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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhou, Jun, Rong, Ximing, Molokeev M. S., Wang, Yulong, Yun, Xiangyan, Xu, Denghui, Li, Xiong
Заглавие : Alloying Cs+ into Rb2ZrCl6:Te4+ toward highly efficient and stable perovskite variants
Коллективы : Beijing Natural Science FoundationBeijing Natural Science Foundation [2214068]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [61705003]; Beijing Technology and Business University Research Team Construction Project [PXM2019_014213_000007, PXM2020_014213_000017]
Место публикации : Mat. Chem. Front. - 2021. - Vol. 5, Is. 13. - P.4997-5003. - ISSN 2052-1537(eISSN), DOI 10.1039/d1qm00302j
Примечания : Cited References: 37. - This work is supported by Beijing Natural Science Foundation (No. 2214068), the National Natural Science Foundation of China (No. 61705003), and the Beijing Technology and Business University Research Team Construction Project (No. PXM2019_014213_000007 and PXM2020_014213_000017)
Предметные рубрики: TELLER
PHOTOLUMINESCENCE
TELLURIUM(IV)
COMPLEXES
PHOSPHORS
Аннотация: Doping or alloying in perovskites and perovskite variants provides a promising way for modulating the electronic and photoluminescence properties and the structural stability. In this work, a series of yellow-emitting Rb2−xCsxZrCl6:Te4+ solid solution phosphors were prepared by a hydrothermal method, and their broad emission is assigned to the triplet 3P1–1S0 self-trapped excitons (STEs). Upon increasing the alloying ion Cs+, the yellow emission can be greatly enhanced by a stronger Jahn–Teller distortion. Moreover, Cs2ZrCl6:Te4+ shows a high photoluminescence quantum yield (PLQY), and impressive thermal and anti-water stability. This doping–alloying strategy presents a new direction towards designing lead-free, high-performance and stable perovskite derivatives.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Wei, Y.i., Yang, Hang, Gao, Zhiyu, Xing, Gongcheng, Molokeev M. S., Li, Guogang
Заглавие : Bismuth activated full spectral double perovskite luminescence materials by excitation and valence control for future intelligent LED lighting
Место публикации : Chem. Commun. - 2020. - Vol. 56, Is. 64. - P.9170-9173. - ISSN 1359-7345, DOI 10.1039/d0cc03975f. - ISSN 1364-548X(eISSN)
Примечания : Cited References: 27. - This work was supported by the National Natural Science Foundation of China (Grant No. 51672259) and the Fundamental Research Funds for the National Universities, China University of Geosciences (Wuhan) (No. 1910491T02)
Предметные рубрики: PHOTOLUMINESCENCE
PHOSPHORS
Bi3+
MODULATION
CRYSTAL
Аннотация: A novel La2Mg1.14Zr0.86O6:Bi3+ double perovskite phosphor with excitation-induced blue/green photoluminescence tuning is reported. By designing Bi3+ → Eu3+ energy transfer, single-composition white light with wide-scale adjustable corrected color temperatures (CCTs) is successfully achieved. This work initiates a new insight to explore phosphors with excitation-induced photoluminescence tuning and wide CCT control for future intelligent LED lighting.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Guan, Ming, Zheng, Hong, Huang, Zhaohui, Ma, Bin, Molokeev M. S., Huang, Saifang, Mei, Lefu
Заглавие : Ca/Sr ratio dependent structure and up-conversion luminescence of (Ca1-xSrx)In2O4 : Yb3+/Ho3+ phosphors
Место публикации : RSC Adv.: Royal Society of Chemistry, 2015. - Vol. 5, Is. 73. - P.59403-59407. - ISSN 2046-2069, DOI 10.1039/c5ra08467a
Примечания : Cited References:25. - 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 no. 2652014125, 2652013128, 2652013043), and the Research Fund for the Doctoral Program of Higher Education of China (Grant no. 20130022110006).
Предметные рубрики: CO-DOPED CAIN2O4
ENERGY-TRANSFER
PHOTOLUMINESCENCE
EMISSION
SRIN2O4
Аннотация: Up-conversion (UC) phosphors of (Ca1-xSrx)In2O4 : Yb3+/Ho3+ (x = 0, 0.1, 0.3, 0.5, 0.7, 0.9, 1.0) were prepared. Based on the crystal structure evolution of these series solid solution samples, which were characterized by Rietveld refinement, the variation of UC luminescent properties was discussed in detail. Sr and Ca occupied one position and Yb/Ho dissolved in the In ion site in the (Ca1-xSrx)In2O4 lattice. With increasing Sr substituting Ca atoms, the cell parameters and cell volumes of these samples increased linearly, and distortions of (Ca/Sr)O-8 polyhedron were formed. The distortions on crystal structures showed a negative relation with UC luminescent intensities in these series phosphors.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Shi P. L., Xia, Zhiguo, Molokeev M. S., Atuchin V. V.
Заглавие : Crystal chemistry and luminescence properties of red-emitting CsGd1−xEux(MoO4)2 solid-solution phosphors
Место публикации : Dalton Trans.: Royal Society of Chemistry, 2014. - Vol. 43, Is. 25. - P.9669-9676. - ISSN 1477-9226, DOI 10.1039/C4DT00339J. - ISSN 1477-9234
Примечания : Cited References: 46. - The present work was supported by the National Natural Science Foundations of China (grant no. 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 Fundamental Research Funds for the Central Universities (2-9-2014-044), and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306). V. V. A. gratefully acknowledges the Ministry of Education and Science of the Russian Federation for the financial support.
Предметные рубрики: WHITE-LIGHT
VIBRATIONAL PROPERTIES
HYDROTHERMAL SYNTHESIS
SINGLE-CRYSTALS
DIODES
EFFICIENCY
PHOTOLUMINESCENCE
CSGD(MOO4)2
MORPHOLOGY
GROWTH
Аннотация: Scheelite related alkali-metal rare-earth double molybdate compounds with a general formula of ALn(MoO4)2 can find wide application as red phosphors. The crystal chemistry and luminescence properties of red-emitting CsGd1−xEux(MoO4)2 solid-solution phosphors have been evaluated in the present paper. A detailed analysis of the structural properties indicates the formation of isostructural scheelite-type CsGd1−xEux(MoO4)2 solid-solutions over the composition range of 0 ≤ x ≤ 1. The photoluminescence emission (PL) and excitation (PLE) spectra, and the decay curves were measured for this series of compounds. The critical doping concentration of Eu3+ is determined to be x = 0.6 in order to realize the maximum emission intensity. The emission spectra of the as-obtained CsGd(1−x)Eux(MoO4)2 phosphors show narrow high intensity red lines at 592 and 615 nm upon excitation at 394 or 465 nm, revealing great potential for applications in white light-emitting diode devices.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xia Y., Chen J., Liu Y.-G., Molokeev M. S., Guan M., Huang Z., Fang M.
Заглавие : Crystal structure evolution and luminescence properties of color tunable solid solution phosphors Ca2+xLa8-x(SiO4)6-x(PO4)xO2:Eu2+
Место публикации : Dalton Trans.: Royal Society of Chemistry, 2016. - Vol. 45, Is. 3. - P.1007-1015. - ISSN 14779226 (ISSN), DOI 10.1039/c5dt03786g
Примечания : Cited References: 42. - This work was sponsored by National Natural Science Foundation of China (Grant No. 51472223), the Program for New Century Excellent Talents in University of Ministry of Education of China (Grant No. NCET-12-0951) and the Fundamental Research Funds for the Central Universities (Grant No. 2652015020).
Предметные рубрики: LIGHT-EMITTING-DIODES
WHITE-LIGHT
ENERGY-TRANSFER
SILICATE GLASS
SINGLE-PHASE
EU2+
LEDS
PHOTOLUMINESCENCE
EMISSION
UV
Аннотация: A series of apatite solid solution phosphors Ca2+xLa8-x(SiO4)6-x(PO4)xO2:Eu2+ (x = 0,2,4,6) were synthesized by a conventional higherature solid-state reaction. The phase purity was examined using XRD, XPS and XRF. The crystal structure information, such as the concentration, cell parameters and occupation rate, was analyzed using a Rietveld refinement, demonstrating that the Eu2+ activated the Ca2La8(SiO4)6O2 and Ca8La2(PO4)6O2 to form continuous solid solution phosphors. Different behaviors of luminescence evolution in response to structural variation were verified among the series of phosphors. Two kinds of Eu2+ ion sites were proved using low temperature PL spectra (8k) and room temperature decay curves. The substitution of large La3+ ions by small Ca2+ ions induced a decreased crystal field splitting of the Eu2+ ions, which caused an increase in emission energy from the 5d excited state to the 4f ground state and a resultant blue-shift from 508 nm to 460 nm. Therefore, with the crystal structure evolution, the emitted color of the series of phosphors could be tuned from green to blue by adjusting the ratio of Ca/La. © 2016 The Royal Society of Chemistry.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Yang, Zhiyu, Zhao, Yifei, Zhou, Yayun, Qiao, Jianwei, Chuang, Yu-Chun, Molokeev M. S., Xia, Zhiguo
Заглавие : Giant red-shifted emission in (Sr,Ba)Y2O4:Eu2+ phosphor toward broadband near-infrared luminescence
Коллективы : International Cooperation Project of National Key Research and Development Program of China [2021YFE0105700]; National Natural Science Foundations of ChinaNational Natural Science Foundation of China (NSFC) [51972118, 51961145101]; Guangzhou Science & Technology Project [202007020005]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01X137]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]
Место публикации : Adv. Funct. Mater. - 2022. - Vol. 32, Is. 1. - Ст.2103927. - ISSN 1616-301X, DOI 10.1002/adfm.202103927. - ISSN 1616-3028(eISSN)
Примечания : Cited References: 60. - This research was supported by the International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), National Natural Science Foundations of China (Grant No. 51972118 and 51961145101), Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003
Предметные рубрики: LIGHT-SOURCES
PHOTOLUMINESCENCE
TRANSITION
CE3+
BLUE
SUBSTITUTION
Аннотация: Near-infrared (NIR) light-emitting diodes (LEDs) light sources are desirable in photonic, optoelectronic, and biological applications. However, developing broadband red and NIR-emitting phosphors with good thermal stability is always a challenge. Herein, the synthesis of Eu2+-activated SrY2O4 red phosphor with high photoluminescence quantum efficiency and broad emission band ranging from 540 to 770 nm and peaking at 620 nm under 450 nm excitation is designed. Sr/Ba substitution in SrY2O4:Eu2+ has been further utilized to achieve tunable emission by modifying the local environment, which facilitates the giant red-shifted emission from 620 to 773 nm while maintaining the outstanding thermal stability of SrY2O4:Eu2+. The NIR emission is attributed to the enhanced Stokes shift and crystal field strength originated from the local structural distortions of [Y1/Eu1O6] and [Y2/Eu2O6]. The investigation in charge distribution around Y/Eu provides additional insight into increasing covalency to tune the emission toward the NIR region. As-fabricated NIR phosphor-converted LEDs demonstration shows its potential in night-vision technologies. This study reveals the NIR luminescence mechanism of Eu2+ in oxide-based hosts and provides a design principle for exploiting Eu2+-doped NIR phosphors with good thermal stability.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhu L., Huang Z., Molokeev M. S., Min X., Liu Y., Fang M., Wu X.
Заглавие : Influence of cation substitution on the crystal structure and luminescent properties in apatite structural Ba4.97- xSrx(PO4)3Cl:0.03Eu2+ phosphors
Место публикации : Chem. Phys. Lett.: Elsevier, 2016. - Vol. 658. - P.248-253. - ISSN 00092614 (ISSN), DOI 10.1016/j.cplett.2016.06.061
Примечания : Cited References: 23. - This present work was supported by the National Natural Science Foundations of China (Grant Nos. 51472222 and 51372232), the Fundamental Research Funds for the Central Universities (Grant No. 2652015310), and the Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20130022110006).
Предметные рубрики: PHOTOLUMINESCENCE
ENERGY
Ce3+
Sr
UV
Ключевые слова (''Своб.индексиров.''): substitution--apatite--ba4.97- xsrx(po4)3cl:0.03eu2+--luminescence
Аннотация: A series of apatite-type phosphors Ba4.97- xSrx(PO4)3Cl:Eu2+(x = 0, 0.5, 1.0, 1.5, 2.0) were synthesized by the high temperature solid-state reaction method, and its luminescence properties were investigated in detail. It can be found that a red shift of the emission peak wavelength emerged from 439 to 462 nm with the continuous introduction of Sr2+ into the crystal lattice which has been simulated by a crystal-field model. The red shift is explained by the distortion in the crystal structure through X-ray diffraction and the Rietveld refinement analysis. According to a recently raised structural model, Eu2+ ions are surrounded by O atoms, PO4 tetrahedrons and Ba/Sr ions. After introducing Sr2+ into the lattice, the interatomic distance between Ba/Sr atoms and Eu2+ was expected to become shorter, resulting in a distortion of the inner EuOn polyhedrons. Then the crystal field strength surrounding Eu2+ was increased, finally resulting in the red shift. © 2016 Published by Elsevier B.V.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Gaochao, Molokeev M. S., Xia, Zhiguo
Заглавие : Structural rigidity control toward Cr3+-based broadband near-infrared luminescence with enhanced thermal stability
Коллективы : International Cooperation Project of the National Key Research and Development Program of China [2021YFE0105700]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [51972118, 51961145101]; Guangzhou Science & Technology Project [202007020005]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01X137]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]
Место публикации : Chem. Mat. - 2022. - Vol. 34, Is. 3. - P.1376-1384. - ISSN 0897-4756, DOI 10.1021/acs.chemmater.1c04131. - ISSN 1520-5002(eISSN)
Примечания : Cited References: 59. - This work was supported by the International Cooperation Project of the National Key Research and Development Program of China (2021YFE0105700) , National Natural Science Foundation of China (Nos.: 51972118 and 51961145101) , Guangzhou Science & Technology Project (202007020005) , and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137) . This work was also funded by RFBR according to the research Project No. 19-52-80003
Предметные рубрики: PHOSPHOR
PHOTOLUMINESCENCE
EFFICIENT
EMISSION
CR3+
Аннотация: Broadband near-infrared (NIR) light sources based on phosphor-converted light-emitting diodes (pc-LEDs) are desirable for biochemical analysis and medical diagnosis applications; however, the development of target NIR phosphor is still a challenge. Herein, broadband NIR phosphors, Cr3+-activated CaSc1–xAl1+xSiO6 (λem = 950 nm), are designed and optimized by chemical substitution toward enhanced quantum efficiency and thermal stability. Structural and spectral analyses along with density functional theory calculations reveal that Sc3+/Al3+ substitution contributes to enhancing the structural rigidity and the local symmetry of the [Sc/AlO6] octahedron so that the nonradiative relaxation of Cr3+ emission centers is suppressed significantly. The as-fabricated phosphor-in-glass-based NIR LED light source demonstrates great potential in the detection of alcohol concentration. This study provides a local structure design principle for exploring NIR phosphors with enhanced thermal stability and will also stimulate further studies on material discovery and quantitative analysis of NIR spectroscopy.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ji H., Wang L., Molokeev M. S., Hirosaki N., Huang Z., Xia Z., Ten Kate O. M., Liu L., Xie R.
Заглавие : New garnet structure phosphors, Lu3-xYxMgAl3SiO12:Ce3+ (x = 0-3), developed by solid solution design
Место публикации : J. Mater. Chem. C: Royal Society of Chemistry, 2016. - Vol. 4, Is. 12. - P.2359-2366. - ISSN 20507534 (ISSN), DOI 10.1039/c6tc00089d
Примечания : 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.
Предметные 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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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ji H., Huang Z., Xia, Zhiguo, Molokeev M. S., Chen M., Atuchin V. V., Fang M., Liu Y., Wu, Xiaowen
Заглавие : 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
Место публикации : J. Am. Ceram. Soc. - 2015. - Vol. 98, Is. 10. - P.3280-3284. - ISSN 0002-7820, DOI 10.1111/jace.13787
Примечания : 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.
Предметные 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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