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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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    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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    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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    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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    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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    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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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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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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    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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