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1.
Insights into Ba4Si6O16
structure and photoluminescence tuning of Ba4Si6O16:Ce3+,Eu2+ phosphors / Chen M. [et al.]> // J. Mater. Chem. C. - 2015. -
Vol. 3
,
Is. 48
. - P. 12477-12483,
DOI
10.1039/c5tc03271g. - Cited References: 39. - This work was supported by the National Natural Science Foundations of China (Grant No. 51572023 and 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306), and Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1). . - ISSN 2050-7534
Перевод заглавия:
Исследования структуры Ba4Si6O16 и люминесцентных свойств Ba4Si6O16:Ce3+,Eu2+
РУБ
Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
LIGHT-EMITTING-DIODES
ENERGY-TRANSFER
LUMINESCENCE PROPERTIES
WHITE-LIGHT
GLASS-CERAMICS
BA PHOSPHORS
EMISSION
GREEN
EU2+
FLUORESCENCE
Аннотация:
The versatile polymorphism and chemical compositions of barium silicates have been studied for a long time and their crystal structures have been established. Herein, we focused on the understanding of the crystal structure of the Ba4Si6O16 phase and the structural correlation of Ba4Si6O16 and Ba2Si3O8; moreover, the luminescence properties of Ce3+,Eu2+-co-activated Ba4Si6O16 phosphors have been discussed. Ba4Si6O16:Ce3+,Eu2+ phosphors show tunable blue-
green
emission upon excitation with 365 nm ultraviolet (UV) light. The blue emission originates from Ce3+, whereas the bluish-
green
emission is ascribed to Eu2+, and variation in the emission peak wavelength from 442 to 497 nm can be achieved by properly tuning the Ce3+/Eu2+ ratio. Energy transfer from Ce3+ to Eu2+ in the Ba4Si6O16 host has been validated by the variation of emission spectra as well as the variation of Ce3+ decay lifetimes with increasing Eu2+ concentration, and the energy transfer mechanism is demonstrated to be a resonant type via a dipole-dipole process. The results suggest that Ba4Si6O16:Ce3+,Eu2+ phosphors are potential candidates as a blue-
green
component for UV-excited white light-emitting diodes. © 2015 The Royal Society of Chemistry.
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Держатели документа:
Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Доп.точки доступа:
Chen M.; Xia Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu Q.
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2.
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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3.
Preparation, structure, and
up-conversion luminescence of Yb3+/Er3+ codoped SrIn2O4 phosphors / M. Guan [et al.]> // J. Am. Ceram. Soc. - 2015. -
Vol. 98
,
Is. 4
. - P. 1182-1187,
DOI
10.1111/jace.13415. - Cited References:26. - This present work was supported by the National Natural Science Foundations of China (grant no. 51202226), the Fundamental Research Funds for the Central Universities (grant nos. 292014125,2652013128, 2652013043), and the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006). . - ISSN 0002. - ISSN 1551-2916
Перевод заглавия:
Синтез, структура и ап-конверсионная люминесценция SrIn2O4 допированного Yb3+/Er3+
РУБ
Materials Science, Ceramics
Рубрики:
CORE-SHELL NANOPARTICLES
DOPED CaIn2O4
GREEN
Er3+
EMISSION
GLASSES
Аннотация:
SrIn2O4, which shows lower phonon energy than CaIn2O4, is not only a good photocatalyst but also can be an excellent up-conversion (UC) host to exhibits UC luminescence. In this work, Yb3+ and/or Er3+ doped SrIn2O4 phosphors were synthesized, and their UC luminescence properties were studied and compared with those in the CaIn2O4 host. The structure of SrIn2O4: 0.01Er3+ and SrIn2O4: 0.1Yb3+/0.01Er3+ samples were refined by the Rietveld method and found to that SrIn2O4: 0.1Yb3+/0.01Er3+ showed increasing unit cell parameters and cell volume, indicating In3+ sites were substituted successfully by Yb3+ and/or Er3+ ions. From the UC luminescence spectra and diffuse reflection spectra, Er3+-doped SrIn2O4 showed very weak luminescence due to ground state absorption of Er3+; Yb3+/Er3+ codoped SrIn2O4 presented strong
green
(550 nm) and red (663 nm) UC emissions which were assigned to energy transfer from Yb3+ transition 2F7/2→2F5/2 to the Er3+ transition 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2. Comparing with CaIn2O4, Yb3+/Er3+ codoped SrIn2O4 showed obvious advantages with higher UC luminescent intensity. The pumping powers study showed that UC emissions in Yb3+/Er3+ codoped SrIn2O4 were attributed to energy transfer of Yb3+→Er3+ with a two-photon process. The possible UC luminescent mechanism of Yb3+/Er3+-doped SrIn2O4 was discussed.
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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, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia
Univ Auckland, Dept Chem & Mat Engn, Auckland 1142, New Zealand
Доп.точки доступа:
Guan, Ming; Zheng, Hong; Mei, Lefu; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xie, Jing; Yang, Tao; Wu, Xiaowen; Huang, Saifang; Huang, Zhaohui
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4.
Preparation, crystal structure
and up-conversion luminescence of Er3+, Yb3+ co-doped Gd2(WO4)3 / M. Yin [et al.]> // RSC Adv. - 2015. -
Vol. 5
,
Is. 89
. - P. 73077-73082,
DOI
10.1039/c5ra12959a. - Cited References: 43. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51472223), the Fundamental Research Funds for the Central Universities (Grant No. 2652015008), and New Century Excellent Talents in University of Ministry of Education of China (Grant No. NCET-12-0951). . - ISSN 2046-2069
Перевод заглавия:
Синтез, кристаллическая структура и люминесценция с апконверсией Gd2(WO4)3 содопированного Er3+, Yb3+
РУБ
Chemistry, Multidisciplinary
Рубрики:
HYDROTHERMAL SYNTHESIS
ENERGY-TRANSFER
RED PHOSPHORS
NANOCRYSTALS
EMISSION
GREEN
HO
TEMPERATURE
TUNGSTATES
TM
Аннотация:
Up-conversion (UC) phosphors Gd2(WO4)3:Er3+/Yb3+ were synthesized by a high temperature solid-state reaction method. The crystal structure of Gd2(WO4)3:3% Er3+/10% Yb3+ was refined by Rietveld method and it was showed that Er3+/Yb3+ were successfully doped into the host lattice replacing Gd3+. Under 980 nm laser excitation, intense
green
and weak red emissions centered at around 532 nm, 553 nm, and 669 nm were observed, which were assigned to the Er3+ ion transitions of 4H11/2 → 4I15/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2, respectively. The optimum Er3+ doping concentration was determined as 3 mol% when the Yb3+ concentration was fixed at 10 mol%. The pump power study indicated that the energy transfer from Yb3+ to Er3+ in Er3+, Yb3+ co-doped Gd2(WO4)3 was a two-photon process, and the related UC mechanism of energy transfer was discussed in detail. This journal is © The Royal Society of Chemistry.
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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, China University of GeosciencesBeijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Доп.точки доступа:
Yin, Mengyan; Liu, Yangai; Mei, Lefu; Molokeev, M. S.; Молокеев, Максим Сергеевич; Huang, Zhaohui; Fang, Minghao
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5.
Eu2+ site preferences
in the mixed cation K2BaCa(PO4)2 and thermally stable luminescence / J. W. Qiao [et al.]> // J. Am. Chem. Soc. - 2018. -
Vol. 140
,
Is. 30
. - P. 9730-9736,
DOI
10.1021/jacs.8b06021. - Cited References: 40. - This work is supported by the National Natural Science Foundation of China (No. 51722202, 91622125, 51572023, and 11574003), Natural Science Foundations of Beijing (2172036) and M.M. acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 0002-7863
Перевод заглавия:
Предпочтительное положение ионов Eu2+ в смешанных катионах K2BaCa(PO4)2 и термически стабильная люминесценция
РУБ
Chemistry, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
SOLID-SOLUTION
PHOSPHORS
GREEN
BLUE
Аннотация:
Site preferences of dopant Eu2+ on the locations of K+, Ba2+, and Ca2+ in the mixed cation phosphate K2BaCa(PO4)2 (KBCP) are quantitatively analyzed via a combined experimental and theoretical method to develop a blue-emitting phosphor with thermally stable luminescence. Eu2+ ions are located at K2 (M2) and K3 (M3) sites of KBCP, with the latter occupation relatively more stable than the former, corresponding to emissions at 438 and 465 nm, respectively. KBCP:Eu2+ phosphor exhibits highly thermal stable luminescence even up to 200 °C, which is interpreted as due to a balance between thermal ionization and recombination of Eu2+ 5d excited-state centers with the involvement of electrons trapped at crystal defect levels. Our results can initiate more exploration of activator site engineering in phosphors and therefore allow predictive control of photoluminescence tuning and thermally stable luminescence for emerging applications in white LEDs.
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Держатели документа:
Univ Sci & Technol Beijing, Beijing Municipal Key Lab New Energy Mat & Techno, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
Anhui Normal Univ, Dept Phys, Anhui Key Lab Optoelect Mat Sci & Technol, Wuhu 241000, Anhui, Peoples R China.
RAS, SB, KSC, Lab Crystal Phys,Kirensky Inst Phys,Fed Res Ctr, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan.
Доп.точки доступа:
Qiao, Jianwei; Ning, Lixin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chuang, Yu-Chun; Liu, Quanlin; Xia, Zhiguo
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6.
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.
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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
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