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1.


   
    Ultraviolet fluorescence of coelenteramide and coelenteramide-containing fluorescent proteins. Experimental and theoretical study / R. R. Alieva [et al.] // J. Photochem. Photobiol. B Biol. - 2016. - Vol. 162. - P. 318-323, DOI 10.1016/j.jphotobiol.2016.07.004. - Cited References: 49. - This work was supported by the state budget allocated to the fundamental research at the Russian Academy of Sciences (project No 01201351504); the Russian Foundation for Basic Research, Grant No 15-43-04377-sibir; and Russian president's grant NSh-7559.2016.2. . - ISSN 1011-1344
РУБ Biochemistry & Molecular Biology + Biophysics
Рубрики:
DENSITY-FUNCTIONAL THEORY
   ELECTRON-EXCITED-STATES

   PHOTOPROTEIN OBELIN

   DISCHARGED-OBELIN

   LIGHT-EMITTERS

   BIOLUMINESCENCE

   AEQUORIN

   LUMINESCENCE

   MECHANISM

   CHEMILUMINESCENCE

Кл.слова (ненормированные):
Coelenteramide -- Fluorescent protein -- Discharged photoproteins -- Obelin -- Aequorin -- Fluorescence -- Excitation energy -- Fluorescence -- B3LYP
Аннотация: Coelenteramide-containing fluorescent proteins are products of bioluminescent reactions of marine coelenterates. They are called ‘discharged photoproteins’. Their light-induced fluorescence spectra are variable, depending considerably on external conditions. Current work studies a dependence of light-induced fluorescence spectra of discharged photoproteins obelin, aequorin, and clytin on excitation energy. It was demonstrated that photoexcitation to the upper electron-excited states (260–300 nm) of the discharged photoproteins initiates a fluorescence peak in the near UV region, in addition to the blue-green emission. To characterize the UV fluorescence, the light-induced fluorescence spectra of coelenteramide (CLM), fluorophore of the discharged photoproteins, were studied in methanol solution. Similar to photoproteins, the CLM spectra depended on photoexcitation energy; the additional peak (330 nm) in the near UV region was observed in CLM fluorescence at higher excitation energy (260–300 nm). Quantum chemical calculations by time depending method with B3LYP/cc-pVDZ showed that the conjugated pyrazine-phenolic fragment and benzene moiety of CLM molecule are responsible for the additional UV fluorescence peak. Quantum yields of CLM fluorescence in methanol were 0.028 ± 0.005 at 270–340 nm photoexcitation. A conclusion was made that the UV emission of CLM might contribute to the UV fluorescence of the discharged photoproteins. The study develops knowledge on internal energy transfer in biological structures – complexes of proteins with low-weight aromatic molecules. © 2016 Elsevier B.V.

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Держатели документа:
Institute of Biophysics SB RAS, Akademgorodok 50/50, Krasnoyarsk, Russian Federation
Institute of Physics SB RAS, Akademgorodok 50/38, Krasnoyarsk, Russian Federation
Siberian Federal University, Svobodny Prospect 79, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Alieva, R. R.; Tomilin, F. N.; Томилин, Феликс Николаевич; Kuzubov, A. A.; Кузубов, Александр Александрович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Kudryasheva, N. S.
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2.


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

   LUMINESCENCE

   PHOTOLUMINESCENCE

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

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Держатели документа:
South China Univ Technol, Sch Mat Sci & Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Guangzhou 510640, Peoples R China.
Fed Res Ctr KSC SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Agr Univ, Coll Mat & Energy, Guangdong Prov Engn Technol Res Ctr Opt Agr, Guangzhou 510642, Peoples R China.

Доп.точки доступа:
Liu, Gaochao; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lei, Bingfu; Xia, Zhiguo
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3.


   
    Tunable photoluminescence in Sb3+-doped zero-dimensional hybrid metal halides with intrinsic and extrinsic self-trapped excitons / J. Zhou, M. Z. Li, M. S. Molokeev [et al.] // J. Mater. Chem. C. - 2020. - Vol. 8, Is. 15. - P. 5058-5063, DOI 10.1039/d0tc00391c. - Cited References: 33. - This work is supported by the National Natural Science Foundation of China (No. 51722202, 51961145101, 51972118, 21576002 and 61705003), Fundamental Research Funds for the Central Universities (D2190980), the Guangdong Provincial Science & Technology Project (2018A050506004), and Beijing Technology and Business University Research Team Construction Project (No. PXM2019_014213_000007). This work was also funded by RFBR according to the Research Project No. 19-52-80003. . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Перестраиваемая фотолюминесценция в нульмерных гибридных металлогалогенидах, легированных Sb3 +, с внутренними и внешними автолокализованными экситонами
РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
WHITE-LIGHT EMISSION
   LUMINESCENCE

   PEROVSKITES

   CS2NASCCL6

   CS2NAYCL6

Аннотация: Dopants in luminescent metal halides provide an alternative way for photoluminescence tuning towards versatile optical applications. Here we report a trivalent antimony (Sb3+)-doped single crystalline 0D metal halide with the composition of (C9NH20)9[Pb3Cl11](ZnCl4)2:Sb3+. This compound possessed the coexistence of two emission centers including intrinsic and extrinsic self-trapped excitons (STEs), which are ascribed to [Pb3Cl11]5− clusters and triplet STEs formed by the 3P1–1S0 transition of Sb3+. By regulating the Sb3+ concentration, the emission can be tuned from green to yellow and finally to orange, which would help to develop optically pumped white light-emitting diodes (WLEDs) with different photometric characteristics. Moreover, this dopant-induced extrinsic STE approach presents a new direction towards tuning the luminescence properties of 0D metal halides, and may find application in environmentally-friendly, high-performance metal halide light emitters.

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Держатели документа:
Beijing Technol & Business Univ, Sch Sci, Beijing 100048, Peoples R China.
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
RAS, SB, 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, Jun; Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Sun, Jiayue; Xu, Denghui; Xia, Zhiguo
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4.


   
    The trigonal polymorph of strontium tetraborate, beta-SrB4O7 [Text] / A. D. Vasiliev, A. V. Cherepakhin, A. I. Zaitsev // Acta Crystallogr. Sect. E.-Struct Rep. Online. - 2010. - Vol. 66, Part 6. - PI48-U132, DOI 10.1107/S1600536810019069. - Cited Reference Count: 22. - Гранты: We thank the State Program for Support of Leading Scientific Schools (grant LS-4645.2010.2.). - Финансирующая организация: Leading Scientific Schools [LS-4645.2010.2] . - JUN. - ISSN 1600-5368
Рубрики:
CRYSTAL-STRUCTURE
   SRB4O7

   LUMINESCENCE

   MODEL

Кл.слова (ненормированные):
Tetra
Аннотация: The asymmetric unit of the title compound, beta-SrB4O7, contains five Sr atoms (three located on a threefold rotation axis), twelve B and 21 O atoms. The structure is made up from BO3 triangles and BO4 tetrahedra in a 1:1 ratio. Pairs of BO3 triangles are linked to BO4 tetrahedra via common corners, forming chains. These chains are further linked to adjacent chains through corner-sharing, leading to a three-dimensional framework with channels running parallel to [001]. The Sr2+ ions reside in the channels and exhibit strongly distorted polyhedra The density of the beta-polymorph is considerably lower than that of beta-SrB4O7, which is constructed solely from BO4 tetrahedra.

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Держатели документа:
Inst Phys SB RAS, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660041, Russia

Доп.точки доступа:
Vasiliev, Alexander D.; Cherepakhin, Alexander V.; Zaitsev, Alexander I.
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5.


   
    Spectroscopic properties of HoAl3(BO3)4 single crystal / D. A. Ikonnikov [et al.] // Opt. Mater. - 2014. - Vol. 37. - P. 257–261, DOI 10.1016/j.optmat.2014.05.036. - Cited References: 30. - The work was supported by Grant of the Ministry of Education and Science of the Russian Federation for Siberian Federal University, the Russian Foundation for Basic Research Grants 12-02-00026, 14-02-00219 and 13-02-00825, by the Russian President Grant SS-2886.2014.2, and by SB RAS Project No. 43. . - ISSN 0925. - ISSN 1873-1252
   Перевод заглавия: Спектроскопические свойства монокристалла HoAl3(BO3)4
РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
RARE-EARTH IONS
   OPTICAL-PROPERTIES

   Ho3+ IONS

   ABSORPTION

   INTENSITIES

   EMISSION

   GLASSES

   SPECTRA

   LUMINESCENCE

   PARAMETERS

Кл.слова (ненормированные):
Absorption -- Luminescence -- Holmium -- Huntite -- Judd-Ofelt
Аннотация: The Judd–Ofelt theory has been applied to analyze absorption spectra of Ho3+ ion in HoAl3(BO3)4 measured in spectral range 300–700 nm at room temperature. The Judd–Ofelt spectroscopic parameters have been determined as: Ω2 = 18.87 x 10 -20 cm2, Ω4 = 17.04 x 10 -20 cm2, Ω6 = 9.21 x 10 -20 cm2. These parameters have been used to calculate radiative lifetimes and branching ratios of the luminescence manifolds. Three luminescent bands were found in the spectral range 450–700 nm ascribed to transitions from the 5F5, (5F4, 5S2) and 3K8 states to the ground state 5I8. Experimental intensities of these luminescence transitions were compared with those calculated by using Judd–Ofelt theory and the system of kinetic equations for populations of starting luminescing states. Probabilities of radiativeless transitions were evaluated from this comparison.

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Держатели документа:
Siberian Fed Univ, Krasnoyarsk, Russia
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Ikonnikov, D. A.; Malakhovskii, A. V.; Малаховский, Александр Валентинович; Sukhachev, A. L.; Сухачев, Александр Леонидович; Temerov, V. L.; Темеров, Владислав Леонидович; Krylov, A. S.; Крылов, Александр Сергеевич; Bovina, A. F.; Бовина, Ася Федоровна; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Ministry of Education and Science of the Russian Federation for Siberian Federal University; Russian Foundation for Basic Research Grants [12-02-00026, 14-02-00219, 13-02-00825]; Russian President Grant [SS-2886.2014.2]; SB RAS Project [43]
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6.


   
    Spectroscopic properties of ErAl3(BO3)4 single crystal / A. V. Malakhovskii [et al.] // Chem. Phys. - 2014. - Vol. 428. - P. 137–143, DOI 10.1016/j.chemphys.2013.11.008. - Cited References: 43. - The work was supported by the Russian Foundation for Basic Researches grant 12-02-00026, by the Russian President Grants SS-1044.2012.2 and 4828.2012.2, by project No 3.9.5 PSB RAS, and by the Ministry of Education and Science of Russian Federation grant 8365 . - ISSN 0301-0104. - ISSN 1873-4421
   Перевод заглавия: Спектроскопические свойства монокристалла ErAl3(BO3)4
РУБ Chemistry, Physical + Physics, Atomic, Molecular & Chemical
Рубрики:
RARE-EARTH IONS
   GREEN UP-CONVERSION

   ER3+ IONS

   MICROCHIP LASER

   ABSORPTION INTENSITIES

   YAL3(BO3)4 CRYSTAL

   OPTICAL-ABSORPTION

   FIELD ANALYSIS

   GROWTH

   LUMINESCENCE

Кл.слова (ненормированные):
Rare earth compounds -- Er3+ -- Spectroscopic properties -- Judd-Ofelt analysis -- Luminescence
Аннотация: Single crystal of ErAl3(BO3)4 was grown and its structure was studied. Polarized absorption spectra of ErAl3(BO3)4 single crystal were measured in the spectral range 1670–330 nm (6000–30000 cm−1). The Judd–Ofelt spectroscopic parameters have been determined: Ω2 = 4.87 × 10−20 cm2, Ω4 = 2.49 × 10−20 cm2, Ω6 = 2.72 × 10−20 cm2. These parameters have been used to calculate the radiative transition probabilities, the multiplet luminescence branching ratios and the fluorescence life times of the manifolds. The luminescence spectra due to transitions 2H11/2 → 4I15/2 (526 nm), 4S3/2 → 4I15/2 (548 nm), 4F9/2 → 4I15/2 (662 nm), 2H11/2 → 4I13/2 + 4I9/2 → 4I15/2 (800 nm) and 4S3/2 → 4I13/2 (855 nm) were recorded in α, σ and π polarizations. The most intensive luminescence belonged to 4S3/2 → 4I15/2 transition (548 nm).
Поляризованные спектры поглощения ErAl3 (BO3) 4 монокристалла были измерены в спектральном диапазоне 1670-330 нм (6000-30000 см-1). Спектроскопические параметры Джадда-Офельта были определены как: Ω2 = 4,87 • 10-20 см2, Ω4 = 2.49 • 10-20 см2, Ω6 = 2,72 • 10-20 см2. Параметры были использованы для расчета вероятностей излучающих переходов, мультиплетные отношения люминесценции раскола и времена жизни мультиплетов. Спектры люминесценции за счет переходов 2П11 / 2 → 4I15 / 2 (526 нм), 4S3 / 2 → 4I15 / 2 (548 нм), 4F9 / 2 → 4I15 / 2 (662 нм), 2П11 / 2 → 4I13 / 2 + 4I9 / 2 → 4I15 / 2 (800 нм) и 4S3 / 2 → 4I13 / 2 (855 нм) были записаны в α, σ и π поляризации. Наиболее интенсивное свечение принадлежало переходу 4S3 / 2 → 4I15 / 2 (548 нм).

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Доп.точки доступа:
Malakhovskii, A. V.; Малаховский, Александр Валентинович; Kutsak, T. V.; Куцак, Т. В.; Sukhachev, A. L.; Сухачев, Александр Леонидович; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Gudim, Irina A.; Гудим, Ирина Анатольевна; Molokeev, M. S.; Молокеев, Максим Сергеевич
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7.


   
    Solvatochromic Photoluminescent Effects in All-Inorganic Manganese(II)-Based Perovskites by Highly Selective Solvent-Induced Crystal-to-Crystal Phase Transformations / H. Xiao, P. P. Dang, X. H. Yun [et al.] // Angew. Chem. Int. Edit. - 2021. - Vol. 60, Is. 7. - P. 3699-3707, DOI 10.1002/anie.202012383. - Cited References: 85. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018) . - ISSN 1433-7851. - ISSN 1521-3773
РУБ Chemistry, Multidisciplinary
Рубрики:
LEAD-FREE
   HALIDE PEROVSKITE

   NANOCRYSTALS

   MN2+

   LUMINESCENCE

Кл.слова (ненормированные):
lead-free materials -- low-dimensional perovskites -- luminescence -- manganese -- phase transitions
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, 5625 Renmin St, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Hefei 230026, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, Wuhan 430074, Peoples R China.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr,KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Xiao, Hui; Dang, Peipei; Yun, Xiaohan; Li, Guogang; Wei, Y.i.; Xiao, Xiao; Zhao, Yajie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cheng, Ziyong; Lin, Jun
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8.


   
    Quality of the rare earth aluminum borate crystals for laser applications, probed by high-resolution spectroscopy of the Yb3+ ion / K. N. Boldyrev [et al.] // Opt. Mater. - 2012. - Vol. 34, Is. 11. - P. 1885-1889, DOI 10.1016/j.optmat.2012.05.021. - Cited References: 20. - This work was supported by the Russian Academy of Sciences under the Programs for Basic Research, the Russian Foundation for Basic research under Grants No 10-02-01071-a and No 09-02-00171-a, and by the Ministry of Education and Science under Grant HIII-4828.2012.2. . - ISSN 0925-3467
РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
GROWTH
   Y1-XYBXAL3(BO3)4

   LUMINESCENCE

   FREQUENCY

   CENTERS

Кл.слова (ненормированные):
Ytterbium -- Aluminum borates -- Impurities -- High-resolution spectroscopy -- UV edge
Аннотация: A comparative study was performed of the low-temperature high-resolution absorption spectra of the Yb3+ probe in R1−xYbxAl3(BO3)4 (R = Y, Tm, Lu) crystals grown by flux technique independently in four different laboratories using different solvents. We show that the incorporation of solvent components into the crystal in the course of crystallization gives rise to spectral satellites of the Yb3+ 0(2F7/2) → 0′(2F5/2) absorption lines and assign particular satellites to the Yb3+ centers near the bismuth and molybdenum impurities (which decrease the transparency of YAB in the UV spectral range). We suggest this spectroscopic method for a rapid analysis of the quality of UV laser crystals and for improvement of growth technologies.

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Держатели документа:
[Boldyrev, K. N.
Popova, M. N.] RAS, Inst Spect, Troitsk 142190, Moscow Region, Russia
[Bettinelli, M.] Univ Verona, Dept Biotechnol, I-37134 Verona, Italy
[Bettinelli, M.] UdR Verona, INSTM, I-37134 Verona, Italy
[Temerov, V. L.
Gudim, I. A.
Bezmaternykh, L. N.] RAS, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
[Loiseau, P.
Aka, G.] ENSCP, CNRS, LCMCP, UMR 7574, F-75005 Paris, France
[Leonyuk, N. I.] Moscow MV Lomonosov State Univ, Fac Geol, Moscow 119899, Russia

Доп.точки доступа:
Boldyrev, K. N.; Popova, M. N.; Bettinelli, M.; Temerov, V. L.; Темеров, Владислав Леонидович; Gudim, Irina A.; Гудим, Ирина Анатольевна; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Loiseau, P.; Aka, G.; Leonyuk, N. I.
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9.


   
    Phase transformation in Ca3(PO4)2:Eu2+ via the controlled quenching and increased Eu2+ content: Identification of new cyan-emitting α-Ca3(PO4)2:Eu2+ phosphor / H. Ji [et al.] // J. Am. Ceram. Soc. - 2015. - Vol. 98, Is. 10. - P. 3280-3284, DOI 10.1111/jace.13787. - Cited References: 23. - This work was partly supported by the National Natural Science Foundations of China (grant nos. 51272242, 51472222, 51511130035), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), and the Russian Foundation for Basic Research (grant no. 15-52-53080 GFEN_a). VVA was partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 0002-7820
   Перевод заглавия: Фазовый переход в Ca3(PO4)2:Eu2+ посредством контролируемой закалки и увеличения концентрации Eu2+: Идентификация нового голубого люминофора α-Ca3(PO4)2:Eu2+
РУБ Materials Science, Ceramics
Рубрики:
NEUTRON POWDER DIFFRACTION
   SOLID-SOLUTION PHOSPHORS

   CRYSTAL-STRUCTURE

   DIODES

   PHOTOLUMINESCENCE

   LUMINESCENCE

   TRANSITION

   ALPHA

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

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Держатели документа:
School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing, China
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk, Russian Federation
Functional Electronics Laboratory, Tomsk State University, Tomsk, Russian Federation
Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk, Russian Federation

Доп.точки доступа:
Ji, H.; Huang, Z.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chen, M.; Atuchin, V. V.; Fang, M.; Liu, Y.; Wu, Xiaowen
}
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10.


   
    Phase formation upon crystallization of SrO center dot 2B(2)O(3) glasses / A. I. Zaitsev [et al.] // Crystallogr. Rep. - 2011. - Vol. 56, Is. 1. - P44-51, DOI 10.1134/S1063774511010263. - Cited Reference Count: 21 . - JAN. - ISSN 1063-7745
Рубрики:
STRONTIUM TETRABORATE
   LUMINESCENCE

   SRB4O7

   GROWTH

Кл.слова (ненормированные):
crystalline form -- crystalline formation -- crystalline phasis -- glass surfaces -- phase formations -- thermal analysis -- thermal stability -- crystalline materials -- crystallization -- glass -- thermoanalysis -- thermodynamic stability -- metastable phases
Аннотация: The crystallization of SrO center dot 2B(2)O(3) glasses has been studied. Four different crystalline formations were found to form simultaneously and independently on the glass surface: stable alpha-SrB4O7 crystals and metastable crystalline forms (beta-SrB4O7, Sr4B14O25, and spherulites (presumably, mixtures of crystalline phases)). The ranges of thermal stability of the newly formed metastable phases have been established using thermal analysis.

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Держатели документа:
Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660041, Russia

Доп.точки доступа:
Zaitsev, A. I.; Зайцев, Александр Иванович; Zamkov, A. V.; Замков, Анатолий Васильевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cherepakhin, A. V.; Черепахин, Александр Владимирович; Koroleva, N. S.
}
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11.


   
    Phase formation of (Y,Ce)2BaAl4SiO12 yellow microcrystal-glass phosphor for blue LED pumped white lighting / H. P. Ji [et al.] // Ceram. Int. - 2017. - Vol. 43, Is. 8. - P. 6425-6429, DOI 10.1016/j.ceramint.2017.02.055. - Cited References:12. - This study was partially supported by the National Natural Science Foundations of China (Grants No. 51272259, 51572232 and 51561135015). R.X. was partially supported by the JSPS KAKENHI (No. 15K06448). M.M. was partially supported by the Russian Foundation for Basic Research (Grant No. 15-52-53080) H.J. thanks the China Scholarship Council (CSC) for scholarship support. . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Образование фаз желтых люминофоров микрокристалл-стекло для белых светодиодов с накачкой синим цветом
РУБ Materials Science, Ceramics
Рубрики:
LUMINESCENCE
   EVOLUTION

Кл.слова (ненормированные):
Phosphor -- WLED -- Photoluminescence -- Cathodoluminescence
Аннотация: The (Y,Ce)2BaAl4SiO12 phosphor, a garnet-structured blue-to-yellow color convertor for WLED, exhibits an interesting “microcrystal-glass powder” feature, which can be regarded as the 4th form for phosphor, in addition to the “ceramic powder phosphor”, the “single crystal phosphor” and the “glass-ceramic phosphor”. The structure exhibits luminescent microcrystals embedding in non-luminescent glass matrix: the spherical crystals are mainly arranged around the glass phase forming a “necklace” pattern, while the individual crystals show a “core-shell” architecture regarding the luminescence intensity variation. Further combining the phase evolution evidence evaluated by Rietveld refinement, we propose the formation mechanism for such unique morphology/structure as a two-stage process, including an initial nucleation by solid state reaction and following liquid-assisted crystal growth, instead of a precipitation-crystallization process.

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Beijing 100083, Peoples R China.
Natl Inst Mat Sci, Sialon Grp, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan.
Natl Inst Mat Sci, Nano Device Characterizat Grp, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan.
China Jiliang Univ, Coll Opt & Elect Technol, Hangzhou 310018, Zhejiang, Peoples R China.
RAS, SB, KSC, Lab Crystal Phys,Kirensky Inst Phys,Fed Res Ctr, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Xiamen Univ, Coll Mat, Xiamen, Peoples R China.

Доп.точки доступа:
Ji, Haipeng; Cho, Yujin; Wang, L.e.; Hirosaki, Naoto; Molokeev, M. S.; Молокеев, Максим Сергеевич; Huang, Zhaohui; Xie, Rong-Jun
}
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12.


   
    Optical functional units in zero-dimensional metal halides as a paradigm of tunable photoluminescence and multicomponent chromophores / M. Z. Li, M. S. Molokeev, J. Zhao, Z. G. Xia // Adv. Opt. Mater. - 2020. - Vol. 8, Is. 8. - Ст. 1902114, DOI 10.1002/adom.201902114. - Cited References: 38. - This work was supported by the National Natural Science Foundation of China (Nos. 51961145101, 51722202, and 51972118), Fundamental Research Funds for the Central Universities (D2190980), the Guangdong Provincial Science & Technology Project (2018A050506004), and this work was also funded by RFBR according to the Research Project No. 19-52-80003 . - ISSN 2195-1071
   Перевод заглавия: Оптические функциональные элементы в 0D металлгалогенидах как парадигма перестраиваемой фотолюминесценции многокомпонентных хромофоров
РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
PEROVSKITES
   LUMINESCENCE

   ABSORPTION

   EMISSION

Кл.слова (ненормированные):
hybrid metal halides -- optical functional applications -- structural design
Аннотация: Zero-dimensional (0D) organic–inorganic hybrid luminescent metal halides have many promising optoelectronic applications; however, the single building unit in the 0D framework restricts their multimode optical control and photoluminescence tuning. Thus, it remains urgent but challenging to rationally design distinct anionic polyhedral with different optical functions and further expand this family by an equivalent cation substitution and halogen replacement. Herein, (C9NH20)9[Pb3X11](MX4)2 (X = Br and Cl, M = Mn, Fe, Co, Ni, Cu, and Zn) is successfully synthesized verifying the rationality of the design philosophy, and the optical characterizations demonstrate the effects of X‐position anions and M‐position cations on luminescence process. Intriguingly, both [Pb3X11]5− and [MX4]2− perform as inorganic building units in this 0D system and optically active centers, in which the former leads to high‐efficiency broad‐band yellow/green emission originating from self‐trapped excitons and the as‐observed multicomponent chromophores are derived from the absorption of the latter in the visible light region. The present work highlights the importance of different optical functional units showing synergistic effects on the physical properties and inspires future studies to explore multifunctional application of 0D luminescent metal halides.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, 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:
Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Xia, Zhiguo
}
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13.


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

   Photoluminescence

   Ce3+

   Substitution

   Discovery

   Oxygen

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

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

Доп.точки доступа:
Ji, H.; Wang, L.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Hirosaki, N.; Huang, Z.; Xia, Z.; Ten Kate, O. M.; Liu, L.; Xie, R.
}
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14.


   
    Multiple substitution strategies toward tunable luminescence in Lu2MgAl4SiO12:Eu2+ phosphors / Z. Ming, J. Qiao, M. S. Molokeev [et al.] // Inorg. Chem. - 2020. - Vol. 59, Is. 2. - P. 1405-1413, DOI 10.1021/acs.inorgchem.9b03142. - Cited References: 31. - This research is supported by the National Natural Science Foundation of China (Grants 51972118, 51722202, and 51572023), Natural Science Foundations of Beijing (Grant 2172036), and Fundamental Research Funds for the Central Universities (Grant FRF-TP-18-002C1) . - ISSN 0020-1669. - ISSN 1520-510X
   Перевод заглавия: Стратегии множественного замещения для перестраиваемой люминесценции в люминофорах Lu2MgAl4SiO12:Eu2+
Рубрики:
Physical and chemical processes
   Phosphors

   Luminescence

   Cations

   Ions

Аннотация: The equivalent or heterovalent substitution strategy is an efficient way to stimulate photoluminescence tuning or to optimize the luminescence performances of phosphor materials. Garnet-type compounds receive much attention as phosphor hosts because of their flexible structural frameworks. Herein, a garnet-type Lu2MgAl4SiO12:Eu2+ phosphor with broad-band blue-green emission is first explored with two-site occupation by varying the Eu2+ content. Two host-substitution approaches to controlling the luminescence behavior of Lu2MgAl4SiO12:Eu2+ phosphor are implemented. The cation substitution strategy of Ca2+ for Mg2+ achieves tunable emission from 463 to 503 nm together with broadening emission bands in Lu2Mg1–yCayAl4SiO12:Eu2+ phosphors. Moreover, chemical unit cosubstitution of [Ca2+–Ge4+] replacing [Lu3+–Al3+] results in Lu2–zCazMgAl4–zGezSiO12:Eu2+ phosphors, which induce a red shift of the emission peak of about 60 nm and a broadening in the emission spectra with increasing Ca2+ and Ge4+ concentrations. The possible photoluminescence tuning mechanism is ascribed to the coordination sphere variation in the EuO8 polyhedron depending on the changing neighboring cations. The proposed approaches on equivalent or heterovalent substitution can contribute to the development of Eu2+-activated garnet-type phosphors with regulation of the luminescence performance and further initiate research discovering new phosphors for white-light-emitting diodes.

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Держатели документа:
School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing 100083, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Siberian Federal University, Krasnoyarsk, 660041, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russia
Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, 9300, South Africa
State Key Laboratory of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641, China

Доп.точки доступа:
Ming, Zhiqiang; Qiao, Jianwei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Swart, Hendrik C.; Xia, Zhiguo
}
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15.


   
    Morphology and phase transformation from NaCaSiO3OH to Na2Ca2Si2O7 and photoluminescence evolution: Via Eu3+/Tb3+ doping / M. Chen [et al.] // Chem. Commun. - 2016. - Vol. 52, Is. 75. - P. 11292-11295, DOI 10.1039/c6cc06375f. - Cited References: 26. - The present work was supported by the National Natural Science Foundation of China (Grant No. 51572023 and 51272242), the Fundamental Research Funds for the Central Universities (FRF-TP-15-003A2) and the Russian Foundation for Basic Research (Grant No. 15-52-53080 GFEN_a). . - ISSN 1359-7345
   Перевод заглавия: Морфология и фазовый переход из NaCaSiO3OH в Na2Ca2Si2O7 и преобразование люминесценции при допировании Eu3+/Tb3+
РУБ Chemistry, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
   ENERGY-TRANSFER

   SPECTROSCOPIC PROPERTIES

   PHOSPHORS

   LUMINESCENCE

Аннотация: A facile and controllable ethanol/water aided hydrothermal process was developed to prepare the NaCaSiO3OH:Tb3+/Eu3+ phosphor. The morphologies were in situ constructed with the phase transformation from NaCaSiO3OH to Na2Ca2Si2O7, and the intrinsic crystal structural transformation mechanism and the dependence of their photoluminescence tuning on the Tb3+/Eu3+ ratio have been discussed. © 2016 The Royal Society of Chemistry.

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

Доп.точки доступа:
Chen, M.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Q.
}
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16.


   
    Monoclinic SmAl3(BO3)4: synthesis, structural and spectroscopic properties / A. S. Oreshonkov, N. P. Shestakov, M. S. Molokeev [et al.] // Acta Crystallogr. B. - 2020. - Vol. 76. - P. 654-660, DOI 10.1107/S2052520620008781. - Cited References: 38. - Funding for this research was provided by: Russian Foundation for Basic Research (grant Nos. 18-03-00750, 18-05-00682 and 18-32-20011 to AO) . - ISSN 2052-5206
   Перевод заглавия: Моноклинный SmAl3(BO3)4: синтез, структура и спектроскопические свойства
РУБ Chemistry, Multidisciplinary + Crystallography
Рубрики:
Optical-properties
   Luminescence

   Spectra

   Crystals

   Sm

Кл.слова (ненормированные):
IR spectroscopy -- monoclinic structure -- luminescence -- Raman spectroscopy -- X-ray diffraction -- crystal structure
Аннотация: Single crystals of SmAl3(BO3)4 were synthesized by the group growth on seeds method. The crystal structure was solved using a single-crystal experiment and the purity of the bulk material was proved by the Rietveld method. This borate crystallizes in the monoclinic C2/c space group with unit-cell parameters a = 7.2386 (3), b = 9.3412 (5), c = 11.1013 (4) Å and β = 103.2240 (10)°. IR and Raman spectroscopic analyses confirmed the monoclinic structure of SmAl3(BO3)4. Under 532.1 nm excitation, luminescence spectra exhibit bands assignable to the transitions from 4G5/2 to 6H5/2, 6H7/2, 6H9/2 and 6H11/2. The similarity of the luminescence spectra of the trigonal and monoclinic poly­morphs is explained by the minor role of Sm—O bond distortion and the primary role of rotational distortion of SmO6 octa­hedra. The smaller covalency of the Sm—O bond in alumoborates is deduced in comparison with galloborates. Calorimetric measurements did not reveal high-temperature structural phase transitions up to a temperature of 720 K.

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Держатели документа:
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Mol Spect, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Engn & Construct, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk, Russia.
Siberian Fed Univ, Sch Engn Phys & Radio Elect, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Coherent Opt, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Radiospect & Spintron, Krasnoyarsk 660036, Russia.
Russian Acad Sci, Inst Automat & Electrometry, Novosibirsk 630090, Russia.
Fed Res Ctr KSC SB RAS, Dept Mol Elect, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660074, Russia.
Tyumen State Univ, Dept Inorgan & Phys Chem, Tyumen 625003, Russia.
Ind Univ Tyumen, Dept Gen & Special Chem, Tyumen 625000, Russia.

Доп.точки доступа:
Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Shestakov, N. P.; Шестаков, Николай Петрович; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Gudim, I. A.; Гудим, Ирина Анатольевна; Temerov, V. L.; Темеров, Владислав Леонидович; Adichtchev, S. V.; Pugachev, A. M.; Nemtsev, I. V.; Немцев, Иван Васильевич; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич; Denisenko, Y. G.; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [18-03-00750, 18-05-00682, 18-32-20011]
}
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17.


   
    Manifestations of Structural Phase Transitions in a Rb2KLuF6 Crystal in Its Raman Spectra / A. S. Krylov [et al.] // Opt. Spectrosc. - 2019. - Vol. 126, Is. 4. - P. 341-345, DOI 10.1134/S0030400X1904012X. - Cited References: 27. - This work was supported by the Russian Foundation for Basic Research, project nos. 16-02-00102, 18-02-00754. . - ISSN 0030-400X. - ISSN 1562-6911
РУБ Optics + Spectroscopy
Рубрики:
SCATTERING
   ELPASOLITES

   LUMINESCENCE

   TRANSFORMATIONS

   FLUORIDES

Аннотация: The Raman spectra of an Rb2KLuF6 crystal are studied in the temperature range from 8 to 375 K, which includes two phase transitions: one of which proceeds from a cubic to a tetragonal phase, while the other transition takes place from a tetragonal to a monoclinic phase. An analysis of the temperature dependences of parameters of spectral lines shows that the former transition is of the second kind, while the latter transition is of the first kind, close to the tricritical point. It is shown that the structural phase transitions in the Rb2KLuF6 double perovskite are not associated with disordering. The former transition is associated with rotations of LuF6 octahedra around the fourth-order axis, while the latter transition is related with rotations of octahedra and displacements of rubidium ions.

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Публикация на русском языке Проявление структурных фазовых переходов в кристалле Rb2KLuF6 в спектрах комбинационного рассеяния света [Текст] / А. С. Крылов [и др.] // Оптика и спектроскопия. - 2019. - Т. 126 Вып. 4. - С. 423-427

Держатели документа:
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Krylov, A. S.; Крылов, Александр Сергеевич; Vtyurin, A. N.; Втюрин, Александр Николаевич; Voronov, V. N.; Воронов, Владимир Николаевич; Krylova, S. N.; Крылова, Светлана Николаевна; Russian Foundation for Basic Research [16-02-00102, 18-02-00754]
}
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18.


   
    Learning from a mineral structure toward an ultra-narrow-band blue-emitting silicate phosphor RbNa3(Li3SiO4)4:Eu2+ / H. X. Liao [et al.] // Angew. Chem. - Int. Edit. - 2018. - Vol. 57, Is. 36. - P. 11728-11731, DOI 10.1002/anie.201807087. - Cited References: 22. - This work was supported by the National Natural Science Foundations of China (Grant Nos. 51722202, 91622125 and 51572023), and Natural Science Foundations of Beijing (2172036), and M.S.M. acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 1433-7851. - ISSN 1521-3773
   Перевод заглавия: Обучение от минеральной структуры к ультраузкополосному синему силикатному люминофору RbNa3(Li3SiO4)4:Eu2+
РУБ Chemistry, Multidisciplinary
Рубрики:
RED PHOSPHORS
   COLOR-GAMUT

   LUMINESCENCE

Кл.слова (ненормированные):
luminescence -- minerals -- phosphors -- rigid structure -- silicates
Аннотация: Learning from natural mineral structures is an efficient way to develop potential host lattices for applications in phosphor converted (pc)LEDs. A narrow‐band blue‐emitting silicate phosphor, RbNa3(Li3SiO4)4:Eu2+ (RNLSO:Eu2+), was derived from the UCr4C4‐type mineral model. The broad excitation spectrum (320–440 nm) indicates this phosphor can be well matched with the near ultraviolet (n‐UV) LED chip. Owing to the UCr4C4‐type highly condensed and rigid framework, RNLSO:Eu2+ exhibits an extremely small Stokes shift and an unprecedented ultra‐narrow (full‐width at half‐maximum, FWHM=22.4 nm) blue emission band (λem=471 nm) as well as excellent thermal stability (96 %@150 °C of the initial integrated intensity at 25 °C). The color gamut of the as‐fabricated (pc)LEDs is 75 % NTSC for the application in liquid crystal displays from the prototype design of an n‐UV LED chip and the narrow‐band RNLSO:Eu2+ (blue), β‐SiAlON:Eu2+ (green), and K2SiF6:Mn4+ (red) components as RGB emitters.

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
Fed Res Ctr KSC SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Liao, Hongxu; Zhao, Ming; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Quanlin; Xia, Zhiguo
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19.


   
    Heat capacity and thermodynamic properties of crystalline SrB4O7 / N. V. Moiseev [et al.] // Inorg. Mater. - 2012. - Vol. 48, Is. 5. - P. 504-507, DOI 10.1134/S0020168512050123. - Cited References: 24. - This work was supported in part by the RF President's Grants Council (grant no. NSh-4645.2010.2), the RF Ministry of Education and Science (analytical departmental targeted program Development of the Scientific Potential of Higher Education Institutions, grant no. RNP 2.1.1/10747), Bryansk State University (project no. 1.1.11), and the Physical Sciences Division of the Russian Academy of Sciences (Physics of Advanced Materials and Structures Program, project no. 2.5.2). . - ISSN 0020-1685
РУБ Materials Science, Multidisciplinary
Рубрики:
STRONTIUM TETRABORATE
   SINGLE-CRYSTALS

   LUMINESCENCE

Аннотация: The heat capacity of a strontium tetraborate (SrB4O7) single crystal has been determined in the temperature range 55-300 K by adiabatic calorimetry, and its Debye characteristic temperature, entropy change, enthalpy increment, and phonon mean free path have been calculated as functions of temperature.

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Публикация на русском языке Теплоемкость и термодинамические свойства кристаллического SrB4O7 [Текст] / Н. В. Моисеев [и др.] // Неорган. матер. - 2012. - Т. 48 № 5. - С. 588-591

Держатели документа:
[Moiseev, N. V.
Popov, P. A.
Solomennik, V. D.] Petrovskii State Univ, Bryansk 241036, Russia
[Zaitsev, A. I.
Cherepakhin, A. V.] Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Moiseev, N. V.; Popov, P. A.; Solomennik, V. D.; Zaitsev, A. I.; Зайцев, Александр Иванович; Cherepakhin, A. V.; Черепахин, Александр Владимирович
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20.


   
    Facile synthesis of the desired red phosphor Li2Ca2Mg2Si2N6:Eu2+ for high CRI white LEDs and plant growth LED device / X. Yang [et al.] // J. Am. Ceram. Soc. - 2020. - Vol. 103, Is. 3. - P. 1773-1781, DOI 10.1111/jace.16858. - Cited References: 34. - National Natural Science Foundations of China, Grant/Award Number: 21671070 and 51802101; Project GDUPS; Natural Science Foundation of Guangdong Province, Grant/Award Number: 2018A030310217; Guangzhou Science & Technology Project, Grant/Award Number: 201704030086; Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams; National Undergraduate Innovation and Entrepreneurship Training Program granted for Gening Xie, Grant/Award Number: 201910564035 . - ISSN 0002-7820. - ISSN 1551-2916
   Перевод заглавия: Простой синтез красного люминофора Li2Ca2Mg2Si2N6: Eu2+, необходимого для белых светодиодов с высоким CRI, и светодиодных устройств для роста растений
РУБ Materials Science, Ceramics
Рубрики:
IN-GLASS
   LUMINESCENCE

   PERFORMANCE

   EFFICIENT

   EMISSION

   ROUTE

Кл.слова (ненормированные):
high CRI white LEDs -- Li2Ca2Mg2Si2N6:Eu2+ -- phosphor -- plant growth LED device
Аннотация: The red emission with suitable peak wavelength and narrow band is acutely required for high color rendering index (CRI) white LEDs without at the cost of the luminous efficacy. Herein, the Li2Ca2Mg2Si2N6:Eu2+ red phosphor was prepared with facile solid‐state method using Ca3N2, Mg3N2, Si3N4, Li3N, and Eu2O3 as the safety raw materials under atmospheric pressure for the first time, which shows red emission peaking at 638 nm with full width at half maximum (FWHM) of 62 nm under blue light irradiation and becomes the desired red phosphor to realize the balance between luminous efficacy and high CRI in white LEDs. The morphology, structure, luminescence properties, thermal quenching behavior, and chromaticity stability of the Li2Ca2Mg2Si2N6:Eu2+ phosphor are investigated in detail. Concentration quenching occurs when the Eu2+ content exceeds 1.0 mol%, whereas high‐temperature photoluminescent measurements show a 32% drop from the room‐temperature efficiency at 423 K. In view of the excellent luminescence performances of Li2Ca2Mg2Si2N6:Eu2+ phosphor, a white LEDs with CRI of 91 as a proof‐of‐concept experiment was fabricated by coating the title phosphor with Y3Al5O12:Ce3+ on a blue LED chip. In addition, the potential application of the title phosphor in plant growth LED device was also demonstrated. All the results indicate that Li2Ca2Mg2Si2N6:Eu2+ is a promising red‐emitting phosphor for blue LED‐based high CRI white LEDs and plant growth lighting sources.

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Держатели документа:
South China Agr Univ, Coll Hort, Guangzhou, Guangdong, Peoples R China.
South China Agr Univ, Coll Mat & Energy, Guangdong Prov Engn Technol Res Ctr Opt Agr, Guangzhou 510642, Guangdong, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk, Russia.

Доп.точки доступа:
Yang, Xiang; Zhang, Y.u.; Zhang, Xuejie; Chen, Jian; Huang, Haisen; Wang, Dongsheng; Chai, Xirong; Xie, Gening; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhang, Haoran; Liu, Yingliang; Lei, Bingfu
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