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    Two-site Cr3+ occupation in the MgTa2O6:Cr3+ phosphor toward broad-band near-infrared emission for vessel visualization / G. C. Liu, M. S. Molokeev, B. F. Lei, Z. G. Xia // J. Mater. Chem. C. - 2020. - Vol. 8, Is. 27. - P. 9322-9328, DOI 10.1039/d0tc01951h. - Cited References: 52. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51972118, 51961145101 and 51722202), Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science & Technology Project (202007020005), the Guangdong Provincial Science & Technology Project (No. 2018A050506004), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003. . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Заселение Cr3+ двух кристаллографических позиций в люминофоре MgTa2O6:Cr3+ для широкополосного ближнего инфракрасного излучения используемого для визуализации сосудов

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
LIGHT-SOURCES
   PHOSPHOR
   LUMINESCENCE
   PHOTOLUMINESCENCE
Аннотация: Near-infrared (NIR) phosphor-converted light-emitting diodes (pc-LEDs) have great potential in photonic, optoelectronic and biological applications, while the discovery of a broad-band NIR phosphor still remains a challenge. Here, we report a novel Cr3+-activated MgTa2O6 phosphor with an asymmetrical emission band ranging from 700 to 1150 nm and a large full width at half maximum (FWHM) of 140 nm upon 460 nm blue light excitation. The broad spectrum is assigned to the overlap of two bands centered at 910 and 834 nm, which originate from the spin-allowed transition of 4T2 → 4A2 for different Cr3+ ions located in the two six-coordinated crystallographic sites of Mg2+ and Ta5+, respectively. The distribution of blood vessels and bones in human palm and wrist is observed with the assistance of a commercial NIR camera and a fabricated pc-LED, which demonstrates that the MgTa2O6:Cr3+ phosphor is promising in biological applications.

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Держатели документа:
South China Univ Technol, Sch Mat Sci & Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Guangzhou 510640, 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.
South China Agr Univ, Coll Mat & Energy, Guangdong Prov Engn Technol Res Ctr Opt Agr, Guangzhou 510642, Peoples R China.

Доп.точки доступа:
Liu, Gaochao; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lei, Bingfu; Xia, Zhiguo
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Synthesis and luminescence properties of Li2O–Y2O3–TeO2:Eu3+ tellurite glass / V. V. Atuchin [et al.] // Mater. Chem. Phys. - 2014. - Vol. 147, Is. 3. - P. 1191-1194, DOI 10.1016/j.matchemphys.2014.07.003. - Cited References: 26. - This study is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0254-0584. - ISSN 1879-3312

РУБ Materials Science, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
   SPECTROSCOPIC PROPERTIES
   OPTICAL-PROPERTIES
   ENERGY-TRANSFER
   CERAMICS
   Eu3+
   PHOTOLUMINESCENCE
   TEMPERATURE
   EMISSION
   PHOSPHOR
Кл.слова (ненормированные):
Glasses -- Heat treatment -- Photoluminescence spectroscopy -- Optical properties
Аннотация: The Eu3+-doped red-orange emitting phosphor of tellurite glass 0.25Li2O–0.20Y2O3–0.5TeO2–0.05Eu2O3 has been synthesized by the melt quenching method. The amorphous nature of the glass has been verified by XRD measurements. The photoluminescence excitation and emission spectra, the luminescence decay curves have been investigated for the composition. The phosphor can be efficiently excited by the near UV light to realize the intense narrow red emission line (611 nm) corresponding to forced electric dipole transition 5D0 → 7F2 of Eu3+ ions. The Li2O–Y2O3–TeO2:Eu3+glass phosphor is a potential red-orange emitting candidate for the application in WLEDs.

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Держатели документа:
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 & Dielect Mat, Novosibirsk 630090, Russia
SB RAS, Inst Geol & Mineral, Lab High Pressure Minerals & Diamond Deposits, Novosibirsk 630090, Russia
Novosibirsk State Univ, Dept Appl Phys, Novosibirsk 630090, Russia
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Atuchin, V. V.; Yelisseyev, A. P.; Galashov, E. N.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ministry of Education and Science of the Russian Federation
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    Structure and luminescence properties of Eu2+ doped LuxSr2-xSiNxO4-x phosphors evolved from chemical unit cosubstitution / Z. Xia [et al.] // J. Mater. Chem. C. - 2016. - Vol. 4, Is. 6. - P. 1336-1344, DOI 10.1039/c5tc04222d. - Cited References: 32. - This work was supported by the National Natural Science Foundation of China (Grant No. 51572023 and 51272242), 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 Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, CAS (RERU2015022), and Fundamental Research Funds for the Central Universities (FRF-TP-15-003A2). . - ISSN 2050-7534
   Перевод заглавия: Структура и люминесцентные свойства люминофора LuxSr2-xSiNxO4-x полученного в результате со-замещения химических блоков и допированного Eu2+

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
SOLID-SOLUTION PHOSPHORS
   WHITE-LIGHT
   PHOTOLUMINESCENCE
   SUBSTITUTION
   DISCOVERY
   TRANSITIONLEDS
   EVOLUTION
   HOST
   LEDS
Аннотация: The design scheme of the chemical unit cosubstitution of [Lu3+-N3-] for [Sr2+-O2-] in Sr2SiO4:Eu2+ has been put into practice to discover the new phosphor systems with tunable luminescence properties, and the structures and photoluminescence tuning of yellow-emitting LuxSr2-xSiNxO4-x:Eu2+ phosphors have been investigated. Crystal structures of LuxSr2-x-ySiNxO4-x:yEu2+ samples were resolved using the Rietveld method, suggesting that the as-prepared Sr2SiO4 belonged to monoclinic symmetry (P21/n) of β-phase Sr2SiO4, while Sr1.97Eu0.03SiO4 and Sr1.965Eu0.03Lu0.005SiO3.995N0.005 belonged to orthorhombic symmetry (Pnma) of α-Sr2SiO4. The emission peaks of LuxSr1.97-xSiNxO4-x:0.03Eu2+ phosphors were red-shifted from 563 to 583 nm upon increasing the [Lu3+-N3-] substitution content from x = 0 to x = 0.005, furthermore, the PL emission peaks of Lu0.005Sr1.965-ySiN0.005O3.995:yEu2+ also showed a red-shift from 583 nm to 595 nm with increasing Eu2+ concentration (y = 0.03, 0.07, 0.10 and 0.15), and their corresponding red-shift mechanism has been discussed. The temperature dependent luminescence results further verified that the introduction of [Lu3+-N3-] for [Sr2+-O2-] in Sr2SiO4:Eu2+ can improve the thermal stability of the photoluminescence, which indicated that the LuxSr2-x-ySiNxO4-x:yEu2+ phosphors have potential applications in white light-emitting diodes (wLEDs). © 2016 The Royal Society of Chemistry.

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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
School of Materials Sciences and Technology, China University of Geosciences, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation

Доп.точки доступа:
Xia, Z.; Miao, S.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chen, M.; Liu, Q.
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    Structural evolution induced preferential occupancy of designated cation sites by Eu2+ in M5(Si3O9)2 (M = Sr, Ba, Y, Mn) phosphors / Y. Wei [et al.] // RSC Adv. - 2016. - Vol. 6, Is. 62. - P. 57261-57265, DOI 10.1039/c6ra11681g. - Cited References: 28. - This project is financially supported by the National Natural Science Foundation of China (Grants No. NSFC 21301162, 21571162, 60977013, 91433110, U1301242, 21221061), the National College Students' Innovative Training Program (Nos. 201510491109, 201610491067, 201610491070), and the Ministry of Science and Technology of Taiwan (No. MOST 104-2917-1-564-060). Zewei Quan acknowledges the funding support (FRG-SUSTC1501A-17) from South University of Science and Technology of China. . - ISSN 2046-2069
   Перевод заглавия: Структурная трансформация, вызванная преимущественной заселенностью обозначенных катионных позиций ионами Eu2+ в люминофорах M5(Si3O9)2 (M = Sr, Ba, Y, Mn)

РУБ Chemistry, Multidisciplinary
Рубрики:
LUMINESCENCE PROPERTIES
   RED LUMINESCENCE
   UP-CONVERSION
   WHITE LEDS
   PHOTOLUMINESCENCE
   NANOPHOSPHORS
   YELLOW
   WLEDS
Аннотация: In this paper, we present new insight into a changing Eu2+ crystallographic site preference in Eu-doped M5(Si3O9)2 (M = Sr, Ba, Y, Mn), which is related to the structural variation induced by M cation substitutions. The effect of the local structural geometry on the luminescence properties of Eu2+ is revealed. By substitution of Ba2+ for Sr2+, the lattice expansion is restricted to specific cation sites, resulting in the abrupt blue shifted emission of Eu2+ ions. The abnormal blue shift on replacing Sr2+ with Mn2+ is attributed to the preferential 6-fold coordination for Mn2+ that moves the Eu2+ ions to other sites. The results elucidate the mechanisms of emission band adjustment by local site coordination change and it can be potentially extended to crystals which properties are sensitive to local lattice variations. © 2016 The Royal Society of Chemistry.

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Держатели документа:
Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, China
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, China
Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, CC Utrecht, Netherlands
Department of Chemistry, South University of Science and Technology of China, Shenzhen Guangdong, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
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, 2 Pirogov Str., Novosibirsk, Russian Federation
National Synchrotron Radiation Research Center, Hsinchu, Taiwan

Доп.точки доступа:
Wei, Y.; Lin, C. C.; Quan, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Chan, T. -S.; Liang, Y.; Lin, J.; Li, G.
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    Strong Electron Correlations Determine Energetic Stability and Electronic Properties of Er-Doped Goldberg-Type Silicon Quantum Dots / P. V. Avramov [et al.] // J. Phys. Chem. C. - 2009. - Vol. 113, Is. 36. - P. 15964-15968, DOI 10.1021/jp904996e. - Cited Reference Count: 43. - Гранты: This work was supported by a CREST (Core Research for Evolutional Science and Technology) grant in the Area of High Performance Computing for Multiscale and Multiphysics Phenomena from the Japan Science and Tcchnology Agency (JST) and a collaborative RFBR-JSPS Grant 0902-92107-Phi. One of the authors (S.I.) also acknowledges support by the Program for Improvement of Research Environment for Young Researchers from Special Coordination Funds for Promoting Science and Technology (SCF) commissioned by the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan. - Финансирующая организация: Japan Science and Tcchnology Agency (JST); RFBR-JSPS Grant; Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan . - SEP 10. - ISSN 1932-7447
Рубрики:
IMPLANTED POROUS SILICON
   AUGMENTED-WAVE METHOD
   MU M LUMINESCENCE
   SI NANOCRYSTALS
   THIN-FILMS
   BASIS-SET
   ERBIUM
   PHOTOLUMINESCENCE
   DENSITY
   PSEUDOPOTENTIALS
Кл.слова (ненормированные):
Ab initio -- Atomic structure -- Density functionals -- Empirical pseudo-potential -- Endohedrals -- Energetic stability -- Er-doped -- Erbium complexes -- Erbium ion -- Experimental data -- Hartree-fock -- Many body perturbation theory -- Mass centers -- Perturbation approach -- Plane wave -- Pseudopotentials -- Quantum Dot -- Silicon quantum dots -- Strong binding -- Strong electron correlations -- Theoretical result -- Crystal atomic structure -- Electron correlations -- Electron density measurement -- Electronic properties -- Electronic structure -- Erbium -- Perturbation techniques -- Structural optimization -- Semiconductor quantum dots
Аннотация: Atomic and electronic structures of Goldberg-type silicon quantum dots and their endohedral erbium complexes were studied using ab initio and plane wave pseudopotential density functional and Moller-Plesset many-body perturbation theories. During atomic structure optimizations, the erbium ions occupy mass centers inside the central hollows of quantum dots of different symmetries. It was found that strong electron correlations within the Er 4f shell taken into account by empirical pseudopotential and post-Hartree-Fock perturbation approaches are responsible for strong binding of Er ions to quantum dots. We elucidate the effects of symmetry and discuss theoretical results in comparison to available experimental data,

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http://pubs.acs.org/doi/abs/10.1021/jp904996e.
Держатели документа:
SB RAS, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660041, Russia
Natl Inst Adv Ind Sci & Technol, RICS, Tsukuba, Ibaraki 3058568, Japan
Nagoya Univ, Inst Adv Res, Nagoya, Aichi 4648602, Japan
Nagoya Univ, Dept Chem, Nagoya, Aichi 4648602, Japan
Kyoto Univ, Fukui Inst Fundamental Chem, Sakyo Ku, Kyoto 6068103, Japan

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

РУБ Chemistry, Multidisciplinary
Рубрики:
LUMINESCENCE PROPERTIES
   CE3+
   ENERGY
   PHOTOLUMINESCENCE
   TRANSITION
Кл.слова (ненормированные):
light-emitting diodes -- red-emitting phosphors -- silicates -- site occupancy
Аннотация: Establishing an effective design principle in solid-state materials for a blue-light-excited Eu2+-doped red-emitting oxide-based phosphors remains one of the significant challenges for white light-emitting diodes (WLEDs). Selective occupation of Eu2+ in inorganic polyhedra with small coordination numbers results in broad-band red emission as a result of enhanced crystal-field splitting of 5d levels. Rb3YSi2O7:Eu exhibits a broad emission band at λmax=622 nm under 450 nm excitation, and structural analysis and DFT calculations support the concept that Eu2+ ions preferably occupy RbO6 and YO6 polyhedra and show the characteristic red emission band of Eu2+. The excellent thermal quenching resistance, high color-rendering index Ra (93), and low CCT (4013 K) of the WLEDs clearly demonstrate that site engineering of rare-earth phosphors is an effective strategy to target tailored optical performance.

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

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

РУБ Chemistry, Multidisciplinary
Рубрики:
LUMINESCENCE PROPERTIES
   CE3+
   ENERGY
   PHOTOLUMINESCENCE
   TRANSITION
Кл.слова (ненормированные):
light-emitting diodes -- red-emitting phosphors -- silicates -- site occupancy
Аннотация: Establishing an effective design principle in solid-state materials for a blue-light-excited Eu2+-doped red-emitting oxide-based phosphors remains one of the significant challenges for white light-emitting diodes (WLEDs). Selective occupation of Eu2+ in inorganic polyhedra with small coordination numbers results in broad-band red emission as a result of enhanced crystal-field splitting of 5d levels. Rb3YSi2O7:Eu exhibits a broad emission band at λmax=622 nm under 450 nm excitation, and structural analysis and DFT calculations support the concept that Eu2+ ions preferably occupy RbO6 and YO6 polyhedra and show the characteristic red emission band of Eu2+. The excellent thermal quenching resistance, high color-rendering index Ra (93), and low CCT (4013 K) of the WLEDs clearly demonstrate that site engineering of rare-earth phosphors is an effective strategy to target tailored optical performance.

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

Доп.точки доступа:
Qiao, Jianwei; Ning, Lixin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chuang, Yu-Chun; Zhang, Qinyuan; Poeppelmeier, Kenneth R.; Xia, Zhiguo
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    Preparation and luminescence properties of the blue-emitting phosphor BaBPO5:Eu2+ / L. Zhang [et al.] // Sci. Adv. Mater. - 2016. - Vol. 8, Is. 5. - P. 1086-1092, DOI 10.1166/sam.2016.2704. - Cited References: 22. - This work was financially supported by the National Natural Science Foundation of China (NSFC Grant no. 51172216) and the Fundamental Research Funds for the Central Universities (Grant no. 2652015022). . - ISSN 1947-2935
   Перевод заглавия: Синтез и люминесцентные свойства синего люминофора BaBPO5:Eu2+

РУБ Nanoscience & Nanotechnology + Physics, Applied + Physics, Applied
Рубрики:
Energy-transfer
   Diodes
   Ions
   Eu3+
   Photoluminescence
   Reduction
   Tb3+
Кл.слова (ненормированные):
BaBPO5 -- Eu2+ -- Phosphor -- White light emitting diodes
Аннотация: Blue-emitting BaBPO5:xEu2+ phosphors were prepared by a high-temperature solid-state reaction route. The crystal phase, luminescence properties, lifetime, and thermal stability were investigated, respectively. The phase analysis indicated that BaBPO5 crystallize with the structure of stillwellite-type compounds. Under the excitation at 310 nm, the phosphor exhibited an asymmetric broad-band blue emission with peak at 410 nm, which was ascribed to the 4f-5d transition of Eu2+. It was further calculated that the dipole-dipole interactions were responsible for a concentration quenching effect in BaBPO5:xEu2+ phosphors at x = 0.08. The lifetime decreased with the increasing concentration of Eu2+ ions. The temperature-dependent emission spectra indicated an excellent thermal stability of the BaBPO5:0.08Eu2+ samples. Surface morphology and CIE coordinate were also investigated. All the properties assessed indicated that the developed blue-emitting BaBPO5:Eu2+ phosphor is a good candidate for application in white-light emitting diodes. © 2016 by American Scientific Publishers.

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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences (Beijing), Beijing, China
National Engineering Research Center for Rare Earth Materials, General Research Institute for Nonferrous Metals, Grirem Advanced Materials Co., Ltd., 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:
Zhang, L.; Fang, M.; Huang, Z.; Liu, Y.; Min, X.; Tang, H.; Chen, K.; Guan, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич
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    Phase transformation in Ca3(PO4)2:Eu2+ via the controlled quenching and increased Eu2+ content: Identification of new cyan-emitting α-Ca3(PO4)2:Eu2+ phosphor / H. Ji [et al.] // J. Am. Ceram. Soc. - 2015. - Vol. 98, Is. 10. - P. 3280-3284, DOI 10.1111/jace.13787. - Cited References: 23. - This work was partly supported by the National Natural Science Foundations of China (grant nos. 51272242, 51472222, 51511130035), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), and the Russian Foundation for Basic Research (grant no. 15-52-53080 GFEN_a). VVA was partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0002-7820
   Перевод заглавия: Фазовый переход в Ca3(PO4)2:Eu2+ посредством контролируемой закалки и увеличения концентрации Eu2+: Идентификация нового голубого люминофора α-Ca3(PO4)2:Eu2+

РУБ Materials Science, Ceramics
Рубрики:
NEUTRON POWDER DIFFRACTION
   SOLID-SOLUTION PHOSPHORS
   CRYSTAL-STRUCTURE
   DIODES
   PHOTOLUMINESCENCE
   LUMINESCENCE
   TRANSITION
   ALPHA
Аннотация: A case of phosphor is reported where the cooling rate parameter significantly influences the luminescence property. By quenching the sample after the higherature solid-state reaction at 1250°C, we successfully prepared the Eu2+-doped α form Ca3(PO4)2 (α-TCP:Eu2+) as a new kind of bright cyan-emitting phosphor. The unusual emission color variation (from cyan to blue) depends on the cooling rate after sintering and Eu2+ doping level as it was observed in the TCP-based phosphors. By the Rietveld analysis, it is revealed that the cyan- and blue-emitting phosphors are two different TCP forms crystallizing in the monoclinic (space group P21/a, α-TCP) and the rhombohedral structure (space group R3c, β-TCP), respectively. Upon 365 nm UV light excitation, α-TCP:Eu2+ exhibits an asymmetric broad-band cyan emission peaking at 480 nm, while β-TCP:Eu2+ displays a relatively narrow-band blue emission peaking at 416 nm. The Eu2+-doping in Ca3(PO4)2 shifts the upper temperature limit of the stable structural range of β form from 1125°C to ≥1250°C. Moreover, the crystal structures of α/β-TCP:Eu2+ were compared in the aspects of compactness and cation site sets. The emission thermal stability of α/β-TCP:Eu2+ was comparatively characterized and the difference was related to the specific host structural features. © 2015 The American Ceramic Society.

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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing, China
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
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.; Huang, Z.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chen, M.; Atuchin, V. V.; Fang, M.; Liu, Y.; Wu, Xiaowen
}
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10.

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

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

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National Laboratory of Mineral Materials, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, School of Materials Science and Technology, China University of Geosciences (Beijing), Beijing, China
Sialon Group, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Japan
College of Optical and Electronic Technology, China Jiliang University, Hangzhou, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China

Доп.точки доступа:
Ji, H.; Wang, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Hirosaki, N.; Huang, Z.; Xia, Z.; Ten Kate, O. M.; Liu, L.; Xie, R.
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