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    Шабанов, Александр Васильевич.
    Особенности усиления электромагнитного поля и увеличение плотности фотонных состояний в растительных фотонно-кристаллических структурах / А. В. Шабанов, М. А. Коршунов, Е. Р. Буханов // Комп. оптика. - 2019. - Т. 43, № 2. - С. 231-237 ; Comput. Opt., DOI 10.18287/2412-6179-2019-43-2-231-237. - Библиогр.: 29 . - ISSN 0134-2452. - ISSN 2412-6179
   Перевод заглавия: Features of the amplification of the electromagnetic field and the density of states of photonic crystal structures in plants

РУБ Optics
Рубрики:
BLUE IRIDESCENCE
   LIGHT
   COLOR
   PULSE
   BAND
Кл.слова (ненормированные):
фотонный кристалл -- дефектная мода -- фотонная запрещенная зона -- слоистые периодические структуры -- плотность фотонных состояний -- photonic crystal -- defect mode -- photonic band gap -- layered periodic structures -- density of states
Аннотация: Проведены расчёты с использованием метода трансфер матриц одномерных фотонных кристаллов с низким контрастом и разнопериодными асимметричными структурами. Такие структуры были найдены во многих растениях. При состыковке двух последовательно соединённых подрешёток с разными периодами отмечается увеличение амплитуды электромагнитного поля и плотности фотонных состояний внутри структуры и их изменение в зависимости от асимметрии толщин подрешёток.
Calculations were performed using the transfer matrix of one-dimensional photonic crystals with low contrast and asymmetric structures of different periods. Such structures have been found in many plants. When joining two successively connected sublattices with different periods, an increase is observed in the amplitude of the electromagnetic field and the density of photon states inside the structure, and their change depends on the asymmetry of the thickness of the sublattices.

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Держатели документа:
Институт физики им. Л.В. Киренского, ФИЦ КНЦ СО РАН, Красноярск, Россия
ФИЦ КНЦ СО РАН, Красноярск, Россия

Доп.точки доступа:
Коршунов, Михаил Анатольевич; Korshunov, M. A.; Буханов, Евгений Романович; Bukhanov E. R.; Shabanov, A. V.

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    Understanding perceived color through gradual spectroscopic variations in electrochromism / S. Mishra [et al.] // Indian J. Phys. - 2019. - Vol. 93, Is. 7. - P. 927-933, DOI 10.1007/s12648-018-1353-7. - Cited References: 34. - Authors acknowledge financial support from the Department of Science and Technology (DST), Govt. of India. Authors are thankful to Dr. K. V. Adarsh (IISER Bhopal) for Raman measurements. Authors thank Prof. V.D. Vankar (IIT Delhi) for useful discussions. Authors (AC and DKP) are thankful to MHRD and CSIR (Govt. of India), respectively, for providing fellowships. Support received from DST under FIST scheme (grant number: SR/FST/PSI-225/2016) is also acknowledged. . - ISSN 0973-1458. - ISSN 0974-9845
   Перевод заглавия: Понимание воспринимаемого цвета через постепенные спектроскопические изменения в электрохромизме

РУБ Physics, Multidisciplinary
Рубрики:
3 REDOX FORMS
   TUNGSTEN-OXIDE
   RAMAN-SPECTRA
   VIOLOGEN
   SALTS
Кл.слова (ненормированные):
Viologen -- Raman spectroscopy -- Electrochromism -- UV-Vis
Аннотация: A bias-dependent in situ Raman scattering and UV–Vis absorption spectroscopic change has been correlated with the corresponding color change of an electrochromic device in an attempt to explain how to understand the relationship between actual perceived color and its absorption/transmittance spectra. For this, the bias across an electrochromic device was increased gradually, rather than abruptly turning ON and OFF, to see subtle variations in Raman and absorption spectra due to bias. Raman scattering establishes that viologen changes its oxidation state reversibly between two redox species (EV2+ to EV+•) as a result of bias-induced dynamic redox process. A gradual variation in Raman and absorption spectra, which shows maximum absorption corresponding to the yellow light, accompanies similar variation in color change of the device as visible by naked eye. These spectroscopic results are correlated with the perceived blue color, in the reflected light, by the eye to understand the actual reason behind this. Maximum absorption of yellow light by the device resulting in blue appearance has been explained using the concept of additive and subtractive primary colors.

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Держатели документа:
Indian Inst Technol Indore, Discipline Phys & MEMS, Mat Res Lab, Simrol 453552, India.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Univ Alberta, Natl Inst Nanotechnol, Edmonton, AB, Canada.

Доп.точки доступа:
Mishra, S.; Yogi, P.; Chaudhary, A.; Pathak, D. K.; Saxena, S. K.; Krylov, A. S.; Крылов, Александр Сергеевич; Sagdeo, P. R.; Kumar, R.; Department of Science and Technology (DST), Govt. of India; MHRD; CSIR (Govt. of India); DST under FIST scheme [SR/FST/PSI-225/2016]
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    Ultra-broad-band-excitable Cu(I)-based organometallic halide with near-unity emission for light-emitting diode applications / J. Huang, B. Su, E. Song [et al.] // Chem. Mater. - 2021. - Vol. 33, Is. 12. - P. 4382-4389, DOI 10.1021/acs.chemmater.1c00085. - Cited References: 43. - This research was supported by the National Natural Science Foundation of China (Grant Nos. 51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science and Technology Project (202007020005), International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). The reported study was also funded by RFBR according to research project no. 19-52-80003 . - ISSN 0897-4756
   Перевод заглавия: Металлоорганический галогенид на основе Cu (I) со сверхширокополосным возбуждением и излучением с квантовым выходом близким к единице для применения в светодиодах
Кл.слова (ненормированные):
Crown ethers -- Hybrid materials -- Light -- Luminescence -- Metal halide lamps -- Metal halides -- Organic light emitting diodes (OLED) -- Organometallics -- Sodium compounds -- Application prospect -- Excitation characteristics -- Green emission bands -- High color rendering index -- Luminescence mechanisms -- Luminescent material -- Photoluminescence quantum yields -- White light emitting diodes -- Copper compounds
Аннотация: Low-dimensional hybrid metal halides demonstrate broad-band emission and high photoluminescence quantum yield (PLQY) acting as excellent candidates for a new generation of luminescent materials in lighting fields. However, most luminescent metal halides can only be excited by ultraviolet radiation, and the discovery of high-efficient emitters with broad-band excitation characteristics, especially upon efficient blue light irradiation, is a challenge. Herein, a zero-dimensional (0D) Cu(I)-based organometallic halide (18-crown-6)2Na2(H2O)3Cu4I6 (CNCI) was prepared with a green emission band centered at 536 nm and a near-unity PLQY (91.8%) upon excitation of 450 nm. Importantly, the ultrabroad excitation band covering a 300-500 nm range was observed in CNCI, and the luminescence mechanism has been discussed in detail. A white light-emitting diode (WLED) was fabricated with high luminous efficiency of 156 lm/W and a high color rendering index of 89.6. This work provides guidance for designing high-performance luminescent metal halides with suitable excitation characteristics and also promotes the application prospects of such materials in WLED fields.

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Держатели документа:
The 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
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
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation

Доп.точки доступа:
Huang, J.; Su, B.; Song, E.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.
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Two-color display based on polymer dispersed liquid crystals films / V. A. Gunyakov, V. A. Zhuikov, V. Ya. Zyryanov [et al.] // First Summer European Liquid Crystal Conference : abstracts. - Vilnius, 1991. - Vol. 1. - P. 90

Доп.точки доступа:
Gunyakov, V. A.; Гуняков, Владимир Алексеевич; Zhuikov, V. A.; Жуйков, Владимир Александрович; Zyryanov, V. Ya.; Зырянов, Виктор Яковлевич; Smorgon, S. L.; Сморгон, Сергей Леонидович; Shabanov, V. F.; Шабанов, Василий Филиппович; Summer European Liquid Crystals conference(1 ; 1991 ; Aug. 19-25 ; Vilnius)
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    Temperature and Eu2+-doping induced phase selection in NaAlSiO4 polymorphs and the controlled yellow/blue emission / M. Zhao [et al.] // Chem. Mater. - 2017. - Vol. 29, Is. 15. - P. 6552-6559, DOI 10.1021/acs.chemmater.7b02548. - Cited References: 48. - The present work was supported by the National Natural Science Foundation of China (Grants 91622125 and 51572023 and 11574003), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-16-002A3). L.N. acknowledges the support from the Special and Excellent Research Fund of Anhui Normal University. . - ISSN 0897-4756
   Перевод заглавия: Фазовый переход индуцированный температурой и допированием Eu2+ в NaAlSiO4, и контролируемое излучение желтого/голубого света
Кл.слова (ненормированные):
Chemical modification -- Coordination reactions -- Europium -- Light emitting diodes -- Photoluminescence -- Functional properties -- High color rendering index -- Local coordination structures -- Near ultraviolet excitations -- Structural transformation -- Synthesis temperatures -- Temperature dependent -- White light emitting diodes -- Density functional theory
Аннотация: The union of temperature-dependent phase transition and relating structural transformation via modification of chemical compositions is of fundamental importance for the discovery of new materials or their functional properties optimization. Herein, the synthesis temperature and Eu2+-doping content induced phase selection and variations of the local structures in nepheline, low-carnegieite and high-carnegieite types of NaAlSiO4 polymorphs were studied in detail. The luminescence of Eu2+ in low-carnegieite and nepheline phases shows blue (460 nm) and yellow (540 nm) broad-band emissions, respectively, under near-ultraviolet excitation. The photoluminescence evolution can be triggered by the different synthesis temperatures in relation to the Eu2+-doping concentration, as corroborated by density functional theory calculations on the local coordination structures and corresponding mechanical stabilities in terms of the Debye temperature. The fabricated white light-emitting diode device with high color rendering index demonstrates that the multicolor phosphors from one system provides a new gateway for the photoluminescence tuning. © 2017 American Chemical Society.

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Держатели документа:
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 Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Anhui Key Laboratory of Optoelectronic Materials Science and Technology, Department of Physics, Anhui Normal University, Wuhu, Anhui, China

Доп.точки доступа:
Zhao, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ning, L.; Liu, Q.
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    Synthesis and luminescence properties of blue-emitting phosphor Li3c2(PO4)3:Er2+ / S. X. Yu [et al.] // ECS J. Solid State Sci. Technol. - 2014. - Vol. 3, Is. 8. - P. R159-R163, DOI 10.1149/2.0071408jss. - Cited References: 33. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51002146, No. 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635) and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306). Z. G. Xia is also grateful for the financial support from University of Science and Technology Beijing. V.V.A. gratefully acknowledge the Ministry of Education and Science of the Russian Federation for the financial support. . - ISSN 2162-8769. - ISSN 2162-8777
   Перевод заглавия: Синтез и люминесцентные свойства синего люминофора Li3Sc2(PO4)3:Eu2+

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
ENERGY-TRANSFER
   PHOTOLUMINESCENCE PROPERTIES
   INORGANIC-COMPOUNDS
   EMISSION COLOR
   FULL-COLOR
   DIODES
   Eu2+
   IONS
   LEDS
   Tb
Аннотация: A new blue-emitting phosphor Li3Sc2(PO4)3:Eu2+ was synthesized by a high temperature solid-state reaction method, and the crystal structure and photoluminescence properties were investigated in detail. The preferred crystallographic position of the Eu2+ ions in the Li3Sc2(PO4)3 host were determined from the structural analysis and spectroscopic properties. The as-prepared phosphor gave an intense blue emission band centered at 439 nm with the CIE coordinate of (0.1540, 0.0317) upon the excitation of the near ultraviolet light. The critical quenching concentration of Eu2+ in Li3Sc2(PO4)3:Eu2+ was about 15 mol%, and the corresponding concentration quenching mechanism was verified to be the dipole-quadrupole interaction. The fluorescence lifetime of Eu2+ emission and the thermal stable luminescence property have been investigated. Li3Sc2(PO4)3:Eu2+ was found to be a promising candidate as a blue-emitting n-UV convertible phosphor for the application in white light emitting diodes (w-LEDs).

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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 & Dielectr Mat, Novosibirsk 630090, Russia

Доп.точки доступа:
Yu, Shixin; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Miao, Hao; Atuchin, V. V.
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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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    Structure and color-tunable luminescence properties of Ce3+ and Tb3+-activated Mg2La8(SiO4)6O2 phosphors based on energy transfer behavior / Y. Zhang [et al.] // J. Solid State Chem. - 2017. - Vol. 255. - P. 36-41, DOI 10.1016/j.jssc.2017.07.026. - Cited References: 45. - This present work was supported by the National Natural Science Foundations of China (Grant no. 41172053), the Fundamental Research Funds for the Central Universities (Grant nos. 2652016083 and 2652016037), and Science and Technology Innovation Fund of the China University of Geosciences (Beijing). . - ISSN 0022-4596
   Перевод заглавия: Структура и управляемые люминесцентные свойства Ce3+ и Tb3+-активированных Mg2La8(SiO4)6O2 люминофоров, основанные на передаче энергии
Кл.слова (ненормированные):
Crystal structure -- Luminescence properties -- Phosphors -- Apatite structure
Аннотация: A series of novel luminescent emission-tunable phosphors Mg2La8(SiO4)6O2:Ce3+,Tb3+ (MLS:Ce3+,Tb3+) have been prepared by a solid-state reaction. The phase formation was firstly confirmed through X-ray diffraction technique and refined by the Rietveld method. The MLS:Ce3+,Tb3+ phosphors, which crystallized in apatite-type hexagonal phase, exhibited a broad excitation band ranging from 200 to 400 nm and several emission bands centered at 426 nm and 551 nm. Energy transfer from Ce3+ to Tb3+ ions via a dipole-dipole mechanism occurred in the as-synthesized phosphors upon ultraviolet (UV) excitation. The energy transfer efficiency increases with increasing doping content of Tb3+ ions, which was confirmed by the luminescence spectra and fluorescence decay curves of corresponding ions simultaneously. The energy transfer critical distance was calculated and evaluated by both the concentration quenching and spectral overlap methods. The chromaticity of emission-tunable phosphors was also characterized by the Commission International de l'eclairage (CIE) chromaticity indexes, and the color tone can be tuned from blue (0.179, 0.122) to green (0.267, 0.408) by controlling the ratio of Ce3+/Tb3+. © 2017 Elsevier Inc.

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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, Krasnoyarsk, Russian Federation
Institute of Physics, Polish Academy of Sciences, Al. Lotnikow 32/46, Warsaw, Poland
Siberian Federal University, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Zhang, Y.; Liu, H.; Mei, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wang, Y.; Huang, Z.
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    Strategy to construct high thermal-stability narrow-band green-emitting Si-CDs@MAs phosphor for wide-color-gamut backlight displays / J. Chen, X. Zou, W. Li [et al.] // Adv. Opt. Mater. - 2022. - Vol. 10, Is. 21. - Ст. 2200851, DOI 10.1002/adom.202200851. - Cited References: 47. - The work was supported by the Ministry of Science and Technology of China (No. G2021030022L), the Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams (No. 2021KJ122), the National Natural Science Foundations of China (No. 52102042), the Independent Research and Development Projects of Maoming Laboratory (No. 2021ZZ004), the Key Realm R&D Program of Guangdong Province (No. 2021B0707010003), the Guangzhou Science & Technology Project (Nos. 202007020005 and 202103000059), the Guangdong Provincial Science and Technology Project (Nos. 2021A0505050006 and 2022A1515010229), and the Project of GDUPS (2018) for B.L. . - ISSN 2195-1071
   Перевод заглавия: Стратегия создания узкополосного люминофора Si-CD@MAs с высокой термостабильностью, излучающего зеленый свет, для дисплеев с подсветкой с широкой цветовой гаммой
Кл.слова (ненормированные):
carbon dots -- low thermal quenching -- narrowband -- photoluminescence -- WLED backlights
Аннотация: Developing innovative narrow-band green-emitting phosphors featuring low thermal quenching and eco-friendliness for white light-emitting diode (WLED) backlights is a pivotal challenge. Benefitting from narrowband and low toxicity of green-emitting silanized carbon dots (Si-CDs), an efficient confinement and protection strategy through embedding Si-CDs in mesoporous aluminas (MAs) is proposed to construct MAs and Si-CDs composites (Si-CDs@MAs) with superior luminescence properties. Si-CDs@MAs phosphor exhibits green emission at 526 nm with narrow full width at half maximum of 51 nm, zero-thermal quenching even up to 423 K (104.1%@423 K of the emission peak intensity at 298 K), and the internal quantum efficiency of 64.46%. Compared with broad-band yellow-emitting solid-state Si-CDs (S-Si-CDs), the thermal stability, photostability, and water stability of Si-CDs@MAs phosphor are remarkably improved due to surface protection. The WLED backlight is fabricated with optimized Si-CDs@MAs phosphor, which shows high luminous efficacy of 117.43 lm W?1 and wide color gamut (107% NTSC). Furthermore, this work provides the design principles of realizing stable narrow-band solid-state fluorescence carbon dots, suggesting its great potential for wide-color-gamut display application.

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Держатели документа:
Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangzhou, 510642, China
Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Guangdong, Maoming, 525100, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Siberian Branch of the Russian Academy of Sciences (SB RAS), Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Chen, J.; Zou, X.; Li, W.; Zhang, H.; Zhang, X.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Y.; Lei, B.
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10.

    Probing Eu2+ luminescence from different crystallographic sites in Ca10M(PO4)7:Eu2+ (M = Li, Na, and K) with β-Ca3(PO4)2-type structure / M. Chen [et al.] // Chem. Mater. - 2017. - Vol. 29, Is. 17. - P. 7563-7570, DOI 10.1021/acs.chemmater.7b02724. - Cited References: 34. - The present work was supported by the National Natural Science Foundation of China (Grants 51722202, 91622125, and 51572023), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-16-002A3). C.C.L. and C.C.S. acknowledge the financial support from the Ministry of Science and Technology of Taiwan (Contract No. MOST 104-2113-M-027-007-MY3), and M. Molokeev acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 0897-4756
   Перевод заглавия: Исследование люминесценции Eu2+ в разных кристаллографических положениях в Ca10M(PO4)7:Eu2+ (M = Li, Na and K) со структурой типа beta-Ca3(PO4)2
Кл.слова (ненормированные):
Calcium -- Doping (additives) -- Excited states -- Light emission -- Lithium -- Luminescence -- Phosphors -- Photoluminescence -- Positive ions -- Rietveld refinement -- Single crystals -- Color tuning -- Crystallographic sites -- Different distributions -- Emission bands -- Local environments -- Long wavelength bands -- Luminescent centers -- Power diffraction data -- Europium
Аннотация: Eu2+ local environments in various crystallographic sites enable the different distributions of the emission and excitation energies and then realize the photoluminescence tuning of the Eu2+ doped solid state phosphors. Herein we report the Eu2+-doped Ca10M(PO4)7 (M = Li, Na, and K) phosphors with β-Ca3(PO4)2-type structure, in which there are five cation crystallographic sites, and the phosphors show a color tuning from bluish-violet to blue and yellow with the variation of M ions. The difference in decay rate monitored at selected wavelengths is related to multiple luminescent centers in Ca10M(PO4)7:Eu2+, and the occupied rates of Eu2+ in Ca(1), Ca(2), Ca(3), Na(4), and Ca(5) sites from Rietveld refinements using synchrotron power diffraction data confirm that Eu2+ enters into four cation sites except for Ca(5). Since the average bond lengths d(Ca-O) remain invariable in the Ca10M(PO4)7:Eu2+, the drastic changes of bond lengths d(M-O) and Eu2+ emission depending on the variation from Li to Na and K can provide insight into the distribution of Eu2+ ions. It is found that the emission band at 410 nm is ascribed to the occupation of Eu2+ in the Ca(1), Ca(2), and Ca(3) sites with similar local environments, while the long-wavelength band (466 or 511 nm) is attributed to Eu2+ at the M(4) site (M = Na and K). We show that the crystal-site engineering approach discussed herein can be applied to probe the luminescence of the dopants and provide a new method for photoluminescence tuning.

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Держатели документа:
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 Crystal Physics, Kirensky Institute of Physics, Federal Research Center, KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Institute of Organic and Polymeric Materials, National Taipei University of Technology, Taipei, Taiwan
National Synchrotron Radiation Research Center, Hsinchu, Taiwan

Доп.точки доступа:
Chen, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lin, C. C.; Su, C.; Chuang, Y. -C.; Liu, Q.
}
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11.

    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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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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12.

    Photoluminescence of monoclinic Li3AlF6 crystals under vacuum ultraviolet and soft X-ray excitations / V. A. Pustovarov [et al.] // Opt. Mater. - 2015. - Vol. 49. - P. 201-207, DOI 10.1016/j.optmat.2015.09.011. - Cited References: 49. - This work was partly supported by the Ministry of Education and Science of the Russian Federation (the basic part of the government mandate); Center of Excellence "Radiation and Nuclear Technologies" (Competitiveness Enhancement Program of Ural Federal University, Russia), HASYLAB DESY (Projects Nos. 20110843, 20080119EC), European Social Fund ("Mobilitas" program, MJD219), Estonian Research Council (Institutional Research Funding IUT02-26) and Baltic Science Link project coordinated by the Swedish Research Council, VR . - ISSN 0925-3467
   Перевод заглавия: Люминесценция моноклинных кристаллов Li3AlF6 под вакуумным ультрафиолетом и мягким рентгеновским излучением

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
LiBaAlF6 single-crystals
   F-type centers
   LiBaF3 crystals
   Color-centers
   Recombination luminescence
   Rietveld refinement
   VUV spectroscopy
   Trapped excitons
   Energy-transfer
   Pure
Кл.слова (ненормированные):
Li3AlF6 -- Time-resolved luminescence -- VUV spectroscopy -- Defects
Аннотация: Using Bridgman technique we have grown monoclinic β-LiAF crystals suitable for optical studies, performed XRD-identification and Rietveld refinement of the crystal structure and carried out a photoluminescence study upon vacuum ultraviolet (VUV) and extreme ultraviolet (XUV)-excitations, using the low-temperature (T = 7.2 K) time-resolved VUV-spectroscopy technique. The intrinsic PL emission band at 340–350 nm has been identified as due to radiative recombination of self-trapped excitons. The electronic structure parameters were determined: bandgap E g ≈ 12.5 eV, energy threshold for creation of unrelaxed excitons 11.8 eV < E n < 12.5 eV . The PL emission bands at 320–325 and 450 nm were attributed to luminescence caused by lattice defects. We have discovered an efficient excitation of PL emission bands in the energy range of interband transitions ( E ex > 13.5 eV), as well as in the energy range of core transitions at 130 eV. We have revealed UV–VUV PL emission bands at 170 and 208 nm due to defects. A reasonable assumptions about the origin of the UV–VUV bands were discussed.

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Ural Federal University, 19, Mira Street, Yekaterinburg, Russian Federation
Institute of Physics, University of Tartu, 14c, Ravila Street, Tartu, Estonia
Kirensky Institute of Physics, SB RAS, Akademgorodok 50, Krasnoyarsk, Russian Federation
Far Eastern State Transport University, 47, Serysheva Street, Khabarovsk, Russian Federation
Institute of Geology and Mineralogy, SB RAS, 43, Russkaya Street, Novosibirsk, Russian Federation
Novosibirsk National Research University, 2, Pirogova Street, Novosibirsk, Russian Federation

Доп.точки доступа:
Pustovarov, V. A.; Пустоваров В. А.; Ogorodnikov, I. N.; Огородников И. Н.; Omelkov, S. I.; Омелков С. И.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Kozlov, A. V.; Козлов А. В.; Isaenko, L. I.; Исаенко Л. И.
}
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13.

Origin of color centers in the flux-grown europium gallium garnet / A. S. Aleksandrovsky [et al.] // J. Appl. Phys. - 2008. - Vol. 103, Is. 8. - Ст. 83102, DOI 10.1063/1.2902365. - Cited References: 7 . - ISSN 0021-8979

РУБ Physics, Applied
Рубрики:
SPECTRA
IONS
Кл.слова (ненормированные):
Absorption -- Europium alloys -- Garnets -- Ultraviolet radiation -- Calcium-free flux -- Flux-grown europium gallium garnet -- Color centers
Аннотация: Europium gallium garnet (EuGG) single crystals were grown from fluxes with various contents. Optical absorption spectra of EuGG grown from a flux containing calcium show an additional band in the ultraviolet and blue regions of the spectra as compared to the case of a calcium-free flux. Mossbauer spectra of the samples grown from the fluxes with different additives show no signs of other valence states of the europium ions except for 3+. However, they indicate changes in the crystal field due to the entrance of additive ions. The nature of the additional absorption must be the same as that for calcium-doped gadolinium gallium garnet, i.e., anion vacancies. Mossbauer isotope shifts and quadrupole splitting for EuGG are determined. (C) 2008 American Institute of Physics.

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Держатели документа:
[Aleksandrovsky, A. S.
Arkhipkin, V. G.
Bezmaternykh, L. N.
Gudim, I. A.
Krylov, A. S.] LV Kirenskii Inst Phys, Krasnoyarsk 660036, Russia
[Aleksandrovsky, A. S.
Arkhipkin, V. G.
Bezmaternykh, L. N.
Gudim, I. A.
Krylov, A. S.] Siberian Fed Univ, Krasnoyarsk 660079, Russia
[Vagizov, F.] Texas A&M Univ, Dept Phys, College Stn, TX 77840 USA
ИФ СО РАН
L. V. Kirensky Institute of Physics, Siberian Federal University, Akademgorodok, Krasnoyarsk 660036, Russian Federation
Department of Physics, Texas A and M University, College Station, TX 77840, United States

Доп.точки доступа:
Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Arkhipkin, V. G.; Архипкин, Василий Григорьевич; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Gudim, I. A.; Гудим, Ирина Анатольевна; Krylov, A. S.; Крылов, Александр Сергеевич; Vagizov, F.
}
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14.

    Near-infrared luminescence and color tunable chromophores based on Cr3+-Doped Mullite-Type Bi2(Ga,Al)4O9 solid solutions / C. Liu [et al.] // Inorg. Chem. - 2015. - Vol. 54, Is. 4. - P. 1876-1882, DOI 10.1021/ic502779d. - Cited References: 26. - The present work was supported by the National Natural Science Foundations of China (Grants 51002146, 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in 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 0020-1669
   Перевод заглавия: Ближняя инфракрасная люминесценция и перестраиваемые цвет хромофоры построенные на допированных Cr3+ твердых растворах Bi2(Ga,Al)4O9 со структурой муллита.

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
PERSISTENT LUMINESCENCE
   PHOSPHORS
   PIGMENT
   GARNET
   OXIDES
   FIELD
   RED
Аннотация: Cr3+-activated mullite-type Bi2Ga(4-x)AlxO9 (x = 0, 1, 2, 3, and 4) solid solutions were prepared by the solid state reaction, and their spectroscopic properties were investigated in conjunction with the structural evolution. Under excitation at 610 nm, Bi2[Ga(4-y)Aly]3.97O9:0.03Cr3+ (y = 0, 1, 2, 3, and 4) phosphors exhibited broad-band near-infrared (NIR) emission peaking at ?710 nm in the range 650?850 nm, and the optimum Cr3+ concentrations and concentration quenching mechanism were determined. Except for the interesting NIR emission, the body color changed from white (at x = 0) to green (at x = 0.08) for Bi2Ga4?xO9:xCr3+, and from light yellow (at x = 0) to deep brown (at x = 0.08) for Bi2Al4?xO9:xCr3+, respectively. Moreover, as a result of variable Al/Ga ratio, the observed body color for Bi2[Ga(4-y)Aly]3.97O9:0.03Cr3+ (y = 0, 1, 2, 3, and 4) varied from deep brown to green. The relationship between the observed colors and their diffuse reflectance spectra were also studied for the understanding of the different absorption bands. The results indicated that Cr3+-doped Bi2Ga(4-x)AlxO9 solid solutions appeared as the bifunctional materials with NIR phosphors and color-tunable pigments.

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

Доп.точки доступа:
Liu, C.; Xia, Zhiguo; Chen, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.
}
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15.

    Modulation of Bi3+ luminescence from broadband green to broadband deep red in Lu2WO6 by Gd3+ doping and its applications in high color rendering index white LED and near-infrared LED / X. Wang, X. Feng, M. S. Molokeev [и др.] // Dalton Trans. - 2023. - Vol. 52, Is. 9. - P. 2619-2630, DOI 10.1039/D2DT03751C. - Cited References: 4. - This work is supported in part by the Project of Education Department of Liaoning Province (Grant No. LQ2019014) and he Natural Science Foundation of Liaoning Province (Grant No. 2020-MS-286). The authors are thankful for the support for the 4B9A Beamline from the Beijing Synchrotron Radiation Facility (BSRF) (Project No. 2021-BEPC-PT-005290). The authors would like to thank Siqi Liu from Shiyanjia Lab ( . - ISSN 1477-9226. - ISSN 1477-9234
   Перевод заглавия: Модуляция люминесценции Bi3+ от широкополосного зеленого до широкополосного темно-красного в Lu2WO6 с помощью легирования Gd3+ и его применение в белых светодиодах с высоким индексом цветопередачи и светодиодах ближнего инфракрасного диапазона
Аннотация: Phosphors that exhibit tunable broadband emissions are highly desired in multi-functional LEDs, including pc-WLEDs and pc-NIR LEDs. In this work, broadband emissions were obtained and modulated in the unexpectedly wide spectral range of 517–609 nm for (Lu0.99−xGdxBi0.01)2WO6 phosphors by tuning the Gd3+ content (x = 0–0.99). The effects of Gd3+ doping on phase constituents, particle morphology, crystal structure, and photoluminescence were systematically investigated. Broadband green emission was obtained from Gd3+-free (Lu0.99Bi0.01)2WO6 phosphors (x = 0), whose emission intensity was enhanced by 50% with 5 at% Gd3+ (x = 0.05). The phase transition happened when x 0.50 and the broadband red-NIR emission was obtained when x = 0.75–0.99. Three luminescence centers were proved to be responsible for the broadband green emissions via crystal structure, spectral fitting and fluorescence decay analysis. A pc-WLED with a high color rendering index (Ra = 91.3), a stable emission color, and a low color temperature (3951 K) was fabricated from the (Lu0.94Gd0.05Bi0.01)2WO6 broadband green phosphor, and an LED device that simultaneously emits high color rendering index white light and NIR light was obtained with the (Gd0.99Bi0.01)2WO6 broadband red-NIR phosphor. Night vision and noninvasive imaging were also demonstrated using the latter LED device.

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Держатели документа:
College of Chemistry and Materials Engineering, Bohai University, Jinzhou, Liaoning 121007, China
Research Center for Functional Materials, National Institute for Materials Science, Tsukuba, Ibaraki 305-0044, Japan
Laboratory of Crystal Physics, Kirensky Institute of Physics, FRC KSC SB RAS, Krasnoyarsk 660036, Russia
Research and Development Department, Kemerovo State University, Kemerovo 650000, Russia
Siberian Federal University, Krasnoyarsk 660041, Russia
Jilin Engineering Laboratory for Quantum Information Technology, Institute for Interdisciplinary Quantum Information Technology, Jilin Engineering Normal University, Changchun 130052, China

Доп.точки доступа:
Wang, Xuejiao; Feng, Xiaowen; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zheng, Huiling; Wang, Qiushi; Xu, Chunyan; Li, Ji-Guang
}
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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.

    Layered hydroxyl sulfate: Controlled crystallization, structure analysis, and green derivation of multi-color luminescent (La,RE)2O2SO4 and (La,RE)2O2S phosphors (RE = Pr, Sm, Eu, Tb, and Dy) / X. Wang [et al.] // Chem. Eng. J. - 2016. - Vol. 302. - P. 577-586, DOI 10.1016/j.cej.2016.05.089. - Cited References: 50. - This work is supported in part by the National Natural Science Foundation of China (Grants Nos. 51172038, 51302032, and U1302272), the Fundamental Research Fund for the Central Universities (Grant No. N140204002), Grants-in-Aid for Scientific Research (KAKENHI No. 26420686), and the Russian Foundation for Basic Research (15-52-53080). X.J. Wang acknowledges financial support from the China Scholarship Council for her overseas Ph.D. study (Contract No. 201406080035) and the assistance of Q. Q. Zhu (University of Science and Technology of China) for his help with calcination. . - ISSN 1385-8947
   Перевод заглавия: Слоистые гидроксил сульфаты: контролируемая кристаллизация, структурный анализ, и зеленый синтез мультицветных люминофоров (La,RE)2O2SO4 и (La,RE)2O2S (RE=Pr, Sm, Eu, Tb, and Dy)

РУБ Engineering, Environmental + Engineering, Chemical
Рубрики:
PHOTOLUMINESCENCE PROPERTIES
   OXYSULFATE/OXYSULFIDE SYSTEMS
   CRYSTAL-STRUCTURE
   OXYGEN-STORAGE
   Ln
   NANOCOMPOSITES
   EMISSION
   CAPACITY
   FAMILY
   FABRICATION
Кл.слова (ненормированные):
Sulfate type layered rare earth hydroxide -- Luminescence -- Oxysulfate -- Oxysulfide
Аннотация: The two important groups of Ln2O2SO4 and Ln2O2S compounds are traditionally synthesized with the involvements of environmentally harmful sulfur-containing reagents. We developed in this work a unique green approach for their synthesis, using Ln2(OH)4SO4·2H2O layered hydroxyl sulfate as the precursor (Ln-241 phase). Phase selective crystallization of La-241 under both atmospheric pressure and hydrothermal conditions was firstly optimized, followed by transformation into La2O2S and La2O2SO4 by controlled calcination. Rietveld structure refinement was performed for La-241, La(OH)SO4, La2O2SO4, and La2O2S, and the crystal structure and cell parameters of La-241 were originally reported. The photoluminescence performances of several important activators (Pr3+, Sm3+, Eu3+, Tb3+, and Dy3+) in the two hosts, in terms of excitation, emission, quantum yield, and color coordinates of emission, were thoroughly investigated, and multi-color luminescence including bright red, green, orange red, and yellow was obtained under ultraviolet excitation. Detailed investigations of Tb3+ photoluminescence revealed that the lack of 5D3 emission in La2O2S and the gradual quenching of 5D3 blue emission at a higher Tb3+ content (hence decreasing I488/I545 ratio and changing color coordinates) in La2O2SO4 were suggested to be due to thermal activation of the 5D3 electrons into the conduction band and cross relaxation between adjacent Tb3+, respectively. The synthesis approach developed in this work for La2O2SO4 and La2O2S, with water vapor as the only exhaust gas, is environmentally benign and holds great potential in the facile synthesis of analogous compounds of other lanthanides. © 2016 Elsevier B.V.

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Держатели документа:
Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), School of Materials Science and Engineering, Northeastern University, Shenyang, Liaoning, China
Advanced Materials Processing Unit, National Institute for Materials Science, Tsukuba, Ibaraki, Japan
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:
Wang, X.; Li, J. -G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhu, Q.; Li, X.; Sun, X.
}
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18.

Hybrid anchoring for a color-reflective dual-frequency cholesteric liquid crystal device switched by low voltages / Y. C. Hsiao [et al.] // Opt. Mater. Express. - 2015. - Vol. 5, Is. 11. - P. 2715-2720, DOI 10.1364/OME.5.002715. - Cited References:17. - This work was financially sponsored by the Ministry of Science and Technology, Taiwan, under grant No. 103-2923-M-009-003-MY3, by the Russian Foundation for Basic Research (project No. 14-02-31248), and by the Siberian Branch of the Russian Academy of Sciences (SB RAS) through an NSC-SB-RAS joint project between Taiwan and Russia . - ISSN 2159-3930

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
Photonic structure
Drive scheme
Modulation
Аннотация: Cholesteric liquid crystal (CLC) materials used in electro-optical (EO) devices are characterized by high operating voltage and slow response speed, which hinders their further development in display applications. Dual-frequency CLCs (DFCLCs) can solve the problem of slow bistable transition, but the operating voltage is still high, especially in color-reflective DFCLC cells. Here we report a simple approach to lowering the switching voltage as well as to shortening the response time. This technique adopts hybrid surface treatment to modulate the structural arrangement of CLC molecules. Both planar-and vertical-alignment layers are employed and coated on one and the other substrates separately to improve the electro-optical properties of DFCLCs. We show that the threshold voltage for switching can be decreased to as low as 5 V and the shortest response time is measured to be 0.8 ms, which renders CLC EO devices including displays more practical for commercial purpose.

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Держатели документа:
Natl Chiao Tung Univ, Coll Photon, Inst Imaging & Biomed Photon, Tainan 71150, Taiwan.
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Lab Nonlinear Opt & Spect, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Hsiao, Yu-Cheng; Timofeev, I. V.; Тимофеев, Иван Владимирович; Zyryanov, V. Ya.; Зырянов, Виктор Яковлевич; Lee, Wei; Ministry of Science and Technology, Taiwan [103-2923-M-009-003-MY3]; Russian Foundation for Basic Research [14-02-31248]; Siberian Branch of the Russian Academy of Sciences (SB RAS) through an NSC-SB-RAS joint project between Taiwan and Russia
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19.

    Green-emitting Bi3+-doped La2SrSc2O7 phosphor for pc-WLED lighting: Luminescent properties and energy transfer strategy / W. Yan, Y. Wei, M. S. Molokeev [et al.] // J. Alloys Compd. - 2022. - Vol. 908. - Ст. 164621, DOI 10.1016/j.jallcom.2022.164621. - Cited References: 63. - This work was supported by the National Natural Science Foundation of China (Grant Nos. 52072349) . - ISSN 0925-8388
   Перевод заглавия: Зеленый люминофор La2SrSc2O7, легированный Bi3+, для светодиодного освещения: люминесцентные свойства и стратегия передачи энергии
Кл.слова (ненормированные):
Green phosphor -- Bi3+ -- Energy transfer strategy -- Color tuning -- Pc-WLED devices
Аннотация: The crystal structure, photoluminescence properties, thermal stability and corresponding mechanisms of the novel Bi3+, Eu3+-doped La2SrSc2O7 (LSS) phosphors have been measured and analyzed in details. The emission spectrum of LSS: 1.0%Bi3+ phosphor shows a novel green emission centered at 530 nm under 340 nm excitation, which is attributed to the 3P1→1S0 transition of Bi3+ ions. By designing Bi3+→Eu3+energy transfer strategy, luminescence colors of LSS: 1.0%Bi3+, yEu3+ (y = 0–5.0%) phosphors can be tuned from green to orange with increasing Eu3+ concentration, which achieve multiple emission colors in LSS host. The photoluminescence decay curves, average decay lifetimes, energy transfer efficiency and time-resolved emission spectra of LSS: 1.0%Bi3+, yEu3+ (y = 0–5.0%) phosphors prove the existence of energy transfer from Bi3+ to Eu3+. The prototype pc-WLED device with green-emitting LSS: 1.0%Bi3+ possesses high color rendering index (CRI = 96.0) and low correlated color temperature (CCT = 4306 K). These results provide clear evidences that LSS: Bi3+and LSS: 1.0%Bi3+, Eu3+ phosphors would be novel promising green-to-orange tunable phosphor candidates for pc-WLED applications.

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Держатели документа:
Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices, Hubei University of Arts and Science, Hubei, Xiangyang, 441053, China
Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, 388 Lumo Road, Wuhan, 430074, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, FRC KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Yan, W.; Wei, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wang, S.; Li, G.
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20.

    Enhanced luminescence performance of CaO:Ce3+,Li+,F- phosphor and its phosphor-in-glass based high-power warm LED properties / J. Deng [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 15. - P. 4077-4086, DOI 10.1039/c8tc00813b. - Cited References: 44. - The present study was supported by the National Natural Science Foundation of China (Grant No. 21671070), the Project for Construction of High-level University in Guangdong Province, the Teamwork Projects funded by the Guangdong Natural Science Foundation (Grant No. S2013030012842), the Guangzhou Science & Technology Project (No. 201704030086) and the Open Project Fund from Key Laboratory of Advanced of Materials of Yunnan Province (No. 2018KF01). . - ISSN 2050-7534
   Перевод заглавия: Улучшенные характеристики люминесценции CaO: Ce3 +, Li +, F- люминофора и мощные тепловые свойства светодиодной лампы, созданной на его основе
Кл.слова (ненормированные):
Correlated color temperature -- Critical concentration -- Doping concentration -- Enhanced luminescence -- High color rendering index -- High power white LED -- High temperature solid-state reaction -- Thermal and chemical stabilities
Аннотация: To obtain white light-emitted diodes (wLEDs) with a low correlated color temperature (CCT) and a high color rendering index (CRI), red-emission is indispensable in their emission spectra. Herein, CaO:Ce3+,Li+,F- yellow phosphors with more red spectral component have been prepared via a high temperature solid-state reaction. As compared to the F- undoped samples, CaO:Ce3+,Li+,F- phosphor have lower critical doping concentration of Ce3+ and show stronger luminescence. At the critical concentration, a quantum efficiency of 66.4% and enhanced thermal and chemical stability were obtained in CaO:Ce3+,Li+,F-. Furthermore, a CaO:Ce3+,Li+,F--based phosphor-in-glass (PiG) using the red-emitting glass system with the composition of SiO2-Na2CO3-Al2O3-CaO:Eu3+ as the host material was constructed and used for high-power white LED applications. Such PiG samples with different phosphor doping concentrations can satisfy various light color demands and display higher reliability than the CaO:Ce3+,Li+,F- phosphor. An optimal PiG-based wLED exhibits color coordinates of (0.3769, 0.3386), a CCT of 3774 K, a CRI of 82.5 and a LE of 73.1 when the mass ratio of phosphor to glass matrix was 7:50 in PiG. Moreover, such PiG-based wLED also showed acceptable color stability under different drive currents. All the above results demonstrate that CaO:Ce3+,Li+,F- can be expected to be a potential alternative yellow phosphor for blue light excited PiG based warm wLEDs, particularly for high-power devices.

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Держатели документа:
Guangdong Provincial Engineering Technology Research Center for Optical Agricultural, College of Materials and Energy, South China Agricultural University, Guangzhou, 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
Siberian Federal University, Krasnoyarsk, Russian Federation
Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming, China
Department of Physics, Georgia Southern University, Statesboro, GA, United States

Доп.точки доступа:
Deng, J.; Zhang, H.; Zhang, X.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Qiu, J.; Liu, Y.; Lei, B.; Ma, L.; Wang, X.
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