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    Novel Cr3+-doped garnet phosphor with broadband efficient far-red emission for photochrome matching plant-lighting / X. Dai, X. Zou, H. Zhang [et al.] // Adv. Opt. Mater. - 2024. - Vol. 12, Is. 11. - Ст. 2302380, DOI 10.1002/adom.202302380. - Cited References: 54. - The work was supported by the National Natural Science Foundations of China (No. 12274144), the Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams (No. 2023KJ122), the Key Realm R&D Program of Guangdong Province (No. 2021B0707010003), the Guangdong Provincial Science and Technology Project (No. 2022A1515010229), and the Project of GDUPS (2018) for Prof. Bingfu LEI . - ISSN 2195-1071
   Перевод заглавия: Новый гранатовый люминофор, легированный Cr3+, с широкополосным эффективным излучением в дальнем красном диапазоне для фотохромного освещения растений
Кл.слова (ненормированные):
Ca2YAl3–xGe2O12:xCr3+ -- garnets -- plant growth LEDs -- pc-LEDs -- photoluminescence
Аннотация: Cr3+-doped phosphors are highly recognized in various fields for their remarkable luminous efficiency and spectral flexibility, including modern agriculture and horticulture. However, the shortage of suitable Cr3+-doped phosphors for far-red LED devices has inhibited their popularization in plant lighting. Herein, an innovative Cr3+-doped phosphor Ca2YAl3Ge2O12:Cr3+ (CYAG:Cr3+), achieving a broad far-red emission at 770 nm upon 450 nm blue light excitation is designed. The optimal CYAG:Cr3+ phosphor exhibits a high internal quantum yield of 78.2% and low thermal-quenching behavior of 85%@373 K. Thus, the fabricated phosphor-converted LEDs (pc-LEDs) for plant far-red lighting have a high output power of 33.3 mW and photovoltaic conversion efficiency of 11.5% at 100 mA. The potential of CYAG:Cr3+ in plant lighting is assessed by supplementing the far-red lighting of Italian lettuce with fabricated pc-LEDs, and the biomass of Italian lettuce is significantly increased by 33%. The successful development of CYAG:Cr3+ phosphors provides a high-quality option for plant far-red light devices and further stimulates the development of new Cr3+-doped plant-lighting phosphors.

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Держатели документа:
Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangdong, Guangzhou, 510642, China
Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Guangdong, Maoming, 25100, China
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk, 660036, Russian Federation
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Physics and Optoelectronics, South China University of Technology, Guangzhou, 510641, China

Доп.точки доступа:
Dai, X.; Zou, X.; Zhang, H.; Chen, W.; Yang, C.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.; Liu, Y.; Zhang, X.; Zheng, M.; Lei, B.
}
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Temperature/component-dependent luminescence in lead-free hybrid metal halides for temperature sensor and anti-counterfeiting / G. Zhou, Y. Wang, Y. Mao [et al.] // Adv. Funct. Mater. - 2024. - Ст. 2401860, DOI 10.1002/adfm.202401860. - Cited References: 89. - G.J.Z. and Y.T.W. contributed equally to this work. This work was supported by the National Natural Science Foundation of China (No.52202177, 22271211), Fundamental Research Program of Shanxi Province (No.20210302124054), Science and Technology Innovation Project of Colleges and Universities in Shanxi Province (No.2021L262), 1331 Project of Shanxi Province, Postgraduate Innovation Project of Shanxi Province (No.2023KY462), and supported by the Ministry of Science and High Education of Russian Federation (No.FSRZ-2023-0006). The authors would like to thank Prof. Haijun Jiao, Leibniz-Institut für Katalyse e.V., Germany, for the theoretical support on the electron-transition mechanism . - Article in press. - ISSN 1616-301X. - ISSN 1616-3028
Кл.слова (ненормированные):
electron-transition -- hybrid metal halides -- optical-functional applications -- self-trapped excitons -- tunable photoluminescence
Аннотация: Hybrid metal halides (HMHs) have emerged as a promising platform for optically functional crystalline materials, but it is extremely challenging to thoroughly elucidate the electron transition coupled to additional ligand emission. Herein, to discover sequences of lead-free HMHs with distinct optically active metal cations are aimed, that is, Sb3+ (5s2) with the lone-pair electron configuration and In3+ (4d10) with the fully-filled electron configuration. (Me2NH2)4MCl6·Cl (Me = −CH3, M = Sb, In) exhibits the superior temperature/component-dependent luminescence behaviors resulting from the competition transition between triplet-states (Tn-S0) self-trapped excitons (STEs) of inorganic units and singlet-state (S1-S0) of organic cations, which is manipulated by the optical activity levels of [SbCl6]3− and [InCl6]3−. The bonding differences between Sb3+/In3+ and Cl− in terms of electronic excitation and hybridization are emphasized, and the different electron-transition mechanisms are established according to the PL spectra at the extreme temperature of 5 to 305 K and theoretical calculations. By fine-tuning the B-site Sb3+/In3+ alloying, the photoluminescence quantum yield (PLQY = 81.5%) and stability are optimized at 20% alloying of Sb3+. This research sheds light on the rules governing PL behaviors of HMHs, as well as exploring the optical-functional application of aviation temperature sensors and access-control systems.

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Держатели документа:
Key Laboratory of Magnetic Molecules and Magnetic Information Materials (Ministry of Education), School of Chemistry and Material Science, Shanxi Normal University, Taiyuan 030031, P. R. China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
International Research Center of Spectroscopy and Quantum Chemistry-IRC SQC, Siberian Federal University, Krasnoyarsk 660041, Russia
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, Guangdong Engineering Technology Research and Development Center of Special Optical Fiber Materials and Devices, School of Physics and Optoelectronics, South China University of Technology, Guangzhou, Guangdong 510641, P. R. China
College of Chemistry & Chemical Engineering, Key Laboratory of Interface Science and Engineering in Advanced Material, Ministry of Education, Taiyuan University of Technology, Taiyuan, Shanxi 030024, P. R. China

Доп.точки доступа:
Zhou, G.; Wang, Y.; Mao, Y.; Guo, C.; Zhang, J.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.; Zhang, X.-M.
}
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    Two organic-inorganic manganese(II) halide hybrids containing protonated N,N’-dialkylthioureas with efficient green-emission / N. N. Golovnev, M. A. Gerasimova, I. A. Ostapenko [et al.] // J. Mol. Struct. - 2023. - Vol. 1277. - Ст. 134851, DOI 10.1016/j.molstruc.2022.134851. - Cited References: 42. - The reported study was funded by RFBR according to the research project № 19-52-80003. X-ray data from single crystals and powders were obtained with the analytical equipment of Krasnoyarsk Center of collective use of SB RAS . - ISSN 0022-2860
   Перевод заглавия: Два металорганических галогенида марганца(II), содержащие протонированные N,N'-диалкилтиомочевины с эффективным зеленым излучением
Кл.слова (ненормированные):
Zero-dimensional hybrid manganese(II) halides -- N,N′-alkylthioureas -- Synthesis -- Structure -- Photoluminescence -- Quantum yield -- X-ray diffraction
Аннотация: Luminescent (C5H13N2S)2[MnBr4] (1) and (C7H17N2S)2[MnBr4] (2) (C5H12N2S = N,N′-diethylthiourea, C7H16N2S = N,N′-diisopropylthiourea) were prepared via solvothermal method, and the structures of these compounds have been resolved using X-ray single crystal diffraction. The structures consist of electrostatically bound MnBr42− anions and organic C5H13N2S+ and C7H17N2S+ cations. The intermolecular N−H···Br and N−H···S hydrogen bonds additionally stabilize crystal structures of 1-2. Upon excitation over broadband covering the range 265 to 515 nm, these compounds show green emission peaking at 526 nm for 1 and 522 nm for 2, which is assigned to the 4T1→ 6A1 electronic transition of Mn2+ from isolated within the crystal structures MnBr42− tetrahedra. The photoluminescence quantum yield (PLQY) of powder 1 is 97 ± 7% for excitation at 440 nm and that of powder 2 is 83 ± 7% for excitation at 365 nm. The high PLQY indicates the absence of noticeable concentration quenching at shortest Mn···Mn distance of 8.11 and 8.73 Å between Mn2+ ions within the structures of 1 and 2. The high-performance photoluminescence of 0D (C5H13N2S)2[MnBr4] and (C7H17N2S)2[MnBr4] compounds demonstrated promising applications in photonics.

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Держатели документа:
Siberian Federal University, Krasnoyarsk 660041, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russia

Доп.точки доступа:
Golovnev, Nicolay N.; Gerasimova, Marina A.; Ostapenko, Ivan A.; Zolotov, Andrey O.; Molokeev, M. S.; Молокеев, Максим Сергеевич
}
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Manganese luminescent centers of different valence in yttrium aluminum borate crystals / A. Molchanova, K. Boldyrev, N. Kuzmin [et al.] // Materials. - 2023. - Vol. 16, Is. 2. - Ст. 537, DOI 10.3390/ma16020537. - Cited References: 49. - This work was supported in part by the Russian Science Foundation under Grant No. 21-72-00134. K.B. and M.P. acknowledge financial support from the Ministry of Science and Higher Education of Russia under Grant 0039-2019-0004 . - ISSN 1996-1944
Кл.слова (ненормированные):
manganese -- YAl3(BO3)4:Mn crystal -- XANES spectroscopy -- high-resolution optical spectroscopy -- photoluminescence
Аннотация: We present an extensive study of the luminescence characteristics of Mn impurity ions in a YAl3(BO3)4:Mn crystal, in combination with X-ray fluorescence analysis and determination of the valence state of Mn by XANES (X-ray absorption near-edge structure) spectroscopy. The valences of manganese Mn2+(d5) and Mn3+(d4) were determined by the XANES and high-resolution optical spectroscopy methods shown to be complementary. We observe the R1 and R2 luminescence and absorption lines characteristic of the 2E ↔ 4A2 transitions in d3 ions (such as Mn4+ and Cr3+) and show that they arise due to uncontrolled admixture of Cr3+ ions. A broad luminescent band in the green part of the spectrum is attributed to transitions in Mn2+. Narrow zero-phonon infrared luminescence lines near 1060 nm (9400 cm−1) and 760 nm (13,160 cm−1) are associated with spin-forbidden transitions in Mn3+: 1T2 → 3T1 (between excited triplets) and 1T2 → 5E (to the ground state). Spin-allowed 5T2 → 5E Mn3+ transitions show up as a broad band in the orange region of the spectrum. Using the data of optical spectroscopy and Tanabe–Sugano diagrams we estimated the crystal-field parameter Dq and Racah parameter B for Mn3+ in YAB:Mn as Dq = 1785 cm−1 and B = 800 cm−1. Our work can serve as a basis for further study of YAB:Mn for the purposes of luminescent thermometry, as well as other applications.

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Держатели документа:
Institute of Spectroscopy, Russian Academy of Sciences, Troitsk, 108840 Moscow, Russia
Landau Phystech School of Physics and Research, Moscow Institute of Physics and Technology, 141701 Dolgoprudny, Russia
Faculty of Geology, Lomonosov Moscow State University, 119991 Moscow, Russia
National Research Center “Kurchatov Institute”, 123182 Moscow, Russia
Federal Scientific Research Center “Crystallography and Photonics”, Russian Academy of Sciences, 119333 Moscow, Russia
Kirensky Institute of Physics, Siberian Branch of the Russian Academy of Sciences, Akademgorodok, 660036 Krasnoyarsk, Russia
Branch “Aprelevka Department of VNIGNI”, Federal State Budgetary Institution “All-Russian Research Geological Oil Institute”, 143360 Aprelevka, Russia

Доп.точки доступа:
Molchanova, A.; Boldyrev, K.; Kuzmin, N.; Veligzhanin, A.; Khaydukov, K.; Khaydukov, E.; Kondratev, O.; Gudim, I. A.; Гудим, Ирина Анатольевна; Mikliaeva, E.; Popova, M.
}
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    Site occupation engineering toward giant red-shifted photoluminescence in (Ba,Sr)2LaGaO5:Eu2+ phosphors / Yu Chen, Zh. Yang, J. Jin [et al.] // Chem. Mater. - 2023. - Vol. 35, Is. 20. - P. 8714-8721, DOI 10.1021/acs.chemmater.3c01980. - Cited References: 35. - This research was supported by the National Key Research and Development Program of China (2021YFB3500401 and 2021YFE0105700), the National Natural Science Foundations of China (Grant Nos. 51972118 and 52102169), the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137), the China Postdoctoral Science Foundation (2021M691053), and the Young Elite Scientists Sponsorship Program by China Association for Science and Technology (No. YESS20200053). This work was also 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. 075-15-2022-314 . - ISSN 0897-4756. - ISSN 1520-5002
   Перевод заглавия: Управление заселенностью позиций для получения фотолюминесценции в люминофорах (Ba,Sr)2LaGaO5:Eu2+ с большим красным смещением
Аннотация: Exploring oxide-based red-emitting phosphors is essential for improving the color rendering index (Ra) and reducing the correlated color temperature (CCT) of white-light-emitting diode (LED) lighting sources. Especially, it is challenging to design Eu2+ red emission in inorganic solids. Here, the Eu2+-activated oxide phosphor Sr2LaGaO5:Eu2+ was synthesized with red emission peaking at 618 nm under 450 nm excitation. The crystal structure and spectral analysis indicate that Eu2+ tends to occupy [Sr1/LaO8] polyhedrons with a smaller coordination number, resulting in a large crystal field splitting at the 5d level and realizing the broadband 4f–5d red emission. When Sr is substituted by Ba atoms, density functional theory calculations verify that Ba tends to enter [Sr2O10] with a large coordination number, further giving rise to the lattice distortion and a giant spectral redshift (618–800 nm). The white LED device fabricated by mixing red Sr1.8Ba0.2GaO5:Eu2+ and green Lu3Al5O12:Ce3+ phosphors exhibits a high color rendering index (Ra = 92.1) and a low color-dependent temperature (CCT = 4570 K). This study will give guidance for exploring new Eu2+ activated oxide-based red phosphors as well as achieving tunable emission through cations’ substitution.

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The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, Guangdong Engineering Technology Research and Development Center of Special Optical Fiber Materials and Devices, School of Materials Science and Engineering, South China University of Technology,Guangzhou 510641, P. R. China
Department of Mathematics and Physics,Chongqing Universityof Posts and Telecommunications, Chongqing 400065,China
Collegeof Physics, Taiyuan University of Technology, 030024 Taiyuan, China
Laboratory of Crystal Physics, Kirensky Institute of Physics,Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
World-Class Research Center “Advanced Digital Technologies”, Universityof Tyumen, Tyumen 625003, Russia
Department of Physics, University of the Free State, Bloemfontein ZA-9300, South Africa

Доп.точки доступа:
Chen, Yu; Yang, Zhiyu; Jin, Jiance; Qiao, Jianwei; Wang, Yuzhen; Molokeev, M. S.; Молокеев, Максим Сергеевич; Swart, Hendrik C.; Xia, Zhiguo
}
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    Liu, Gaochao.
    Structural rigidity control toward Cr3+-based broadband near-infrared luminescence with enhanced thermal stability / G. C. Liu, M. S. Molokeev, Z. G. Xia // Chem. Mat. - 2022. - Vol. 34, Is. 3. - P. 1376-1384, DOI 10.1021/acs.chemmater.1c04131. - 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 . - ISSN 0897-4756. - ISSN 1520-5002
   Перевод заглавия: Контроль структурной жесткости для получения широкополосной люминесценции в ближней инфракрасной области на основе Cr3+ с повышенной термической стабильностью

РУБ Chemistry, Physical + Materials Science, Multidisciplinary
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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Держатели документа:
South China Univ Technol, Sch Mat Sci & Engn, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, State Key Lab Luminescent Mat & Devices, Guangzhou 510640, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
South China Univ Technol, Sch Phys & Optoelect, Guangzhou 510641, Peoples R China.

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo; 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]
}
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    Shining Mn4+ in 0D organometallic fluoride hosts towards highly efficient photoluminescence / H. Ming, Y. F. Zhao, Y. Y. Zhou [et al.] // Adv. Opt. Mater. - 2022. - Vol. 10, Is. 7. - Ст. 2102141, DOI 10.1002/adom.202102141. - Cited References: 40. - This work is financially supported by the National Science Foundation of China (Grants Nos. 51472088, 51972117, and U1601205), Basic and Applied Basic Research Foundation of Guangdong Province (2021A1515012415), Guangzhou Science and Technology Planning Project (202002030098 and 202102020125), and Fundamental Research Funds for the Central Universities (2020ZYGXZR050). This work was also funded by RFBR according to the research project No. 19-52-80003 . - ISSN 2195-1071
   Перевод заглавия: Свечение Mn4+ в 0D металлоорганических фторидных матрицах для высокоэффективной фотолюминесценции

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
RED PHOSPHOR
Кл.слова (ненормированные):
fluoride phosphors -- high efficiency -- Mn -- 4+-doped -- white light-emitting diodes
Аннотация: The design and discovery of Mn4+-activated fluoride phosphors that can secure both high luminescence efficiency and short fluorescence lifetime simultaneously are crucial and urgent for constructing high-quality wide-color gamut (WCG) backlight display applications. Herein, a series of brand-new Mn4+-activated narrow-band red-emitting phosphors with both high external quantum efficiency (EQE, >50%) and short fluorescence lifetime (τ ≤ 3.8 ms) are designed by introducing Mn4+ into newfound tetramethylammonium (Me4N)-based organometallic fluoride (Me4N)2BF6 (B = Ge, Ti, Zr) hosts. These intriguing properties of Mn4+ arise from the larger steric hindrance of (Me4N)+ cations and low local structure symmetry in the 0D (Me4N)2BF6, as verified by the structural and spectral analyses. (Me4N)2GeF6:Mn4+, as a representative, shows a high EQE of ≈64.6% and a short lifetime of ≈3.78 ms. A prototype projector with superb performance is assembled by employing a remote (Me4N)2GeF6:Mn4+-based white light-emitting diode with high luminous efficiency (≈143.09 lm W−1) and WCG (≈112.02% National Television System Committee (NTSC)) to demonstrate their great potentials for backlight applications. The research brings up a promising alternative as the host materials for Mn4+-doped fluoride phosphors and provides a deeper understanding on the correlation between structure and luminescence.

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Держатели документа:
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ Technol, Guangdong Engn Technol Res & Dev Ctr Special Opt, Guangzhou 510641, Guangdong, Peoples R China.
City Univ Hong Kong, Dept Chem, Hong Kong 999077, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
South China Univ Technol, Sch Phys & Optoelect, Guangzhou 510641, Guangdong, Peoples R China.

Доп.точки доступа:
Ming, Hong; Zhao, Yifei; Zhou, Yayun; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wang, Yuanjing; Zhang, Shuai; Song, Enhai; Ye, Shi; Xia, Zhiguo; Zhang, Qinyuan
}
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    Competitive site occupation toward improved quantum efficiency of SrLaScO4:Eu red phosphors for warm white LEDs / Z. Y. Yang, G. C. Liu, Y. F. Zhao [et al.] // Adv. Opt. Mater. - 2022. - Vol. 10. Is. 6. - Ст. 2102373, DOI 10.1002/adom.202102373. - Cited References: 42. - This research was supported by the International Cooperation Project of National Key Research and Development Program of China (Program No. 2021YFE0105700), National Natural Science Foundation of China (Grant Nos. 51972118 and 51961145101), Guangzhou Science & Technology Project (Project No. 202007020005), the State Key Laboratory of Luminescent Materials and Devices (Grant No. Skllmd-2021-09), China Postdoctoral Science Foundation (Grant No. 2021M691053), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (Program No. 2017BT01X137). This work was also funded by RFBR according to the research Project No. 19-52-80003 and the NRF International: SA/China Joint Research Programme 2021 - CHIN2002265 06921 UID 132785 . - ISSN 2195-1071
   Перевод заглавия: Конкурентное заселение позиций для повышения квантовой эффективности красных люминофоров SrLaScO4:Eu для тепло-белых светодиодов

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
LUMINESCENCE
   EUROPIUM
   BLUE
   EU2+
   STABILIZATION
   EPR
Кл.слова (ненормированные):
light-emitting diodes -- photoluminescence -- red emission
Аннотация: The discovery of Eu2+-doped high-efficiency red phosphors remains a vital challenge for white light-emitting diode (WLED) applications. It is therefore urgent to find effective strategies managing the oxidation state to help reduce Eu3+ to Eu2+ and accordingly increase the photoluminescence quantum yield (PLQY). Herein, a new red-emitting SrLaScO4:Eu phosphor is designed, and the PLQY is enhanced from 13% to 67% under 450 nm excitation by employing (NH4)2SO4-assisted sintering. Combined structural analysis, optical spectroscopy, and theoretical calculation reveal that predominant Eu2+ prefers to occupy the Sr2+ sites in the SrLaScO4 enabling red emission, and a competitive site occupation of Eu3+ in La3+ can be restrained, and the reduction mechanism of Eu3+ to Eu2+ originating from the (NH4)2SO4 addition is analyzed. The fabricated WLED device using red-emitting SrLaScO4:Eu and yellow-emitting Y3(Al,Ga)5O12:Ce3+ exhibits a high color-rendering index of 86.7 at a low correlated color temperature of 4005 K. This work provides a feasible reduction strategy for guiding the development of high-efficiency Eu2+-doped red phosphor for WLED applications.

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South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China.
City Univ Hong Kong, Dept Chem, Kowloon, Hong Kong 999077, Peoples R China.
KSC SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Fed Res Ctr, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
Univ Free State, Dept Phys, POB 339, ZA-9300 Bloemfontein, South Africa.
South China Univ Technol, Sch Phys & Optoelect, Guangzhou 510641, Peoples R China.

Доп.точки доступа:
Yang, Zhiyu; Liu, Gaochao; Zhao, Yifei; Zhou, Yayun; Qiao, Jianwei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Swart, Hendrik C.; Xia, Zhiguo; International Cooperation Project of 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]; State Key Laboratory of Luminescent Materials and Devices [Skllmd-2021-09]; China Postdoctoral Science FoundationChina Postdoctoral Science Foundation [2021M691053]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01X137]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]; NRF International: SA/China Joint Research Programme 2021 [CHIN2002265 06921 UID 132785]
}
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    Machine learning analysis and discovery of zero-dimensional ns2 metal halides toward enhanced photoluminescence quantum yield / M. S. Molokeev, B. B. Su, A. S. Aleksandrovsky [et al.] // Chem. Mat. - 2022. - Vol. 34, Is. 2. - P. 537-546, DOI 10.1021/acs.chemmater.1c02725. - Cited References: 66. - This work is supported by the National Natural Science Foundation of China (51961145101 and 51972118), International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), Guangzhou Science and 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 . - ISSN 0897-4756. - ISSN 1520-5002
   Перевод заглавия: Машинное обучение и открытие нульмерных ns2 металлогалогенидов для увеличения квантового выхода фотолюминесценции

РУБ Chemistry, Physical + Materials Science, Multidisciplinary
Рубрики:
RANDOM FOREST
   CRYSTAL-STRUCTURE
   TIN BROMIDE
   CLASSIFICATION
Аннотация: The dependence of photoluminescence quantum yield (PLQY) on the crystal structure of existing zero-dimensional ns2 metal halides is analyzed with the help of principal component analysis and random forest methods. The primary role of the distance between metal ions in different compounds is revealed, and the influence of other structural features such as metal-halogen distance and the distortion of metal-halogen polyhedrons are quantified. Accordingly, the two previously unknown Sb3+-based zero-dimensional metal halides were synthesized to verify the obtained model. Experimental studies of the two compounds demonstrated good agreement with the predictions, and the PLQY of (C10H16N)2SbCl5 is found to be 96.5%. Via machine learning analysis, we demonstrate that concentration quenching is the main factor that determines PLQY for all s2 ion metal halides, which will accelerate the discovery of new luminescence metal halides.

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Держатели документа:
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China.
RAS, KSC, SB, Lab Coherent Opt,Kirensky Inst Phys,Fed Res Ctr, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Dept Res & Dev, Kemerovo 650000, Russia.

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Su, Binbin; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Golovnev, Nicolay N.; Plyaskin, M. E.; Пляскин, Михаил Е.; Xia, Zhiguo
}
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10.

    Photoluminescence of pefloxacindi-ium manganese(II) and zinc(II) tetrahalides / N. N. Golovnev, M. A. Gerasimova, M. S. Molokeev [et al.] // J. Mol. Struct. - 2022. - Vol. 1248. - Ст. 131468, DOI 10.1016/j.molstruc.2021.131468. - Cited References: 42. - The research was funded by RFBR, Krasnoyarsk Territory and Krasnoyarsk Regional Fund of Science, project number 20-43-240007. Authors thank the Centre for Equipment Joint User of School of Petroleum and Natural Gas Engineering of Siberian Federal University, Institute of Chemistry and Chemical Technology SB RAS for their technical support . - ISSN 0022-2860
   Перевод заглавия: Фотолюминесценция тетрагалогенидов марганца(II) и цинка(II) пефлоксацина
Кл.слова (ненормированные):
Manganese and zinc halides -- Pefloxacin -- Ionic compounds -- Photoluminescence -- X-ray diffraction -- Thermal decomposition
Аннотация: Mn2+-based hybrid materials have become the hotspot of current research studies owing to their high photoluminescence quantum yield (PLQY), low-cost, environmental friendliness and stability. For the first time, we report the hydrothermal synthesis of two lead-free zero-dimensional luminescent organic-inorganic hybrid compounds, PefH2[MnBr4] (1) and PefH2[MnCl4] (2) (Pef = pefloxacin). They were characterized by elemental analysis, TG-DSC, single-crystal and powder XRD. Compounds 1–2 exhibit a distorted tetrahedral geometry around the manganese(II) metal center, which is isolated from the same centers by bulky pefloxacindi-ium (PefH22+) ions with a Mn···Mn distance of 7.3 Å. Their structures are stabilized by N—H···O, O—H···X (X = Br, Cl), C—H···O and C—H···X hydrogen bands and π–π stacking interaction. Thermal decomposition starts at T › 230°С for 1 and T › 210°С for 2 and proceeds for several stages. Upon UV excitation compounds exhibit a bright green emission with a moderate PLQY of 45% for 1 and 30% for 2. The influence of the halide ion and metal ion on the photoluminescence properties of isostructural compounds PefH2[MX4] (M = Mn, Zn and X = Br, Cl) is discussed.

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Siberian Federal University, 79 Svobodny Prospect, Krasnoyarsk, 660041, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, bld. 38 Akademgorodok 50, Krasnoyarsk, 660036, Russian Federation
Department of Physics, Far Eastern State Transport University, 47 Seryshev Str., Khabarovsk, 680021, Russian Federation
Research and Development Department, Kemerovo State University, 6 Krasnaya Str., Kemerovo, 650000, Russian Federation

Доп.точки доступа:
Golovnev, N. N.; Gerasimova, M. A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Plyaskin, M. E.; Baronin, M. E.
}
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11.

    Giant red-shifted emission in (Sr,Ba)Y2O4:Eu2+ phosphor toward broadband near-infrared luminescence / Z. Y. Yang, Y. F. Zhao, Y. Y. Zhou [et al.] // Adv. Funct. Mater. - 2022. - Vol. 32, Is. 1. - Ст. 2103927, DOI 10.1002/adfm.202103927. - 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 . - ISSN 1616-301X. - ISSN 1616-3028
   Перевод заглавия: Излучение с гигантским красным смещением в люминофоре (Sr,Ba)Y2O4: Eu2 + для широкополосной люминесценции в ближней инфракрасной области

РУБ Chemistry, Multidisciplinary + Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Applied + Physics, Condensed Matter
Рубрики:
LIGHT-SOURCES
   PHOTOLUMINESCENCE
   TRANSITION
   CE3+
   BLUE
   SUBSTITUTION
Кл.слова (ненормированные):
near-infrared emission -- photoluminescence -- red emission
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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South China Univ Technol, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, State Key Lab Luminescent Mat & Devices, Sch Mat Sci & Engn, Guangzhou 510641, Peoples R China.
Natl Synchrotron Radiat Res Ctr, Mat Sci Grp, Sci Res Div, Hsinchu 300, Taiwan.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.

Доп.точки доступа:
Yang, Zhiyu; Zhao, Yifei; Zhou, Yayun; Qiao, Jianwei; Chuang, Yu-Chun; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo; 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]
}
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12.

Temperature dependent structural, dielectric, Raman, piezoresponse and photoluminescence investigations in sol-gel derived BCZT ceramics / I. Coondoo, A. Krylov, D. K. Sharma [et al.] // Mater. Chem. Phys. - 2022. - Vol. 277. - Ст. 125526, DOI 10.1016/j.matchemphys.2021.125526. - Cited References: 82. - I.C. and J.S.K would like to acknowledge financial assistance by national funds (OE), through FCT – Fundação para a Ciência e a Tecnologia, I.P., in the scope of the framework contract foreseen in the numbers 4, 5 and 6 of the article 23, of the Decree-Law 57/2016, of August 29, changed by Law 57/2017, of July 19. This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020 & UIDP/50011/2020, financed by national funds through the FCT/MCTES. This work was partially developed within the scope of the project i3N, UIDB/50025/2020 & UIDP/50025/2020, financed by national funds through the FCT/MEC. Part of this work (A.K.) was supported by the Ministry of Science and Higher Education of the Russian Federation (grant no. 075-15-2021-588). This research used resources of the Ural Center for Shared Use “Modern nanotechnology”, Ural federal University, Russia and the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS”. The authors thank Dr. Gonzalo Irurueta, Center for Mechanical Engineering and Automation, University of Aveiro, Portugal and Dr. E. Venkata Ramana, Department of Physics, University of Aveiro, Portugal . - ISSN 0254-0584
Кл.слова (ненормированные):
Lead-free piezoelectrics -- Sol-gel -- Phase transitions -- Raman spectroscopy -- PFM -- Photoluminescence
Аннотация: 0.5Ba(Ti0.8Zr0.2)O3-0.5(Ba0.7Ca0.3)TiO3 [50BZT-50BCT or BCZT] based compounds have been the focus of a lot of research, particularly motivated by their high piezoelectric effect. However, the literature lacks an elaborate investigation of the phase transition behavior in BCZT ceramics obtained by wet chemistry processing. Here, we present an in-depth study on the temperature dependence of x-ray diffraction (XRD), Raman scattering, dielectric properties, local piezoresponse and photoluminescence (PL) to investigate the sequence of phase transitions in the BCZT ceramic synthesized via a chemical route. Phase formation was determined by Rietveld analysis of XRD data, while compositional homogeneity and elemental quantification of the compound was validated using energy dispersive x-ray spectroscopy (EDX) and x-ray photoelectron spectroscopy (XPS) studies. Detailed fitting of XPS data indicated the existence of Ti3+ species (∼6%) in the prepared BCZT. Phase transitions were examined by analyzing the modifications in the XRD profile of Bragg reflection {200} and anomalies observed in the temperature variation of dielectric and Raman spectra studied over a wide temperature range starting from 10K to beyond Curie temperature. Crystallographic transformation temperatures obtained from dielectric measurement agreed well with those assessed from the temperature evolution of Raman spectra. In addition to other transitions, Raman scattering results revealed the existence of a transition from to phase near −175 °C, a transition that has not been interpreted in BCZT (and generally not observed in parent BaTiO3 compound). The luminescence response was studied by photoluminescence (PL) spectroscopy in the temperature range 15–300 K. The position of the PL peak was observed to shift with temperature and discontinuities in the wavelength shift were noted near phase transitions. Evolution of domain morphology with temperature was examined by piezoresponse force microscopy technique. Consolidated results assign the phase sequence in sol-gel derived BCZT as: R(R3c)→-175±10°CR(R3m)→-50±10°CO→40±10°CT→120±10°CC.

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Держатели документа:
Department of Physics & CICECO – Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
DEMaC & CICECO – Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal
School of Natural Sciences and Mathematics, Ural Federal University, Ekaterinburg, 620026, Russian Federation
I3N-Aveiro, Department of Physics, University of Aveiro, Aveiro, 3810-193, Portugal
Physical Materials Science and Composite Materials Centre, Research School of Chemistry & Applied Biomedical Sciences, National Research Tomsk Polytechnic University, Tomsk, 634050, Russian Federation

Доп.точки доступа:
Coondoo, I.; Krylov, A. S.; Крылов, Александр Сергеевич; Sharma, D. K.; Krylova, S. N.; Крылова, Светлана Николаевна; Alikin, D.; Kumar, J. S.; Mirzorakhimov, A.; Melnikova, N.; Soares, M. J.; Kholkin, A. L.
}
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13.

    New double nonlinear-optical borate Rb3SmB6O12: Synthesis, structure and spectroscopic properties / V. Atuchin, A. Subanakov, A. Aleksandrovsky [et al.] // J. Alloys Compd. - 2022. - Vol. 905. - Ст. 164022, DOI 10.1016/j.jallcom.2022.164022. - Cited References: 65. - This work was supported by the Ministry of Science and Higher Education of Russia (project 0273-2021-0008) and the Russian Science Foundation (project 21-19-00046, in part of conceptualization). Also, this study was partly funded by RFBR (project No. 20–33-90188а) and State assignment Basic Project of IA&E SB RAS No 121032400052-6 . - ISSN 0925-8388
   Перевод заглавия: Новый двойной нелинейно-оптический борат Rb3SmB6O12: синтез, структура и спектроскопические свойства
Кл.слова (ненормированные):
Borate -- Crystal structure -- Raman -- Photoluminescence
Аннотация: New noncentrosymmetric alkali rare-earth double borate Rb3SmB6O12 was found in the ternary system Rb2O–Sm2O3–B2O3. The Rb3SmB6O12 powder was prepared by the solid state reaction method at 750 °C for 40 h and the crystal structure was obtained by the Rietveld method. Rb3SmB6O12 crystallized in space group R32 with unit cell parameters a = 13.4874 (3) and c = 30.9398 (6) Å, V = 4874.2 (2) Å3, Z = 15. In the three-dimensional framework structure of Rb3SmB6O12, each [B5O10]5− group is linked to four different Sm-O polyhedra and, likewise, each Sm-O polyhedron is connected to four neighboring [B5O10]5− groups. The Sm-O polyhedra are formed by the face-sharing linked SmO6 octahedra. Rb+ cations are located in large cavities of the framework structure. From the thermal stability measurements, the incongruent melting of Rb3SmB6O12 is observed at 1104 K with as high melting enthalpy as Hm = –161.5 J/g. The nonlinear optical response of Rb3SmB6O12 tested via SHG is estimated to be similar to that of K3YB6O12. The Raman spectrum of Rb3SmB6O12 is mainly governed by the vibrations of BO4 and BO3 borate groups observed over the wavenumber range of 287–1550 cm–1. The spectral bands below 270 cm–1 were attributed to rotational, translational and mixed vibrations of Rb3SmB6O12 structural units. The luminescence spectrum of Sm3+ ions in the specific local environment of the Rb3SmB6O12 crystal lattice shows the ability to control the individual band intensity ratio originating from 4G5/2 level.

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Держатели документа:
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation
Department of Applied Physics, Novosibirsk State University, Novosibirsk, 630090, Russian Federation
Department of Industrial Machinery Design, Novosibirsk State Technical University, Novosibirsk, 630073, Russian Federation
Laboratory of Oxide Systems, Baikal Institute of Nature Management, SB RAS, Ulan-Ude, 670047, Russian Federation
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
School of Engineering and Construction, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Condensed Matter Spectroscopy, Institute of Automation and Electrometry, Novosibirsk, 630090, Russian Federation

Доп.точки доступа:
Atuchin, V.; Subanakov, A.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Bazarov, B.; Bazarova, J.; Krylov, A. S.; Крылов, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Pugachev, A.
}
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14.

    Exploration of the crystal structure and thermal and spectroscopic properties of monoclinic praseodymium sulfate Pr2(SO4)3 / Y. G. Denisenko, V. V. Atuchin, M. S. Molokeev [et al.] // Molecules. - 2022. - Vol. 27, Is. 13. - Ст. 3966, DOI 10.3390/molecules27133966. - Cited References: 95. - This research was funded by the Russian Science Foundation (project 21-19-00046, in part of conceptualization). Some parts of the experiments were performed in the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” . - ISSN 1420-3049
   Перевод заглавия: Исследование кристаллической структуры, термических и спектроскопических свойств моноклинного сульфата празеодима Pr2(SO4)3
Кл.слова (ненормированные):
praseodymium sulfate -- crystal structure -- thermal analysis -- thermal expansion anisotropy -- photoluminescence -- band structure -- vibrational properties
Аннотация: Praseodymium sulfate was obtained by the precipitation method and the crystal structure was determined by Rietveld analysis. Pr2(SO4)3 is crystallized in the monoclinic structure, space group C2/c, with cell parameters a = 21.6052 (4), b = 6.7237 (1) and c = 6.9777 (1) Å, β = 107.9148 (7)°, Z = 4, V = 964.48 (3) Å3 (T = 150 °C). The thermal expansion of Pr2(SO4)3 is strongly anisotropic. As was obtained by XRD measurements, all cell parameters are increased on heating. However, due to a strong increase of the monoclinic angle β, there is a direction of negative thermal expansion. In the argon atmosphere, Pr2(SO4)3 is stable in the temperature range of T = 30–870 °C. The kinetics of the thermal decomposition process of praseodymium sulfate octahydrate Pr2(SO4)3·8H2O was studied as well. The vibrational properties of Pr2(SO4)3 were examined by Raman and Fourier-transform infrared absorption spectroscopy methods. The band gap structure of Pr2(SO4)3 was evaluated by ab initio calculations, and it was found that the valence band top is dominated by the p electrons of oxygen ions, while the conduction band bottom is formed by the d electrons of Pr3+ ions. The exact position of ZPL is determined via PL and PLE spectra at 77 K to be at 481 nm, and that enabled a correct assignment of luminescent bands. The maximum luminescent band in Pr2(SO4)3 belongs to the 3P0 → 3F2 transition at 640 nm.

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Держатели документа:
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen, 625003, Russian Federation
Department of General and Special Chemistry, Industrial University of Tyumen, Tyumen, 625000, Russian Federation
Institute of Inorganic and Analytical Chemistry, Justus-Liebig-University Giessen, Giessen, 35392, Germany
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, 630090, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation
Department of Applied Physics, Novosibirsk State University, Novosibirsk, 630090, Russian Federation
Department of Industrial Machinery Design, Novosibirsk State Technical University, Novosibirsk, 630073, Russian Federation
R&D Center “Advanced Electronic Technologies”, Tomsk State University, Tomsk, 634034, Russian Federation
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
School of Engineering Physics and Radio Electronics, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
School of Engineering and Construction, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Institute of Automation and Electrometry, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation
Research Department, Northern Trans-Ural Agricultural University, Tyumen, 625003, Russian Federation
Center for Materials Research (LaMa), Justus-Liebig-University Giessen, Giessen, 35392, Germany

Доп.точки доступа:
Denisenko, Y. G.; Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Sedykh, A. E.; Khritokhin, N. A.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Shestakov, N. P.; Шестаков, Николай Петрович; Adichtchev, S. V.; Pugachev, A. M.; Sal’nikova, E. I.; Andreev, O. V.; Razumkova, I. A.; Muller-Buschbaum, K.
}
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15.

    Strategy to construct high thermal-stability narrow-band green-emitting Si-CDs@MAs phosphor for wide-color-gamut backlight displays / J. Chen, X. Zou, W. Li [et al.] // Adv. Opt. Mater. - 2022. - Vol. 10, Is. 21. - Ст. 2200851, DOI 10.1002/adom.202200851. - Cited References: 47. - The work was supported by the Ministry of Science and Technology of China (No. G2021030022L), the Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams (No. 2021KJ122), the National Natural Science Foundations of China (No. 52102042), the Independent Research and Development Projects of Maoming Laboratory (No. 2021ZZ004), the Key Realm R&D Program of Guangdong Province (No. 2021B0707010003), the Guangzhou Science & Technology Project (Nos. 202007020005 and 202103000059), the Guangdong Provincial Science and Technology Project (Nos. 2021A0505050006 and 2022A1515010229), and the Project of GDUPS (2018) for B.L. . - ISSN 2195-1071
   Перевод заглавия: Стратегия создания узкополосного люминофора Si-CD@MAs с высокой термостабильностью, излучающего зеленый свет, для дисплеев с подсветкой с широкой цветовой гаммой
Кл.слова (ненормированные):
carbon dots -- low thermal quenching -- narrowband -- photoluminescence -- WLED backlights
Аннотация: Developing innovative narrow-band green-emitting phosphors featuring low thermal quenching and eco-friendliness for white light-emitting diode (WLED) backlights is a pivotal challenge. Benefitting from narrowband and low toxicity of green-emitting silanized carbon dots (Si-CDs), an efficient confinement and protection strategy through embedding Si-CDs in mesoporous aluminas (MAs) is proposed to construct MAs and Si-CDs composites (Si-CDs@MAs) with superior luminescence properties. Si-CDs@MAs phosphor exhibits green emission at 526 nm with narrow full width at half maximum of 51 nm, zero-thermal quenching even up to 423 K (104.1%@423 K of the emission peak intensity at 298 K), and the internal quantum efficiency of 64.46%. Compared with broad-band yellow-emitting solid-state Si-CDs (S-Si-CDs), the thermal stability, photostability, and water stability of Si-CDs@MAs phosphor are remarkably improved due to surface protection. The WLED backlight is fabricated with optimized Si-CDs@MAs phosphor, which shows high luminous efficacy of 117.43 lm W?1 and wide color gamut (107% NTSC). Furthermore, this work provides the design principles of realizing stable narrow-band solid-state fluorescence carbon dots, suggesting its great potential for wide-color-gamut display application.

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Держатели документа:
Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangzhou, 510642, China
Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Guangdong, Maoming, 525100, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Siberian Branch of the Russian Academy of Sciences (SB RAS), Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Chen, J.; Zou, X.; Li, W.; Zhang, H.; Zhang, X.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Y.; Lei, B.
}
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16.

    Multiple strategies to approach high-efficiency luminescence controllable in blue/cyan/green-emitting Bi3+-activated phosphors / P. Gao, Q. Li, S. Li [et al.] // J. Phys. Chem. C. - 2022. - Vol. 126, Is. 21. - P. 9195-9206, DOI 10.1021/acs.jpcc.2c02560. - Cited References: 53. - The authors would like to gratefully acknowledge funds from the National Natural Science Foundation of China (grant no. 51974123), the Distinguished Youth Foundation of Hunan Province (grant no.2020JJ2018), the Key R&D projects in Hunan Province (2020WK2016, 2020SK2032, 2021SK2047, and 2022NK2044), the Natural Science Foundation of Hunan Province, China (grant no. 2021JJ40261), the Hunan High Level Talent Gathering Project (2019RS1077 and 2020RC5007), the Scientific Research Fund of Hunan Provincial Education Department (19C0903), the Natural Sciences Foundation of Hunan Agricultural University, China (grant no. 19QN11), the Hunan Provincial Key Laboratory of Crop Germplasm Innovation and Resource Utilization Science Foundation (19KFXM12), the Changsha Science and Technology Plan (KH2005114, KH2201428), and the College Students’ Innovative Training (S202110537012) . - ISSN 1932-7447
   Перевод заглавия: Многочисленные стратегии достижения высокоэффективной управляемой люминесценции в синих/голубых/зеленых Bi3+-активированных люминофорах
Кл.слова (ненормированные):
Energy transfer -- Luminescence -- Blue phosphors -- Emitting phosphors -- High quality -- Higher efficiency -- Multiple strategy -- Optical tuning -- Performance -- Photoluminescence spectrum -- Red green blues -- White light emitting diodes
Аннотация: Cyan gap is a major block in achieving high-quality white light-emitting diodes (WLEDs). Hence, a novel cyan-emitting phosphor Sr2GdGaO5/0.02Bi3+ with optical tuning performance is synthesized based on the local crystal field regulation strategy surrounding the luminescence center. With the substitution of Al3+ for Ga3+, the photoluminescence (PL) spectra of Sr2GdGa1–xAlxO5/0.02Bi3+ (0 ≤ x ≤ 1) phosphors adjust from cyan (466 nm) to blue (450 nm). Moreover, such a Ba2+ doping adjusts the PL spectra of Sr2–xBaxGdGaO5/0.02Bi3+ (0 ≤ x ≤ 0.5) phosphors from cyan (466 nm) to green (482 nm). These phenomena are contributed to the crystal field splitting and nephelauxetic effect. The energy transfer from Bi3+ to Eu3+ is realized by co-doping Bi3+ and Eu3+ ions in the A2GdBO5/Bi3+ (A = Sr, Ba; B = Ga, Al) host materials, and two single-phase white phosphors Sr2GdGaO5/0.02Bi3+, 0.05Eu3+ and Sr1.5Ba0.5GdGaO5/0.02Bi3+, 0.05Eu3+ are obtained. Finally, a WLED with high color rendering index (Ra = 93.6) is prepared by using red/green/blue (RGB) phosphors and Sr2GdGaO5/0.02Bi3+ phosphor, which is higher than that of the WLED prepared by RGB phosphors (Ra = 86.7), indicating that Sr2GdGaO5/0.02Bi3+ phosphor can close the cyan gap. These results provide multiple strategies in achieving luminescence controllable and WLED.

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Держатели документа:
School of Chemistry and Materials Science, Hunan Agricultural University, Changsha, 410128, China
Hunan Optical Agriculture Engineering Technology Research Center, Changsha, 410128, China
College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, 410128, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Gao, P.; Li, Q.; Li, S.; Gai, S.; Li, Y.; Ma, Y.; Zhang, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhou, Z.; Xia, M.
}
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17.

A high thermal stability Cr3+-doped gallate far red phosphor for plant lighting: structure, luminescence enhancement and application prospect / C. Zhou, L. Peng, Z. H. Kong [et al.] // J. Mater. Chem. C. - 2022. - Vol. 10, Is. 15. - P. 5829-5839, DOI 10.1039/d2tc00614f. - Cited References: 39. - The authors would like to gratefully acknowledge funds from the National Natural Science Foundation of China (Grant no. 51974123), the Distinguished Youth Foundation of Hunan Province (Grant no. 2020JJ2018), Key R & D projects in Hunan Province (2020WK2016 & 2020SK2032), the Hunan High Level Talent Gathering Project (2019RS1077 & 2020RC5007), the Natural Sciences Foundation of Hunan Agricultural University (19QN11), the Hunan Provincial Key Laboratory of Crop Germplasm Innovation and Resource Utilization Science Foundation (19KFXM12), the Changsha Science and technology plan (KH2005114), the Scientific Research Fund of Hunan Provincial Education Department (19C0903) and the Innovation Training Program for College Students of Hunan Province (No. S202010537012) . - ISSN 2050-7526. - ISSN 2050-7534

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
EMITTING PHOSPHOR
TUNING PHOTOLUMINESCENCE
LEDS
Аннотация: Cationic substitution is a common material modification strategy. Generally, it follows the principles of radius matching, valency equilibrium and stoichiometric substitution. However, radius-mismatched, nonstoichiometric-ratio ion substitution can achieve unexpected experimental results. Such unexpected results are very important for expanding the research of materials, but the modification mechanism is still unclear. In this work, the optical performance of ZnGa2O4:0.02Cr3+ (ZGO:0.02Cr3+) is effectively regulated by chemical unit cosubstitution (Ge4+–Li+/Na+ for Ga3+–Zn2+) and excess cation substitution synergetic strategies, and the thermal stability is retained at 97.7% at room temperature and 150 °C. Ge4+–Li+ and Ge4+–Na+ replace the lattice position of Ga3+–Zn2+ to enhance the photoluminescence (PL) intensity and quantum efficiency (QE) of ZGO:0.02Cr3+. The optimal doping contents of Ge4+–Li+ and Ge4+–Na+ are all 0.3 mol (PL intensity is 130.3% and 153.4% and QE = 77.4% and 85.1%). With further addition of Li+ ions, the emission intensity and QE continued to increase to 176.4% and 83.8%, respectively. The synergistic effect of the mechanism on optical properties is explained via Rietveld refinement, optical band gap energy and thermoluminescence. Finally, LED devices were fabricated by using the ZGO:0.02Cr3+,0.03Ge4+,0.11Li+ phosphor to investigate the effect on plant growth. The growth period was reduced and the fruit quality was improved in dwarf potted tomato, which shows the application prospect in plant growth of the ZGO:0.02Cr3+ phosphor.

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Держатели документа:
Hunan Agr Univ, Sch Chem & Mat Sci, Changsha 410128, Peoples R China.
Hunan Opt Agr Engn Technol Res Ctr, Changsha 410128, Peoples R China.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Sun Yat Sen Univ, Sch Chem, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Guangdong, Peoples R China.

Доп.точки доступа:
Zhou, Cheng; Peng, L.u.; Kong, Zihui; Wu, Meihan; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhou, Zhi; Wang, Jing; Xia, Mao
}
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18.

    Zero-Dimensional Organic Copper(I) Iodide Hybrid with High Anti-Water Stability for Blue-Light-Excitable Solid-State Lighting / B. Su, J. Jin, Y. Peng [et al.] // Adv. Opt. Mater. - 2022. - Vol. 10, Is. 12. - Ст. 2102619, DOI 10.1002/adom.202102619. - Cited References: 55. - This work was supported by the National Natural Science Foundation of China (Nos.: 51961145101 and 51972118), Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program(2017BT01×137). This work was also funded by RFBR according to the research Project No.19-52-80003 . - ISSN 2195-1071
   Перевод заглавия: Нульмерный металлорганический гибрид йодида меди(I) с высокой водостойкостью для ламп, возбуждаемых синим светом
Кл.слова (ненормированные):
anti-water stability -- copper(I) iodide cluster -- light-emitting diodes -- photoluminescence -- zero-dimensional metal halides
Аннотация: The discovery of rare-earth free luminescent materials with blue-light-excitable characteristic is of great importance for solid-sate lighting applications. Herein, a Cu(I)-based 0D luminescent hybrid (1,3-dppH2)2Cu4I8∙H2O is synthesized by a facile solution method, and it shows the orange-red emission peaking at 625 nm upon 460 nm excitation. The structure-related luminescence mechanism has been elaborated by experimental and theoretical investigations. Moreover, the emission intensity remains unchanged even after continuous water treatment for 60 days due to the improved structural stability originating from intermolecular π–π interaction between organic cations. A warm white light-emitting diode (LED) device with the color rendering index of 91.4% has been fabricated by combining the 440 nm LED chip, green-emitting Lu3Al5O12:Ce3+, and (1,3-dppH2)2Cu4I8∙H2O. This work provides a new design route towards 0D cuprous halide materials and will initiate more exploration of their intrinsic luminescence mechanism.

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Держатели документа:
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Engineering, South China University of Technology, Guangzhou, 510641, China
School of Physics and Optoelectronics, South China University of Technology, Guangzhou, 510641, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Engineering Physics and Radioelectronic, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation

Доп.точки доступа:
Su, B.; Jin, J.; Peng, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Yang, X.; Xia, Z.
}
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19.

Triplet-triplet energy transfer from Bi3+to Sb3+in zero-dimensional indium hybrids via a B-site co-doping strategy toward white-light emission / Q. Ren, J. Zhang, M. S. Molokeev [et al.] // Inorg. Chem. Front. - 2022. - Vol. 9, Is. 22. - P. 5960-5968, DOI 10.1039/d2qi01631a. - Cited References: 60. - This work was supported by the Natural Science Foundation of Shanxi Province (No. 20210302124054), the National Natural Science Foundation of China (No. 21871167), the Science and Technology Innovation Project of Colleges and Universities in Shanxi Province (No. 2021L262), the 1331 Project of Shanxi Province and the Postgraduate Innovation Project of Shanxi Normal University (No. 2021XSY040), and funded by RFBR according to the research project No. 19-52-80003 . - ISSN 2052-1553
Кл.слова (ненормированные):
Co-doping -- Doping strategies -- Lightemitting diode -- Lone pair -- Low dimensional -- Photoluminescence properties -- Triplet-triplet energy transfer -- White light emission -- Widely tunable -- Zero-dimensional -- Metal halides
Аннотация: Low-dimensional metal halides have emerged as promising platforms for the development of new-generation phosphor-converted light emitting diodes (pc-LEDs), in which zero-dimensional (0D) hybrids with lone-pair ns2 states, in particular, show unprecedented competitiveness owing to their fascinating photoluminescence (PL) properties. Herein, we designed a novel 0D indium hybrid, (C20H20P)2InCl5, and proposed a co-doping strategy to incorporate Bi3+ (6s2) and Sb3+ (5s2) ions into this indium hybrid. Widely tunable emissions from blue to red are achieved, which are assigned to the triplet self-trapped excitons (STEs) (3P1 → 1S0) of Bi3+ (476 nm) and Sb3+ (658 nm), respectively. Importantly, an uncommon triplet–triplet energy transfer from Bi3+ to Sb3+ contributes to tunable dual emissions, and enables a single-phase cool white-light emission under ultraviolet (UV) excitation. Moreover, the energy transfer mechanism is discussed clearly by fluorescence photon dynamic analysis and DFT calculations. This work provides a deeper insight into triplet–triplet energy transfer, as well as presents a new model system for tuning the PL behaviours of ns2 configuration dopants.

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Держатели документа:
Key Laboratory of Magnetic Molecules and Magnetic Information Materials (Ministry of Education), School of Chemistry and Material Science, Shanxi Normal University, Taiyuan, 030031, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center Ksc Sb Ras, Krasnoyarsk, 660036, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
College of Chemistry & Chemical Engineering, Key Laboratory of Interface Science and Engineering in Advanced Material, Ministry of Education, Taiyuan University of Technology, Shanxi, Taiyuan, 030024, China

Доп.точки доступа:
Ren, Q.; Zhang, J.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhou, G.; Zhang, X. -M.
}
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20.

    Manipulation of Cl/Br transmutation in zero-dimensional Mn2+-based metal halides toward tunable photoluminescence and thermal quenching behaviors / G. J. Zhou, Z. Y. Liu, M. S. Molokeev [et al.] // J. Mater. Chem. C. - 2021. - Vol. 9, Is. 6. - P. 2047-2053, DOI 10.1039/d0tc05137c. - Cited References: 56. - The present work was financially supported by the Natural Science Foundation of China (21871167), and 1331 Project of Shanxi Province and the Postgraduate Innovation Project of Shanxi Normal University (2019XBY018), and funded by RFBR according to the research project no. 19-52-80003 . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Манипуляции перестановок Cl/Br в нульмерных галогенидах металлов на основе Mn2+ для настраиваемой фотолюминесценции и ослабления термического тушения

РУБ Materials Science, Multidisciplinary + Physics, Applied

Аннотация: Low-dimensional-networked metal halides are attractive for the screening of emitters applied in solid-state lighting and displays, but the lead toxicity and poor stability are obstacles that must be overcome in industrial applications. Herein, we aim at the discovery of bright and stable photoluminescence in zero-dimensional (0D) Mn2+-based metal halides. By manipulation of Cl/Br transmutation, the nature of the halogen can be confirmed as a pivotal factor to tune the PL behaviors, and the optimum Mn2+ emission with a high PLQY of 99.8% and a short lifetime of 0.372 ms can be achieved in (C24H20P)2MnBr4. The thermal quenching behaviors have been discussed in depth, indicating that the synergistic effect of good chemical stability of organic groups, a long Mn⋯Mn distance of 10.447 Å and a relatively large activation energy (ΔE = 0.277 eV) provides a platform for achieving excellent thermal stability in (C24H20P)2MnBr4. Moreover, the as-fabricated white LED device with a high luminous efficacy of 118.9 lm W−1 and a wide color gamut of 105.3% National Television System Committee (NTSC) shows that (C24H20P)2MnBr4 can be employed as a desirable narrow-band green emitter for LED displays. This work provides a new understanding of fine tailoring halogens, and proposes a feasible approach to achieving high thermal stability emitters toward the targeted practical applications.

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Держатели документа:
Shanxi Normal Univ, Sch Chemist & Mat Sci, Key Lab Magnet Mol & Magnet Informat Mat, Minist Educ, Linfen 041004, Shanxi, Peoples R China.
Huazhong Univ Sci & Technol, Wuhan Natl Lab Optoelect, Wuhan 430074, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Peoples R China.

Доп.точки доступа:
Zhou, Guojun; Liu, Zhiyang; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xiao, Zewen; Xia, Zhiguo; Zhang, Xian-Ming
}
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