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    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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Synthesis and luminescence properties of Li2O–Y2O3–TeO2:Eu3+ tellurite glass / V. V. Atuchin [et al.] // Mater. Chem. Phys. - 2014. - Vol. 147, Is. 3. - P. 1191-1194, DOI 10.1016/j.matchemphys.2014.07.003. - Cited References: 26. - This study is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0254-0584. - ISSN 1879-3312

РУБ Materials Science, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
   SPECTROSCOPIC PROPERTIES
   OPTICAL-PROPERTIES
   ENERGY-TRANSFER
   CERAMICS
   Eu3+
   PHOTOLUMINESCENCE
   TEMPERATURE
   EMISSION
   PHOSPHOR
Кл.слова (ненормированные):
Glasses -- Heat treatment -- Photoluminescence spectroscopy -- Optical properties
Аннотация: The Eu3+-doped red-orange emitting phosphor of tellurite glass 0.25Li2O–0.20Y2O3–0.5TeO2–0.05Eu2O3 has been synthesized by the melt quenching method. The amorphous nature of the glass has been verified by XRD measurements. The photoluminescence excitation and emission spectra, the luminescence decay curves have been investigated for the composition. The phosphor can be efficiently excited by the near UV light to realize the intense narrow red emission line (611 nm) corresponding to forced electric dipole transition 5D0 → 7F2 of Eu3+ ions. The Li2O–Y2O3–TeO2:Eu3+glass phosphor is a potential red-orange emitting candidate for the application in WLEDs.

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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, Inst Geol & Mineral, Lab High Pressure Minerals & Diamond Deposits, Novosibirsk 630090, Russia
Novosibirsk State Univ, Dept Appl Phys, Novosibirsk 630090, Russia
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Atuchin, V. V.; Yelisseyev, A. P.; Galashov, E. N.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ministry of Education and Science of the Russian Federation
}
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    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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    Discovery of new solid solution phosphors via cation substitution-dependent phase transition in M-3(PO4)2:Eu2+ (M =Ca/Sr/Ba) quasi-binary sets / H. P. Ji [et al.] // J. Phys. Chem. C. - 2015. - Vol. 119, Is. 4. - P. 2038-2045, DOI 10.1021/jp509743r. - Cited References:48. - This work was supported by the National Natural Science Foundations ofChina (Grant Nos. 51032007, 51002146, and 51272242), the Research Fundfor 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 Ministryof Education of China (NCET-12-0950), the Beijing Nova Program(Z131103000413047), and Beijing Youth Excellent Talent Program(YETP0635). V.V.A. acknowledges the Ministry of Education and Science ofthe Russian Federation for financial support. . - ISSN 1932-7447
   Перевод заглавия: Открытие новых твердых растворов люминофоров посредством фазовых переходов при замещении катионов в квазибинарных составах M3(PO4)2:Eu2+ (M = Ca/Sr/Ba)

РУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
LUMINESCENCE PROPERTIES
ENERGY-TRANSFER
Аннотация: The cation substitution-dependent phase transition was used as a strategy to discover new solid solution phosphors and to efficiently tune the luminescence property of divalent europium (Eu2+) in the M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) quasi-binary sets. Several new phosphors including the greenish-white SrCa2(PO4)2:Eu2+, the yellow Sr2Ca(PO4)2:Eu2+, and the cyan Ba2Ca(PO4)2:Eu2+ were reported, and the drastic red shift of the emission toward the phase transition point was discussed. Different behavior of luminescence evolution in response to structural variation was verified among the three M3(PO4)2:Eu2+ joins. Sr3(PO4)2 and Ba3(PO4)2 form a continuous isostructural solid solution set in which Eu2+ exhibits a similar symmetric narrow-band blue emission centered at 416 nm, whereas Sr2+ substituting Ca2+ in Ca3(PO4)2 induces a composition-dependent phase transition and the peaking emission gets red shifted to 527 nm approaching the phase transition point. In the Ca3?xBax(PO4)2:Eu2+ set, the validity of crystallochemical design of phosphor between the phase transition boundary was further verified. This cation substitution strategy may assist in developing new phosphors with controllably tuned optical properties based on the phase transition.

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Держатели документа:
China Univ Geosci, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Sch Mat Sci & Technol, Natl Lab Mineral Mat, 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
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:
Ji, Haipeng; Huang, Zhaohui; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Fang, Minghao; Liu, Yangai
}
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    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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    Comparative investigations of the crystal structure and photoluminescence property of eulytite-type Ba3Eu(PO4)3 and Sr3Eu(PO4)3 / H. P. Ji [et al.] // Dalton Trans. - 2015. - Vol. 44, Is. 16. - P. 7679-7686, DOI 10.1039/c4dt03887h. - Cited References:65. - This work was supported by the National Natural Science Foundations of China (grant no. 51032007, no. 51002146, no. 51272242), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), Natural Science Foundations of Beijing (2132050), and the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047) and Beijing Youth Excellent Talent Program (YETP0635). VVA is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 1477. - ISSN 1477-9234
   Перевод заглавия: Сравнительный анализ кристаллических структур и люминесцентных свойств Ba3Eu(PO4)3 и Sr3Eu(PO4)3. со структурой эвлитина

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
LIGHT-EMITTING-DIODES
DOPED Sr3Gd(PO4(3 PHOSPHOR
EFFICIENT
Аннотация: In this study, the Ba3Eu(PO4)3 and Sr3Eu(PO4)3 compounds were synthesized and the crystal structures were determined for the first time by Rietveld refinement using powder X-ray diffraction (XRD) patterns. Ba3Eu(PO4)3 crystallizes in cubic space group I3d, with cell parameters of a = 10.47996(9) Å, V = 1151.01(3) Å3 and Z = 4; Ba2+ and Eu3+ occupy the same site with partial occupancies of 3/4 and 1/4, respectively. Besides, in this structure, there exists two distorted kinds of the PO4 polyhedra orientation. Sr3Eu(PO4)3 is isostructural to Ba3Eu(PO4)3 and has much smaller cell parameters of a = 10.1203(2) Å, V = 1036.52(5) Å3. The bandgaps of Ba3Eu(PO4)3 and Sr3Eu(PO4)3 are determined to be 4.091 eV and 3.987 eV, respectively, based on the UV–Vis diffuse reflectance spectra. The photoluminescence measurements reveal that, upon 396 nm n-UV light excitation, Ba3Eu(PO4)3 and Sr3Eu(PO4)3 exhibit orange-red emission with two main peaks at 596 nm and prevailing 613 nm, corresponding to the 5D0 → 7F1 and 5D0 → 7F2 transitions of Eu3+, respectively. The dynamic disordering in the crystal structures contributes to the broadening of the luminescence spectra. The electronic structure of the phosphates was calculated by the first-principles method. The analysis elucidats that the band structures are mainly governed by the orbits of phosphorus, oxygen and europium, and the sharp peaks of the europium f-orbit occur at the top of the valence bands.

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, 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.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Chinese Acad Sci, Tech Inst Phys & Chem, Beijing Ctr Crystal R&D, Key Lab Funct Crystals & Laser Technol, Beijing 100190, Peoples R China.
Univ Chinese Acad Sci, Beijing 100049, Peoples R China.
Russian Acad Sci, Inst Semicond Phys, SB RAS, 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:
Ji, Haipeng; Huang, Zhaohui; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Jiang, Xingxing; Lin, Zheshuai; Atuchin, V. V.
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    Synthesis, crystal structure, and enhanced luminescence of garnet-type Ca3Ga2Ge3O12:Cr3+ by codoping Bi3+ / C. Y. Liu [et al.] // J. Am. Ceram. Soc. - 2015. - Vol. 98, Is. 6. - P. 1870-1876, DOI 10.1111/jace.13553. - Cited References:24. - This work was supported by the National Natural Science Foundations of China (grant nos. 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 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 0002. - ISSN 1551-2916
   Перевод заглавия: Синтез, кристаллическая структура и улучшенная люминесценция граната Ca3Ga2Ge3O12:Cr3+ содопированного Bi3+

РУБ Materials Science, Ceramics
Рубрики:
LIGHT-EMITTING-DIODES
   INFRARED PERSISTENT LUMINESCENCE
   ENERGY-TRANSFER
   PHOSPHOR
   RED
   NANOPARTICLES
   EFFICIENCY
Аннотация: Garnet-type compound Ca3Ga2Ge3O12 and Cr3+-doped or Cr3+/Bi3+ codped Ca3Ga2Ge3O12 phosphors were prepared by a solid-state reaction. The crystal structure of Ca3Ga2Ge3O12 host was studied by X-ray diffraction (XRD) analysis and further determined by the Rietveld refinement. Near-infrared (NIR) photoluminescence (PL) and long-lasting phosphorescence (LLP) emission can be observed from the Cr3+-doped Ca3Ga2Ge3O12 sample, and the enhanced NIR PL emission intensity and LLP decay time can be realized in Cr3+/Bi3+ codped samples. The optimum concentration of Cr3+ in Ca3Ga2Ge3O12 phosphor was about 6 mol%, and optimum Bi3+ concentration induced the energy-transfer (ET) process between Bi3+ and Cr3+ ions was about 30 mol%. Under different excitation wavelength from 280 to 453 nm, all the samples exhibit a broadband emission peaking at 739 nm and the intensity of NIR emission increases owing to the ET behavior from Bi3+ to Cr3+ ions. The critical ET distance has been calculated by the concentration-quenching method. The thermally stable luminescence properties were also studied and the introduction of Bi3+ can also improve the thermal stability of the NIR emission.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China.
SB RAS, LV Kirensky Phys Inst, Lab Crystal Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Liu, Chengyin; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Quanlin
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    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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    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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10.

    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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