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    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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    A novel single-phase white light emitting phosphor Ca9La(PO4)5(SiO4)F2:Dy3+: Synthesis, crystal structure and luminescence properties / H. Liu [et al.] // RSC Adv. - 2016. - Vol. 6, Is. 29. - P. 24577-24583, DOI 10.1039/c5ra23348h. - Cited References: 33. - We gratefully acknowledge the financial support by the National Natural Science Foundations of China (Grant no. 41172053), the Fundamental Research Funds for the Central Universities (Grant no. 2652013043), and Science and Technology Innovation Fund of the China University of Geosciences (Beijing). . - ISSN 2046-2069
   Перевод заглавия: Новый однофазный люминофор Ca9La(PO4)5(SiO4)F2:Dy3+, излучающий белый свет: синтез, кристаллическая структура и люминесцентные свойства

РУБ Chemistry, Multidisciplinary
Рубрики:
Energy-transfer
   Diodes
   LEDs
   Emission
   Ions
   Excitation
   Ce3+
   Eu2+
   Ln
Аннотация: A novel single-phase white light emitting phosphor Ca9La(PO4)5(SiO4)F2:Dy3+ was prepared through traditional high-temperature solid state technology. The crystal structures of Ca9La(PO4)5(SiO4)F2 with or without Dy3+ ions were refined by the Rietveld method. The diffuse reflection spectra, excitation spectra, emission spectra, and decay times were characterized to investigate the photoluminescence properties for application in white light-emitting diodes. The results showed that the Ca9La(PO4)5(SiO4)F2:Dy3+ phosphor could efficiently assimilate n-UV light and emit blue (∼485 nm) and yellow light (∼580 nm), originating from the f-f transitions of Dy3+. The critical Dy3+ quenching concentration (QC) was determined to be about 15 mol%, and the corresponding QC mechanism was verified to be the dipole-dipole interaction. Additionally, the emission colors of all samples were located close to the ideal white light region, and the optimal chromaticity coordinates and correlated color temperature (CCT) were determined to be (x = 0.338, y = 0.336) and 5262 K. All the above results indicate that the as-prepared Ca9La(PO4)5(SiO4)F2:Dy3+ phosphor could serve as a promising candidate for white-light n-UV-LEDs. © The Royal Society of Chemistry 2016.

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Держатели документа:
Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science 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:
Liu, H.; Liao, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Guo, Q.; Zhang, Y.; Mei, L.
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    Crystal structure and luminescence properties of green-emitting Sr1−xAl12O19:xEu2+ phosphors / B. Ma [et al.] // Ceram. Int. - 2016. - Vol. 42, Is. 5. - P. 5995-5999, DOI 10.1016/j.ceramint.2015.12.149. - Cited References: 30. - This work was supported by the National Natural Science Foundation of China (Grant nos. 51032007 and 51372232) and the Fundamental Research Funds for the Central Universities (Grant no. 2652015024). . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Кристаллическая структура и люминесцентные свойства зеленого люминофора Sr1-xAl12O19:xEu2+

РУБ Materials Science, Ceramics
Рубрики:
COLOR-TUNABLE PHOSPHOR
   ENERGY-TRANSFER
   Dy3+ PHOSPHORS
   NEAR-UV
   Eu2+
   DIODES
   PHASE
   STATE
   Ce3+
Кл.слова (ненормированные):
Crystal structure -- Magnetoplumbite -- Phosphor
Аннотация: In this paper, a series of novel luminescent Sr1−xAl12O19:xEu2+ phosphors were synthesized by a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, as well as the decay curves were investigated. The quenching concentration of Eu2+ in SrAl12O19 was about 0.15 (mol). Upon excitation at 378 nm, the composition-optimized Sr0.85Al12O19:0.15Eu2+ exhibited strong broad-band green emission at 530 nm with the CIE chromaticity (0.2917, 0.5736). The results indicate that Sr1−xAl12O19:xEu2+ phosphors have potential applications as green-emitting phosphors for UV-pumped white-light LEDs.

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Beijing 100083, Peoples R China.
SB RAS, Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Ma, Bin; Guo, Q. F.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lv, Zhenfei; Yao, Jun; Mei, Lefu; Huang, Zhaohui
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    New garnet structure phosphors, Lu3-xYxMgAl3SiO12:Ce3+ (x = 0-3), developed by solid solution design / H. Ji [et al.] // J. Mater. Chem. C. - 2016. - Vol. 4, Is. 12. - P. 2359-2366, DOI 10.1039/c6tc00089d. - Cited References: 33. - This work was partly supported by the National Natural Science Foundation of China (Grant No. 51511130035, 51272259, 61575182, 51572232 and 51561135015) and the Russian Foundation for Basic Research (Grant No. 15-52-53080). H. J. thanks the China Scholarship Council (CSC) for providing a scholarship to support his study in NIMS. . - ISSN 2050-7534
   Перевод заглавия: Новые люминофоры со структурой граната, Lu3-xYxMgAl3SiO12:Ce3+ (x = 0-3), полученные как твердые растворы

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
Particle-diagnosis approach
   Luminescence
   Photoluminescence
   Ce3+
   Substitution
   Discovery
   Oxygen
Аннотация: New garnet phosphors, Lu3−xYxMgAl3SiO12:Ce3+ (x = 0–3), which can be efficiently excited by blue light and emit the yellow-orange light, were developed using the solid solution design strategy combining the chemical unit substitution and the cation substitution. Crystal structures of the four compounds were reported for the first time via the Rietveld refinement of their powder XRD patterns. All phosphors show the general cubic garnet structure with the space group Iad. The specific occupancy of Lu/Y, Al/Mg, Al/Si and O atoms in different positions was identified. The evolution of cell parameters and Y/Lu/Ce–O bond lengths were identified. Photoluminescence properties were evaluated on aspects of emission/excitation spectra, internal/external quantum efficiency and thermal emission stability. Under the 450 nm blue light excitation, the phosphors exhibit bright yellow color emission, peaking in the 575–597 nm spectral range. The internal and external quantum efficiency can reach 83% and 58%, respectively. The emission red-shift in response to the Y/Lu ratio variation was discussed in relation to the local structure evolution. The phosphors are relatively promising to act as wavelength converter of blue light in white light emitting diodes.

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Держатели документа:
National Laboratory of Mineral Materials, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, School of Materials Science and Technology, China University of Geosciences (Beijing), Beijing, China
Sialon Group, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Japan
College of Optical and Electronic Technology, China Jiliang University, Hangzhou, 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 Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China

Доп.точки доступа:
Ji, H.; Wang, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Hirosaki, N.; Huang, Z.; Xia, Z.; Ten Kate, O. M.; Liu, L.; Xie, R.
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    Crystal structure and luminescence properties of novel Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphor with apatite structure / Q. F. Guo [et al.] // Ceram. Int. - 2016. - Vol. 42, Is. 10. - P. 11687-11691, DOI 10.1016/j.ceramint.2016.04.086. - Cited References:26. - This present work is supported by the National Natural Science Foundation of China (Grant no. 41172053). . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Кристаллическая структура и люминесцентные свойства нового люминофора Sr10-x(SiO4)3(SO4)3O:xEu2+ со структурой апатита

РУБ Materials Science, Ceramics
Рубрики:
Light-Emitting-Diodes
   Energy-transfer
   Tunable phosphor
   LEDs
   Eu-2+
   Ions
   Ce3+
Кл.слова (ненормированные):
Crystal structure -- Apatite -- Phosphor
Аннотация: In this paper, a series of novel luminescent Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphors with apatite structure were synthesized by a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, as well as the PL thermal stability were investigated. Sr9.92(SiO4)3(SO4)3O:0.08Eu2+ phosphor exhibits better thermal quenching resistance, retaining the luminance of 66.55% at 150 °C compared with that at 25 °C. The quenching concentration of Eu2+ in Sr10(SiO4)3(SO4)3O was about 0.08 (mol) with the dipole–quadrupole interaction. The Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphors exhibited a broad-band green emission at 538 nm upon excitation at 396 nm. The results indicate that Sr10−x(SiO4)3(SO4)3O:xEu2+ phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs.

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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.
SB RAS, Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Guo, Q. F.; Ma, B.; Liao, L. B.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Mei, L. F.; Liu, H. K.
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    Influence of cation substitution on the crystal structure and luminescent properties in apatite structural Ba4.97- xSrx(PO4)3Cl:0.03Eu2+ phosphors / L. Zhu [et al.] // Chem. Phys. Lett. - 2016. - Vol. 658. - P. 248-253, DOI 10.1016/j.cplett.2016.06.061. - Cited References: 23. - This present work was supported by the National Natural Science Foundations of China (Grant Nos. 51472222 and 51372232), the Fundamental Research Funds for the Central Universities (Grant No. 2652015310), and the Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20130022110006). . - ISSN 0009-2614
   Перевод заглавия: Влияние катионного замещения на кристаллическую структуру и люминесценные свойства в апатите Ba4.97-xSrx(PO4)3Cl:0.03Eu2+

РУБ Chemistry, Physical + Physics, Atomic, Molecular & Chemical
Рубрики:
PHOTOLUMINESCENCE
   ENERGY
   Ce3+
   Sr
   UV
Кл.слова (ненормированные):
Substitution -- Apatite -- Ba4.97- xSrx(PO4)3Cl:0.03Eu2+ -- Luminescence
Аннотация: A series of apatite-type phosphors Ba4.97- xSrx(PO4)3Cl:Eu2+(x = 0, 0.5, 1.0, 1.5, 2.0) were synthesized by the high temperature solid-state reaction method, and its luminescence properties were investigated in detail. It can be found that a red shift of the emission peak wavelength emerged from 439 to 462 nm with the continuous introduction of Sr2+ into the crystal lattice which has been simulated by a crystal-field model. The red shift is explained by the distortion in the crystal structure through X-ray diffraction and the Rietveld refinement analysis. According to a recently raised structural model, Eu2+ ions are surrounded by O atoms, PO4 tetrahedrons and Ba/Sr ions. After introducing Sr2+ into the lattice, the interatomic distance between Ba/Sr atoms and Eu2+ was expected to become shorter, resulting in a distortion of the inner EuOn polyhedrons. Then the crystal field strength surrounding Eu2+ was increased, finally resulting in the red shift. © 2016 Published by Elsevier B.V.

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Держатели документа:
School of Materials Science and Technology, National Laboratory of Mineral Materials, 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, L.; Huang, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Min, X.; Liu, Y.; Fang, M.; Wu, X.
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    Structure evolution and photoluminescence of Lu3(Al,Mg)2(Al,Si)3O12:Ce3+ phosphors: New yellow-color converters for blue LED-driven solid state lighting / H. Ji [et al.] // J. Mater. Chem. C. - 2016. - Vol. 4, Is. 28. - P. 6855-6863, DOI 10.1039/c6tc00966b. - Cited References: 44. - This work was partially supported by the National Natural Science Foundations of China (Grant No. 51511130035, 51272259, 61575182, 51561135015, and 51572232) and the Russian Foundation for Basic Research (Grant No. 15-52-53080). We are also grateful to financial support from the JSPS KAKENHI (No. 15K06448). H. J. thanks the China Scholarship Council (CSC) for scholarship support. V. V. A. was partially supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 2050-7534
   Перевод заглавия: Изменения структуры и фотолюминесценция люминофоров Lu3(Al,Mg)2(Al,Si)3O12:Ce3+: новый желтый преобразователь голубого света, получаемого от твердотельных светодиодов
Рубрики:
WHITE LEDS
   LUMINESCENCE PROPERTIES
   EMITTING-DIODES
   GARNET PHOSPHORS
   SUBSTITUTION
   Ce3+
   PHASE
   Ca
Аннотация: This paper reports the development of new phosphors using the chemical unit cosubstituting solid solution design strategy. Starting from Lu3Al5O12, the Al3+-Al3+ couple in respective octahedral and tetrahedral coordination was simultaneously substituted by a Mg2+-Si4+ pair forming the Lu3(Al2-xMgx)(Al3-xSix)O12:Ce3+ (x = 0.5-2.0) series; as a result, the CeO8 polyhedrons were compressed and the emission got red-shifted from green to yellow together with the broadening. The evolution of, the unit cell, the local structural geometry as well as the optical properties of Ce3+ in these garnet creations, in response to the gradual Mg-Si substitution for Al-Al, were studied by combined techniques of structural refinement and luminescence measurements. The new composition Lu2.97Ce0.03Mg0.5Al4Si0.5O12 was comprehensively evaluated regarding its potential application in blue LED-driven solid state white lighting: the maximum emission is at 550 nm under ?ex = 450 nm; the internal and external quantum efficiencies can reach 85% and 49%, respectively; a 1-phosphor-converted wLED lamp fabricated using the as-prepared phosphor exhibits the luminous efficacy of 105 lm W-1, the correlated color temperature of 6164 K and the color rendering index (Ra) of 75.6. The new solid solution composition series is open for further optimization to enhance the competence for commercial consideration. © 2016 The Royal Society of Chemistry.

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Держатели документа:
National Laboratory of Mineral Materials, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, School of Materials Science and Technology, China University of Geosciences (Beijing), Beijing, China
Sialon Group, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Japan
College of Optical and Electronic Technology, China Jiliang University, Hangzhou, 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
College of Materials, Xiamen University, Xiamen, China
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
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.; Wang, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Hirosaki, N.; Xie, R.; Huang, Z.; Xia, Z.; Ten Kate, O. M.; Liu, L.; Atuchin, V. V.
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    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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    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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10.

    Giant red-shifted emission in (Sr,Ba)Y2O4:Eu2+ phosphor toward broadband near-infrared luminescence / Z. Y. Yang, Y. F. Zhao, Y. Y. Zhou [et al.] // Adv. Funct. Mater. - 2022. - Vol. 32, Is. 1. - Ст. 2103927, DOI 10.1002/adfm.202103927. - Cited References: 60. - This research was supported by the International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), National Natural Science Foundations of China (Grant No. 51972118 and 51961145101), Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003 . - ISSN 1616-301X. - ISSN 1616-3028
   Перевод заглавия: Излучение с гигантским красным смещением в люминофоре (Sr,Ba)Y2O4: Eu2 + для широкополосной люминесценции в ближней инфракрасной области

РУБ Chemistry, Multidisciplinary + Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Applied + Physics, Condensed Matter
Рубрики:
LIGHT-SOURCES
   PHOTOLUMINESCENCE
   TRANSITION
   CE3+
   BLUE
   SUBSTITUTION
Кл.слова (ненормированные):
near-infrared emission -- photoluminescence -- red emission
Аннотация: Near-infrared (NIR) light-emitting diodes (LEDs) light sources are desirable in photonic, optoelectronic, and biological applications. However, developing broadband red and NIR-emitting phosphors with good thermal stability is always a challenge. Herein, the synthesis of Eu2+-activated SrY2O4 red phosphor with high photoluminescence quantum efficiency and broad emission band ranging from 540 to 770 nm and peaking at 620 nm under 450 nm excitation is designed. Sr/Ba substitution in SrY2O4:Eu2+ has been further utilized to achieve tunable emission by modifying the local environment, which facilitates the giant red-shifted emission from 620 to 773 nm while maintaining the outstanding thermal stability of SrY2O4:Eu2+. The NIR emission is attributed to the enhanced Stokes shift and crystal field strength originated from the local structural distortions of [Y1/Eu1O6] and [Y2/Eu2O6]. The investigation in charge distribution around Y/Eu provides additional insight into increasing covalency to tune the emission toward the NIR region. As-fabricated NIR phosphor-converted LEDs demonstration shows its potential in night-vision technologies. This study reveals the NIR luminescence mechanism of Eu2+ in oxide-based hosts and provides a design principle for exploiting Eu2+-doped NIR phosphors with good thermal stability.

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Держатели документа:
South China Univ Technol, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, State Key Lab Luminescent Mat & Devices, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China.
Natl Synchrotron Radiat Res Ctr, Mat Sci Grp, Sci Res Div, Hsinchu 300, Taiwan.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.

Доп.точки доступа:
Yang, Zhiyu; Zhao, Yifei; Zhou, Yayun; Qiao, Jianwei; Chuang, Yu-Chun; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo; International Cooperation Project of National Key Research and Development Program of China [2021YFE0105700]; National Natural Science Foundations of ChinaNational Natural Science Foundation of China (NSFC) [51972118, 51961145101]; Guangzhou Science & Technology Project [202007020005]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01X137]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]
}
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