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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chen K., Gao P., Zhang Z., Ma Y., Luo Z., Molokeev M. S., Zhou Zh., Xia M.
Заглавие : Zero-thermal-quenching broadband yellow-emitting Bi3+-activated phosphors based on metal to metal charge transfer
Колич.характеристики :9 с
Место публикации : J. Alloys Compd. - 2024. - Vol. 986. - Ст.174112. - ISSN 09258388 (ISSN), DOI 10.1016/j.jallcom.2024.174112. - ISSN 18734669 (eISSN)
Примечания : Cited References: 52. - The authors would like to gratefully acknowledge funds from the National Natural Science Foundation of China (Grant No. 51974123), the Key R & D Projects in Hunan Province (2021SK2047 and 2022NK2044), the Wangcheng Science and Technology Plan (KJ221017) and the Science and Technology Innovation Program of Hunan Province (2022WZ1022). The work was supported by the Ministry of Science and Higher Education of the Russian Federation as part of World-class Research Center program: "Advanced Digital Technologies", contract no. 075-15-2020-935. Superior Youth Project of the Science Research Project of Hunan Provincial Department of Education (22B0211)
Аннотация: Bi3+-activated phosphors have been proven to have potential applications foreground in white light-emitting diodes (WLED), plant growth lamps and temperature sensing. Therefore, it is urgent to exploit high-efficiency Bi3+-activated phosphors. Herein, a novel broadband yellow-emitting phosphor Ba2GdGaO5:Bi3+ with high internal quantum efficiency (IQE = 77%) was obtained based on metal to metal charge transfer (MMCT) between Bi3+ ground state and Gd3+ excited states. The photoluminescence excitation (PLE) spectrum and photoluminescence (PL) spectrum range from 225 nm to 400 nm and 400 nm to 700 nm, respectively, which can avoid the reabsorption phenomenon efficiently. Besides, Ba2GdGaO5:Bi3+ has superior thermal stability and it shows zero-thermal-quenching at 150 °C. The K+ doping hardly changes the thermal stability and can improve the PL intensity to 133.1% when the K+ concentration is 2%. Finally, a phosphor-convert WLED (pc-WLED) was simply synthesized by Ba2GdGaO5:Bi3+ and BaMgAl10O17:Eu2+ (BAM:Eu2+) phosphors. The doping of Eu3+ can significantly enhance the color rendering index (CRI, from 88.1 to 91.5) and reduce the correlated color temperature (CCT, from 4911 K to 4014 K). The above experimental results demonstrated that the phosphor has great application prospect in WLED.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ikonnikov D. A., Voronov V. N., Molokeev M. S., Aleksandrovsky A. S.
Заглавие : Upconversion luminescence of CsScF4 crystals doped with erbium and ytterbium
Коллективы : Russian Foundation for Basic Research [15-52-53080]; Russian President [SS-7612.2016.2, 0358-2015-0012, II.2P]
Место публикации : Opt. Mater.: Elsevier Science, 2016. - Vol. 60. - P.584-589. - ISSN 0925-3467, DOI 10.1016/j.optmat.2016.09.016. - ISSN 1873-1252(eISSN)
Примечания : Cited References:33. - The authors are grateful to D. L. Chertkova for excellent technical assistance. The work was partially supported by the Russian Foundation for Basic Research Grant 15-52-53080, by the Russian President Grant SS-7612.2016.2, and by Project No0358-2015-0012 of SB RAS Program NoII.2P.
Предметные рубрики: MODULATED STRUCTURE
LANTHANIDE
NANOCRYSTALS
PHOSPHORS
Ключевые слова (''Своб.индексиров.''): fluoride crystals--erbium--ytterbium--up-conversion--luminescence--crystal structure--power dependence--pump wavelength dependence
Аннотация: Tetragonal CsScF4 crystals doped with (5 at.%) Er and Er/Yb (0.5 at.%/5 at.%) are grown and their crystal structure is determined to belong to Pmmn space group. Er and Yb ions are shown to occupy distorted octahedral Sc sites with the center of inversion. Bright visible upconversion luminescence was observed under 970-980 nm pumping with red (4F9/2), yellow (4S3/2) and green (2H11/2) bands of comparable intensity. UCL tuning curves maximize at 972 nm (CSF:Er) and at 969.7 nm (CSF:Er,Yb) pumping wavelengths. Different ratios between yellow-green and red luminescence intensities in CSF:Er and CSF:Er, Yb are explained by contribution of cross-relaxation in CSF:Er UCL UC in CSF:Er is a three stage process while UC in CSF:Er, Yb is a two stage process. The peculiarities of power dependences are explained by the power-dependent repopulation between starting levels of UC. (C) 2016 Elsevier B.V. All rights reserved.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Wei Y., Qu X., Li G., Cheng Z., Molokeev M. S., Lin C. C., Chan T. -S., Chang C. -K., Chuang Y. -C., Lin J.
Заглавие : Ultra-narrow band blue emission of Eu2+ in halogenated (Alumino)borate systems based on high lattice symmetry
Место публикации : J. Am. Ceram. Soc. - 2019. - Vol. 102. - P.2353– 2369. - ISSN 00027820 (ISSN) , DOI 10.1111/jace.16127
Примечания : Cited References: 63. - This work was supported by the National Natural Science Foundation of China (Grant Nos. 51672259, 51672265, 21521092, 51750110511), Engineering Research Center of Nano-Geomaterials of Ministry of Education, China University of Geosciences (Wuhan) (No. NGM2016KF002), the Ministry of Science and Technology of Taiwan (Contract No. MOST 104-2113-M-027-007-MY3), the Key Research Program of Frontier Sciences, CAS (Grant No. YZDY-SSW-JSC018), and projects for science and technology development plan of Jilin province (20170414003GH), the Program for Jiangmen Innovative Reasearch Team (No.[2017]385),major program of basic research and applied research of Guangdong Province (2017KZDXM083) and the Russian Science Foundation (Grant No. 17-12-01047).
Ключевые слова (''Своб.индексиров.''): blue emission--high symmetry--phosphors--ultra-narrow band--wleds
Аннотация: Phosphor materials with ultra‐high color purity are highly desired in backlit display and WLEDs. How to achieve high‐purity three‐primary emission in rare earth ions activated inorganic phosphors has become a hot topic. Herein, we reported ultra‐narrow band and highly efficient blue‐violet‐emitting Eu2+‐doped Ba2B5O9X (fwhm = 31 nm) and NaBa4(AlB4O9)2X3 (X = Cl, Br) (fwhm = 43 nm) phosphors with peak positions around 424‐437 nm. Especially, the color purity of Ba2B5O9Cl:Eu sample even exceeded 97%, its internal quantum efficiency could achieve 87%. The EXANES analysis revealed that the Eu mainly existed in the form of +2. According to the Rietveld structural refinement, extraordinarily narrow band emission should be attributed to the highly symmetric lattice structures with the flower‐like polyhedrons in the studied (alumino)borate matrix. Significantly, the color gamut of as‐prepared blue phosphor combined with the standard green and red phosphors was almost close to that of Rec. 2020 display standard. In addition, cation substitution strategy in NaBa4(AlxB5‐xO9)2Cl3 (x = 0‐4) and NaBa4(GayB5‐yO9)2Cl3 (y = 0‐3) samples successfully achieved spectra adjustment, and the underlying mechanism was proposed. All these results demonstrate that the as‐prepared phosphors could be superior blue‐emitting candidates for backlit display as well as WLEDs.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhou, Guojun, Jiang, Xingxing, Zhao, Jing, Molokeev M. S., Lin, Zheshuai, Liu, Quanlin, Xia, Zhiguo
Заглавие : Two-dimensional-layered perovskite ALaTa2O7:Bi3+ (A = K and Na) phosphors with versatile structures and tunable photoluminescence
Место публикации : ACS Appl. Mater. Interfaces. - 2018. - Vol. 10, Is. 29. - P.24648-24655. - ISSN 1944-8244, DOI 10.1021/acsami.8b08129
Примечания : Cited References: 48. - The authors acknowledge the support from the National Natural Science Foundation of China (Nos. 51722202, 91622125, and 51572023) and the Natural Science Foundations of Beijing (2172036) and RFBR (17-52-53031).
Предметные рубрики: GENERALIZED GRADIENT APPROXIMATION
YELLOW-EMITTING PHOSPHOR
Ключевые слова (''Своб.индексиров.''): 2d-layered perovskite--bi3+ emission--ion exchange--photoluminescence tuning--white light leds
Аннотация: Topological chemical reaction methods are indispensable for fabricating new materials or optimizing their functional properties, which is particularly important for two-dimensional (2D)-layered compounds with versatile structures. Herein, we demonstrate a low-temperature (∼350 °C) ion exchange approach to prefabricate metastable phosphors ALa1–xTa2O7:xBi3+ (A = K and Na) with RbLa1–xTa2O7:xBi3+ serving as precursors. The as-prepared ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) share the same Dion–Jacobson type 2D-layered perovskite phase, and photoluminescence analyses show that ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) phosphors exhibit broad emission bands peaking at 540, 550, and 510 nm, respectively, which are attributed to the nonradiative transition of Bi3+ from excited state 3P1 or 3P0 to ground state 1S0. The various Bi3+ local environments at the crystallographic sites enable the different distributions of emission and excitation spectra, and the photoluminescence tuning of ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) phosphors are realized through alkali metal ion exchange. Notably, the combination of superior trivalent bismuth emission and low-temperature ion exchange synthesis leads to a novel yellow-emitting K(La0.98Bi0.02)Ta2O7 phosphor which is successfully applied in a white LED device based on a commercially available 365 nm LED chip. Our realizable cases of this low-temperature ion exchange strategy could promote exploration into metastable phosphors with intriguing properties.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xia Z., Liu G., Wen J., Mei Z., Balasubramanian M., Molokeev M. S., Peng L., Gu L., Miller D. J., Liu Q., Poeppelmeier K. R.
Заглавие : Tuning of photoluminescence by cation nanosegregation in the (CaMg)x(NaSc)1-xSi2O6 solid solution
Место публикации : J. Am. Chem. Soc.: American Chemical Society, 2016. - Vol. 138, Is. 4. - P.1158-1161. - ISSN 00027863 (ISSN), DOI 10.1021/jacs.5b12788
Примечания : Cited References: 23. - Work performed by Z.X. and Q.L. was supported by the National Natural Science Foundation of China (51272242 and 51572023), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), and the Beijing Nova Program (Z131103000413047). Work performed by G.L., J.W., Z.M., M.B., and D.J.M. at Argonne National Laboratory was supported by the Office of Basic Energy Sciences of the U.S. Department of Energy (DOE) through Grant DE-AC02-06CH11357 for research on heavy elements chemistry and materials sciences. TEM was accomplished in part at the Center for Nanoscale Materials, a DOE Office of Science User Facility under Contract DE-AC02-06CH11357. Sector 20 operations at APS are supported by DOE and the Canadian Light Source, with additional support from the University of Washington. G.L. acknowledges travel support from the CAS/SAFEA International Partnership Program for Creative Research Teams. K.R.P. gratefully acknowledges support from the National Science Foundation (DMR-1307698).
Предметные рубрики: SPINODAL DECOMPOSITION
ENERGY-TRANSFER
EXSOLUTION
CLINOPYROXEN
NANOCRYSTALS
SEGREGATION
MECHANISMS
PYROXENESS
JERVISITE
PHOSPHORS
Аннотация: Controlled photoluminescence tuning is important for the optimization and modification of phosphor materials. Herein we report an isostructural solid solution of (CaMg)x(NaSc)1-xSi2O6 (0 < x < 1) in which cation nanosegregation leads to the presence of two dilute Eu2+ centers. The distinct nanodomains of isostructural (CaMg)Si2O6 and (NaSc)Si2O6 contain a proportional number of Eu2+ ions with unique, independent spectroscopic signatures. Density functional theory calculations provided a theoretical understanding of the nanosegregation and indicated that the homogeneous solid solution is energetically unstable. It is shown that nanosegregation allows predictive control of color rendering and therefore provides a new method of phosphor development. © 2016 American Chemical Society.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chen M., Xia Z., Molokeev M. S., Wang T., Liu Q.
Заглавие : Tuning of photoluminescence and local structures of substituted cations in xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7:Eu2+ phosphors
Место публикации : Chem. Mater.: American Chemical Society, 2017. - Vol. 29, Is. 3. - P.1430-1438. - ISSN 08974756 (ISSN), DOI 10.1021/acs.chemmater.7b00006
Примечания : Cited References: 37. - The present work was supported by the National Natural Science Foundation of China (Grants 91622125 and 51572023), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-15-003A2).
Ключевые слова (''Своб.индексиров.''): calcium--energy transfer--europium--light emission--lithium--luminescence--phosphors--photoionization--photoluminescence--single crystals--composition ranges--crystal-field splitting--luminescence measurements--non-linear variation--photoionization process--polyhedra distortion--rare earth doped solids--temperature dependent--solid solutions
Аннотация: Local structure modification in solid solution is an essential part of photoluminescence tuning of rare earth doped solid state phosphors. Herein we report a new solid solution phosphor of Eu2+-doped xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7 (0 ≤ x ≤ 1), which share the same β-Ca3(PO4)2 type structure in the full composition range. Depending on the x parameter variation in xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7:Eu2+, the vacancies generated in the M(4) site enable the nonlinear variation of cell parameters and volume, and this increases the magnitude of M(4)O6 polyhedra distortion. The local structure modulation around the Eu2+ ions causes different luminescent behaviors of the two-peak emission and induces the photoluminescence tuning. The shift of the emission peaks in the solid solution phosphors with different compositions has been discussed. It remains invariable at x ≤ 0.5, but the red-shift is observed at x 0.5 which is attributed to combined effect of the crystal field splitting, Stokes shift, and energy transfer between Eu2+ ions. The temperature-dependent luminescence measurements are also performed, and it is shown that the photoionization process is responsible for the quenching effect.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Lim C. S., Aleksandrovsky A. S., Molokeev M. S., Oreshonkov A. S., Ikonnikov D. A., Atuchin V. V.
Заглавие : Triple molybdate scheelite-type upconversion phosphor NaCaLa(MoO4)3:Er3+/Yb3+: Structural and spectroscopic properties
Место публикации : Dalton Trans.: Royal Society of Chemistry, 2016. - Vol. 45, Is. 39. - P.15541-15551. - ISSN 14779226 (ISSN), DOI 10.1039/c6dt02378a
Примечания : Cited References: 71
Ключевые слова (''Своб.индексиров.''): light emission--optical properties--phosphors--sol-gel process--sol-gels--tungstate minerals--after-heat treatment--crystallized particles--homogeneous morphology--photoluminescence emission--spectroscopic property--triple molybdates--up-conversion emission--upconversion phosphors--optical emission spectroscopy
Аннотация: Triple molybdate NaCaLa(1-x-y)(MoO4)3:xEr3+,yYb3+ (x = y = 0, x = 0.05 and y = 0.45, x = 0.1 and y = 0.2, x = 0.2 and y = 0) phosphors were successfully synthesized for the first time by the microwave sol-gel method. Well-crystallized particles formed after heat treatment at 900 °C for 16 h showed a fine and homogeneous morphology with particle sizes of 2-3 ?m. The structures were refined by the Rietveld method in the space group I41/a. The optical properties were examined comparatively using photoluminescence emission and Raman spectroscopy. Under excitation at 980 nm, the NaCaLa0.7(MoO4)3:0.1Er3+,0.2Yb3+ and NaCaLa0.5(MoO4)3:0.05Er3+,0.45Yb3+ particles exhibited a strong 525 nm emission band, a weaker 550 nm emission band in the green region, and three weak 655 nm, 490 nm and 410 nm emission bands in the red, blue and violet regions. The pump power dependence and Commission Internationale de L'Eclairage chromaticity of the upconversion emission intensity were evaluated in detail. © 2016 The Royal Society of Chemistry.
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Вид документа : Статья из журнала
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Автор(ы) : Lim C. S., Aleksandrovsky A. S., Molokeev M. S., Oreshonkov A. S., Atuchin V. V.
Заглавие : The modulated structure and frequency upconversion properties of CaLa2(MoO4)4:Ho3+/Yb3+ phosphors prepared by microwave synthesis
Место публикации : Phys. Chem. Chem. Phys.: Royal Society of Chemistry, 2015. - Vol. 17, Is. 29. - P.19278-19287. - ISSN 1463-9076, DOI 10.1039/c5cp03054d
Примечания : Cited References: 63. - This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2014-046024). VVA, ASA and ASO are partially supported by the Ministry of Education and Science of the Russian Federation.
Аннотация: CaLa2−x(MoO4)4:Ho3+/Yb3+ phosphors with the doping concentrations of Ho3+ and Yb3+ (x = Ho3+ + Yb3+, Ho3+ = 0.05; Yb3+ = 0.35, 0.40, 0.45 and 0.50) have been successfully synthesized by the microwave sol–gel method. The modulated and averaged crystal structures of CaLa2−x(MoO4)4:Ho3+/Yb3+ molybdates have been found by the Rietveld method, and the upconversion photoluminescence properties have been investigated. The synthesized particles, being formed after the heat-treatment at 900 °C for 16 h, showed a highly crystallized state. Under the excitation at 980 nm, CaLa2−x(MoO4)4:Ho3+/Yb3+ particles exhibited strong 545 and 655 nm emission bands in the green and red regions. When the Yb3+:Ho3+ ratios are 9:1 and 10:1, the UC intensity of CaLa1.5(MoO4)4:Yb0.45/Ho0.05 and CaLa1.45(MoO4)4:Yb0.50/Ho0.05 particles is the highest for different bands. The CIE coordinates calculated for CaLa2−x(MoO4)4:Ho3+/Yb3+ phosphors are related to the yellow color field. The Raman spectrum of undoped CaLa2(MoO4)4 has revealed about 13 narrow lines. The strongest band observed at 906 cm−1 was assigned to the ν1 symmetric stretching vibration of MoO4 tetrahedra. The spectra of the samples doped with Ho and Yb, as obtained under the 514.5 nm excitation, were dominated by Ho3+ luminescence over the wavenumber range of 700 cm−1 preventing the recording of the Raman spectra.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Jiang C., Brik M. G., Li L., Li L., Peng J., Wu J., Molokeev M. S., Wong K. -L., Peng M.
Заглавие : The electronic and optical properties of a narrow-band red-emitting nanophosphor K2NaGaF6:Mn4+ for warm white light-emitting diodes
Место публикации : J. Mater. Chem. C. - 2018. - Vol. 6, Is. 12. - P.3016-3025. - ISSN 20507534 (ISSN), DOI 10.1039/c7tc05098d
Примечания : Cited References: 55. - We acknowledge the financial support received from the Program for Innovative Research Team in University of Ministry of Education of China (Grant No. IRT_17R38), the Key Program of Guangzhou Scientific Research Special Project (Grant No. 201607020009), the National Natural Science Foundation of China (Grant No. 51672085, 51322208, 3160440), and the Fundamental Research Funds for the Central Universities. M. G. Brik acknowledges the supports received from the Recruitment Program of High-end Foreign Experts (Grant No. GDW20145200225), the Programme for the Foreign Experts offered by Chongqing University of Posts and Telecommunications, Ministry of Education and Research of Estonia, (Project PUT430) and European Regional Development Fund (Project TK141), and the Guest Professorship at Kyoto University (Prof. S. Tanabe laboratory). The first-principles calculations were carried out using the resources provided by the Wroclaw centre for Networking and Supercomputing (http://wcss.pl; Grant No. WCSS#10117290).
Ключевые слова (''Своб.индексиров.''): energy efficiency--gallium compounds--light emission--light emitting diodes--manganese--manganese compounds--optical properties--phosphors--precipitation (chemical)--quenching--rietveld refinement--sodium compounds
Аннотация: Recently, as a key red component in the development of warm white light-emitting diodes (WLEDs), Recently, as a key red component in the development of warm white light-emitting diodes (WLEDs), Mn4+-doped fluorides with narrow red emission have sparked rapidly growing interest because they improve color rendition and enhance the visual energy efficiency. Herein, a red nanophosphor, K2NaGaF6:Mn4+, with a diameter of 150-250 nm has been synthesized using a simple co-precipitation method. Rietveld refinement reveals that it crystallizes in the space group Fm3m with the cell parameter a = 8.25320(4) Å. The exchange charge model (ECM) has been used to calculate the energy levels of Mn4+ ions in K2NaGaF6, which match well with the experimental spectra. The as-synthesized phosphor exhibits a narrow red emission at around 630 nm (spin-forbidden 2Eg → 4A2 transition of Mn4+ ions) when excited at 365 nm (4A2g → 4T1g) and 467 nm (4A2g → 4T2g), with a quantum efficiency (QE) of 61% and good resistance to thermal quenching. Based on the structure, the formation mechanism of ZPL has been discussed. In addition, the concentration-dependent decay curves of Mn4+ in K2NaGaF6 were fitted using the Inokuti-Hirayama model, suggesting that the dipole-dipole interactions determine the concentration quenching. Finally, encouraged by the good performance, a warm LED with a CRI of 89.4 and CCT of 3779 K was fabricated by employing the title nanophosphor as the red component. Our findings suggest that K2NaGaF6:Mn4+ can be a viable candidate for the red phosphor used in warm WLEDs.
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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chen C. -T., Lin T. -J., Molokeev M. S., Liu W. -R.
Заглавие : Synthesis, luminescent properties and theoretical calculations of novel orange-red-emitting Ca2Y8(SiO4)6O2:Sm3+ phosphors for white light-emitting diodes
Место публикации : Dyes Pigm. - 2018. - Vol. 150. - P.121-129. - ISSN 01437208 (ISSN), DOI 10.1016/j.dyepig.2017.10.047
Примечания : Cited References: 61. - This research was supported by Minister of Science and Technology under contract no. MOST 105-2622-E-033-003-CC2 and MOST 104-2628-E-033-002-MY3.
Ключевые слова (''Своб.индексиров.''): ca2y8(sio4)6o2--photoluminescence--phosphor--solid state reaction
Аннотация: The novel orange-red-emitting Ca2Y8(SiO4)6O2:Sm3+ phosphors (CYSO:Sm3+) were synthesized via conventional a solid state reaction. The crystal structure and atomic coordinates of CYSO:Sm3+ was characterized by Rietveld refinement. Luminesce properties of as-synthesized CYSO:Sm3+ phosphors are carried out by PL/PLE, decay life time, thermal quenching as well as reflectance spectrometer and LED fabrications. The results indicates that composition-optimized CYSO:1%Sm3+ exhibits orange-red emission peaks located on 564, 601, 608 and 648 nm attributed to the transitions of 4G5/2 → 6H5/2, 4G5/2 → 6H7/2, 4G5/2 → 6H7/2 and 4G5/2 → 6H9/2, respectively. The decay lifetime of CYSO:Sm3+ phosphors was in the range of 0.37–1.10 ms. The temperature-dependent photoluminescence is decreased to 80% from room temperature to 150 °C, which is superior to that of commercial red phsophpr-Y2O3:Eu3+. The results of LED fabrication by combing 405 chips and blue/green phosphors are demonstrated in this study. Finally, from viewpoint of theoretical calculations, band structure and density of state for CYSO and CYSO:Sm3+ are studied by first principles calculations. All the results indicate that CYSO:Sm3+ phosphors could be a potential material for white light-emitting diodes.
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11.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Atuchin V. V., Aleksandrovsky A. S., Chimitova O. D., Gavrilova T. A., Krylov A. S., Molokeev M. S., Oreshonkov A. S., Bazarov B. G., Bazarova J. G.
Заглавие : Synthesis and spectroscopic properties of monoclinic α-Eu2(MoO4)3
Коллективы : Ministry of Education and Science of the Russian Federation
Место публикации : J. Phys. Chem. C: American Chemical Society, 2014. - Vol. 118, Is. 28. - P.15404-15411. - ISSN 1932-7447, DOI 10.1021/jp5040739
Примечания : Cited References: 63. - This study is partly supported by the Ministry of Education and Science of the Russian Federation.
Предметные рубрики: RARE-EARTH MOLYBDATES
VIBRATIONAL PROPERTIES
LUMINESCENCE PROPERTIES
CRYSTAL-STRUCTURE
PHASE-TRANSITIONS
TRIPLE MOLYBDATE
SINGLE-CRYSTAL
X-RAY
PHOSPHORS
EUROPIUM
Аннотация: The microcrystals of monoclinic europium molybdate, alpha-Eu-2(MoO4)(3), have been fabricated by solid-state synthesis at T = 753-1273 K for 300 h. The crystal structure of alpha-Eu-2(MoO4)(3) has been refined by the Rietveld method and was found to belong to the space group C2/c with unit cell parameters a = 7.5576(1), b = 11.4709(2), c = 11.5158(2) angstrom, and beta = 109.278(1)degrees (R-B = 3.39%). About 40 narrow Raman lines have been observed in the Raman spectrum of the alpha-Eu-2(MoO4)(3) powder sample. The luminescence spectra of alpha-Eu-2(MoO4)(3) under excitation at 355 and 457.9 nm reveal domination of induced electric dipole transition D-5(0) - F-7(2) and the presence of ultranarrow lines at D-5(0) - F-7(0) and D-5(1) - F-7(0) transitions.
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12.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xia, Zhiguo, Miao S., Chen M., Molokeev M. S., Liu Q.
Заглавие : Structure, crystallographic sites, and tunable luminescence properties of Eu2+ and Ce3+/Li+-activated Ca1.65Sr0.35SiO4 phosphors
Место публикации : Inorg. Chem.: American Chemical Society, 2015. - Vol. 54, Is. 16. - P.7684-7691. - ISSN 0020-1669, DOI 10.1021/acs.inorgchem.5b00455
Примечания : Cited References: 26. - The present work was supported by the National Natural Science Foundations of China (Grants 51002146, 51272242); Natural Science Foundations of Beijing (2132050); the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950); the Beijing Nova Program (Z131103000413047); the Beijing Youth Excellent Talent Program (YETP0635); the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306); and the Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1).Cover image: Artwork representing main idea of this article
Аннотация: Eu2+ and Ce3+/Li+ singly doped and Eu2+/Ce3+/Li+-codoped Ca1.65Sr0.35SiO4 phosphors have been synthesized by a solid-state reaction method. The crystal structure was determined by Rietveld refinement to verify the formation of the αL′-Ca2SiO4 phase with the Sr addition into Ca2SiO4, and the preferred crystallographic positions of the Eu2+ and Ce3+/Li+ ions in Ca1.65Sr0.35SiO4 were analyzed based on a comparison of the unit-cell volumes and the designed chemical compositions of undoped isostructural compounds Ca(2-x)SrxSiO4 (x = 0.25, 0.35, 0.45, 0.55 and 0.65). Ce3+/Li+ singly activated Ca1.65Sr0.35SiO4 phosphors exhibit strong absorption in the range of 250-450 nm and a blue emission peak centered at about 465 nm. When Eu2+ ions are codoped, the emission colors of Ca1.65Sr0.35SiO4:Ce3+,Li+,Eu2+ phosphors under the irradiation of 365 nm can be finely tuned from blue to green through the energy transfer from Ce3+ to Eu2+. The involved energy-transfer process between Ce3+ and Eu2+ and the corresponding mechanism are discussed in detail. The reported Ca1.65Sr0.35SiO4:Ce3+,Li+,Eu2+ phosphor might be a candidate for color-tunable blue-green components in the fabrication of near-ultraviolet-pumped white-light-emitting diodes (WLEDs). © 2015 American Chemical Society.
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13.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ji H., Wang L., Molokeev M. S., Hirosaki N., Xie R., Huang Z., Xia Z., Ten Kate O. M., Liu L., Atuchin V. V.
Заглавие : Structure evolution and photoluminescence of Lu3(Al,Mg)2(Al,Si)3O12:Ce3+ phosphors: New yellow-color converters for blue LED-driven solid state lighting
Место публикации : J. Mater. Chem. C: Royal Society of Chemistry, 2016. - Vol. 4, Is. 28. - P.6855-6863. - ISSN 20507534 (ISSN), DOI 10.1039/c6tc00966b
Примечания : Cited References: 44. - This work was partially supported by the National Natural Science Foundations of China (Grant No. 51511130035, 51272259, 61575182, 51561135015, and 51572232) and the Russian Foundation for Basic Research (Grant No. 15-52-53080). We are also grateful to financial support from the JSPS KAKENHI (No. 15K06448). H. J. thanks the China Scholarship Council (CSC) for scholarship support. V. V. A. was partially supported by the Ministry of Education and Science of the Russian Federation.
Предметные рубрики: WHITE LEDS
LUMINESCENCE PROPERTIES
EMITTING-DIODES
GARNET PHOSPHORS
SUBSTITUTION
Ce3+
PHASE
Ca
Аннотация: This paper reports the development of new phosphors using the chemical unit cosubstituting solid solution design strategy. Starting from Lu3Al5O12, the Al3+-Al3+ couple in respective octahedral and tetrahedral coordination was simultaneously substituted by a Mg2+-Si4+ pair forming the Lu3(Al2-xMgx)(Al3-xSix)O12:Ce3+ (x = 0.5-2.0) series; as a result, the CeO8 polyhedrons were compressed and the emission got red-shifted from green to yellow together with the broadening. The evolution of, the unit cell, the local structural geometry as well as the optical properties of Ce3+ in these garnet creations, in response to the gradual Mg-Si substitution for Al-Al, were studied by combined techniques of structural refinement and luminescence measurements. The new composition Lu2.97Ce0.03Mg0.5Al4Si0.5O12 was comprehensively evaluated regarding its potential application in blue LED-driven solid state white lighting: the maximum emission is at 550 nm under ?ex = 450 nm; the internal and external quantum efficiencies can reach 85% and 49%, respectively; a 1-phosphor-converted wLED lamp fabricated using the as-prepared phosphor exhibits the luminous efficacy of 105 lm W-1, the correlated color temperature of 6164 K and the color rendering index (Ra) of 75.6. The new solid solution composition series is open for further optimization to enhance the competence for commercial consideration. © 2016 The Royal Society of Chemistry.
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14.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xia Z., Miao S., Molokeev M. S., Chen M., Liu Q.
Заглавие : Structure and luminescence properties of Eu2+ doped LuxSr2-xSiNxO4-x phosphors evolved from chemical unit cosubstitution
Место публикации : J. Mater. Chem. C: Royal Society of Chemistry, 2016. - Vol. 4, Is. 6. - P.1336-1344. - ISSN 20507534 (ISSN), DOI 10.1039/c5tc04222d
Примечания : 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).
Предметные 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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15.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhang Y., Liu H., Mei L., Molokeev M. S., Wang Y., Huang Z.
Заглавие : Structure and color-tunable luminescence properties of Ce3+ and Tb3+-activated Mg2La8(SiO4)6O2 phosphors based on energy transfer behavior
Место публикации : J. Solid State Chem. - 2017. - Vol. 255. - P.36-41. - ISSN 00224596 (ISSN), DOI 10.1016/j.jssc.2017.07.026
Примечания : Cited References: 45. - This present work was supported by the National Natural Science Foundations of China (Grant no. 41172053), the Fundamental Research Funds for the Central Universities (Grant nos. 2652016083 and 2652016037), and Science and Technology Innovation Fund of the China University of Geosciences (Beijing).
Ключевые слова (''Своб.индексиров.''): crystal structure--luminescence properties--phosphors--apatite structure
Аннотация: A series of novel luminescent emission-tunable phosphors Mg2La8(SiO4)6O2:Ce3+,Tb3+ (MLS:Ce3+,Tb3+) have been prepared by a solid-state reaction. The phase formation was firstly confirmed through X-ray diffraction technique and refined by the Rietveld method. The MLS:Ce3+,Tb3+ phosphors, which crystallized in apatite-type hexagonal phase, exhibited a broad excitation band ranging from 200 to 400 nm and several emission bands centered at 426 nm and 551 nm. Energy transfer from Ce3+ to Tb3+ ions via a dipole-dipole mechanism occurred in the as-synthesized phosphors upon ultraviolet (UV) excitation. The energy transfer efficiency increases with increasing doping content of Tb3+ ions, which was confirmed by the luminescence spectra and fluorescence decay curves of corresponding ions simultaneously. The energy transfer critical distance was calculated and evaluated by both the concentration quenching and spectral overlap methods. The chromaticity of emission-tunable phosphors was also characterized by the Commission International de l'eclairage (CIE) chromaticity indexes, and the color tone can be tuned from blue (0.179, 0.122) to green (0.267, 0.408) by controlling the ratio of Ce3+/Tb3+. © 2017 Elsevier Inc.
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16.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhu J., Xia, Zhiguo, Zhang Y., Molokeev M. S., Liu Q.
Заглавие : Structural phase transitions and photoluminescence properties of Eu3+ doped Ca(2-x)BaxLaNbO6 phosphors
Место публикации : Dalton Trans.: Royal Society of Chemistry, 2015. - Vol. 44, Is. 42. - P.18536-18543. - ISSN 1477-9226, DOI 10.1039/c5dt03430b
Примечания : Cited References: 27. - The present work was supported by the National Natural Science Foundation of China (Grant No. 51272027, 51472028 and 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306)
Предметные рубрики: Double-perovskite
Luminescence properties
Thermal-stability
Crystal-chemistry
Red phosphors
White LEDs
Symmetry
Band
Ta
Ln
Аннотация: Crystal structures of the series of double perovskites Ca(2-x)BaxLaNbO6:Eu3+ phosphors have been examined by powder X-ray diffraction and Rietveld refinements. Ca2LaNbO6 has a monoclinic (P21/n) and Ba2LaNbO6 has a monoclinic (C2/m) structure. The structural phases of Ca(2-x)BaxLaNbO6:Eu3+ samples are divided into three sections depending on different Ca/Ba ratios: (1) monoclinic phase (P21/n) as Ca2LaNbO6 in the range of x = 0-0.1, (2) mixed phases containing Ca2LaNbO6 and Ba2LaNbO6 between 0.15 and 1.2, and (3) monoclinic phase (C2/m) as Ba2LaNbO6 for x = 1.4-2. Eu3+ ions act as the structural probes to study the structural phase transitions, and the evolution of the photoluminescence properties and thermal stability behaviours has been also comparatively investigated depending on different structural symmetries from Ca2LaNbO6 to Ba2LaNbO6 phase. The strong red emission from 5D0-7F2 peaking at 618 nm can be found in Ca2LaNbO6:Eu3+ phosphors, which is attributed to the low crystal field effect of the activator ions located in the highly distorted [Lao8] polyhedra sites. The composition-optimized phosphors can find applications in white light emitting diodes (LEDs).
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17.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chen M., Xia Z., Molokeev M. S., Liu Q.
Заглавие : Structural phase transformation and luminescent properties of Ca2-xSrxSiO4:Ce3+ orthosilicate phosphors
Место публикации : Inorg. Chem.: American Chemical Society, 2015. - Vol. 54, Is. 23. - P.11369-11376. - ISSN 00201669 (ISSN), DOI 10.1021/acs.inorgchem.5b01955
Примечания : 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)
Предметные 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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18.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Wei Y., Lin C. C., Quan Z., Molokeev M. S., Atuchin V. V., Chan T. -S., Liang Y., Lin J., Li G.
Заглавие : Structural evolution induced preferential occupancy of designated cation sites by Eu2+ in M5(Si3O9)2 (M = Sr, Ba, Y, Mn) phosphors
Место публикации : RSC Adv.: Royal Society of Chemistry, 2016. - Vol. 6, Is. 62. - P.57261-57265. - ISSN 20462069 (ISSN), DOI 10.1039/c6ra11681g
Примечания : 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.
Предметные 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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19.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Fang M. -H., Mahlik S., Lazarowska A., Grinberg M., Molokeev M. S., Sheu H. -S., Lee J. -F., Liu R. -S.
Заглавие : Structural Evolution and Effect of the Neighboring Cation on the Photoluminescence of Sr(LiAl3)1−x(SiMg3)xN4:Eu2+ Phosphors
Место публикации : Angew. Chem. Int. Ed. - 2019. - Vol. 58, Is. 23. - P.7767-7772. - ISSN 14337851 (ISSN), DOI 10.1002/anie.201903178
Примечания : Cited References: 23. - This work was supported by the Ministry of Science and Technology of Taiwan (Contract Nos. MOST 107‐2113‐M‐002‐008‐MY3 and MOST 107–2923‐M‐002‐004‐MY3). This work was supported by the National Science Centre Poland grant Opus no. 2016/23/B/ST3/03911 and the National Centre for Research and Development Poland Grant (No. PL‐TW/V/1/2018).
Предметные рубрики: Solid-Solution Phosphors
Аннотация: In this study, a series of Sr(LiAl3)1−x(SiMg3)xN4:Eu2+ (SLA‐SSM) phosphors were synthesized by a solid‐solution process. The emission peak maxima of SLA‐SSM range from 615 nm to 680 nm, which indicates structural differences in these materials. 7Li solid‐state NMR spectroscopy was utilized to distinguish between the Li(1)N4 and Li(2)N4 tetrahedra in SLA‐SSM. Differences in the coordination environments of the two Sr sites were found which explain the unexpected luminescent properties. Three discernible morphologies were detected by scanning electron microscopy. Temperature‐dependent photoluminescence and decay times were used to understand the diverse environments of europium ions in the two strontium sites Sr1 and Sr2, which also support the NMR analysis. Moreover, X‐ray absorption near‐edge structure studies reveal that the Eu2+ concentration in SLA‐SSM is much higher than that in in SrLiAl3N4:Eu2+ and SrSiMg3N4:Eu2+ phosphors. Finally, an overall mechanism was proposed to explain the how the change in photoluminescence is controlled by the size of the coordinated cation.
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20.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhang Z., Ma C., Gautier R., Molokeev M. S., Liu Q., Xia Z.
Заглавие : Structural confinement toward giant enhancement of red emission in Mn2+-based phosphors
Место публикации : Adv. Funct. Mater. - 2018. - Vol. 28, Is. 41. - Ст.1804150. - ISSN 1616301X (ISSN), DOI 10.1002/adfm.201804150
Примечания : Cited References: 26. - The present work was supported by the National Natural Science Foundation of China (Grants 51722202, 91622125, and 51572023), Natural Science Foundations of Beijing (2172036), and by Russian Foundation for Basic Research according to the research project 17‐52‐53031, and by the French National Agency for Research (ANR Young Researchers, ANR‐16‐CE08‐0003‐01, Combi‐SSL project). C.‐G.M. thanks supports from China Scholarship Council (CSC File No. 201607845015) and Wenfeng High‐end Talents Project of CQUPT (Grant No. W2016‐01). The authors would like thank Dr. Shuao Wang, Professor of Soochow University, for supplying the single crystal data collection.
Аннотация: Structural confinement effect on a pair of Eu2+ and Mn2+ optical centers is developed to realize the greatly enhanced red emission attributed to the 4T1(4G)–6A1(6S) transition of Mn2+ ions. Sr9Mn1.26(2)Li0.24(2)(PO4−δ)7 , when it is doped with Eu2+, emerges as a new red‐emitting phosphor, and the intensity dependence of such a red emission on the trace amounts of Eu2+ doping is quantitatively analyzed with a combined experimental and theoretical methods. The modeling result confirms the validity of this proposed design strategy, and the intrinsic high‐efficient Eu2+–Mn2+ energy transfer process can be elucidated by the structural confinement effect featured as some Sr (Eu) close to Mn atoms. The results can initiate the exploration of Mn2+‐based red phosphors for pc‐white light‐emitting diodes applications, and such a strategy can be easily expanded to other systems, thus opening a new perspective for the development of luminescence materials.
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