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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Ying, Rong, Ximing, Li, Mingze, Molokeev M. S., Zhao, Jing, Xia, Zhiguo
Заглавие : Incorporating rare-earth terbium(III) ions into Cs2AgInCl6:Bi nanocrystals toward tunable photoluminescence
Место публикации : Angew. Chem. - 2020. - Vol. 132, Is. 28. - P.11731-11737. - ISSN 1521-3757(eISSN), DOI 10.1002/ange.202004562
Примечания : Cited References: 43
Предметные рубрики: HALIDE DOUBLE PEROVSKITE
LEAD-FREE
LANTHANIDE
STABILITY
EMISSION
Аннотация: The incorporation of impurity ions or doping is a promising method for controlling the electronic and optical properties and the structural stability of halide perovskite nanocrystals (NCs). Herein, we establish relationships between rare‐earth ions doping and intrinsic emission of lead‐free double perovskite Cs2AgInCl6 NCs to impart and tune the optical performances in the visible light region. Tb3+ ions were incorporated into Cs2AgInCl6 NCs and occupied In3+ sites as verified by both crystallographic analyses and first‐principles calculations. Trace amounts of Bi doping endowed the characteristic emission (5D4→7F6‐3) of Tb3+ ions with a new excitation peak at 368 nm rather than the single characteristic excitation at 290 nm of Tb3+. By controlling Tb3+ ions concentration, the emission colors of Bi‐doped Cs2Ag(In1−xTbx)Cl6 NCs could be continuously tuned from green to orange, through the efficient energy‐transfer channel from self‐trapped excitons to Tb3+ ions. Our study provides the salient features of the material design of lead‐free perovskite NCs and to expand their luminescence applications.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhou J., Chen Y., Jiang C., Milicevic B., Molokeev M. S., Brik M. G., Bobrikov I. A., Yan J., Li J., Wu M.
Заглавие : High moisture resistance of an efficient Mn4+-activated red phosphor Cs2NbOF5:Mn4+ for WLEDs
Место публикации : Chem. Eng. J. - 2021. - Vol. 405. - Ст.126678. - ISSN 13858947 (ISSN), DOI 10.1016/j.cej.2020.126678
Примечания : Cited References: 43. - This work was financially supported by grants from the National Natural Science Foundation of China (No. 51802359, 21801254, 51902354) and its Joint Funds of Yunnan and Guangdong Province (No. U1702254 and No. U1801253), Special Fund of Guangdong Province Project for Applied Science and Technology Research and Development (No. 2017B090917001), Guangdong Basic and Applied Basic Research Foundation (No. 2020A1515010556), the Fundamental Research Funds for the Central Universities (No. 19lgpy123), and China Postdoctoral Science Foundation (No. 2019M663230). M. G. Brik thanks the supports from the National Recruitment Program of High-end Foreign Experts (No. GDT20185200479 and GDW20145200225), the Programme for the Foreign Experts (No. W2017011) and Wenfeng High-end Talents Project (No. W2016-01) offered by Chongqing University of Posts and Telecommunications (CQUPT) , Estonian Research Council grant PUT PRG111, and European Regional Development Fund (TK141)
Аннотация: Mn4+-activated fluoride red phosphors, the most important red phosphors for warm white light emitting diodes (LEDs), usually suffer from inherent poor moisture resistance which is a major obstacle to their long-lasting outdoor applications in a high humidity environment. Surface modification of phosphors by coating with either organic or inorganic shells is an effective way to improve waterproof stability. However, the coating procedure usually has a negative impact on the luminous efficacy due to the increased passivation shell thickness. In this work, Mn4+-activated oxyfluoroniobate (Cs2NbOF5), a highly efficient phosphor with internal quantum efficiency of ca. 82%, has been successfully synthesized and it is interesting to note that Cs2NbOF5:Mn4+ can exhibit remarkably improved waterproof stability even without surface coating compared to well-accepted commercial fluoride red-emitting phosphor, K2SiF6:Mn4+. The results obtained indicate that Nb5+ ions inside red phosphor play a crucial role in improving the water-resistant performance of Mn4+, which provides a new concept for overcoming the downside of their waterproof in humid conditions and maintaining the luminescence efficiency. In the final phase white LEDs with a high luminous efficacy of 174 lm/W (higher than commercial fluoride red phosphors), low correlated color temperature (3164 K) and high color rendering index (Ra = 90 and R9 = 85) have been fabricated using Cs2NbOF5:Mn4+.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Denisenko Y. G., Atuchin V. V., Molokeev M. S., Wang N., Jiang X., Aleksandrovsky A. S., Krylov A. S., Oreshonkov A. S., Sedykh A. E., Volkova S. S., Lin Z., Andreev O. V., Muller-Buschbaum K.
Заглавие : Negative thermal expansion in one-dimension of a new double sulfate AgHo(SO4)2 with isolated SO4 tetrahedra
Место публикации : J. Mater. Sci. Technol. - 2021. - Vol. 76. - P.111-121. - ISSN 10050302 (ISSN), DOI 10.1016/j.jmst.2020.10.026
Примечания : Cited References: 55. - This work was financially supported by the Russian Foundation for Basic Research (Nos. 18-02-00754 and 18-32-20011 ), the National Scientific Foundations of China (No. 11974360 ) and the Russian Science Foundation (No. 19-42-02003 , in the part of conceptualization). M.S. Molokeev, A.S. Aleksandrovsky, A.S. Krylov, and A.S. Oreshonkov are grateful to Basic Project of the Ministry of Science of the Russian Federation in part of XRD, luminescent and Raman studies. IR-spectrometry was performed using resources of the Research Resource Center "Natural Resource Management and Physico-Chemical Research". Use of equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center «Krasnoyarsk Science Center SB RAS» is acknowledged
Аннотация: A double holmium-silver sulfate was obtained for the first time. The temperature intervals for the formation and stability of the compound were determined by differential scanning calorimetry. The crystal structure of AgHo(SO4)2 was determined by Rietveld method. The X-ray diffraction (XRD) analysis showed that the compound crystallizes in the monoclinic syngony, space group P21/m, with the unit cell parameters a = 4.71751 (4) Å, b = 6.84940 (6) Å and c = 9.89528 (9) Å, β = 95.1466 (4)°, V = 318.448 (5) Å3, Z = 2, RB = 1.55 %, T = 303 K. Two types of sulfate tetrahedra were found in the structure, which significantly affected the spectral properties in the infrared range. In the temperature range of 143−703 K, a negative thermal expansion along the b direction accompanied by a positive thermal expansion along the a and c directions was observed. It was established that negative thermal expansion is the result of the deformation of sulfate tetrahedra, which is affected by the movement of holmium and silver atoms. The excitation in the blue spectral range (457.9 nm) produces a luminescence in light blue (489 nm), green (545 nm) and red (654 nm) spectral ranges, and the latter two were of comparable intensity that is favorable for WLED sources. The observed luminescent band distribution is ascribed to the specific crystal field at Ho3+ ion sites rather than a variation of radiationless probability.
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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) : Gai S., Zhu H., Gao P., Zhou C., Kong Z., Molokeev M. S., Qi Z., Zhou Z., Xia M.
Заглавие : Structure analysis, tuning photoluminescence and enhancing thermal stability on Mn4+-doped La2-xYxMgTiO6 red phosphor for agricultural lighting
Место публикации : Ceram. Int. - 2020. - Vol. 46, Is. 12. - P.20173-20182. - ISSN 02728842 (ISSN), DOI 10.1016/j.ceramint.2020.05.095
Примечания : Cited References: 40. - The authors would like to gratefully acknowledge funds from the National Natural Science Foundation of China (Grant No. 21706060 , 51703061 , 51974123 ), the Hunan Graduate Research and Innovation Project (Grant No. CX2018B396 ), the Hunan provincial Engineering Technology Research Center for Optical Agriculture (Grant No. 2018TP2003 ), the Scientific Research Fund of Hunan Provincial Education Department (15K058, 19C0903), the Natural Sciences Foundation of Hunan agricultural university, China (Grant No. 19QN11), the Science and Technology project of Changsha (KH1801219) and the Huxiang high level talent gathering project (2019RS1077)
Аннотация: Currently, phosphor-converted LEDs (pc-LEDs) are revolutionizing the industry of plant growth lighting. To meet the requirements of this technology, phosphors with tunable photoluminescence, high thermal stability and luminous intensity are required. Herein, we found that the simple substitution of yttrium for lanthanum in La2MgTiO6:Mn4+ (LMT:Mn4+) system could satisfy above three criteria simultaneously. The photoluminescence properties can be regulated by continuously controlling the chemical composition of La2-xYxMgTiO6:Mn4+ solid solution. The La sites are occupied by Y ions, causing a significant blue shift in the emission spectra which owing to the change of local crystal field strengthen. Meanwhile, the thermal stability and decay lifetimes are also varied due to the variation of local structure and band gap energy. The thermal stability of the material reaches 83.5% at 150 °C, which is better than the reported La2MgTiO6:Mn4+ and Y2MgTiO6:Mn4+ phosphors. The electronic luminescence (EL) of pc-LED devices using La2-xYxMgTiO6:Mn4+ red phosphor is evaluated, which matching the absorption regions of plant pigments well, reflecting the superiority of the studied phosphors in plant growth lighting areas.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Gaochao, Molokeev M. S., Lei, Bingfu, Xia, Zhiguo
Заглавие : Two-site Cr3+ occupation in the MgTa2O6:Cr3+ phosphor toward broad-band near-infrared emission for vessel visualization
Место публикации : J. Mater. Chem. C. - 2020. - Vol. 8, Is. 27. - P.9322-9328. - ISSN 2050-7526, DOI 10.1039/d0tc01951h. - ISSN 2050-7534(eISSN)
Примечания : 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.
Предметные 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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Lai S., Zhao M., Qiao J., Molokeev M. S., Xia Z.
Заглавие : Data-driven photoluminescence tuning in Eu2+-doped phosphors
Место публикации : J. Phys. Chem. Lett. - 2020. - Vol. 11, Is. 14. - P.5680-5685. - ISSN 19487185 (ISSN), DOI 10.1021/acs.jpclett.0c01471
Примечания : Cited References: 34. - 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), Guangzhou Science & Technology Project (202007020005), 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
Предметные рубрики: Phosphors
Luminescence properties
Crystal structure
Ions
Quantum mechanics
Аннотация: Discovery of rare earth phosphors has generally relied on the chemical intuition and time-intensive trial-and-error synthesis; therefore, finding new materials assisted by data-driven computations is urgent. Herein, we utilize a regression model to predict the emission wavelengths of Eu2+-doped phosphors by revealing the relationships between the crystal structure and luminescence property. The emission wavelengths of [Rb(1–x)K(x)]3LuSi2O7:Eu2+ (0 ≤ x ≤ 1) phosphors, as examples for the data-driven photoluminescence tuning, are successfully predicted on the basis of the existing data of only eight systems, also consistent with the experimental results. These phosphors can be excited by blue light and exhibit broad-band red and near-infrared emission ranging from 619 to 737 nm. These findings in Eu2+-doped silicate phosphors indicate that data-driven computations through the regression mode would have bright application in discovering novel phosphors with a target emission wavelengths.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Su B., Song G., Molokeev M. S., Golovnev N. N., Lesnikov M. K., Lin Z., Xia Z.
Заглавие : Role of metal-chloride anions in photoluminescence regulations for hybrid metal halides
Место публикации : J. Phys. Chem. Lett. - 2021. - Vol. 12, Is. 7. - P.1918-1925. - ISSN 19487185 (ISSN), DOI 10.1021/acs.jpclett.1c00182
Примечания : Cited References: 40. - This work is supported by the National Natural Science Foundation of China (51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (D2190980), the 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
Аннотация: Organic–inorganic hybrid metal halides with emissive organic cations are of great interest due to their structural diversity and interesting photophysical properties. Here, we assemble emissive organic cations (EnrofloH22+) with different metal–chloride anions (Pb2Cl62– to Bi2Cl104– to SnCl62–) to form the new single crystal phases, and thus the photoluminescence properties of the metal halides, including Stokes shift, full width at half-maximum (FWHM), and photoluminescence quantum yield (PLQY) have been studied accordingly. (EnrofloH2)SnCl6·H2O, as an example, possesses narrow FWHM and high PLQY, which are caused by the strong π–π stacking and inter- and intramolecular hydrogen bonds interactions. Compared with EnrofloH22+ cation in solution, the interactions generate a restraining effect and increase the rigid degree of EnrofloH22+ cation in the bulk single crystals. Our work clarifies the photophysical properties of the EnrofloH22+ organic cations by constructing the inter- and intramolecular interactions and boosts the further study of organic–inorganic hybrid metal halides materials with different luminescence mechanisms.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Yang, Zhiyu, Zhou, Yayun, Qiao, Jianwei, Molokeev M. S., Xia, Zhiguo
Заглавие : Rapid synthesis of red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors and the tunable photoluminescence via Sr/Ba substitution
Место публикации : Adv. Opt. Mater. - 2021. - Vol. 9. Is. 16. - Ст.2100131. - ISSN 2195-1071, DOI 10.1002/adom.202100131
Примечания : Cited References: 44. - Z.Y. and Y.Z. contributed equally to this work. This research was supported by the National Natural Science Foundations of China (Grant Nos. 51972118 and 51961145101), International Cooperation Project of National Key Research and Development Program of China (No. 2021YFE0105700), Guangzhou Science & Technology Project (No. 202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (No. 2017BT01x137). This work was also funded by RFBR according to the research Project No. 19-52-80003
Предметные рубрики: LUMINESCENCE PROPERTIES
THERMAL-STABILITY
EU2+
GREEN
EU3+
SR
Аннотация: Discovering new Eu2+-doped red-emitting phosphors in oxide-based materials is a challenge for white light-emitting diode (WLED) applications. Herein, a highly efficient high-frequency induction heating method is employed to rapidly prepare the red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors peaking at 614 nm and exhibiting a high photoluminescence quantum yield of 78.4% under the excitation of 440 nm. The structural and spectral analyses suggest that Eu2+ ions tend to enter the [Sc1/Ga1O6] and [Ga2O6] polyhedrons with small coordination numbers, leading to the broadband red emission originated from large crystal field splitting of Eu2+ 5d level. The chemical substitution of Ba in the Sr site enhances the thermal stability and helps to the photoluminescence tuning from 614 to 728 nm in SrBaSc0.5Ga1.5O5:Eu2+. The WLED device fabricated by blending the red Sr1.7Ba0.3Sc0.5Ga1.5O5:Eu2+ and yellow Y3(Al, Ga)5O12:Ce3+ phosphors shows a high color-rendering index (Ra = 91.1), and low color-correlated temperature (CCT = 4750 K). This study aims to provide a new synthesis method and design principle for guiding the development of Eu2+-doped oxide-based red phosphors with low preparation cost; moreover, the photoluminescence tuning strategy via cation substitutions is essential to achieve tunable emission, even the near-infrared luminescence.
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10.

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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