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1.


   
    Microwave sol-gel synthesis, microstructural and spectroscopic properties of scheelite-type ternary molybdate upconversion phosphor NaPbLa(MoO4)3:Er3+/Yb3+ / C. S. Lim [et al.] // J. Alloys Compd. - 2020. - Vol. 826. - Ст. 152095, DOI 10.1016/j.jallcom.2019.152095. - Cited References: 53. - This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (2018R1D1A1A09082321). This study was supported by the Russian Science Foundation (19-42-02003, in part of conceptualization). Also, this study was supported by RFBR (18-32-20011, 18-03-00750). . - ISSN 0925-8388. - ISSN 1873-4669
   Перевод заглавия: Микроволновый золь-гель синтез, микроструктурные и спектроскопические свойства апконверсионного люминофора тройного молибдата NaPbLa(MoO4)3:Er3+/Yb3+ со структурой шеелита
Кл.слова (ненормированные):
Optical materials -- Chemical synthesis -- Molybdate -- Raman spectroscopy -- X-ray diffraction -- Phosphors
Аннотация: New ternary molybdate NaPbLa(1-x-y)(MoO4)3:xEr3+,yYb3+ (x = y = 0, x = 0.05 and y = 0.35, 0.4, 0.45 and 0.5) phosphors were successfully fabricated by the MSG (microwave sol-gel) method, and the microstructural and spectroscopic properties were characterized. The crystal structure of NaPbLa(MoO4)3 (NPLM) was defined by Rietveld analysis in space group I41/a with unit cell parameters a = 5.3735(2) and c = 11.8668(4) Å, V = 342.65(3) Å3, Z = 4 (RB = 6.64%). The unit cell volume of NaPbLa(MoO4)3 (NPLM) was intermediate between those of NaLa(MoO4)2 and PbMoO4. Under the 980 nm excitation, upconverted yellowish-green emissions at transitions from 2H11/2 and 4S3/2 were observed. No concentration quenching in the subsystem of donor ions at the content up to 50 at.% and no cross-relaxation losses in the subsystem of acceptor ions at the concentrations as high as 5 at. % were verified. The individual chromaticity points for the NaPbLa(MoO4)3:Er3+,Yb3+ phosphors, corresponding to the equal-energy point in the standard CIE diagram, revealed yellowish-green emissions.

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Держатели документа:
Department of Aerospace Advanced Materials & Chemical Engineering, Hanseo University, Seosan, 356-706, Republic of Korea
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Department of Photonics and Laser Technologies, Siberian Federal University, Krasnoyarsk, 660041, Russia
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russia
Functional Electronics Laboratory, Tomsk State University, Tomsk, 634050, Russia
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Siberian Federal University, Krasnoyarsk, 660041, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia

Доп.точки доступа:
Lim, Chang Sung; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич
}
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2.


   
    Site-Selective Occupancy of Eu2+ Toward Blue-Light-Excited Red Emission in a Rb3YSi2O7:Eu Phosphor / J. W. Qiao [et al.] // Angew. Chem. - 2019. - Vol. 131, Is. 33. - P. 11645-11650, DOI 10.1002/ange.201905787. - Cited References: 41. - This work is supported by the National Natural Science Foundation of China (51722202, 51572023, and 11574003), Natural Science Foundations of Beijing (2172036), Fundamental Research Funds for the Central Universities (FRF-TP-18-002C1), and the Guangdong Provincial Science & Technology Project (2018A050506004). K.R.P. recognizes that this work was made possible by support from the National Science Foundation, Solid State Materials Chemistry award DMR-1608218. . - ISSN 1521-3757
   Перевод заглавия: Селективное заселение Eu2 + для красного излучения люминофора Rb3YSi2O7: Eu при возбуждении синим светом
РУБ Chemistry, Multidisciplinary
Рубрики:
LUMINESCENCE PROPERTIES
   CE3+

   ENERGY

   PHOTOLUMINESCENCE

   TRANSITION

Кл.слова (ненормированные):
light-emitting diodes -- red-emitting phosphors -- silicates -- site occupancy
Аннотация: Establishing an effective design principle in solid-state materials for a blue-light-excited Eu2+-doped red-emitting oxide-based phosphors remains one of the significant challenges for white light-emitting diodes (WLEDs). Selective occupation of Eu2+ in inorganic polyhedra with small coordination numbers results in broad-band red emission as a result of enhanced crystal-field splitting of 5d levels. Rb3YSi2O7:Eu exhibits a broad emission band at λmax=622 nm under 450 nm excitation, and structural analysis and DFT calculations support the concept that Eu2+ ions preferably occupy RbO6 and YO6 polyhedra and show the characteristic red emission band of Eu2+. The excellent thermal quenching resistance, high color-rendering index Ra (93), and low CCT (4013 K) of the WLEDs clearly demonstrate that site engineering of rare-earth phosphors is an effective strategy to target tailored optical performance.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
Anhui Normal Univ, Minist Educ, Key Lab Funct Mol Solids, Anhui Key Lab Optoelect Mat Sci & Technol, Wuhu 241000, Peoples R China.
RAS, Kirensky Inst Phys, Lab Crystal Phys, Fed Res Ctr,KSC,SB, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China.
Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA.

Доп.точки доступа:
Qiao, Jianwei; Ning, Lixin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chuang, Yu-Chun; Zhang, Qinyuan; Poeppelmeier, Kenneth R.; Xia, Zhiguo
}
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3.


   
    Designing high-performance LED phosphors by controlling the phase stability via a heterovalent substitution strategy / C. Cheng [et al.] // Adv. Opt. Mater. - 2020. - Vol. 8, Is. 2. - Ст. 1901608, DOI 10.1002/adom.201901608. - Cited References: 31 . - ISSN 2195-1071
Кл.слова (ненормированные):
phosphors -- photoluminescence -- white light-emitting diodes
Аннотация: Phosphor-converted white light-emitting diodes (LEDs) are currently playing key roles in the lighting and display industries and trigger urgent demands for the discovery of “good” phosphors with high quantum efficiency, improved thermal stability, and controllable excitation/emission properties. Herein, a general and efficient heterovalent substitution strategy is demonstrated in K2HfSi3O9:Eu2+ achieved by Ln3+ (Ln = Gd, Tb, Dy, Tm, Yb, and Lu) doping to optimize luminescence properties, and as an example, the Lu3+ substitution leads to improvement of emission intensity and thermal stability, as well as tunable emission color from blue to cyan. The structural stability and Eu2+ occupation via Lu3+ doping have been revealed by the structural elaboration and density functional theory calculations, respectively. It is shown that heterovalent substitution allows predictive control of site preference of luminescent centers and therefore provides a new method to optimize the solid-state phosphors for LEDs.

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Держатели документа:
The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, 100083, China
Anhui Key Laboratory of Optoelectric Materials Science and Technology, Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Normal University, Wuhu, Anhui 241000, China
Institute of Microstructure and Property of Advanced Materials, Beijing University of Technology, Beijing, 100124, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
National Synchrotron Radiation Research Center, Hsinchu, 300, Taiwan
State Key Laboratory of Luminescent Materials and Devices and Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, South China University of Technology, Guangzhou, 510641, China

Доп.точки доступа:
Cheng, C.; Ning, L.; Ke, X.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wang, Z.; Zhou, G.; Chuang, Y. -C.; Xia, Z.
}
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4.


   
    Site-Selective Occupancy of Eu2+ Toward Blue-Light-Excited Red Emission in a Rb3YSi2O7:Eu Phosphor / J. W. Qiao [et al.] // Angew. Chem. Int. Edit. - 2019. - Vol. 58, Is. 33. - P. 11521-11526, DOI 10.1002/anie.201905787. - Cited References: 41. - This work is supported by the National Natural Science Foundation of China (51722202, 51572023, and 11574003), Natural Science Foundations of Beijing (2172036), Fundamental Research Funds for the Central Universities (FRF-TP-18-002C1), and the Guangdong Provincial Science & Technology Project (2018A050506004). K.R.P. recognizes that this work was made possible by support from the National Science Foundation, Solid State Materials Chemistry award DMR-1608218. . - ISSN 1433-7851. - ISSN 1521-3773
   Перевод заглавия: Селективное заселение Eu2 + для красного излучения люминофора Rb3YSi2O7: Eu при возбуждении синим светом
РУБ Chemistry, Multidisciplinary
Рубрики:
LUMINESCENCE PROPERTIES
   CE3+

   ENERGY

   PHOTOLUMINESCENCE

   TRANSITION

Кл.слова (ненормированные):
light-emitting diodes -- red-emitting phosphors -- silicates -- site occupancy
Аннотация: Establishing an effective design principle in solid-state materials for a blue-light-excited Eu2+-doped red-emitting oxide-based phosphors remains one of the significant challenges for white light-emitting diodes (WLEDs). Selective occupation of Eu2+ in inorganic polyhedra with small coordination numbers results in broad-band red emission as a result of enhanced crystal-field splitting of 5d levels. Rb3YSi2O7:Eu exhibits a broad emission band at λmax=622 nm under 450 nm excitation, and structural analysis and DFT calculations support the concept that Eu2+ ions preferably occupy RbO6 and YO6 polyhedra and show the characteristic red emission band of Eu2+. The excellent thermal quenching resistance, high color-rendering index Ra (93), and low CCT (4013 K) of the WLEDs clearly demonstrate that site engineering of rare-earth phosphors is an effective strategy to target tailored optical performance.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
Anhui Normal Univ, Minist Educ, Key Lab Funct Mol Solids, Anhui Key Lab Optoelect Mat Sci & Technol, Wuhu 241000, Peoples R China.
RAS, Kirensky Inst Phys, Lab Crystal Phys, Fed Res Ctr,KSC,SB, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China.
Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA.

Доп.точки доступа:
Qiao, Jianwei; Ning, Lixin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chuang, Yu-Chun; Zhang, Qinyuan; Poeppelmeier, Kenneth R.; Xia, Zhiguo
}
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5.


   
    Polyhedron Transformation toward Stable Narrow-Band Green Phosphors for Wide-Color-Gamut Liquid Crystal Display / H. Liao [et al.] // Adv. Funct. Mater. - 2019. - Vol. 29, Is. 30. - Ст. 1901988, DOI 10.1002/adfm.201901988. - Cited References: 34. - The present work was supported by the National Natural Science Foundations of China (Grant Nos. 51722202, 91622125, and 51572023), Natural Science Foundations of Beijing (2172036), Fundamental Research Funds for the Central Universities (FRF‐TP‐18‐002C1), and the Guangdong Provincial Science & Technology Project (No. 2018A050506004). . - ISSN 1616-301X
   Перевод заглавия: Через преобразование полиэдра к устойчивым узкополосным зеленым люминофорам для жидкокристаллического дисплея с широкой цветовой гаммой
Кл.слова (ненормированные):
light-emitting diodes -- phosphor -- photoluminescence
Аннотация: A robust and stable narrow-band green emitter is recognized as a key enabler for wide-color-gamut liquid crystal display (LCD) backlights. Herein, an emerging rare earth silicate phosphor, RbNa(Li3SiO4)2:Eu2+ (RN:Eu2+) with exceptional optical properties and excellent thermal stability, is reported. The resulting RN:Eu2+ phosphor presents a narrow green emission band centered at 523 nm with a full width at half maximum of 41 nm and excellent thermal stability (102%@425 K of the integrated emission intensity at 300 K). RN:Eu2+ also shows a high quantum efficiency, an improved chemical stability, and a reduced Stokes shift owing to the modified local environment, in which [NaO8] cubes replace [LiO4] squares in RbLi(Li3SiO4)2:Eu2+ via polyhedron transformation. White light-emitting diode (wLED) devices with a wide color gamut (113% National Television System Committee (NTSC)) and high luminous efficacy (111.08 lm W−1) are obtained by combining RN:Eu2+ as the green emitter, K2SiF6:Mn4+ as the red emitter, and blue-emitting InGaN chips. Using these wLEDs as backlights, a prototype 20.5 in. LCD screen is fabricated, demonstrating the bright future of stable RN:Eu2+ for wide-color-gamut LCD backlight application.

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Держатели документа:
The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, 100083, China
State Key Laboratory of Luminescent Materials and Devices and Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, South China University of Technology, Guangzhou, 510641, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Liao, H.; Zhao, M.; Zhou, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.; Zhang, Q.; Xia, Z.
}
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6.


   
    Engineering of K3YSi2O7 to Tune Photoluminescence with Selected Activators and Site Occupancy / J. Qiao [et al.] // Chem. Mater. - 2019. - Vol. 31, Is. 18. - P. 7770-7778, DOI 10.1021/acs.chemmater.9b02990. - Cited References: 48. - This work was supported by the National Natural Science Foundation of China (Nos. 51722202, 51972118 and 51572023), Natural Science Foundations of Beijing (2172036), Fundamental Research Funds for the Central Universities (FRF-TP-18-002C1), and Guangdong Provincial Science & Technology Project (2018A050506004). This work was also supported by the National Science Foundation, Ceramics Program (No. 1911372), and the computational resources were provided by the Extreme Science and Engineering Discovery Environment (XSEDE) supported by the National Science Foundation (No. ACI-1548562). . - ISSN 0897-4756
   Перевод заглавия: Производство K3YSi2O7 для настройки фотолюминесценции с выбранными активаторами и заселением позиций
Кл.слова (ненормированные):
Citrus fruits -- Density functional theory -- Doping (additives) -- Energy gap -- Gallium alloys -- III-V semiconductors -- Indium alloys -- Light -- Light emitting diodes -- Metal ions -- Phosphors -- Photoluminescence -- Rare earths -- Rietveld refinement -- Semiconductor alloys
Аннотация: The luminescence of rare earth ions (Eu2+, Ce3+, and Eu3+)-doped inorganic solids is attractive for the screening of phosphors applied in solid-state lighting and displays and significant to probe the occupied crystallographic sites in the lattice also offering new routes to photoluminescence tuning. Here, we report on the discovery of the Eu- and Ce-activated K3YSi2O7 phosphors. K3YSi2O7:Eu is effectively excited by 450 nm InGaN blue light-emitting diodes (LEDs) and displays an orange-red emission originated from characteristic transitions of both Eu2+ and Eu3+, while K3YSi2O7:Ce3+ shows green emission upon 394 nm near-ultraviolet (NUV) light excitation. Rietveld refinement verifies the successful doping of the activators, and density functional theory (DFT) calculations further support that Eu2+ occupies both K1 and Y2 crystallographic sites, while Ce3+ and Eu3+ only occupy the Y2 site; hence, the broad-band red emission of Eu2+ are attributed to a small DFT band gap (3.69 eV) of K3YSi2O7 host and a selective occupancy of Eu2+ in a highly distorted K1 site and a high crystal field splitting around Y2 sites. The white LEDs device utilizing orange-red-emitting K3YSi2O7:Eu and green-emitting K3YSi2O7:Ce3+ exhibits an excellent CRI of 90.1 at a correlated color temperature of 4523 K. Our work aims at bridging multivalent Eu2+/Eu3+ and Ce3+ site occupancy in the same host to realize photoluminescence tuning and especially exposes new ways to explore new phosphors with multicolor emission pumped by blue and NUV light for white LEDs.

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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, 100083, China
Department of Nanoengineering, University of California, San Diego, 9500 Gilman Drive, San Diego, CA 92093, United States
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
National Synchrotron Radiation Research Center, Hsinchu, 300, Taiwan
State Key Laboratory of Luminescent Materials and Devices, Institute of Optical Communication Materials, South China University of Technology, Guangzhou, 510641, China

Доп.точки доступа:
Qiao, J.; Amachraa, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chuang, Y. -C.; Ong, S. P.; Zhang, Q.; Xia, Z.
}
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7.


   
    Aliovalent substitution toward reinforced structural rigidity in Ce3+-doped garnet phosphors featuring improved performance / T. Hu [et al.] // J. Mater. Chem. C. - 2019. - Vol. 7, Is. 46. - P. 14594-14600, DOI 10.1039/c9tc05354a. - Cited References: 38. - This work was supported by the National Natural Science Foundation of China (No. 51722202 and 51972118), the Guangdong Provincial Science & Technology Project (2018A050506004) and the Fundamental Research Funds for the Central Universities (D2190980). . - ISSN 2050-7534
   Перевод заглавия: Алиовалентное замещение с целью усиления структурной жесткости в люминофорных гранатах, легированных Ce3 + и имеющих улучшенные характеристики
Кл.слова (ненормированные):
Color -- Deterioration -- Efficiency -- Gallium alloys -- Garnets -- III-V semiconductors -- Indium alloys -- Photoluminescence -- Reinforcement -- Rigidity -- Semiconductor alloys -- Thermal Engineering -- Thermodynamic stability
Аннотация: Highly efficient phosphors with thermal stability and color-tunable emission are required for the fabrication of phosphor-converted white light-emitting diodes (pc-WLEDs). Currently developed engineering strategies are generally successful in photoluminescence tuning but, unfortunately, suffer severe deterioration in emission intensity/efficiency and/or thermal stability. Herein, an efficient aliovalent substitution strategy toward reinforced structural rigidity is proposed and demonstrated experimentally. By incorporating Be2+ ion into the garnet-type Lu2SrAl4SiO12:Ce3+ phosphor, the phosphor shows enhanced internal/external quantum efficiency, from 79.2%/26.7% to 84.5%/32.9%, photoluminescence tuning from green (peaking at ∼512 nm) to yellow (peaking at ∼552 nm), and zero thermal quenching, even up to 200 °C. The Be2+ substitution at the Al2/Si2 site enables stable and rigid local surroundings around the Ce3+ activator, which is responsible for the unprecedented performance. In addition, high-quality warm WLED devices with a luminous efficiency of 158.1 lm W-1, correlated color temperature of 3858 K and high color rendering index of 81.7, are obtained by combining Lu2SrAl4SiO12:Ce3+,Be2+ as the yellow emitter, CaAlSiN3:Eu2+ as the red emitter and a blue-emitting InGaN chip. These findings highlight a new strategy for performance optimization of LED phosphors by selecting rigid covalent compounds with further reinforced structural rigidity via aliovalent substitution.

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Держатели документа:
State Key Laboratory of Luminescent Materials and Devices, Institute of Optical Communication Materials, South China University of Technology, Guangzhou, 510641, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Hu, T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.; Zhang, Q.
}
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8.


   
    Data-driven photoluminescence tuning in Eu2+-doped phosphors / S. Lai, M. Zhao, J. Qiao [et al.] // J. Phys. Chem. Lett. - 2020. - Vol. 11, Is. 14. - P. 5680-5685, DOI 10.1021/acs.jpclett.0c01471. - Cited References: 34. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51972118, 51961145101 and 51722202), Fundamental Research Funds for the Central Universities (D2190980), Guangzhou Science & Technology Project (202007020005), Guangdong Provincial Science & Technology Project (No. 2018A050506004), 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 . - ISSN 1948-7185
   Перевод заглавия: Настройка фотолюминесценции люминофоров, легированных Eu2+, за счет анализа базы данных
Рубрики:
Phosphors
   Luminescence properties

   Crystal structure

   Ions

   Quantum mechanics

Аннотация: Discovery of rare earth phosphors has generally relied on the chemical intuition and time-intensive trial-and-error synthesis; therefore, finding new materials assisted by data-driven computations is urgent. Herein, we utilize a regression model to predict the emission wavelengths of Eu2+-doped phosphors by revealing the relationships between the crystal structure and luminescence property. The emission wavelengths of [Rb(1–x)K(x)]3LuSi2O7:Eu2+ (0 ≤ x ≤ 1) phosphors, as examples for the data-driven photoluminescence tuning, are successfully predicted on the basis of the existing data of only eight systems, also consistent with the experimental results. These phosphors can be excited by blue light and exhibit broad-band red and near-infrared emission ranging from 619 to 737 nm. These findings in Eu2+-doped silicate phosphors indicate that data-driven computations through the regression mode would have bright application in discovering novel phosphors with a target emission wavelengths.

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Держатели документа:
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Engineering, South China University of Technology, Guangzhou, 510641, China
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology BeijingBeijing 100083, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Russian Federation

Доп.точки доступа:
Lai, S.; Zhao, M.; Qiao, J.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.
}
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9.


   
    Bismuth activated full spectral double perovskite luminescence materials by excitation and valence control for future intelligent LED lighting / Y. Wei, H. Yang, Z. Y. Gao [et al.] // Chem. Commun. - 2020. - Vol. 56, Is. 64. - P. 9170-9173, DOI 10.1039/d0cc03975f. - Cited References: 27. - This work was supported by the National Natural Science Foundation of China (Grant No. 51672259) and the Fundamental Research Funds for the National Universities, China University of Geosciences (Wuhan) (No. 1910491T02) . - ISSN 1359-7345. - ISSN 1364-548X
   Перевод заглавия: Активированные висмутом люминесцентные материалы двойных перовскитов, с полным спектром излучения, который получается за счет управления возбуждением и валентностью, для интеллектуального светодиодного освещения в будущем
РУБ Chemistry, Multidisciplinary
Рубрики:
PHOTOLUMINESCENCE
   PHOSPHORS

   Bi3+

   MODULATION

   CRYSTAL

Аннотация: A novel La2Mg1.14Zr0.86O6:Bi3+ double perovskite phosphor with excitation-induced blue/green photoluminescence tuning is reported. By designing Bi3+ → Eu3+ energy transfer, single-composition white light with wide-scale adjustable corrected color temperatures (CCTs) is successfully achieved. This work initiates a new insight to explore phosphors with excitation-induced photoluminescence tuning and wide CCT control for future intelligent LED lighting.

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Держатели документа:
China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Wei, Y.i.; Yang, Hang; Gao, Zhiyu; Xing, Gongcheng; Molokeev, M. S.; Молокеев, Максим Сергеевич; Li, Guogang
}
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10.


   
    Enhanced cyan emission and optical tuning of Ca3Ga4O9:Bi3+ for high-quality full-spectrum white light-emitting diodes / D. J. Liu, X. H. Yun, G. G. Li [et al.] // Adv. Opt. Mater. - 2020. - Vol. 8, Is. 22. - Ст. 2001037, DOI 10.1002/adom.202001037. - Cited References: 55. - This work was financially supported by the National Natural Science Foundation of China (NSFC No. 51932009, 51720105015, 51672265, 51672266, 51672257 and 51672259), the Key Research Program of Frontier Sciences, CAS (Grant No. YZDY-SSW-JSC018), Science and Technology Cooperation Project between Chinese and Australian Governments (2017YFE0132300), the Jiangmen Innovative Research Team Program (2017), and the Major Program of Basic Research and Applied Research of Guangdong Province (2017KZDXM083) . - ISSN 2195-1071
   Перевод заглавия: Улучшенное голубое излучение и оптическая настройка Ca3Ga4O9:Bi3+ для получения высококачественных белых светодиодов полного спектра
РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
ENERGY-TRANSFER
   TUNABLE LUMINESCENCE

   PHOSPHOR

   CRYSTAL

   MODULATION

Кл.слова (ненормированные):
cyan-emitting phosphors -- full-spectrum white lighting -- optical tuning -- single-phased white light-emitting diodes
Аннотация: Highly efficient cyan‐emitting phosphor materials are indispensable for closing the cyan gap in spectra of the traditional phosphor‐converted white light‐emitting diodes (WLEDs) to achieve high‐quality full‐spectrum white lighting. In this work, bright cyan‐emitting Ca3Ga4O9 (CGO):0.02Bi3+,0.07Zn2+ phosphor is developed to bridge the cyan gap. Such a Bi3+,Zn2+ codoping enhances the cyan emission of CGO:0.02Bi3+ by 4.1 times due to the influence of morphology and size of phosphor particles, charge compensation and lattice distortion. Interestingly, codoping La3+ ions into the current system can achieve a photoluminescence tuning of CGO:0.02Bi3+ from cyan to yellowish‐green by crystallographic site engineering. Besides, Bi3+–Eu3+ energy transfer is successfully realized in CGO:0.02Bi3+,0.07Zn2+,nEu3+ phosphors and the emission color tuning from cyan to orange is observed. The investigation of thermal quenching behaviors reveals that the incorporation of Zn2+ and La3+ improves the thermal stability of CGO:0.02Bi3+. Finally, CGO:0.02Bi3+,0.07Zn2+,0.10Eu3+ phosphor is employed to obtain a single‐phased warm WLED device. A full‐spectrum WLED device with remarkable color rendering index (Ra) of 97.4 and high luminous efficiency of 69.72 lm W−1 is generated by utilizing CGO:0.02Bi3+,0.07Zn2+ phosphor. This result suggests the important effect of CGO:0.02Bi3+,0.07Zn2+ phosphor on closing the cyan gap, providing new insights of cyan‐emitting phosphors applied in full‐spectrum white lighting.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Engn Res Ctr Nanogeomat, Minist Educ, Wuhan 430074, Peoples R China.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr,KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Shandong Univ, Sch Mat Sci & Engn, Jinan 266071, Peoples R China.
Wuyi Univ, Sch Appl Phys & Mat, Jiangmen 529020, Guangdong, Peoples R China.

Доп.точки доступа:
Liu, Dongjie; Yun, Xiaohan; Li, Guogang; Dang, Peipei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lian, Hongzhou; Shang, Mengmeng; Lin, Jun
}
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11.


   
    Fabrication of Microcrystalline NaPbLa(WO4)3:Yb3+/Ho3+ Phosphors and Their Upconversion Photoluminescent Characteristics / C. S. Lim, V. V. Atuchin, A. S. Aleksandrovsky [et al.] // Kor. J. Mater. Res. - 2019. - Vol. 29, Is. 12. - P. 741-746, DOI 10.3740/MRSK.2019.29.12.741. - Cited References: 28. - This study was supported by the Research Program through the Campus Research Foundation funded by Hanseo University in 2019 (191Yunghap09) and the Russian Science Foundation (19-42-02003). The authors are grateful for the support from RFBR, according to the research project 18-32-20011. . - ISSN 1225-0562. - ISSN 2287-7258
Кл.слова (ненормированные):
yellowish green phosphor -- triple tungstate -- microwave assisted sol-gel -- upconversion characteristics
Аннотация: New triple tungstate phosphors NaPbLa(WO4)3:Yb3+/Ho3+ (x = Yb3+/Ho3+ = 7, 8, 9, 10) are successfully fabricated by microwave assisted sol-gel synthesis and their structural and frequency upconversion (UC) characteristics are investigated. The compounds crystallized in the tetragonal space group I41/a and the NaPbLa(WO4)3 host have unit cell parameters a = 5.3927(1) and c = 11.7961(3) Å, V = 343.05(2) Å3, Z = 4. Under excitation at 980 nm, the phosphors have yellowish green emissions, which are derived from the intense 5S2/ 5F4 → 5I8 transitions of Ho3+ ions in the green spectral range and strong 5F5 → 5I8 transitions in the red spectral range. The optimal Yb3+:Ho3+ ratio is revealed to be x = 9, which is attributed to the quenching effect of Ho3+ ions, as indicated by the composition dependence. The UC characteristics are evaluated in detail under consideration of the pump power dependence and Commission Internationale de L'Eclairage chromaticity. The spectroscopic features of Raman spectra are discussed in terms of the superposition of Ho3+ luminescence and vibrational lines. The possibility of controlling the spectral distribution of UC luminescence by the chemical content of tungstate hosts is demonstrated.

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Держатели документа:
Department of Aerospace Advanced Materials & Chemical Engineering, Hanseo University, Seosan 356-706, Republic of Korea
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090, Russia
Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk 630090, Russia
Research and Development Department, Kemerovo State University, Kemerovo 650000, Russia
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Department of Photonics and Laser Technologies, Siberian Federal University, Krasnoyarsk 660041, Russia
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen 625003, Russia
Department of General and Special Chemistry, Industrial University of Tyumen, Tyumen 625000, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Siberian Federal University, Krasnoyarsk 660041, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk 680021, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Lim, Chang Sung; Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Denisenko, Yuriy G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич
}
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12.


   
    Multiple substitution strategies toward tunable luminescence in Lu2MgAl4SiO12:Eu2+ phosphors / Z. Ming, J. Qiao, M. S. Molokeev [et al.] // Inorg. Chem. - 2020. - Vol. 59, Is. 2. - P. 1405-1413, DOI 10.1021/acs.inorgchem.9b03142. - Cited References: 31. - This research is supported by the National Natural Science Foundation of China (Grants 51972118, 51722202, and 51572023), Natural Science Foundations of Beijing (Grant 2172036), and Fundamental Research Funds for the Central Universities (Grant FRF-TP-18-002C1) . - ISSN 0020-1669. - ISSN 1520-510X
   Перевод заглавия: Стратегии множественного замещения для перестраиваемой люминесценции в люминофорах Lu2MgAl4SiO12:Eu2+
Рубрики:
Physical and chemical processes
   Phosphors

   Luminescence

   Cations

   Ions

Аннотация: The equivalent or heterovalent substitution strategy is an efficient way to stimulate photoluminescence tuning or to optimize the luminescence performances of phosphor materials. Garnet-type compounds receive much attention as phosphor hosts because of their flexible structural frameworks. Herein, a garnet-type Lu2MgAl4SiO12:Eu2+ phosphor with broad-band blue-green emission is first explored with two-site occupation by varying the Eu2+ content. Two host-substitution approaches to controlling the luminescence behavior of Lu2MgAl4SiO12:Eu2+ phosphor are implemented. The cation substitution strategy of Ca2+ for Mg2+ achieves tunable emission from 463 to 503 nm together with broadening emission bands in Lu2Mg1–yCayAl4SiO12:Eu2+ phosphors. Moreover, chemical unit cosubstitution of [Ca2+–Ge4+] replacing [Lu3+–Al3+] results in Lu2–zCazMgAl4–zGezSiO12:Eu2+ phosphors, which induce a red shift of the emission peak of about 60 nm and a broadening in the emission spectra with increasing Ca2+ and Ge4+ concentrations. The possible photoluminescence tuning mechanism is ascribed to the coordination sphere variation in the EuO8 polyhedron depending on the changing neighboring cations. The proposed approaches on equivalent or heterovalent substitution can contribute to the development of Eu2+-activated garnet-type phosphors with regulation of the luminescence performance and further initiate research discovering new phosphors for white-light-emitting diodes.

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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing 100083, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Siberian Federal University, Krasnoyarsk, 660041, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russia
Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, 9300, South Africa
State Key Laboratory of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641, China

Доп.точки доступа:
Ming, Zhiqiang; Qiao, Jianwei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Swart, Hendrik C.; Xia, Zhiguo
}
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13.


   
    Erratum to: fabrication of microcrystalline NaPbLa(WO4)3:Yb3+/Ho3+ phosphors and their upconversion photoluminescent characteristics (vol 29, pg 741, 2019) / C. S. Lim, V. V. Atuchin, A. S. Aleksandrovsky [et al.] // Kor. J. Mater. Res. - 2020. - Vol. 30, Is. 1. - P. 50, DOI 10.3740/MRSK.2020.30.1.50. - Cited References: 1. - This study was supported by the Research Program through the Campus Research Foundation funded by Hanseo University in 2019 (191Yunghap09). . - ISSN 1225-0562. - ISSN 2287-7258
РУБ Materials Science, Multidisciplinary


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Держатели документа:
Hanseo Univ, Dept Aerosp Adv Mat & Chem Engn, Seosan 356706, South Korea.
RAS, Inst Semicond Phys, Lab Opt Mat & Struct, SB, Novosibirsk 630090, Russia.
Novosibirsk State Univ, Lab Semicond & Dielectr Mat, Novosibirsk 630090, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
RAS, Kirensky Inst, Phys Fed Res Ctr, KSC,SB,Lab Coherent Opt, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Photon & Laser Technol, Krasnoyarsk 660041, Russia.
Tyumen State Univ, Dept Inorgan & Phys Chem, Tyumen 625003, Russia.
Ind Univ Tyumen, Dept Gen & Special Chem, Tyumen 625000, Russia.
RAS, Kirensky Inst Phys, Fed Res Ctr, KSC,SB,Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
RAS, Kirensky Inst Phys, Fed Res Ctr, KSC,SB,Lab Mol Spect, Krasnoyarsk 660036, Russia.
Доп.точки доступа:
Lim, Chang Sung; Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Denisenko, Yuriy G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Campus Research Foundation - Hanseo University [191Yunghap09]
}
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14.


   
    Two-dimensional-layered perovskite ALaTa2O7:Bi3+ (A = K and Na) phosphors with versatile structures and tunable photoluminescence / G. J. Zhou [et al.] // ACS Appl. Mater. Interfaces. - 2018. - Vol. 10, Is. 29. - P. 24648-24655, DOI 10.1021/acsami.8b08129. - Cited References: 48. - The authors acknowledge the support from the National Natural Science Foundation of China (Nos. 51722202, 91622125, and 51572023) and the Natural Science Foundations of Beijing (2172036) and RFBR (17-52-53031). . - ISSN 1944-8244
   Перевод заглавия: 2D-слоистые перовскитоподобные люминофоры ALaTa2O7:Bi3+ (A = K and Na) с разнообразными структурами и управляемой люминесценцией.
РУБ Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
GENERALIZED GRADIENT APPROXIMATION
   YELLOW-EMITTING PHOSPHOR

Кл.слова (ненормированные):
2D-layered perovskite -- Bi3+ emission -- ion exchange -- photoluminescence tuning -- white light LEDs
Аннотация: Topological chemical reaction methods are indispensable for fabricating new materials or optimizing their functional properties, which is particularly important for two-dimensional (2D)-layered compounds with versatile structures. Herein, we demonstrate a low-temperature (∼350 °C) ion exchange approach to prefabricate metastable phosphors ALa1–xTa2O7:xBi3+ (A = K and Na) with RbLa1–xTa2O7:xBi3+ serving as precursors. The as-prepared ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) share the same Dion–Jacobson type 2D-layered perovskite phase, and photoluminescence analyses show that ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) phosphors exhibit broad emission bands peaking at 540, 550, and 510 nm, respectively, which are attributed to the nonradiative transition of Bi3+ from excited state 3P1 or 3P0 to ground state 1S0. The various Bi3+ local environments at the crystallographic sites enable the different distributions of emission and excitation spectra, and the photoluminescence tuning of ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) phosphors are realized through alkali metal ion exchange. Notably, the combination of superior trivalent bismuth emission and low-temperature ion exchange synthesis leads to a novel yellow-emitting K(La0.98Bi0.02)Ta2O7 phosphor which is successfully applied in a white LED device based on a commercially available 365 nm LED chip. Our realizable cases of this low-temperature ion exchange strategy could promote exploration into metastable phosphors with intriguing properties.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
Chinese Acad Sci, Tech Inst Phys & Chem, Beijing 100190, Peoples R China.
Univ Chinese Acad Sci, Beijing 100049, Peoples R China.
SB RAS, KSC, Fed Res Ctr, Kirensky Inst Phys,Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Zhou, Guojun; Jiang, Xingxing; Zhao, Jing; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lin, Zheshuai; Liu, Quanlin; Xia, Zhiguo
}
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15.


   
    Eu2+ site preferences in the mixed cation K2BaCa(PO4)2 and thermally stable luminescence / J. W. Qiao [et al.] // J. Am. Chem. Soc. - 2018. - Vol. 140, Is. 30. - P. 9730-9736, DOI 10.1021/jacs.8b06021. - Cited References: 40. - This work is supported by the National Natural Science Foundation of China (No. 51722202, 91622125, 51572023, and 11574003), Natural Science Foundations of Beijing (2172036) and M.M. acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 0002-7863
   Перевод заглавия: Предпочтительное положение ионов Eu2+ в смешанных катионах K2BaCa(PO4)2 и термически стабильная люминесценция
РУБ Chemistry, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
   SOLID-SOLUTION

   PHOSPHORS

   GREEN

   BLUE

Аннотация: Site preferences of dopant Eu2+ on the locations of K+, Ba2+, and Ca2+ in the mixed cation phosphate K2BaCa(PO4)2 (KBCP) are quantitatively analyzed via a combined experimental and theoretical method to develop a blue-emitting phosphor with thermally stable luminescence. Eu2+ ions are located at K2 (M2) and K3 (M3) sites of KBCP, with the latter occupation relatively more stable than the former, corresponding to emissions at 438 and 465 nm, respectively. KBCP:Eu2+ phosphor exhibits highly thermal stable luminescence even up to 200 °C, which is interpreted as due to a balance between thermal ionization and recombination of Eu2+ 5d excited-state centers with the involvement of electrons trapped at crystal defect levels. Our results can initiate more exploration of activator site engineering in phosphors and therefore allow predictive control of photoluminescence tuning and thermally stable luminescence for emerging applications in white LEDs.

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Держатели документа:
Univ Sci & Technol Beijing, Beijing Municipal Key Lab New Energy Mat & Techno, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
Anhui Normal Univ, Dept Phys, Anhui Key Lab Optoelect Mat Sci & Technol, Wuhu 241000, Anhui, Peoples R China.
RAS, SB, KSC, Lab Crystal Phys,Kirensky Inst Phys,Fed Res Ctr, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan.

Доп.точки доступа:
Qiao, Jianwei; Ning, Lixin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chuang, Yu-Chun; Liu, Quanlin; Xia, Zhiguo
}
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16.


   
    Learning from a mineral structure toward an ultra-narrow-band blue-emitting silicate phosphor RbNa3(Li3SiO4)4:Eu2+ / H. X. Liao [et al.] // Angew. Chem. - Int. Edit. - 2018. - Vol. 57, Is. 36. - P. 11728-11731, DOI 10.1002/anie.201807087. - Cited References: 22. - This work was supported by the National Natural Science Foundations of China (Grant Nos. 51722202, 91622125 and 51572023), and Natural Science Foundations of Beijing (2172036), and M.S.M. acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 1433-7851. - ISSN 1521-3773
   Перевод заглавия: Обучение от минеральной структуры к ультраузкополосному синему силикатному люминофору RbNa3(Li3SiO4)4:Eu2+
РУБ Chemistry, Multidisciplinary
Рубрики:
RED PHOSPHORS
   COLOR-GAMUT

   LUMINESCENCE

Кл.слова (ненормированные):
luminescence -- minerals -- phosphors -- rigid structure -- silicates
Аннотация: Learning from natural mineral structures is an efficient way to develop potential host lattices for applications in phosphor converted (pc)LEDs. A narrow‐band blue‐emitting silicate phosphor, RbNa3(Li3SiO4)4:Eu2+ (RNLSO:Eu2+), was derived from the UCr4C4‐type mineral model. The broad excitation spectrum (320–440 nm) indicates this phosphor can be well matched with the near ultraviolet (n‐UV) LED chip. Owing to the UCr4C4‐type highly condensed and rigid framework, RNLSO:Eu2+ exhibits an extremely small Stokes shift and an unprecedented ultra‐narrow (full‐width at half‐maximum, FWHM=22.4 nm) blue emission band (λem=471 nm) as well as excellent thermal stability (96 %@150 °C of the initial integrated intensity at 25 °C). The color gamut of the as‐fabricated (pc)LEDs is 75 % NTSC for the application in liquid crystal displays from the prototype design of an n‐UV LED chip and the narrow‐band RNLSO:Eu2+ (blue), β‐SiAlON:Eu2+ (green), and K2SiF6:Mn4+ (red) components as RGB emitters.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
Fed Res Ctr KSC SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Liao, Hongxu; Zhao, Ming; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Quanlin; Xia, Zhiguo
}
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17.


   
    Co-substitution in Ca1−xYxAl12−xMgxO19 phosphors: local structure evolution, photoluminescence tuning and application for plant growth LEDs / Y. Zheng [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 15. - P. 4217-4224, DOI 10.1039/c8tc00165k. - Cited References: 47. - The present work was supported by the National Natural Science Foundation of China (Grant No. 21671070), the Project for Construction of High-level University in Guangdong Province, and the Teamwork Projects funded by the Guangdong Natural Science Foundation (Grant No. S2013030012842), and the Guangzhou Science & Technology Projects (No. 201704030086, 201605030005), and the reported study was funded by the RFBR according to the research project 17-52-53031. Special Funds for the Cultivation of Guangdong College Students’ Scientific and Technological Innovation (‘‘Climbing Program’’ Special Funds) were granted for Dr Yinjian Zheng. . - ISSN 2050-7534
   Перевод заглавия: Созамещение в Ca1−xYxAl12−xMgxO19 люминофорах: локальная структура, настройка фотолюминесценции и применение светодиодов для роста растений
Кл.слова (ненормированные):
CO substitution -- Crystal structure transformation -- High temperature solid-state reaction -- Lighting systems -- Local structure -- Luminescence measurements -- Structural refinement -- Tunable luminescences
Аннотация: Herein, Mn4+-activated Ca1-xYxAl12-xMgxO19 (x = 0-0.50) solid solutions were prepared using a conventional high-temperature solid-state reaction. Crystal structure transformation via chemical co-substitution of Y3+/Mg2+ for Ca2+/Al3+ was investigated in detail. The optical properties of Ca1-xYxAl12-xMgxO19 (x = 0-0.50) have been reported for the first time using a combination of techniques including structural refinement and luminescence measurements. Co-doping of Mg and Y cations within the CaAl12O19 host in a controlled manner resulted in the as-prepared samples with red/far-red ratio-tunable luminescence properties. The emission bands well-matched with the absorption band of phytochrome. Interestingly, enhanced Mn4+ luminescence can be obtained upon the addition of Mg2+ and Y3+. Unexpectedly, the quantum yields exhibit a slight change when x is in the range from 0.05 to 0.40; this indicates that these solid solutions have significant potential as lighting systems for plant growth.

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Guangdong Provincial Engineering Technology Research Center for Optical Agricultural, College of Materials and Energy, South China Agricultural University, Guangzhou, China
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation

Доп.точки доступа:
Zheng, Y.; Zhang, H.; Xia, Z.; Liu, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lei, B.
}
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18.


   
    Controllable two-dimensional luminescence tuning in Eu2+,Mn2+ doped (Ca,Sr)9Sc(PO4)7 based on crystal field regulation and energy transfer / S. S. Liang [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 25. - P. 6714-6725, DOI 10.1039/c8tc01825a. - Cited References: 63. - This work was financially supported by the National Natural Science Foundation of China (NSFC No. 51672265, 51672266, 21521092, 51750110511, 51672257, and 51672259), the Key Research Program of Frontier Sciences of CAS (Grant No. YZDY-SSW-JSC018), the National Basic Research Program of China (2014CB643803), the Scientific and Technological Department of Jilin Province (Grant No. 20150520029JH and 20170414003GH), Jiangmen Innovative Research Team Program (2017) and Major Program of Basic Research and Applied Research of Guangdong Province (2017KZDXM083), the Russian Science Foundation (Grant No. 17-12-01047), and the Distinguished Scientist Fellowship Program of King Saud University, as well as the Deanship of Scientific Research at King Saud University through research group no. (RG-1939-038). . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Контролируемое двухпараметрическое управление люминесценцией в допированном Eu2+,Mn2+ (Ca,Sr)9Sc(PO4)7, основанное на регуляции кристаллического поля и переноса энергии
РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
SOLID-SOLUTION PHOSPHORS
   LIGHT-EMITTING-DIODES

   CATION SUBSTITUTION

Аннотация: Currently, controllable luminescence tuning and the generation of single component white emission are viable strategies to modify and optimize the luminescence performances of phosphors, which offer appealing prospects for the w-LED lighting industry. In this paper, we designed two-dimensional (2D) tunable color coordinates on the CIE diagram in the Eu2+,Mn2+ doped (Ca,Sr)9xSc(PO4)7 system by a combination of crystal field regulation and the energy transfer method. X-ray powder diffraction (XRD) and Rietveld refinement were utilized to analyze the phase composition and structural variation of the studied phosphors. The transmission electron microscopy (TEM) and photoluminescence spectra were exploited to analyze the generation of nanosegregation. The effects of the schedule of cation substitutions and energy transfer on the photoluminescence properties were investigated in detail. The corresponding luminescence mechanisms of the red-shifted emission with Sr2+ → Ca2+ substitution and Eu2+ → Mn2+ energy transfer were deeply discussed and proposed. In addition, the temperature-dependent thermal quenching behavior and the electroluminescence (EL) performance of the fabricated w-LED devices were also investigated to characterize the prepared Ca9(1−0.03−x−y)Sr9xSc(PO4)7:0.27Eu2+,9yMn2+. Finally, a representative w-LED device composed of a 369 nm UV chip and Ca9(1−0.03−0.02−0.5)Sr4.5Sc(PO4)7:0.27Eu2+,0.18Mn2+ could present excellent EL performance with the parameters CRI = 88, CCT = 3122 K and color coordinate (0.45, 0.44), which could well meet the commercial standard of warm white light. Therefore, our results suggest that this two-step luminescence tuning method is feasible to be applied in other phosphor systems for obtaining efficient white emitting phosphors.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, 388 Lumo Rd, Wuhan 430074, Peoples R China.
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Qingdao Univ, Sch Chem & Chem Engn, Qingdao 266071, Peoples R China.
King Saud Univ, Coll Appl Med Sci, Dept Dent Hlth, Riyadh, Saudi Arabia.
Wuyi Univ, Sch Appl Phys & Mat, Jiangmen 529020, Guangdong, Peoples R China.

Доп.точки доступа:
Liang, S. S.; Dang, P. P.; Li, G. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wei, Y.; Lian, H. Z.; Shang, M. M.; Al Kheraiff, A. A.; Lin, J.
}
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19.


   
    Pure red upconversion luminescence and optical thermometry of Er3+ doped sensitizer-rich SrYbInO4 phosphors / N. Z. Zhang [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 27. - P. 7361-7366, DOI 10.1039/c8tc02565g. - Cited References:34. - The present work was supported by the National Natural Science Foundation of China (Grant 91622125, 51722202 and 51572023) and the Natural Science Foundations of Beijing (2172036), and M. Molokeev acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Чистая красная апконверсионная люминесценция и оптическая термометрия люминофора SrYbInO4 допированного Er3+
РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
TEMPERATURE-SENSING BEHAVIOR
   EMISSION

   NANOCRYSTALS

   LANTHANIDE

Аннотация: Er3+ doped sensitizer-rich SrYbInO4 upconversion phosphors with an orthorhombic structure (Pnma) were synthesized by using a high temperature solid state reaction and their phase structure, site occupation and microstructure have been analyzed. Interestingly, upon the excitation from 980 nm pulsed laser diodes, the SrYbInO4:Er3+ phosphor emitted a nearly pure red emission on account of the 4F9/2 → 4I15/2 transition of Er3+. Additionally, based on the pump power dependence of the upconversion intensity and the schematic diagram of the energy levels, the upconversion mechanism in this system was verified in a two-photon process. The temperature-dependent behaviors of the as-synthesized sample demonstrated the potential for applications in optical thermometry.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Zhang, Ningzi; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Quanlin; Xia, Zhiguo
}
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20.


   
    Crystal structure of NaLuW2O8·2H2O and down/upconversion luminescence of the derived NaLu(WO4)2:Yb/Ln phosphors (Ln = Ho, Er, Tm) / X. Shi [et al.] // Inorg. Chem. - 2018. - Vol. 57, Is. 17. - P. 10791-10801, DOI 10.1021/acs.inorgchem.8b01427. - Cited References: 60 . - ISSN 0020-1669
   Перевод заглавия: Кристаллическая структура NaLuW2O8∙2H2O и люминесценция производных люминофоров NaLu(WO4)2:Yb/Ln (Ln=Ho, Er, Tm)
Аннотация: Hydrothermally reacting Lu(NO)3 and Na2WO4·2H2O at 200 °C and pH = 8 produced the new compound NaLuW2O8·2H2O, which was analyzed via the Rietveld technique to crystallize in the orthorhombic system (space group: Cmmm) with cell parameters a = 21.655(1), b = 5.1352(3), and c = 3.6320(2) Å and cell volume V = 403.87(4) Å3. The crystal structure presents -(NaO6)-(NaO6)- and -(LuO4(H2O)2WO5)-(LuO4(H2O)2WO5)- alternating layers linked together by the O2- ion common to NaO6 octahedron and WO5 triangle bipyramid. Tetragonal structured and phase-pure Na(Lu0.87Ln0.03Yb0.1)(WO4)2 phosphors (Ln = Ho, Er, and Tm) were directly produced by calcining their NaLuW2O8·2H2O analogous precursors at 600 °C for 2 h, followed by a detailed study of their downconversion/upconversion (DC/UC) photoluminescence. It was shown that the UC luminescence is dominated by a red band at ∼650 nm for Ho3+ (5F5 →5I8 transition), green bands at ∼500-575 nm for Er3+ (2H11/2/4S3/2 →4I15/2 transitions) and a blue band at ∼476 nm for Tm3+ (1G4 →3H6 transition), all via a three-photon process. DC luminescence of the phosphors is characterized by a ∼545 nm green emission for Ho3+ (5F4/5S2 →5I8 transition, ex = 453 nm), ∼500-575 nm green emissions for Er3+ (2H11/2/4S3/2 →4I15/2 transitions, ex = 380 nm), and a ∼455 nm blue emission for Tm3+ (1D2 →3F4 transition, ex = 360 nm), with CIE chromaticity coordinates of around (0.27, 0.71), (0.26, 0.72), and (0.15, 0.04), respectively.

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Держатели документа:
Key Laboratory for Anisotropy and Texture of Materials, Ministry of Education, Northeastern University, Shenyang Liaoning, 110819, China
Institute for Ceramics and Powder Metallurgy, School of Materials Science and Engineering, Northeastern University, Shenyang Liaoning, 110819, China
Research Center for Functional Materials, National Institute for Materials Science, Tsukuba Ibaraki, 305-0044, Japan
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
College of New Energy, Bohai University, Jinzhou Liaoning, 121007, China

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