adjust their luminescent properties. However, the underlying mechanisms are still unclear. In this research, a series of (Sr1-xBax)Si2O2N2:Eu (0 ≤ x ≤ 1) compounds were prepared by solid-state reaction, after which systematic emission variations were investigated. The crystal structures of (Sr1-xBax)Si2O2N2:Eu (0 ≤ x ≤ 1) are nominally divided into three sections, namely, Phase 1 (0 ≤ x ≤ 0.65), Phase 2 (0.65 x 0.80), and Phase 3 (0.80 ≤ x ≤ 1) based on the X-ray diffraction measurements. These experimental results are further confirmed by optimizing the crystal structure data with first-principle calculations. Continuous luminescence adjustments from green to yellow are observed in Phase 1 with gradual replacement of Sr2+ with Ba2+, and the abnormal redshift is clarified through extended X-ray absorption fine structure analysis. Sr(Eu)-O/N bond length shrinkage in local structure causes the redshift emission, and the corresponding luminescence mechanism is proposed. Controllable luminescence in Phase 2 (from blue to white) and Phase 3 (from cyan to yellowish green) are observed. Based on the high-resolution transmission electron microscopy and selected area electron diffraction analysis, the two kinds of luminescence tuning are attributed to phase segregation. This study serves as a guide in developing oxonitride luminescent materials with controllable optical properties based on variations in local coordination environments through cation substitutions.
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Держатели документа:
Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China
SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia
SB RAS, Lab Opt Mat & Struct, Inst Semicond Phys, Novosibirsk 630090, Russia
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia
Univ St Andrews, Sch Chem, EaSTCHEM, St Andrews KY16 9ST, Fife, Scotland
Natl Cent Univ, Ctr Neutron Beam Applicat, Zhongli 320, Taiwan
Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
Chongqing Univ Posts & Telecommun, Coll Math & Phys, Chongqing 400065, Peoples R China
Novosibirsk State Univ, Lab Semicond & Dielect Mat, Novosibirsk 630090, Russia
Доп.точки доступа:
Li, G.; Lin, C. C.; Chen, W.-T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Chiang, C.-Y.; Zhou, W.; Wang, C.-W.; Li, W.-H.; Sheu, H.-S.; Chan, T.-S.; Ma, C.; Liu, R.-S.
}
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7.
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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8.
Crystal chemistry and
luminescence properties of red-emitting CsGd1−xEux(MoO4)2 solid-solution
phosphors
/ P. L. Shi [et al.]> // Dalton Trans. - 2014. -
Vol. 43
,
Is. 25
. - P. 9669-9676,
DOI
10.1039/C4DT00339J. - Cited References: 46. - The present work was supported by the National Natural Science Foundations of China (grant no. 51002146, 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), the Fundamental Research Funds for the Central Universities (2-9-2014-044), and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306). V. V. A. gratefully acknowledges the Ministry of Education and Science of the Russian Federation for the financial support. . - ISSN 1477-9226. - ISSN 1477-9234
Перевод заглавия:
Кристаллохимия и люминесцентные свойства твердых растворов люминофоров CsGd1-xEux(MoO4)2, излучающих красный свет
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
WHITE-LIGHT
VIBRATIONAL PROPERTIES
HYDROTHERMAL SYNTHESIS
SINGLE-CRYSTALS
DIODES
EFFICIENCY
PHOTOLUMINESCENCE
CSGD(MOO4)2
MORPHOLOGY
GROWTH
Аннотация:
Scheelite related alkali-metal rare-earth double molybdate compounds with a general formula of ALn(MoO4)2 can find wide application as red
phosphors
. The crystal chemistry and luminescence properties of red-emitting CsGd1−xEux(MoO4)2 solid-solution
phosphors
have been evaluated in the present paper. A detailed analysis of the structural properties indicates the formation of isostructural scheelite-type CsGd1−xEux(MoO4)2 solid-solutions over the composition range of 0 ≤ x ≤ 1. The photoluminescence emission (PL) and excitation (PLE) spectra, and the decay curves were measured for this series of compounds. The critical doping concentration of Eu3+ is determined to be x = 0.6 in order to realize the maximum emission intensity. The emission spectra of the as-obtained CsGd(1−x)Eux(MoO4)2
phosphors
show narrow high intensity red lines at 592 and 615 nm upon excitation at 394 or 465 nm, revealing great potential for applications in white light-emitting diode devices.
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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
RAS, Kirensky Inst Phys, Lab Crystal Phys, SB, Krasnoyarsk 660036, Russia
RAS, Kirensky Inst Phys, Lab Opt Mat & Struct, SB, Novosibirsk 630090, Russia
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia
Novosibirsk State Univ, Lab Semicond & Dielectr Mat, Novosibirsk 630090, Russia
Доп.точки доступа:
Shi, P. L.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.
}
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9.
Phase transformation in
Ca3(PO4)2:Eu2+ via the controlled quenching and increased Eu2+ content: Identification of new cyan-emitting α-Ca3(PO4)2:Eu2+ phosphor / H. Ji [et al.]> // J. Am. Ceram. Soc. - 2015. -
Vol. 98
,
Is. 10
. - P. 3280-3284,
DOI
10.1111/jace.13787. - Cited References: 23. - This work was partly supported by the National Natural Science Foundations of China (grant nos. 51272242, 51472222, 51511130035), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), and the Russian Foundation for Basic Research (grant no. 15-52-53080 GFEN_a). VVA was partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0002-7820
Перевод заглавия:
Фазовый переход в Ca3(PO4)2:Eu2+ посредством контролируемой закалки и увеличения концентрации Eu2+: Идентификация нового голубого люминофора α-Ca3(PO4)2:Eu2+
РУБ
Materials Science, Ceramics
Рубрики:
NEUTRON POWDER DIFFRACTION
SOLID-SOLUTION
PHOSPHORS
CRYSTAL-STRUCTURE
DIODES
PHOTOLUMINESCENCE
LUMINESCENCE
TRANSITION
ALPHA
Аннотация:
A case of phosphor is reported where the cooling rate parameter significantly influences the luminescence property. By quenching the sample after the higherature solid-state reaction at 1250°C, we successfully prepared the Eu2+-doped α form Ca3(PO4)2 (α-TCP:Eu2+) as a new kind of bright cyan-emitting phosphor. The unusual emission color variation (from cyan to blue) depends on the cooling rate after sintering and Eu2+ doping level as it was observed in the TCP-based
phosphors
. By the Rietveld analysis, it is revealed that the cyan- and blue-emitting
phosphors
are two different TCP forms crystallizing in the monoclinic (space group P21/a, α-TCP) and the rhombohedral structure (space group R3c, β-TCP), respectively. Upon 365 nm UV light excitation, α-TCP:Eu2+ exhibits an asymmetric broad-band cyan emission peaking at 480 nm, while β-TCP:Eu2+ displays a relatively narrow-band blue emission peaking at 416 nm. The Eu2+-doping in Ca3(PO4)2 shifts the upper temperature limit of the stable structural range of β form from 1125°C to ≥1250°C. Moreover, the crystal structures of α/β-TCP:Eu2+ were compared in the aspects of compactness and cation site sets. The emission thermal stability of α/β-TCP:Eu2+ was comparatively characterized and the difference was related to the specific host structural features. © 2015 The American Ceramic Society.
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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing, China
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, Russian Federation
Functional Electronics Laboratory, Tomsk State University, Tomsk, Russian Federation
Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk, Russian Federation
Доп.точки доступа:
Ji, H.; Huang, Z.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chen, M.; Atuchin, V. V.; Fang, M.; Liu, Y.; Wu, Xiaowen
}
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10.
Effects of composition
modulation on the luminescence properties of Eu3+ doped Li1-xAgxLu(MoO4)2 solid-solution
phosphors
/ F. Cheng [et al.]> // Dalton Trans. - 2015. -
Vol. 44
,
Is. 41
. - P. 18078-18089,
DOI
10.1039/c5dt02760h. - Cited References: 42. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51272242, 51572023, 51511130035), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), the Funds of the State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences (RERU2015022), and the excellent tutor section of the Fundamental Research Funds for the Central Universities of China University of Geosciences, Beijing (2-9-2015-028). This work was also partly supported by the Russian Foundation for Basic Research (Grant No. 15-52-53080 GFEN_a). . - ISSN 1477-9226
Перевод заглавия:
Влияние модуляции состава на люминесцентные свойства твердотельного люминофора Li1-xAgxLu(MoO4)2 допированного Eu3+
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
RED
PHOSPHORS
PHOTOLUMINESCENCE PROPERTIES
ENERGY-TRANSFER
WHITE LEDS
IONS
NA
POLYMORPHISM
TUNGSTATES
RELAXATION
MOLYBDATES
Аннотация:
Double molybdate scheelite-type solid-solution
phosphors
Li1−xAgxLu1−y(MoO4)2:yEu3+ were synthesized by the solid state reaction method, and their crystal structures and luminescence properties were investigated in detail. The composition modulation and structural evolution of this series of samples were studied and the selected AgEu(MoO4)2, AgLu(MoO4)2, LiLu(MoO4)2 and LiEu(MoO4)2 phases were analyzed based on the Rietveld refinement. Depending on the variation of the Li/Ag ratio in Li1−xAgxLu1−y(MoO4)2:yEu3+
phosphors
, the difference in the luminescence properties of Li1−xAgxLu1−y(MoO4)2:yEu3+
phosphors
was ascribed to two factors, one reason could be assigned to the coupling effect and the nonradiative transition between the energy levels of LixAg1−xLu(MoO4)2 matrices and the activator Eu3+, another could be due to the near ultraviolet energy absorption and transmission efficiency between the charge-transfer (CT) band of O2−–Mo6+ and the 4f → 4f emissive transitions of Eu3+. The ultraviolet-visible diffuse reflection spectra (UV-vis DRS) and Raman spectra analysis were also used to verify the above mechanism.
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Держатели документа:
School of Materials Sciences and Technology, China University of Geosciences, Beijing, China
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing, China
Доп.точки доступа:
Cheng, F.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Jing, X.
}
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11.
Preparation, crystal structure
and up-conversion luminescence of Er3+, Yb3+ co-doped Gd2(WO4)3 / M. Yin [et al.]> // RSC Adv. - 2015. -
Vol. 5
,
Is. 89
. - P. 73077-73082,
DOI
10.1039/c5ra12959a. - Cited References: 43. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51472223), the Fundamental Research Funds for the Central Universities (Grant No. 2652015008), and New Century Excellent Talents in University of Ministry of Education of China (Grant No. NCET-12-0951). . - ISSN 2046-2069
Перевод заглавия:
Синтез, кристаллическая структура и люминесценция с апконверсией Gd2(WO4)3 содопированного Er3+, Yb3+
РУБ
Chemistry, Multidisciplinary
Рубрики:
HYDROTHERMAL SYNTHESIS
ENERGY-TRANSFER
RED
PHOSPHORS
NANOCRYSTALS
EMISSION
GREEN
HO
TEMPERATURE
TUNGSTATES
TM
Аннотация:
Up-conversion (UC)
phosphors
Gd2(WO4)3:Er3+/Yb3+ were synthesized by a high temperature solid-state reaction method. The crystal structure of Gd2(WO4)3:3% Er3+/10% Yb3+ was refined by Rietveld method and it was showed that Er3+/Yb3+ were successfully doped into the host lattice replacing Gd3+. Under 980 nm laser excitation, intense green and weak red emissions centered at around 532 nm, 553 nm, and 669 nm were observed, which were assigned to the Er3+ ion transitions of 4H11/2 → 4I15/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2, respectively. The optimum Er3+ doping concentration was determined as 3 mol% when the Yb3+ concentration was fixed at 10 mol%. The pump power study indicated that the energy transfer from Yb3+ to Er3+ in Er3+, Yb3+ co-doped Gd2(WO4)3 was a two-photon process, and the related UC mechanism of energy transfer was discussed in detail. This journal is © The Royal Society of Chemistry.
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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, China University of GeosciencesBeijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Доп.точки доступа:
Yin, Mengyan; Liu, Yangai; Mei, Lefu; Molokeev, M. S.; Молокеев, Максим Сергеевич; Huang, Zhaohui; Fang, Minghao
}
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12.
Structure, crystallographic sites,
and tunable luminescence properties of Eu2+ and Ce3+/Li+-activated Ca1.65Sr0.35SiO4
phosphors
/ Z. Xia [et al.]> // Inorg. Chem. - 2015. -
Vol. 54
,
Is. 16
. - P. 7684-7691,
DOI
10.1021/acs.inorgchem.5b00455. - Cited References: 26. - The present work was supported by the National Natural Science Foundations of China (Grants 51002146, 51272242); Natural Science Foundations of Beijing (2132050); the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950); the Beijing Nova Program (Z131103000413047); the Beijing Youth Excellent Talent Program (YETP0635); the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306); and the Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1). - Cover image: Artwork representing main idea of this article . - ISSN 0020-1669
Аннотация:
Eu2+ and Ce3+/Li+ singly doped and Eu2+/Ce3+/Li+-codoped Ca1.65Sr0.35SiO4
phosphors
have been synthesized by a solid-state reaction method. The crystal structure was determined by Rietveld refinement to verify the formation of the αL′-Ca2SiO4 phase with the Sr addition into Ca2SiO4, and the preferred crystallographic positions of the Eu2+ and Ce3+/Li+ ions in Ca1.65Sr0.35SiO4 were analyzed based on a comparison of the unit-cell volumes and the designed chemical compositions of undoped isostructural compounds Ca(2-x)SrxSiO4 (x = 0.25, 0.35, 0.45, 0.55 and 0.65). Ce3+/Li+ singly activated Ca1.65Sr0.35SiO4
phosphors
exhibit strong absorption in the range of 250-450 nm and a blue emission peak centered at about 465 nm. When Eu2+ ions are codoped, the emission colors of Ca1.65Sr0.35SiO4:Ce3+,Li+,Eu2+
phosphors
under the irradiation of 365 nm can be finely tuned from blue to green through the energy transfer from Ce3+ to Eu2+. The involved energy-transfer process between Ce3+ and Eu2+ and the corresponding mechanism are discussed in detail. The reported Ca1.65Sr0.35SiO4:Ce3+,Li+,Eu2+ phosphor might be a candidate for color-tunable blue-green components in the fabrication of near-ultraviolet-pumped white-light-emitting diodes (WLEDs). © 2015 American Chemical Society.
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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
School of Materials Sciences and Technology, China University of Geosciences, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Siberian Branch of the Russian Academy of Sciences (SB RAS), Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Доп.точки доступа:
Xia, Zhiguo; Miao, S.; Chen, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.
}
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13.
Color tunable emission
and energy transfer of Ce3+ and Tb3+ co-doped novel La6Sr4(SiO4)6F2
phosphors
with apatite structure / Q. Guo [et al.]> // Mater. Res. Bull. - 2015. -
Vol. 72
. - P. 245-251,
DOI
10.1016/j.materresbull.2015.07.029. - Cited References: 37. - This present work is supported by the National Natural Science Foundations of China (Grant No. 41172053). . - ISSN 0025-5408
Перевод заглавия:
Излучение с управляемым цветом и энергетический переход ионов Ce3+ и Tb3+ при их совместном допировании нового люминофора La6Sr4(SiO4)6F2 со структурой апатита
РУБ
Materials Science, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
LUMINESCENCE PROPERTIES
PHOTOLUMINESCENCE PROPERTIES
EU2+
LEDS
Кл.слова (ненормированные):
Inorganic compounds
--
Luminescence
--
Phosphors
--
Optical properties
--
Crystal structure
Аннотация:
Single-phase La6Sr4(SiO4)6F2: Ce3+, Tb3+ samples with apatite-like structure have been synthesized via solid-state reaction method. The phase structure, luminescence properties, lifetime, the PL thermal stability, as well as the fluorescence decay curves of the samples were investigated to characterize the resulting samples. Effective energy transfer occurs from Ce3+ to Tb3+ in La6Sr4(SiO4)6F2, which shows more intense Blue-Green light under UV light excitation. In addition, a possible mechanism of the energy-transfer from Ce3+ to Tb3+ ion is also proposed. The critical distance RC of Ce3+ to Tb3+ ions in La6Sr4(SiO4)6F2 host was calculated to be 11.878 Å. All the results indicate that La6Sr4(SiO4)6F2:Ce3+, Tb3+
phosphors
have potential applications to be used as near UV-convertible
phosphors
for white light-emitting diodes. © 2015 Elsevier Ltd. All rights reserved.
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Держатели документа:
Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, School of Materials Sciences and Technology, China University of Geosciences, Beijing, China
Laboratory of Crystal Physics, Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Доп.точки доступа:
Guo, Q.; Liao, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Mei, L.; Liu, H.
}
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14.
Insights into Ba4Si6O16
structure and photoluminescence tuning of Ba4Si6O16:Ce3+,Eu2+
phosphors
/ Chen M. [et al.]> // J. Mater. Chem. C. - 2015. -
Vol. 3
,
Is. 48
. - P. 12477-12483,
DOI
10.1039/c5tc03271g. - Cited References: 39. - This work was supported by the National Natural Science Foundations of China (Grant No. 51572023 and 51272242), Natural Science Foundations of Beijing (2132050), 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 New Ceramics and Fine Processing, Tsinghua University (KF201306), and Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1). . - ISSN 2050-7534
Перевод заглавия:
Исследования структуры Ba4Si6O16 и люминесцентных свойств Ba4Si6O16:Ce3+,Eu2+
РУБ
Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
LIGHT-EMITTING-DIODES
ENERGY-TRANSFER
LUMINESCENCE PROPERTIES
WHITE-LIGHT
GLASS-CERAMICS
BA
PHOSPHORS
EMISSION
GREEN
EU2+
FLUORESCENCE
Аннотация:
The versatile polymorphism and chemical compositions of barium silicates have been studied for a long time and their crystal structures have been established. Herein, we focused on the understanding of the crystal structure of the Ba4Si6O16 phase and the structural correlation of Ba4Si6O16 and Ba2Si3O8; moreover, the luminescence properties of Ce3+,Eu2+-co-activated Ba4Si6O16
phosphors
have been discussed. Ba4Si6O16:Ce3+,Eu2+
phosphors
show tunable blue-green emission upon excitation with 365 nm ultraviolet (UV) light. The blue emission originates from Ce3+, whereas the bluish-green emission is ascribed to Eu2+, and variation in the emission peak wavelength from 442 to 497 nm can be achieved by properly tuning the Ce3+/Eu2+ ratio. Energy transfer from Ce3+ to Eu2+ in the Ba4Si6O16 host has been validated by the variation of emission spectra as well as the variation of Ce3+ decay lifetimes with increasing Eu2+ concentration, and the energy transfer mechanism is demonstrated to be a resonant type via a dipole-dipole process. The results suggest that Ba4Si6O16:Ce3+,Eu2+
phosphors
are potential candidates as a blue-green component for UV-excited white light-emitting diodes. © 2015 The Royal Society of Chemistry.
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Держатели документа:
Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, China
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:
Chen M.; Xia Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu Q.
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15.
Structural phase transformation
and luminescent properties of Ca2-xSrxSiO4:Ce3+ orthosilicate
phosphors
/ M. Chen [et al.]> // Inorg. Chem. - 2015. -
Vol. 54
,
Is. 23
. - P. 11369-11376,
DOI
10.1021/acs.inorgchem.5b01955. - Cited References: 38. - The present work was supported by the National Natural Science Foundations of China (Grant Nos. 51572023, 51272242, and 51511130035), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in Univ. of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), and the Funds of the State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences (RERU2015022) . - ISSN 0020-1669
Перевод заглавия:
Структурный фазовый переход и люминесцентные свойства ортосиликата Ca2-xSrxSiO4:Ce3+
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
LIGHT-EMITTING-DIODES
DICALCIUM SILICATE
CRYSTAL-STRUCTURE
SOLID-SOLUTION
BOND-VALENCE
Ce3+
Eu2+
β-Ca2SiO4
GREEN
TEMPERATURE
Аннотация:
The orthosilicate
phosphors
demonstrate great potential in the field of solid-state lighting, and the understanding of the structure-property relationships depending on their versatile polymorphs and chemical compositions is highly desirable. Here we report the structural phase transformation of Ca2-xSrxSiO4:Ce3+ phosphor by Sr2+ substituting for Ca2+ within 0 ≤ x 2. The crystal structures of Ca2-xSrxSiO4:Ce3+ are divided into two groups, namely, β phase (0 ≤ x 0.15) and α′ phase (0.18 ≤ x 2), and the phase transition (β → α′) mechanism originated from the controlled chemical compositions is revealed. Our findings verified that the phase transition Pnma (α′-phase) ↔ P21/n (β-phase) can be ascribed to the second-order type, and Sr2+ ions in Ca2-xSrxSiO4 preferentially occupy the seven-coordinated Ca2+ sites rather than the eight-coordinated sites with increasing Sr2+ content, which was reflected from the Rietveld refinements and further clarified through the difference of the Ca-O bond length in the two polymorphs of Ca2SiO4. The emission peaks of Ce3+ shift from 417 to 433 nm in the composition range of 0 ≤ x ≤ 0.8, and the difference in the decay curves can also verify the phase transformation process. Thermal quenching properties of selected Ca2-xSrxSiO4:Ce3+ samples were evaluated, and the results show that the integral emission intensities at 200 °C maintain 90% of that at room temperature suggesting superior properties for the application as white light-emitting diodes (w-LEDs)
phosphors
. © 2015 American Chemical Society.
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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
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:
Chen, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.
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16.
Pressure-stimulated synthesis and
luminescence properties of microcrystalline (Lu,Y)3Al5O12:Ce3+ garnet
phosphors
/ V. V. Atuchin [et al.]> // ACS Appl. Mater. Interfaces. - 2015. -
Vol. 7
,
Is. 47
. - P. 26235-26243,
DOI
10.1021/acsami.5b08411. - Cited References: 75. - This work was partly supported by the National Natural Science Foundations of China (Grant Nos. 51272242 and 51511130035) and the Russian Foundation for Basic Research (Grant No. 15-52-53080 GFEN_a). V.V.A. was partly supported by the Ministry of Education and Science of the Russian Federation . - ISSN 1944-8244
Перевод заглавия:
Синтез стимулированный давлением и люминесцентные свойства микрокристаллических гранатов (Lu,Y)3Al5O12:Ce3+
РУБ
Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
LASER MASS-SPECTROMETRY
LIGHT-EMITTING-DIODES
WHITE-LIGHT
SINGLE-CRYSTALS
OPTICAL-PROPERTIES
ELECTRONIC-STRUCTURE
VIBRATIONAL PROPERTIES
PHASE-TRANSITIONS
PARTICLE-SIZE
GROWTH
Кл.слова (ненормированные):
synthesis
--
pressure
--
garnet
--
structure
--
luminescence
--
phosphor
Аннотация:
The Lu2.98Ce0.01Y0.01Al5O12 and Y2.99Ce0.01Al5O12
phosphors
were synthesized by solid state reaction at temperature 1623 K and pressure 1.5 × 107 Pa in (95% N2 + 5% H2) atmosphere. Under the conditions, the compounds crystallize in the form of isolated euhedral partly faceted microcrystals ∼19 μm in size. The crystal structures of the Lu2.98Ce0.01Y0.01Al5O12 and Y2.99Ce0.01Al5O12 garnets have been obtained by Rietveld analysis. The photoluminescence (PL) and X-ray excited luminescence (XL) spectra obtained at room temperature indicate broad asymmetric bands with maxima near 519 and 540 nm for Y2.99Ce0.01Al5O12 and Lu2.98Ce0.01Y0.01Al5O12, respectively. The light source was fabricated using the powder Lu2.98Ce0.01Y0.01Al5O12 phosphor and commercial blue-emitting n-UV LED chips (λex = 450 nm). It is found that the CIE chromaticity coordinates are (x = 0.388, y = 0.563) with the warm white light emission correlated color temperature (CCT) of 6400 K and good luminous efficiency of 110 lm/W. © 2015 American Chemical Society.
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Держатели документа:
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russian Federation
Functional Electronics Laboratory, Tomsk State University, Tomsk, Russian Federation
Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk, Russian Federation
Analytical Laboratory, Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russian Federation
Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
Department of Applied Physics, Novosibirsk State University, Novosibirsk, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Laboratory of High Pressure Minerals and Diamond Deposits, Institute of Geology and Mineralogy, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russian Federation
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Доп.точки доступа:
Atuchin, V. V.; Beisel, N. F.; Galashov, E. N.; Mandrik, E. M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Yelisseyev, A. P.; Yusuf, A. A.; Xia, Z.
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17.
Microwave sol–gel synthesis
of CaGd2(MoO4)4:Er3+/Yb3+
phosphors
and their upconversion photoluminescence properties / C. S. Lim [et al.]> // J. Am. Ceram. Soc. - 2015. -
Vol. 98
,
Is. 10
. - P. 3223-3230,
DOI
10.1111/jace.13739. - Cited References:69. - This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2014-046024). VVA and ASA are partially supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0002. - ISSN 1551-2916
Перевод заглавия:
Микроволновый золь-гель синтез люминофоров CaGd2(MoO4)4:Er3+/Yb3+ и их люминесцентные свойства с апконверсией
РУБ
Materials Science, Ceramics
Рубрики:
RED-EMITTING
PHOSPHORS
VIBRATIONAL PROPERTIES
LUMINESCENCE PROPERTIES
WHITE LEDS
SPECTROSCOPIC PROPERTIES
HYDROTHERMAL SYNTHESIS
CRYSTAL-STRUCTURE
ROOM-TEMPERATURE
ENERGY-TRANSFER
SR
Аннотация:
CaGd2(MoO4)4:Er3+/Yb3+
phosphors
with the doping concentrations of Er3+ and Yb3+ (x = Er3+ + Yb3+, Er3+ = 0.05, 0.1, 0.2, and Yb3+ = 0.2, 0.45) have been successfully synthesized by the microwave sol–gel method, and the crystal structure refinement and upconversion photoluminescence properties have been investigated. The synthesized particles, being formed after heat-treatment at 900°C for 16 h, showed a well-crystallized morphology. Under the excitation at 980 nm, CaGd2(MoO4)4:Er3+/Yb3+ particles exhibited strong 525 and 550-nm emission bands in the green region and a weak 655-nm emission band in the red region. The Raman spectrum of undoped CaGd2(MoO4)4 revealed about 15 narrow lines. The strongest band observed at 903 cm−1 was assigned to the ν1 symmetric stretching vibration of MoO4 tetrahedrons. The spectra of the samples doped with Er and Yb obtained under 514.5 nm excitation were dominated by Er3+ luminescence preventing the recording Raman spectra of these samples. Concentration quenching of the erbium luminescence at 2H11/2→4I15/2 and 4S3/2→4I15/2 transitions in the CaGd2(MoO4)4:Er3+/Yb3+ crystal structure was established to be approximately at the 10 at.% doping level.
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Держатели документа:
Hanseo Univ, Dept Adv Mat Sci & Engn, Seosan 356706, South Korea.
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, Kirensky Inst Phys, Lab Coherent Opt, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Photon & Laser Technol, Krasnoyarsk 660079, Russia.
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
SB RAS, Kirensky Inst Phys, Lab Mol Spect, Krasnoyarsk 660036, Russia.
Доп.точки доступа:
Lim, Chang Sung; Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич
}
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18.
Structural phase transitions
and photoluminescence properties of Eu3+ doped Ca(2-x)BaxLaNbO6
phosphors
/ J. Zhu [et al.]> // Dalton Trans. - 2015. -
Vol. 44
,
Is. 42
. - P. 18536-18543,
DOI
10.1039/c5dt03430b. - Cited References: 27. - The present work was supported by the National Natural Science Foundation of China (Grant No. 51272027, 51472028 and 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306) . - ISSN 1477-9226
Перевод заглавия:
Структурные фазовые переходы и фотолюминесцентные свойства люминофоров Ca(2-x)BaxLaNbO6 допированных Eu3+
РУБ
Chemistry, Inorganic & Nuclear
Рубрики:
Double-perovskite
Luminescence properties
Thermal-stability
Crystal-chemistry
Red
phosphors
White LEDs
Symmetry
Band
Ta
Ln
Аннотация:
Crystal structures of the series of double perovskites Ca(2-x)BaxLaNbO6:Eu3+
phosphors
have been examined by powder X-ray diffraction and Rietveld refinements. Ca2LaNbO6 has a monoclinic (P21/n) and Ba2LaNbO6 has a monoclinic (C2/m) structure. The structural phases of Ca(2-x)BaxLaNbO6:Eu3+ samples are divided into three sections depending on different Ca/Ba ratios: (1) monoclinic phase (P21/n) as Ca2LaNbO6 in the range of x = 0-0.1, (2) mixed phases containing Ca2LaNbO6 and Ba2LaNbO6 between 0.15 and 1.2, and (3) monoclinic phase (C2/m) as Ba2LaNbO6 for x = 1.4-2. Eu3+ ions act as the structural probes to study the structural phase transitions, and the evolution of the photoluminescence properties and thermal stability behaviours has been also comparatively investigated depending on different structural symmetries from Ca2LaNbO6 to Ba2LaNbO6 phase. The strong red emission from 5D0-7F2 peaking at 618 nm can be found in Ca2LaNbO6:Eu3+
phosphors
, which is attributed to the low crystal field effect of the activator ions located in the highly distorted [Lao8] polyhedra sites. The composition-optimized
phosphors
can find applications in white light emitting diodes (LEDs).
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Держатели документа:
School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, China
School of Materials Sciences and Technology, China University of Geosciences, Beijing, China
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:
Zhu, J.; Xia, Zhiguo; Zhang, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.
}
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19.
Effect of Al/Si
substitution on the structure and luminescence properties of CaSrSiO4:Ce3+
phosphors
: analysis based on the polyhedra distortion / S. H. Miao [et al.]> // J. Mater. Chem. C. - 2015. -
Vol. 3
,
Is. 18
. - P. 4616-4622,
DOI
10.1039/c5tc00339c. - Cited References:30. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51002146, 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306) and the excellent tutor section of the Fundamental Research Funds for the Central Universities of China University of Geosciences, Beijing (2652015027). - Cover image: Artwork representing main idea of this article . - ISSN 2050. - ISSN 2050-7534
Перевод заглавия:
Эффект замещения Al/Si на структуру и люминесцентные свойства люминофора CaSrSiO4:Ce3+. Анализ основанный на искажении полиэдров
РУБ
Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
LIGHT-EMITTING-DIODES
COLOR-TUNABLE PHOSPHOR
ENERGY-TRANSFER
Аннотация:
Blue-emitting CaSrSiO4:Ce3+,Li+
phosphors
were prepared by a high temperature solid-state method, and the effect of substituting Al3+ for Si4+ in CaSrSiO4:Ce3+,Li+ has been studied. Crystal structures of the as-prepared Ca1−ySr1−ySi1−xAlxO4:yCe3+,yLi+
phosphors
were resolved by the Rietveld method, which suggested that all the samples belonged to the orthorhombic symmetry (Pnma) group of α-CaSrSiO4. The photoluminescence (PL) emission and excitation spectra, the lifetime, and the effect of Al3+ concentration on the PL properties were investigated in detail. The emission peaks of the CaSrSi1−xAlxO4:Ce3+,Li+ (x = 0–0.10)
phosphors
were red-shifted from 452 to 472 nm with increasing Al/Si ratio. The red-shift of the Ce3+ emission is ascribed to the polyhedra distortion of the cations, originating from the variation in the neighboring [(Si,Al)O4] polyhedra, and the detailed mechanism has been discussed.
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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China.
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Доп.точки доступа:
Miao, Shihai; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chen, Mingyue; Zhang, Jie; Liu, Quanlin
}
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20.
Crystal structure and
photoluminescence evolution of La5(Si2+xB1–x)(O13–xNx):Ce3+ solid solution
phosphors
/ Z. G. Xia [et al.]> // J. Phys. Chem. C. - 2015. -
Vol. 119
,
Is. 17
. - P. 9488-9495,
DOI
10.1021/acs.jpcc.5b01211. - Cited References:25. - The present work was supported by the National Natural Science Foundations of China (Grants 51002146 and 51272242), Natural Science Foundations of Beijing (Grant 2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306) and Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1). . - ISSN 1932-7447
Перевод заглавия:
Кристаллическая структура и постепенное изменение фотолюминесценции в твердых растворах La5(Si2+xB1-x)(O13-xNx):Ce3+
РУБ
Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
ENERGY-TRANSFER PROPERTIES
LUMINESCENCE PROPERTIES
TUNABLE
Аннотация:
A series of iso-structural La-5(Si2+xB1-x)(O13-xNx):Ce3+
phosphors
with apatite structure have been prepared. A combination of powder X-ray diffraction and neutron scattering technique was employed to explore the crystal structural evolution and the rigid nature from oxy- to oxynitride-based apatites, and some local structures were also characterized by HRTEM and Si-29 NMR data, respectively. The new La-5(Si2+xB1-x)(O13-xNx):Ce3+ solid solution
phosphors
gave continuously controlled emission from 421 nm [La5Si2BO13:Ce3+, end-member (x = 0)] to 463 nm (La(5)Si3O12N:Ce3+, end-member (x = 1)). Substitution of B3+ and O-2 by Si4+ and N-3 in La-5(Si2+xB1-x)(O13-xNx):Ce3+
phosphors
produced more covalency into the crystal field environment around the Ce3+ ions inducing the red-shifted emission, further improving the thermal stability of the oxynitride-based apatite
phosphors
. The proposed approach from oxy- to oxynitride based iso-structural phases could significantly contribute to future research in designing complex solid solution
phosphors
.
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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
RAS, SB, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
Far Eastern State Transport Univ, Khabarovsk 680021, Russia
Chonnam Natl Univ, Sch Mat Sci & Engn, Kwangju 500757, South Korea
Доп.точки доступа:
Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Im, Won Bin; Unithrattil, Sanjith; Liu, Quanlin
}
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