Главная
Авторизация
Фамилия
Пароль
 

Базы данных


Труды сотрудников ИФ СО РАН - результаты поиска

Вид поиска

Область поиска
в найденном
Формат представления найденных документов:
полныйинформационныйкраткий
Отсортировать найденные документы по:
авторузаглавиюгоду изданиятипу документа
Поисковый запрос: (<.>K=Substitution<.>)
Общее количество найденных документов : 95
Показаны документы с 1 по 10
 1-10    11-20   21-30   31-40   41-50   51-60      
1.
   В37
   K64


    Knyazev, Yu. V.
    The influence of cationic substitution on the magnetic properties of cobalt ludwigite [Manuscript] : Doctoral thesis in physics / Yu. V. Knyazev. - Krasnoyarsk, 2017. - 99 p. - Bibliogr.: P. 54-57. - ISBN 978-5-7638-3771-1
Диссертация . - [S. l. : s. n.]
ГРНТИ
ББК В379.312я031


Диссертация Князев, Юрий Владимирович. Влияние катионного замещения на магнитные свойства кобальтовых людвигитов [Рукопись] : дис. на соиск. уч. степени канд. физ.-мат. наук : 01.04.11 / Ю. В. Князев ; науч. рук. Н. В. Казак, 2016. - 128 с.

Держатели документа:
Библиотека Института физики им. Л.В. Киренского СО РАН
Доп.точки доступа:
Князев, Юрий Владимирович; Siberian Federal University
Экземпляры всего: 1
ДС (1)
Свободны: ДС (1)}
Найти похожие
2.


   
    Rapid synthesis of red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors and the tunable photoluminescence via Sr/Ba substitution / Z. Y. Yang, Y. Y. Zhou, J. W. Qiao [et al.] // Adv. Opt. Mater. - 2021. - Vol. 9. Is. 16. - Ст. 2100131, DOI 10.1002/adom.202100131. - Cited References: 44. - Z.Y. and Y.Z. contributed equally to this work. This research was supported by the National Natural Science Foundations of China (Grant Nos. 51972118 and 51961145101), International Cooperation Project of National Key Research and Development Program of China (No. 2021YFE0105700), Guangzhou Science & Technology Project (No. 202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (No. 2017BT01x137). This work was also funded by RFBR according to the research Project No. 19-52-80003 . - ISSN 2195-1071
   Перевод заглавия: Синтез люминофоров Sr2Sc0.5Ga1.5O5: Eu2+ с красным излучением и перестраиваемая фотолюминесценция за счет замещения Sr/Ba
РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
LUMINESCENCE PROPERTIES
   THERMAL-STABILITY

   EU2+

   GREEN

   EU3+

   SR

Кл.слова (ненормированные):
Eu2+-doped phosphors -- light-emitting diodes -- photoluminescence -- red emission
Аннотация: Discovering new Eu2+-doped red-emitting phosphors in oxide-based materials is a challenge for white light-emitting diode (WLED) applications. Herein, a highly efficient high-frequency induction heating method is employed to rapidly prepare the red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors peaking at 614 nm and exhibiting a high photoluminescence quantum yield of 78.4% under the excitation of 440 nm. The structural and spectral analyses suggest that Eu2+ ions tend to enter the [Sc1/Ga1O6] and [Ga2O6] polyhedrons with small coordination numbers, leading to the broadband red emission originated from large crystal field splitting of Eu2+ 5d level. The chemical substitution of Ba in the Sr site enhances the thermal stability and helps to the photoluminescence tuning from 614 to 728 nm in SrBaSc0.5Ga1.5O5:Eu2+. The WLED device fabricated by blending the red Sr1.7Ba0.3Sc0.5Ga1.5O5:Eu2+ and yellow Y3(Al, Ga)5O12:Ce3+ phosphors shows a high color-rendering index (Ra = 91.1), and low color-correlated temperature (CCT = 4750 K). This study aims to provide a new synthesis method and design principle for guiding the development of Eu2+-doped oxide-based red phosphors with low preparation cost; moreover, the photoluminescence tuning strategy via cation substitutions is essential to achieve tunable emission, even the near-infrared luminescence.

Смотреть статью,
Scopus,
WOS
Держатели документа:
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Engn,Guangdong Engn Technol Res & D, Guangzhou 510641, Guangdong, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Dept Res & Dev, Kemerovo 650000, Russia.
South China Univ Technol, Sch Phys & Optoelect, Guangzhou 510641, Guangdong, Peoples R China.

Доп.точки доступа:
Yang, Zhiyu; Zhou, Yayun; Qiao, Jianwei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo
}
Найти похожие
3.


   
    The effect of iron substitution on the structure and electronic properties of Cr2SiC by theoretical method / J. Olshevskaya, A. Shubin, A. Kovaleva, F. N. Tomilin // International workshop on the properties of functional MAX-materials (2nd FunMax) : book of abstracts / org. com. M. Farle [et al.]. - 2021. - P. 42

Материалы конференции,
Читать в сети ИФ

Доп.точки доступа:
Farle, M. \org. com.\; Ovchinnikov, S. G. \org. com.\; Овчинников, Сергей Геннадьевич; Tarasov, A. S. \org. com.\; Тарасов, Антон Сергеевич; Smolyarova, T. E. \org. com.\; Смолярова, Татьяна Евгеньевна; Olshevskaya, J.; Shubin, A.; Kovaleva, A.; Tomilin, F. N.; Томилин, Феликс Николаевич; International workshop on functional MAX-materials(2 ; 2021 ; Sept. 14-17 ; Krasnoyarsk (on-line)); Kirensky Institute of Physics; Siberian Federal Univercity
}
Найти похожие
4.


   
    Sb3+dopant and halogen substitution triggered highly efficient and tunable emission in lead-free metal halide single crystals / Y. Jing, Y. Liu, X. Jiang [et al.] // Chem. Mater. - 2020. - Vol. 32, Is. 12. - P. 5327-5334, DOI 10.1021/acs.chemmater.0c01708. - Cited References: 46. - This work is supported by the National Natural Science Foundation of China (51961145101, 51972118, and 51722202), Fundamental Research Funds for the Central Universities (FRFTP-18-002C1), Guangzhou Science & Technology Project (202007020005), Guangdong Provincial Science &Technology Project (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 0897-4756
   Перевод заглавия: Высокоэффективное и перестраиваемое излучение в монокристаллах бессвинцовых металлогалогенидов допированных Sb3+
Кл.слова (ненормированные):
Crystal structure -- Excitons -- Lead compounds -- Luminescence -- Metals
Аннотация: Rational doping and compositional control remain significant challenges in designing luminescent metal halides to achieve highly efficient and tunable emission. Here, the air-stable lead-free Cs2InCl5·H2O crystal with a zero-dimensional structure was investigated as a pristine compound to design new luminescence materials. Sb3+-doping in Cs2InCl5·H2O:Sb3+ enabled broadband yellow emission with a photoluminescence quantum yield up to 95.5%. The emission colors can be expanded into the orange-red region by halogen compositional substitution for Cs2InX5·H2O:Sb3+ (X = Cl/Br/I). The optical characterizations along with the theoretical calculations demonstrate that the characteristic singlet and triplet self-trapped exciton emissions of ns2-metal-halide centers account for the tunable luminescence. Moreover, the admirable stability against air and heat pave way for its further applications in white light-emitting diodes and high-resolution fluorescent signs in anticounterfeiting technology. Our achievement in the case of Sb3+-doped Cs2InCl5·H2O represents a successful strategy for developing stable lead-free metal halides with highly efficient emission for versatile optical applications.

Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Держатели документа:
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, China
Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, 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
University of Chinese Academy of Sciences, Beijing, 100049, China
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Technology, South China University of Technology, Guangzhou, 510640, China

Доп.точки доступа:
Jing, Y.; Liu, Y.; Jiang, X.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lin, Z.; Xia, Z.
}
Найти похожие
5.


   
    Effect of R substitution in spin glass RFeTi2O7 compounds / A. Arauzo, J. Bartolome, J. Luzon [et al.] // J. Magn. Magn. Mater. - 2020. - Vol. 515. - Ст. 167273, DOI 10.1016/j.jmmm.2020.167273. - Cited References: 38. - This study has been financed by MECOM Project MAT2014-53921-R, MICINN Project MAT2017-83468-R and Gobierno de Aragón RASMIA E12_17R. Authors would like to acknowledge the use of Servicio General de Apoyo a la Investigación-SAI, Universidad de Zaragoza . - ISSN 0304-8853
   Перевод заглавия: Влияние замещения редкоземельного иона R в спинстекольных соединениях RFeTi2O7
Кл.слова (ненормированные):
Magnetism -- Spin glass -- Anisotropy -- Frustration -- Anisotropic exchange
Аннотация: Zirconolite oxides R3+Fe3+Ti2O7 (R rare earth element) are known to exhibit spin glass behaviour at low temperatures. Here we present a detailed study of these compounds for R = Eu, Gd, Dy, Ho, and Er, together with reviewed previous measurements on Sm, Tb, Tm, Yb and Lu, with the scope of determining the role played by the rare earth on their magnetic properties. They have been investigated using X-ray powder diffraction, and further characterized by magnetization, frequency dependent ac susceptibility and heat capacity measurements. RFeTi2O7 compounds are all isostructural showing orthorhombic structure, space group Pcnb at 300 K. Disorder of the magnetic ions in the RFeTi2O7 lattice induces spin glass behaviour at low temperatures, mainly due to the Fe sublattice. We show that magnetic rare earth ions participate in the spin glass state tuning its properties. The single ion anisotropy of the R3+ ions, excluding exchange interaction with other magnetic ions, has been calculated by ab initio methods, and expressed in terms of the g tensor of the ground doublet or quasi-doublet in Kramers (Sm, Dy, Er, Yb) and non-Kramers (Tb, Ho) ions, respectively, in an effective spin S* = 1/2 model. In the case of R with a singlet ground state (Eu, Tm) or a multiplet state (Gd), the ion is isotropic. We show that the relative increase in the spin-glass temperature ΔTSGR/TSGFe with respect to the LuFeTi2O7, where Lu is non-magnetic, correlates qualitatively with the product of the ratio gz/gJ (R = Tb, Dy, Ho, and Er), or g⊥/gJ (R = Sm), times the ratio of exchange interactions JR,Fe/JFe,Fe determined from the paramagnetic room temperature susceptibility measurements. Besides, for increasing anisotropy the spin glass transition dynamics slows down to values typical of cluster glass. The coercive field below the transition is increased in the same trend. This paper explains the effect of the R-Fe exchange interaction and R single ion anisotropy on the spin-glass behaviour of these compounds.

Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Держатели документа:
Instituto de Nanociencia y Materiales de Aragon (INMA) and Departamento de Fisica de la Materia Condensada, CSIC- Universidad de Zaragoza, Zaragoza, 50009, Spain
Servicio de Medidas Fisicas, Universidad de Zaragoza, Zaragoza, E-50009, Spain
Centro Universitario de la Defensa, Academia General Militar, Zaragoza, Spain
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok, 50/38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Arauzo, A.; Bartolome, J.; Luzon, J.; Drokina, T. V.; Дрокина, Тамара Васильевна; Petrakovskii, G. A.; Петраковский, Герман Антонович; Molokeev, M. S.; Молокеев, Максим Сергеевич
}
Найти похожие
6.


   
    Li/Na substitution and Yb3+ co-doping enabling tunable near-infrared emission in LiIn2SbO6:Cr3+ phosphors for light-emitting diodes / G. Liu, T. Hu, M. S. Molokeev, Z. Xia // iScience. - 2021. - Vol. 24, Is. 4. - Ст. 102250, DOI 10.1016/j.isci.2021.102250. - Cited References: 45. - The present work was supported by the National Natural Science Foundation of China of China (Grant Nos. 51972118 and 51961145101), the Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science & Technology Project (202007020005), the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Pro-gram (2017BT01X137), and RFBR according to the research project No. 19-52-80003 . - ISSN 2589-0042
   Перевод заглавия: Замещение Li/Na и содопирование Yb3+, позволяющее настраивать излучение в ближней инфракрасной области в люминофорах LiIn2SbO6: Cr3+ для светоизлучающих диодов
Кл.слова (ненормированные):
Inorganic Chemistry -- Optical Materials -- Photonics
Аннотация: Near-infrared (NIR) phosphor-converted light-emitting diode (pc-LED) has great potential in non-invasive detection, while the discovery of tunable broadband NIR phosphor still remains a challenge. Here, we report that Cr3+-activated LiIn2SbO6 exhibits a broad emission band ranging from 780 to 1400 nm with a full width at half maximum (FWHM) of 225 nm upon 492 nm excitation. The emission peaks are tuned from 970 to 1020 nm together with considerable broadening of FWHM (∼285 nm) via Li/Na substitution. Depending on Yb3+ co-doping, a stronger NIR fluorescence peak of Yb3+ appears with improved thermal resistance, which is ascribed to efficient energy transfer from Cr3+ to Yb3+. An NIR pc-LED package has been finally designed and demonstrated a remarkable ability to penetrate pork tissues (∼2 cm) so that the insertion depth of a needle can be observed, indicating that the phosphor can be applied in non-destructive monitoring.

Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Держатели документа:
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, Guangdong Engineering Technology Research and Development Center of Special Optical Fiber Materials and Devices, 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:
Liu, G.; Hu, T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.
}
Найти похожие
7.


    Удод, Любовь Викторовна.
    Влияние катионного замещения на магнитные свойства и электрическую поляризацию в системе Bi2(Sn0.9Ме0.1)2O7, Ме =Cr3+, Fe3 / Л. В. Удод, О. Б. Романова // Новое в магнетизме и магнитных материалах : сборник трудов XXIV международной конференции / прогр. ком.: Р. С. Исхаков, С. Г. Овчинников [и др.]. - 2021. - Секция 1: Новые магнитные и родственные им материалы: синтез и физические свойства. - С. 98-101. - Библиогр.: 13. - Исследование выполнено при финансовой поддержке программы No 3.5743.2021/6.7
   Перевод заглавия: Effect of cationic substitution on magnetic properties and electric polarization in the Bi2(Sn0.9Me0.1)2O7, Me = Cr3 +, Fe3 + system
Аннотация: Исследовано влияние гетерогенного замещения ионами Cr3+и Fe3+ на магнитные свойства и электрическую поляризацию пиростанната висмута.Установлена зависимость магнитных свойств от степени заполнения электронных оболочек ионов хрома и железа. Найден гистерезис поляризации в Bi2(Sn0.9Cr0.1)2O7.
The effect of heterogeneous substitution by Cr3+ and Fe3+ ions on the magnetic properties and electric polarization of bismuth pyrostannate is investigated. The dependence of the magnetic properties on the degree of filling of the electron shells of chromium and iron ions has been established. The hysteresis of polarization was found in Bi2(Sn0.9Cr0.1)2O7.

Материалы конференции,
Читать в сети ИФ
Держатели документа:
Институт физики им. Л.В. Киренского СО РАН

Доп.точки доступа:
Исхаков, Рауф Садыкович \прогр. ком.\; Iskhakov, R. S.; Овчинников, Сергей Геннадьевич \прогр. ком.\; Ovchinnikov, S. G.; Романова, Оксана Борисовна; Romanova, O. B.; Udod, L. V.; "Новое в магнетизме и магнитных материалах", международная конференция(24 ; 2021 ; 1-8 июля ; Москва); Научный совет по физике конденсированных сред РАН; МИРЭА - Российский технологический университет; Московский государственный университет им. М.В. Ломоносова; Магнитное общество России
}
Найти похожие
8.


   
    Structural and spectroscopic effects of Li+ substitution for Na+ in LixNa1-xCaGd0.5Ho0.05Yb0.45(MoO4)3 scheelite-type upconversion phosphors / C.-S. Lim, A. S. Aleksandrovsky, M. S. Molokeev [et al.] // Molecules. - 2021. - Vol. 26, Is. 23. - Ст. 7357, DOI 10.3390/molecules26237357. - Cited References: 77. - This study was supported by the Research Program through the Campus Research Foundation funded by Hanseo University in 2021 (211Yunghap06) . - ISSN 1420-3049
   Перевод заглавия: Структурные и спектральные эффекты замещения Na+ ионами Li+ в LixNa1-xCaGd0.5Ho0.05Yb0.45(MoO4)3 шеелитоподобном апконверсионном люминофоре
Кл.слова (ненормированные):
optical materials -- chemical synthesis -- molybdate -- Raman spectroscopy -- X-ray diffraction; phosphors -- phosphors
Аннотация: A set of new triple molybdates, LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45, was successfully manufactured by the microwave-accompanied sol–gel-based process (MAS). Yellow molybdate phosphors LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45 with variation of the LixNa1-x (x = 0, 0.05, 0.1, 0.2, 0.3) ratio under constant doping amounts of Ho3+ = 0.05 and Yb3+ = 0.45 were obtained, and the effect of Li+ on their spectroscopic features was investigated. The crystal structures of LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45 (x = 0, 0.05, 0.1, 0.2, 0.3) at room temperature were determined in space group I41/a by Rietveld analysis. Pure NaCaGd0.5Ho0.05Yb0.45(MoO4)3 has a scheelite-type structure with cell parameters a = 5.2077 (2) and c = 11.3657 (5) Å, V = 308.24 (3) Å3, Z = 4. In Li-doped samples, big cation sites are occupied by a mixture of (Li,Na,Gd,Ho,Yb) ions, and this provides a linear cell volume decrease with increasing Li doping level. The evaluated upconversion (UC) behavior and Raman spectroscopic results of the phosphors are discussed in detail. Under excitation at 980 nm, the phosphors provide yellow color emission based on the 5S2/5F4 → 5I8 green emission and the 5F5 → 5I8 red emission. The incorporated Li+ ions gave rise to local symmetry distortion (LSD) around the cations in the substituted crystalline structure by the Ho3+ and Yb3+ ions, and they further affected the UC transition probabilities in triple molybdates LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45. The complex UC intensity dependence on the Li content is explained by the specificity of unit cell distortion in a disordered large ion system within the scheelite crystal structure. The Raman spectra of LixNa1-xCaGd0.5(MoO4)3 doped with Ho3+ and Yb3+ ions were totally superimposed with the luminescence signal of Ho3+ ions in the range of Mo–O stretching vibrations, and increasing the Li+ content resulted in a change in the Ho3+ multiplet intensity. The individual chromaticity points (ICP) for the LiNaCaGd(MoO4)3:Ho3+,Yb3+ phosphors correspond to the equal-energy point in the standard CIE (Commission Internationale de L’Eclairage) coordinates.

Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Держатели документа:
Department of Aerospace Advanced Materials and Chemical Engineering, Hanseo University, Seosan 31962, Korea
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, 660041 Krasnoyarsk, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, 660041 Krasnoyarsk, Russia
Department of Physics, Far Eastern State Transport University, 680021 Khabarovsk, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
School of Engineering and Construction, Siberian Federal University, 660041 Krasnoyarsk, Russia
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, 630090 Novosibirsk, Russia
Research and Development Department, Kemerovo State University, 650000 Kemerovo, Russia
Department of Industrial Machinery Design, Novosibirsk State Technical University, 630073 Novosibirsk, Russia

Доп.точки доступа:
Lim, Chang-Sung; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Atuchin, V. V.
}
Найти похожие
9.


   
    The Influence Of Anionic Substitution With Structural And Electrical Properties Of Mn - Se - Те Chalkogenides [Text] / S. Aplesnin, O. Romanova, E. Eremin [et al.] // Moscow Int. Symp. on Magnet. (MISM-2011) : Book of abstracts. - 2011. - Ст. 24PO-I2-27. - P. 693

Материалы конференции,
Читать в сети ИФ

Доп.точки доступа:
Aplesnin, S.; Romanova, O.; Eremin, E.; Ryabinkina, L.; Demidenko, O.; Makovetskii, G.; Yanushkevich, K.; Moscow International Symposium on Magnetism(5 ; 2011 ; Aug. ; 21-25 ; Moscow)
}
Найти похожие
10.


   
    Enhanced luminescence properties of Li2MgTiO4: Mn4+, Ge4+ phosphor via single cation substitution for indoor plant cultivation / S. Zhang, S. Gai, X. Zhang [et al.] // Ceram. Int. - 2022. - Vol. 48. Is. 3. - P. 3070-3080, DOI 10.1016/j.ceramint.2021.10.082. - Cited References: 41. - The authors would like to gratefully acknowledge funds from National Natural Science Foundation of China (Grant No. 51974123), the Distinguished Youth Foundation of Hunan Province (Grant No. 2020JJ2018), Key R & D projects in Hunan Province (2020WK2016 & 2020SK2032), Hunan High Level Talent Gathering Project (2019RS1077 & 2020RC5007), the Natural Sciences Foundation of Hunan Agricultural University (19QN11), Hunan Provincial Key Laboratory of Crop Germplasm Innovation and Resource Utilization Science Foundation (19KFXM12), Changsha Science and technology plan (KH2005114), and the Scientific Research Fund of Hunan Provincial Education Department (19C0903) . - ISSN 0272-8842
   Перевод заглавия: Улучшение люминесцентных свойств люминофора Li2MgTiO4: Mn4+, Ge4+ путем замещения одного катиона при выращивании комнатных растений
Кл.слова (ненормированные):
Mn4+ -- Titanate -- Cationic substitution -- Indoor plant cultivation
Аннотация: Red and far-red emitting phosphors have been widely used in phosphor-converted light emitting diode (pc-LED) devices to provide lighting for indoor plant growth, thus achieving desired product qualities. Among the many ways to optimize phosphors’ optical performance, cationic substitution is one of the most effective methods. In this study, red phosphors (Li2MgTi1-x-yO4: xMn4+, yGe4+) were synthesized by high temperature solid state method and the optical performance of phosphors were improved with increasing Ge4+ constituents. In particular, luminescence intensity of Li2MgTiO4: 0.002Mn4+, 0.1Ge4+ increased by 152% under 468 nm excitation, and the thermostability of emission intensity increases from 22% (y = 0) to 43% (y = 0.1), which is about twice as much. Finally, pc-LED device was fabricated via the red phosphor Li2MgTiO4: 0.002Mn4+,0.1Ge4+ coated on a 470 nm ultraviolet chip. By changing the proportion of the phosphor, the electroluminescence spectra of pc-LED device could match well with the absorption regions of plant pigments. Therefore, Li2MgTiO4: 0.002Mn4+, 0.1Ge4+ phosphor has potential application in plant lighting. Furthermore, this work can offer some helpful references for improving luminescent efficiency by simply modulating the chemical composition.

Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Держатели документа:
School of Pharmaceutical Sciences, Jishou University, Jishou, 416000, China
School of Chemistry and Materials Science, Hunan Agricultural University, Changsha, 410128, China
Hunan Provincial Engineering Technology Research Center for Optical Agriculture, Hunan Agricultural University, Changsha, 410128, China
College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, 410128, China
Xiangfeng Tea Group Co. Ltd, No. 139 Tianhua North Road, Changsha, Hunan, China
Hunan Rare Earth Metal Material Research Institute Co. Ltd, No. 108 Longyuan 2nd Road, Longping High-tech Park, Changsha, Hunan, 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

Доп.точки доступа:
Zhang, S.; Gai, S.; Zhang, X.; Xia, M.; Zhou, Z.; Cheng, X.; Yao, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Feng, Q.
}
Найти похожие
 1-10    11-20   21-30   31-40   41-50   51-60      
 

Другие библиотеки

© Международная Ассоциация пользователей и разработчиков электронных библиотек и новых информационных технологий
(Ассоциация ЭБНИТ)