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Scheelite type microcrystalline AgGd(MoO4)2:Yb3+/Ho3+ upconversion yellow phosphors by MES based synthesis and their spectroscopic properties for biomedical applications / Chang Sung LimWon-Chun Oh, A. S. Aleksandrovsky [et al.] // The 15th International conference on multifunctional materials and application. - 2021. - Ст. PO8. - P. 75-76. - Cited References: 4

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Доп.точки доступа:
Chang Sung Lim; Won-Chun Oh; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; International Conference on Multifunctional Materials and Application(15 ; 2021 ; Nov. 25-25 ; Nakhon Si Thammarat Rajabhat University, Thailand)
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Microwave sol-gel derived Ho3+/Yb3+ co-doped NaCaGd(MoO4)3 yellow phosphors and their upconversion photoluminescence properties for optoelectronic devices / Chang Sung LimWon-Chun Oh, A. S. Aleksandrovsky [et al.] // The 15th International conference on multifunctional materials and application. - 2021. - Ст. PO7. - P. 73-74. - Cited References: 4

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Доп.точки доступа:
Chang Sung Lim; Won-Chun Oh; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; International Conference on Multifunctional Materials and Application(15 ; 2021 ; Nov. 25-25 ; Nakhon Si Thammarat Rajabhat University, Thailand)
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    Синтез и фотоэлектрокаталитическая активность анодных наноструктурированных TiO2 пленок / Н. А. Зосько, Т. А. Кенова, А. С. Александровский [и др.] // Журн. СФУ. Химия. - 2021. - Т. 14, № 3. - С. 396-405 ; J. Sib. Fed. Univ. Chem., DOI 10.17516/1998-2836-0249. - Библиогр.: 25. - Работа выполнена в рамках государственного задания ФИЦ КНЦ СО РАН (проект 0287-2021-0023) с использованием оборудования Красноярского регионального центра коллективного пользования ФИЦ КНЦ СО РАН. Авторы выражают признательность Н. Г. Максимову за снятие диффузных спектров отражения и В. Ф. Шабанову за плодотворную дискуссию . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Synthesis and Photoelectrocatalytic Activity of Anodic Nanostructured TiO2 Films
Кл.слова (ненормированные):
фотоэлектрокаталитическая активность -- TiO2 нанотрубки -- анодное окисление -- морфология поверхности -- катодное осаждение -- Cu2O -- photoelectrocatalytic activity -- TiO2 nanotubes -- anodic oxidation -- structure morphology -- electrodeposition -- Cu2O
Аннотация: Методом электрохимического окисления получены наноструктурированные пленки диоксида титана, исследовано влияние напряжения анодирования на морфологию поверхности, оптические и фотоэлектрокаталитические характеристики полученных нанотрубок. Показано, что напряжение анодирования оказывает существенное влияние на структуру нанопленок и, соответственно, на их фотоэлектрокаталитическую активность. Методом катодного осаждения Cu2O на анодированный TiO2 получен фотоанод с гетеропереходом. Установлено, что фотоэлектроактивность такого анода при потенциале 1В (отн. Ag/AgCl/3,5MKCl) на 15% выше, чем активность исходной наноструктурированной TiO2 пленки.
Nanostructured titanium dioxide films were prepared by electrochemical oxidation technique, anodization voltage effect on structure morphology, optical and photoelectrocatalytic performances of the nanotubes were studied. The anodization voltage is shown to significantly affect structure of nanofilms and, accordingly, their photoelectrocatalytic activity. An active heterojunction photoanode was synthesised with electrode position of Cu2O onanodized TiO2. The anode photoelectroact ivity under bias 1V (Ag/AgCl/3,5M KCl) is found to be 15 % higher than that of the original nanostructured TiO2 film.

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Держатели документа:
Институт химии и химической технологии ФИЦ КНЦ СО РАН, Российская Федерация, Красноярск
Институт физики им. Л. В. Киренского ФИЦ КНЦ СО РАН, Российская Федерация, Красноярск
Сибирский федеральный университет, Российская Федерация, Красноярск

Доп.точки доступа:
Зосько, Н. А.; Кенова, Т. А.; Александровский, Александр Сергеевич; Aleksandrovsky, A. S.; Жижаев, А. М.; Таран, О. П.; [02872021-0023]

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    Structural and spectroscopic effects of Li+ substitution for Na+ in LixNa1-xCaGd0.5Ho0.05Yb0.45(MoO4)3 scheelite-type upconversion phosphors / C.-S. Lim, A. S. Aleksandrovsky, M. S. Molokeev [et al.] // Molecules. - 2021. - Vol. 26, Is. 23. - Ст. 7357, DOI 10.3390/molecules26237357. - Cited References: 77. - This study was supported by the Research Program through the Campus Research Foundation funded by Hanseo University in 2021 (211Yunghap06) . - ISSN 1420-3049
   Перевод заглавия: Структурные и спектральные эффекты замещения Na+ ионами Li+ в LixNa1-xCaGd0.5Ho0.05Yb0.45(MoO4)3 шеелитоподобном апконверсионном люминофоре
Кл.слова (ненормированные):
optical materials -- chemical synthesis -- molybdate -- Raman spectroscopy -- X-ray diffraction; phosphors -- phosphors
Аннотация: A set of new triple molybdates, LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45, was successfully manufactured by the microwave-accompanied sol–gel-based process (MAS). Yellow molybdate phosphors LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45 with variation of the LixNa1-x (x = 0, 0.05, 0.1, 0.2, 0.3) ratio under constant doping amounts of Ho3+ = 0.05 and Yb3+ = 0.45 were obtained, and the effect of Li+ on their spectroscopic features was investigated. The crystal structures of LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45 (x = 0, 0.05, 0.1, 0.2, 0.3) at room temperature were determined in space group I41/a by Rietveld analysis. Pure NaCaGd0.5Ho0.05Yb0.45(MoO4)3 has a scheelite-type structure with cell parameters a = 5.2077 (2) and c = 11.3657 (5) Å, V = 308.24 (3) Å3, Z = 4. In Li-doped samples, big cation sites are occupied by a mixture of (Li,Na,Gd,Ho,Yb) ions, and this provides a linear cell volume decrease with increasing Li doping level. The evaluated upconversion (UC) behavior and Raman spectroscopic results of the phosphors are discussed in detail. Under excitation at 980 nm, the phosphors provide yellow color emission based on the 5S2/5F4 → 5I8 green emission and the 5F5 → 5I8 red emission. The incorporated Li+ ions gave rise to local symmetry distortion (LSD) around the cations in the substituted crystalline structure by the Ho3+ and Yb3+ ions, and they further affected the UC transition probabilities in triple molybdates LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45. The complex UC intensity dependence on the Li content is explained by the specificity of unit cell distortion in a disordered large ion system within the scheelite crystal structure. The Raman spectra of LixNa1-xCaGd0.5(MoO4)3 doped with Ho3+ and Yb3+ ions were totally superimposed with the luminescence signal of Ho3+ ions in the range of Mo–O stretching vibrations, and increasing the Li+ content resulted in a change in the Ho3+ multiplet intensity. The individual chromaticity points (ICP) for the LiNaCaGd(MoO4)3:Ho3+,Yb3+ phosphors correspond to the equal-energy point in the standard CIE (Commission Internationale de L’Eclairage) coordinates.

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Department of Aerospace Advanced Materials and Chemical Engineering, Hanseo University, Seosan 31962, Korea
Laboratory of Coherent Optics, Kirensky Institute of Physics Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, 660041 Krasnoyarsk, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, 660041 Krasnoyarsk, Russia
Department of Physics, Far Eastern State Transport University, 680021 Khabarovsk, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
School of Engineering and Construction, Siberian Federal University, 660041 Krasnoyarsk, Russia
Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, 630090 Novosibirsk, Russia
Research and Development Department, Kemerovo State University, 650000 Kemerovo, Russia
Department of Industrial Machinery Design, Novosibirsk State Technical University, 630073 Novosibirsk, Russia

Доп.точки доступа:
Lim, Chang-Sung; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Atuchin, V. V.
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    Quaternary selenides EuLnCuSe3: Synthesis, structures, properties and in silico studies / M. V. Grigoriev, L. A. Solovyov, A. V. Ruseikina [et al.] // Int. J. Mol. Sci. - 2022. - Vol. 23, Is. 3. - Ст. 1503, DOI 10.3390/ijms23031503. - Cited References: 90 . - ISSN 1422-0067
   Перевод заглавия: Четвертичные селениды EuLnCuSe3: синтез, структура, свойства и компьютерное моделирование

РУБ Biochemistry & Molecular Biology + Chemistry, Multidisciplinary
Рубрики:
RARE-EARTH
   CRYSTAL-STRUCTURES
   MAGNETIC-PROPERTIES
   THERMOELECTRIC PERFORMANCE
Кл.слова (ненормированные):
inorganic materials -- ab initio calculations -- magnetic measurements -- lattice dynamics -- vibrational spectroscopy -- optical spectroscopy -- negative magnetization
Аннотация: In this work, we report on the synthesis, in-depth crystal structure studies as well as optical and magnetic properties of newly synthesized heterometallic quaternary selenides of the Eu+2Ln+3Cu+1Se3 composition. Crystal structures of the obtained compounds were refined by the derivative difference minimization (DDM) method from the powder X-ray diffraction data. The structures are found to belong to orthorhombic space groups Pnma (structure type Ba2MnS3 for EuLaCuSe3 and structure type Eu2CuS3 for EuLnCuSe3, where Ln = Sm, Gd, Tb, Dy, Ho and Y) and Cmcm (structure type KZrCuS3 for EuLnCuSe3, where Ln = Tm, Yb and Lu). Space groups Pnma and Cmcm were delimited based on the tolerance factor t’, and vibrational spectroscopy additionally confirmed the formation of three structural types. With a decrease in the ionic radius of Ln3+ in the reported structures, the distortion of the (LnCuSe3) layers decreases, and a gradual formation of the more symmetric structure occurs in the sequence Ba2MnS3 → Eu2CuS3 → KZrCuS3. According to magnetic studies, compounds EuLnCuSe3 (Ln = Tb, Dy, Ho and Tm) each exhibit ferrimagnetic properties with transition temperatures ranging from 4.7 to 6.3 K. A negative magnetization effect is observed for compound EuHoCuSe3 at temperatures below 4.8 K. The magnetic properties of the discussed selenides and isostructural sulfides were compared. The direct optical band gaps for EuLnCuSe3, subtracted from the corresponding diffuse reflectance spectra, were found to be 1.87–2.09 eV. Deviation between experimental and calculated band gaps is ascribed to lower d states of Eu2+ in the crystal field of EuLnCuSe3, while anomalous narrowing of the band gap of EuYbCuSe3 is explained by the low-lying charge-transfer state. Ab initio calculations of the crystal structures, elastic properties and phonon spectra of the reported compounds were performed.

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Держатели документа:
Univ Tyumen, Lab Theory & Optimizat Chem & Technol Processes, Tyumen 625003, Russia.
SB RAS, Inst Chem & Chem Technol, Fed Res Ctr KSC, Krasnoyarsk 660036, Russia.
Univ Tyumen, Inst Chem, Tyumen 625003, Russia.
Siberian Fed Univ, Dept Photon & Laser Technol, Krasnoyarsk 660079, Russia.
RAS, SB, Fed Res Ctr KSC, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Ural Fed Univ, Inst Nat Sci & Math, Mira Str 19, Ekaterinburg 620002, Russia.
Univ Tyumen, Inst Phys & Technol, Tyumen 625003, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660079, Russia.
Siberian Fed Univ, Sch Engn & Construct, Krasnoyarsk 660041, Russia.
Univ Tyumen, Engn Ctr Composite Mat Based Wolfram Cpds & Rare, Tyumen 625003, Russia.
Univ Stuttgart, Inst Inorgan Chem, D-70569 Stuttgart, Germany.
Kurgan State Univ, Adv Mat Ind & Biomed Lab, Sovetskaya Str 63-4, Kurgan 640020, Russia.
Ural Fed Univ, Innovat Ctr Chem & Pharmaceut Technol, Mira Str 19, Ekaterinburg 620002, Russia.

Доп.точки доступа:
Grigoriev, Maxim V.; Solovyov, Leonid A.; Ruseikina, Anna V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Chernyshev, Vladimir A.; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Garmonov, Alexander A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Shestakov, N. P.; Шестаков, Николай Петрович; Matigorov, Alexey V.; Volkova, Svetlana S.; Ostapchuk, Evgeniy A.; Kertman, Alexander V.; Schleid, Thomas; Safin, Damir A.
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Phase matched conversion of radiation in nonlinear photonic crystals of strontium tetraborate / A. S. Aleksandrovsky [et al.] // Proceedings of SPIE - The International Society for Optical Engineering. - 2011. - Vol. 7993: ICONO 2010: International Conference on Coherent and Nonlinear Optics (23 August 2010 through 26 August 2010, Kazan, ) Conference code: 83828, DOI 10.1117/12.872943 . - ISBN 0277786X (ISSN); 9780819485663 (ISBN)
Кл.слова (ненормированные):
nonlinear photonic crystal -- random quasi phase matching -- second harmonic generation -- strontium tetraborate -- average power -- deep uv -- enhancement factor -- fs pulse -- monodomains -- nonlinear photonic crystals -- quasi-phase-matched frequency doubling -- radiation source -- random quasi phase matching -- rotational shift -- second harmonic generation -- tetraborate -- tuning ranges -- band structure -- harmonic generation -- nonlinear optics -- optical materials -- phase matching -- quantum optics -- strontium -- photonic crystals
Аннотация: Random quasi-phase-matched frequency doubling of fs pulses to the deep UV was obtained in 1D nonlinear photonic crystal (NPC) of strontium tetraborate. Tuning range of generated radiation is from 187.5 to 215 nm. The spectrum of generated radiation consists from series of peaks with the width of order of 1 A. These peaks are the manifestation of the NPC band structure. Using fs oscillator as the fundamental radiation source, maximum average power of generated radiation is of order 1 ?W, the enhancement factor with respect to monodomain sample being of order of several hundred. The red rotational shift of NPC band structure is experimentally demonstrated. © 2011 SPIE.

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Держатели документа:
Kirensky Institute of Physics, Akademgorodok 50/38, 660036, Krasnoyarsk, Russian Federation
Siberian Federal University, Svobodniy 79, 660041, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Aleksandrovsky, A.S.; Vyunishev, A.M.; Zaitsev, A.I.; Ikonnikov, A.A.; Pospelov, G.I.; Slabko, V.V.
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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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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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Synthesis, structure, and properties of EuLnCuSe3 (Ln = Nd, Sm, Gd, Er) / O. V. Andreev, V. V. Atuchin, A. S. Aleksandrovsky [et al.] // Crystals. - 2022. - Vol. 12, Is. 1. - Ст. 17, DOI 10.3390/cryst12010017. - Cited References: 60. - The study was funded by the Ministry of Science and Higher Education of the Russian Ferderation (Projects AAAA-A21-121011390011-4 and AAAA-A19-119031890025-9), as well as the Government of the Tyumen Region (grant to non-profit organizations No. 2. 89-don, dated 7 December 2020) . - ISSN 2073-4352

РУБ Crystallography + Materials Science, Multidisciplinary
Рубрики:
RARE-EARTH
   CRYSTAL-STRUCTURE
   MAGNETIC-PROPERTIES
   CHALCOGENIDES
Кл.слова (ненормированные):
rare earth elements -- complex sulfides -- chalcogenides -- crystal structure -- magnetic properties
Аннотация: EuLnCuSe3 (Ln = Nd, Sm, Gd, Er), due to their complex composition, should be considered new materials with the ability to purposefully change the properties. Samples of the EuLnCuSe3 were prepared using Cu, rare earth metal, Se (99.99%) by the ampoule method. The samples were obtained by the crystallization from a melt and annealed at temperatures 1073 and 1273 K. The EuErCuSe3 crystal structure was established using the single-crystal particle. EuErCuSe3 crystallizes in the orthorhombic system, space group Cmcm, KCuZrS3 structure type, with cell parameters a = 4.0555 (3), b = 13.3570 (9), and c = 10.4602 (7) Å, V = 566.62 (6) Å3. In structure EuErCuSe3, erbium ions are coordinated by selenium ions in the octahedral polyhedron, copper ions are in the tetrahedral coordination, europium ions are between copper and erbium polyhedra layers and are coordinated by selenium ions as two-cap trigonal prisms. The optical band gap is 1.79 eV. At 4.7 K, a transition from the ferrimagnetic state to the paramagnetic state was detected in EuErCuSe3. At 85 and 293 K, the compound is in a paramagnetic state. According to XRPD data, EuLnCuSe3 (Ln = Nd, Sm, Gd) compounds have a Pnma orthorhombic space group of the Eu2CuS3 structure type. For EuSmCuSe3, a = 10.75704 (15) Å, b = 4.11120 (5) Å, c = 13.37778 (22) Å. In the series of EuLnCuSe3 compounds, the optical band gap increases 1.58 eV (Nd), 1.58 eV (Sm), 1.72 eV (Gd), 1.79 eV (Er), the microhardness of the 205 (Nd), 210 (Sm), 225 (Gd) 235 ± 4 HV (Er) phases increases, and the thermal stability of the phases increases significantly. According to the measurement data of differential scanning calorimetry, the EuNdCuSe3 decomposes, according to the solid-phase reaction T = 1296 K, ΔH = 8.2 ± 0.8 kJ/mol. EuSmCuSe3 melts incongruently T = 1449 K, ΔH = 18.8 ± 1.9 kJ/mol. For the EuGdCuSe3, two (Tα↔β = 1494 K, ΔHα↔β = 14.8 kJ/mol, Tβ↔γ = 1530 K, ΔHβ↔γ = 4.8 kJ/mol) and for EuErCuSe3 three polymorphic transitions (Tα↔β = 1561 K, ΔHα↔β = 30.3 kJ/mol, Tβ↔γ = 1579 K, ΔHβ↔γ = 4.4 kJ/mol, and Tγ↔δ = 1600 K, ΔHγ↔δ = 10.1 kJ/mol). The compounds melt incongruently at the temperature of 1588 K, ΔHmelt = 17.9 ± 1.8 kJ/mol and 1664 K, ΔHmelt = 25.6 ± 2.5 kJ/mol, respectively. Incongruent melting of the phases proceeds with the formation of a solid solution of EuSe and a liquid phase.

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Держатели документа:
Univ Tyumen, Inst Chem, Tyumen 625003, Russia.
RAS, Inst Semicond Phys, Lab Opt Mat & Struct, SB, Novosibirsk 630090, Russia.
Kemerovo State Univ, Res & Dev Dept, Kemerovo 650000, Russia.
Novosibirsk State Tech Univ, Dept Ind Machinery Design, Novosibirsk 630073, Russia.
RAS, KSC, Fed Res Ctr, Kirensky Inst Phys,SB, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Photon & Laser Technol, Krasnoyarsk 660036, Russia.
Ind Univ Tyumen, Dept Gen & Special Chem, Tyumen 625000, Russia.
RAS, Boreskov Inst Catalysis, SB, Novosibirsk 630090, Russia.
Novosibirsk State Univ, Lab Mol Design & Ecol Safe Technol, Novosibirsk 630090, Russia.
RAS, Inst Solid State Chem, UB, Ekaterinburg 620990, Russia.

Доп.точки доступа:
Andreev, O. V.; Atuchin, V. V.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Denisenko, Y. G.; Zakharov, B. A.; Tyutyunnik, A. P.; Habibullayev, N. N.; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Ulybin, D. A.; Shpindyuk, D. D.; Ministry of Science and Higher Education of the Russian Ferderation [AAAA-A21-121011390011-4, AAAA-A19-119031890025-9]; Government of the Tyumen Region [2. 89-don]
}
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Synthesis, crystal structure, and the optical and thermodynamic properties of PrAlGe2O7 / L. A. Irtyugo, L. T. Denisova, M. S. Molokeev [et al.] // Russ. J. Phys. Chem. A. - 2021. - Vol. 95, Is. 8. - P. 1546-1550, DOI 10.1134/S0036024421080124. - Cited References: 23 . - ISSN 0036-0244. - ISSN 1531-863X

РУБ Chemistry, Physical
Рубрики:
TEMPERATURE HEAT-CAPACITY
   GERMANATES
   SMFEGE2O7
   PR
Кл.слова (ненормированные):
PrAlGe2O7 -- complex oxide compounds -- solid-state synthesis -- crystal structure -- luminescence -- heat capacity -- thermodynamic properties
Аннотация: Germanate PrAlGe2O7 is obtained from initial oxides Pr2O3, Al2O3, and GeO2 via solid-phase synthesis. The crystal structure of the investigated germanate is determined via X-ray diffraction. The luminescence spectra are been determined at room temperature. The effect temperature has on the heat capacity is determined via differential scanning calorimetry. The thermodynamic properties of the complex oxide compound are calculated using the experimental data on Cp = f(T) in the temperature range of 350‒1000 K.

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Публикация на русском языке Синтез, кристаллическая структура, оптические и термодинамические свойства PrAlGe2O7 [Текст] / Л. А. Иртюго, Л. Т. Денисова, М. С. Молокеев [и др.] // Журн. физ. химии. - 2021. - Т. 95 № 8. - С. 1165-1170

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

Доп.точки доступа:
Irtyugo, L. A.; Denisova, L. T.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Denisov, V. M.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Beletskii, V. V.; Sivkova, E. Yu
}
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10.

Синтез, кристаллическая структура, оптические и термодинамические свойства PrAlGe2O7 / Л. А. Иртюго, Л. Т. Денисова, М. С. Молокеев [и др.] // Журн. физ. химии. - 2021. - Т. 95, № 8. - С. 1165-1170, DOI 10.31857/S0044453721080124. - Библиогр.: 23 . - ISSN 0044-4537
Кл.слова (ненормированные):
сложные оксидные соединения -- твердофазный синтез -- кристаллическая структура -- люминесценция -- теплоемкость -- термодинамические свойства
Аннотация: Из исходных оксидов Pr2O3, Al2O3 и GeO2 твердофазным методом синтезирован германат PrAlGe2O7. С использованием рентгеновской дифракции уточнена его кристаллическая структура. Спектры люминесценции измерены при комнатной температуре. Влияние температуры на его теплоемкость определено методом дифференциальной сканирующей калориметрии. По экспериментальным данным Cp = f(T) в области 350–1000 K рассчитаны термодинамические свойства оксидного соединения.

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РИНЦ

Переводная версия Synthesis, crystal structure, and the optical and thermodynamic properties of PrAlGe2O7 [Текст] / L. A. Irtyugo, L. T. Denisova, M. S. Molokeev [et al.] // Russ. J. Phys. Chem. A. - 2021. - Vol. 95 Is. 8.- P.1546-1550

Держатели документа:
Сибирский федеральный университет, Красноярск, Россия
Российская академия наук, Сибирское отделение, Институт физики им. Л.В. Киренского, Красноярск, Россия

Доп.точки доступа:
Иртюго, Л. А.; Денисова, Л. Т.; Молокеев, Максим Сергеевич; Molokeev, M. S.; Денисов, В. М.; Александровский, Александр Сергеевич; Aleksandrovsky, A. S.; Белецкий, В. В.; Сивкова, Е. Ю.
}
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11.

Electronic band structures of NdFe3(BO3)4 and NdGa3(BO3)4 crystals: ab initio calculations / S. Krylova, I. Gudim, A. Aleksandrovsky [et al.] // Ferroelectrics. - 2021. - Vol. 575, Is. 1. - P. 11-17, DOI 10.1080/00150193.2021.1888219. - Cited References: 27. - This work was supported by the Russian Foundation for Basic Research Grant No. 20-42-240009 . - ISSN 0015-0193. - ISSN 1563-5112

РУБ Materials Science, Multidisciplinary + Physics, Condensed Matter
Рубрики:
HOFE3(BO3)4
   TEMPERATURE
   SPECTRA
   GROWTH
Кл.слова (ненормированные):
Borates -- ab initio calculation -- electronic bands -- crystal structure
Аннотация: NdFe3(BO3)4 and NdGa3(BO3)4 crystals are of great interest due to their physical properties. For example, NdFe3(BO3)4 crystal demonstrates magnetodielectric and magnetopiezoelectric effects, and NdGa3(BO3)4 crystal possesses luminescent and nonlinear optical properties. In this work, the properties of these materials are calculated by the plane-wave pseudo-potential method based on density functional theory. The structures of the crystals are optimized. The electronic structure of NdFe3(BO3)4 and NdGa3(BO3)4 are calculated.

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Держатели документа:
Kirensky Inst Phys FRC KSC SB RAS, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.

Доп.точки доступа:
Krylova, S. N.; Крылова, Светлана Николаевна; Gudim, I. A.; Гудим, Ирина Анатольевна; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Vtyurin, A. N.; Втюрин, Александр Николаевич; Krylov, A. S.; Крылов, Александр Сергеевич; Russian Foundation for Basic Research GrantRussian Foundation for Basic Research (RFBR) [20-42-240009]
}
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12.

Evolution of structural, thermal, optical, and vibrational properties of Sc2S3, ScCuS2, and BaScCuS3 semiconductors / N. O. Azarapin, A. S. Oreshonkov, I. A. Razumkova [et al.] // Eur. J. Inorg. Chem. - 2021. - Vol. 2021, Is. 33. - P. 3355-3366, DOI 10.1002/ejic.202100292. - Cited References: 50. - The work was partially carried out using the resources of the Research Resource Center "Natural Resources Management and Physico-Chemical Research" (Tyumen University) with financial support from the Ministry of Science and Higher Education of the Russian Federation (contract No. 05.594.21.0019, UIN RFMEFI59420X0019). The Raman spectroscopic studies were carried out at the collaborative research center for vibrational spectroscopy at ISSC UB RAS (Ekaterinburg, Russia). I.I.L. would like to acknowledge the support from the Research Program No. AAAA-A19-119031890025-9 (ISSC UB RAS). The use of the equipment of Krasnoyarsk Regional Center of Research Equipment of the Federal Research Center "Krasnoyarsk Science Center SB RAS" is acknowledged." The authors are grateful to Dr. Elena V. Vladimirova (ISSC UB RAS) for technical assistance . - ISSN 1434-1948. - ISSN 1099-0682

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
RARE-EARTH
QUATERNARY CHALCOGENIDES
CRYSTAL-STRUCTURES
Кл.слова (ненормированные):
Complex sulfides -- Density functional calculations -- DTA -- Polychalcogenides -- Rare earths
Аннотация: In the present work, we report on the synthesis of Sc2S3, ScCuS2 and BaScCuS3 powders using a method based on oxides sulfidation and modification of their properties. The crystal structures and morphology of samples are verified by XRD and SEM techniques. Thermal stability has been studied by DTA which has revealed that Sc2S3 decomposes to ScS through melting at 1877 K. ScCuS2 and BaScCuS3 melt incongruently at temperatures of 1618 K and 1535 K, respectively. The electronic structure calculations show that the investigated compounds are semiconductors with indirect band gap (Eg). According to the diffuse reflection spectroscopy, Sc2S3, ScCuS2 and BaScCuS3 are wide-bandgap semiconductors featured the Eg values of 2.53 eV, 2.05 eV and 2.06 eV, respectively. The band gap decreases with the introduction of copper (I) and barium cations into the crystal structure of the compounds. Variation of local structure has been verified by Raman and infrared spectroscopy. The calculated vibrational modes of ScCuS2 correspond to CuS4 and Sc−S layer vibrations, even though ScS6 octahedra-like structural units can be found in the structure.

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Держатели документа:
Tyumen State Univ, Dept Inorgan & Phys Chem, Tyumen 625003, Russia.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Lab Mol Spect, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Engn & Construct, Krasnoyarsk 660041, Russia.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
RAS, Fed Res Ctr KSC SB, Inst Chem & Chem Technol, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Ural Branch, Inst Solid State Chem, Ekaterinburg 620990, Russia.

Доп.точки доступа:
Azarapin, N. O.; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Razumkova, I. A.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Maximov, N. G.; Leonidov, I. I.; Shestakov, N. P.; Шестаков, Николай Петрович; Andreev, O. V.; Ministry of Science and Higher Education of the Russian Federation [05.594.21.0019, UIN RFME-FI59420X0019]; ISSC UB RAS [AAAA-A19-119031890025-9]
}
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13.

Спектроскопия комбинационного рассеяния и электронных возбуждений структурно неупорядоченного кристалла FeTiF6∙6H2O / Ю. В. Герасимова, А. С. Александровский, Н. М. Лапташ [и др.] // 7-й Урало-сибирский семинар "Спектроскопия комбинационного рассеяния света" : материалы семинара / прогр. ком. В. Ф. Шабанов, прогр. ком. А. Н. Втюрин, прогр. ком., ред. А. С. Крылов, орг. ком. С. Н. Крылова и др. - 2021. - секция 2: Комбинационное рассеяние в кристаллах. - С. 35-36. - Библиогр.: 2. - Работа выполнена при финансовой поддержке Российского фонда фундаментальных исследований, Правительства Красноярского края и Красноярского краевого фонда науки в рамках исследовательского проекта № 20-42-240014 . - ISBN 978-5-94332-125-2

Материалы конференции,
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Держатели документа:
Институт физики им. Л.В. Киренского СО РАН

Доп.точки доступа:
Шабанов, Василий Филиппович \прогр. ком.\; Shabanov, V. F.; Втюрин, Александр Николаевич \прогр. ком.\; Vtyurin, A. N.; Крылов, Александр Сергеевич \прогр. ком., ред.\; Krylov, A. S.; Крылова, Светлана Николаевна \орг. ком.\; Krylova, S. N.; Герасимова, Юлия Валентиновна; Gerasimova, J. V.; Александровский, Александр Сергеевич; Aleksandrovsky, A. S.; Лапташ, Н. М.; Герасимов, М. А.; Крылов, Александр Сергеевич; Втюрин, Александр Николаевич; "Спектроскопия комбинационного рассеяния света", Урало-сибирский семинар(7 ; 2021 ; 23-25 авг. ; Екатеринбург); Урало-сибирский семинар по спектроскопии комбинационного рассеяния света(7 ; 2021 ; 23-25 авг. ; Екатеринбург); Научный совет по физике конденсированных сред РАН; Научный совет по спектроскопии атомов и молекул РАН; Российское минералогическое общество. Комиссия по рентгенографии, кристаллохимии и спектроскопии; Институт геологии и геохимии им. академика А. Н. Заварицкого УрО РАН; Федеральный исследовательский центр "Красноярский научный центр Сибирского отделения Российской академии наук"; Институт физики им. Л.В. Киренского Сибирского отделения РАН; Институт химии твердого тела УрО РАН; Уральский Федеральный университет им. Первого Президента России Б.Н. Ельцина
}
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14.

    Exploration of the structural, spectroscopic and thermal properties of double sulfate monohydrate NaSm(SO4)2·H2O and its thermal decomposition product NaSm(SO4)2 / Y. G. Denisenko, A. E. Sedykh, S. A. Basova [et al.] // Adv. Powder Technol. - 2021. - Vol. 32, Is. 11. - P. 3943-3953, DOI 10.1016/j.apt.2021.08.009. - Cited References: 81. - This work was partly supported by the Russian Science Foundation (21-19-00046) and Russian Foundation for Basic Research (Grant 19-33-90258\19). The use of the equipment of Krasnoyarsk Regional Center of Research Equipment of the Federal Research Center “Krasnoyarsk Science Center SB RAS” is acknowledged . - ISSN 0921-8831
   Перевод заглавия: Исследование структурных, спектроскопических и термических свойств двойного сульфатного моногидрата NaSm(SO4)2·H2O и продукта его термического разложения NaSm(SO4)2
Кл.слова (ненормированные):
Sulfate -- Thermal decomposition -- Crystal structure -- Raman -- Photoluminescence
Аннотация: Samarium-sodium double sulfate crystalline hydrate NaSm(SO4)2·H2O was obtained by the crystallization from an aqueous solution containing equimolar amounts of ions. The anhydrous salt of NaSm(SO4)2 was formed by a thermally induced release of the equivalent of water from NaSm(SO4)2·H2O. The kinetic parameters of thermal decomposition were determined (Ea = 102 kJ/mol, A = 9·106). The crystal structures of both compounds were refined from the X-ray powder diffraction data. Sulfate hydrate NaSm(SO4)2·H2O crystallizes in the trigonal symmetry, space group P3121 (a = 6.91820(3) and c = 12.8100(1) Å, V = 530.963(7) Å3). The anhydrous salt crystallizes in the triclinic symmetry, space group P-1 (a = 6.8816(2), b = 6.2968(2) and c = 7.0607(2) Å, α = 96.035(1), β = 99.191(1) and γ = 90.986(1)°, V = 300.17(1) Å3). The vibrational properties of compounds are mainly determined by the sulfate group deformations. The luminescence spectra of both sulfates are similar and are governed by the transitions of samarium ions 4G5/2 → 6HJ (J = 5/2, 7/2, 9/2 and 11/2). The anhydrous sulfate is stable up to 1100 K and undergoes an almost isotropic expansion when heated. After 1100 K, the compound decomposes into Sm2(SO4)3 and Na2SO4.

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Держатели документа:
Department of General and Special Chemistry, Industrial University of Tyumen, Tyumen, 625000, Russian Federation
Institute of Inorganic and Analytical Chemistry, Justus-Liebig-University Giessen, Heinrich-Buff-Ring 17, Giessen, 35392, Germany
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen, 625003, Russian Federation
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
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
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
Research Department, Northern Trans-Ural State Agricultural University, Tyumen, 625003, Russian Federation
Laboratory of the Chemistry of Rare Earth Compounds, Institute of Solid State Chemistry, UB RAS, Ekaterinburg, 620137, Russian Federation
Center for Materials Research (LaMa), Justus-Liebig-University Giessen, Heinrich-Buff-Ring 16, Giessen, 35392, Germany

Доп.точки доступа:
Denisenko, Y. G.; Sedykh, A. E.; Basova, S. A.; Atuchin, V. V.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Khritokhin, N. A.; Sal'nikova, E. I.; Andreev, O. V.; Muller-Buschbaum, K.
}
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15.

Spectroscopy of structurally disordered hydrated iron fluoridotitanate in the regions of vibrational and electronic excitations / Y. V. Gerasimova, A. S. Aleksandrovsky, N. M. Laptash [et al.] // Spectrochim. Acta A. - 2022. - Vol. 264. - Ст. 120244, DOI 10.1016/j.saa.2021.120244. - Cited References: 28. - The reported study was funded by Russian Foundation for Basic Research, Government of Krasnoyarsk Territory and Krasnoyarsk Regional Foundation of Science according to the research project “Spectral and magnetic properties of single crystals of transition metal fluoride hexahydrates.” No. 20-42-240014 . - ISSN 1386-1425
Кл.слова (ненормированные):
Hydrated iron fluoridotitanate -- Phase transition -- Order-disorder -- Raman -- Dynamics -- Electronic excitations
Аннотация: Raman and optical absorption spectra of disordered hydrated iron fluoridotitanate (HITF) single crystal were studied. Temperature transformations of the Raman spectra indicate independent ordering processes of the [TiF6]2− and [Fe(H2O)6]2+ complexes below the structural phase transition. The absorption spectrum in the near-infrared and visible ranges includes transitions from the high spin ground state 5T2 of Fe2+ ion to the excited 5E state and a set of excited triplets. Analysis by Tanabe-Sugano method gives crystal field Dq = 490 cm−1 and Racah parameters B = 340 cm−1 and C = 1904 cm−1. Considerable decrease of B parameter as compared to the free ion value indicates a decrease of interelectron repulsion in the disordered neighborhood of Fe2+ ions.

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Держатели документа:
Kirensky Institute of Physics, Siberian Branch of RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Physics and Radio Electronics, Siberian Federal University, Krasnoyarsk, 660079, Russian Federation
Institute of Chemistry, Far Eastern Branch of RAS, Vladivostok, 690022, Russian Federation

Доп.точки доступа:
Gerasimova, Yu. V.; Герасимова, Юлия Валентиновна; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Laptash, N. M.; Gerasimov, M. A.; Герасимов, М. А.; Krylov, A. S.; Крылов, Александр Сергеевич; Vtyurin, A. N.; Втюрин, Александр Николаевич; Dubrovskiy, A. A.; Дубровский, Андрей Александрович
}
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16.

    Crystal structure, vibrational, spectroscopic and thermochemical properties of double sulfate crystalline hydrate [CsEu(H2O)3(SO4)2]·H2O and its thermal dehydration product CsEu(SO4)2 / Y. G. Denisenko, M. S. Molokeev, A. S. Oreshonkov [et al.] // Crystals. - 2021. - Vol. 11, Is. 9. - Ст. 1027, DOI 10.3390/cryst11091027. - Cited References: 103. - This work was partially supported by the Russian Foundation for Basic Research (grant 19-33-90258\19) . - ISSN 2073-4352
   Перевод заглавия: Кристаллическая структура, колебательные, спектроскопические и термохимические свойства двойного сульфатного кристаллического гидрата [CsEu(H2O)3(SO4)2]·H2O и продукта его термической дегидратации CsEu(SO4)2
Кл.слова (ненормированные):
sulfate -- dehydration -- crystal structure -- Raman -- thermal stability -- photoluminescence
Аннотация: Crystalline hydrate of double cesium europium sulfate [CsEu(H2O)3(SO4)2]·H2O was synthesized by the crystallization from an aqueous solution containing equimolar amounts of 1Cs+:1Eu3+:2SO42− ions. Anhydrous salt CsEu(SO4)2 was formed as a result of the thermal dehydration of the crystallohydrate. The unusual effects observed during the thermal dehydration were attributed to the specific coordination of water molecules in the [CsEu(H2O)3(SO4)2]·H2O structure. The crystal structure of [CsEu(H2O)3(SO4)2]·H2O was determined by a single crystal X-ray diffraction analysis, and the crystal structure of CsEu(SO4)2 was obtained by the Rietveld method. [CsEu(H2O)3(SO4)2]·H2O crystallizes in the monoclinic system, space group P21/c (a = 6.5574(1) Å, b = 19.0733(3) Å, c = 8.8364(2) Å, β = 93.931(1)°, V = 1102.58(3) Å3). The anhydrous sulfate CsEu(SO4)2 formed as a result of the thermal destruction crystallizes in the monoclinic system, space group C2/c (a = 14.327(1) Å, b = 5.3838(4) Å, c = 9.5104(6) Å, β = 101.979(3) °, V = 717.58(9) Å3). The vibration properties of the compounds are fully consistent with the structural models and are mainly determined by the deformation of non-rigid structural elements, such as H2O and SO42−. As shown by the diffused reflection spectra measurements and DFT calculations, the structural transformation from [CsEu(H2O)3(SO4)2]·H2O to CsEu(SO4)2 induced a significant band gap reduction. A noticeable difference of the luminescence spectra between cesium europium sulfate and cesium europium sulfate hydrate is detected and explained by the variation of the extent of local symmetry violation at the crystallographic sites occupied by Eu3+ ions, namely, by the increase in inversion asymmetry in [CsEu(H2O)3(SO4)2]·H2O and the increase in mirror asymmetry in CsEu(SO4)2. The chemical shift of the 5D0 energy level in cesium europium sulfate hydrate, with respect to cesium europium sulfate, is associated with the presence of H2O molecules in the vicinity of Eu3+ ion.

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Держатели документа:
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen, 625003, Russian Federation
Laboratory of Crystal Physics, Federal Research Center KSC SB RAS, Kirensky Institute of Physics, Krasnoyarsk, 660036, Russian Federation
Institute of Engineering Physics and Radioelectronic, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation
Laboratory of Molecular Spectroscopy, Federal Research Center KSC SB RAS, Kirensky Institute of Physics, Krasnoyarsk, 660036, Russian Federation
School of Engineering and Construction, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Coherent Optics, Federal Research Center KSC SB RAS, Kirensky Institute of Physics, Krasnoyarsk, 660036, Russian Federation
Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Chemistry of Compounds of Rare-Earth Elements, Institute of Solid State Chemistry, UB RAS, Ekaterinburg, 620137, Russian Federation
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

Доп.точки доступа:
Denisenko, Y. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Azarapin, N. O.; Andreev, O. V.; Razumkova, I. A.; Atuchin, V. V.
}
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17.

Up-Conversion Luminescence of YAl3(BO3)4:(Yb3+,Tm3+) Crystals [Text] / Aleksandrovsky A.S.Gudim I.A. [et al.] // J. Alloys and Compounds. - 2010. - Vol. 496. - PL18-L21

Доп.точки доступа:
Aleksandrovsky, A.S.; Gudim, I.A.; Krylov, A.S.; Malakhovskii, A.V.; Temerov, V.L.
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18.

Nonlinear Photonic Crystals of Strontium Tetraborate: Properties and Conversion of Radiation / Aleksandrovsky A.S.Vyunishev A.M. [et al.] // Proc. SPIE. - 2010. - Vol.7728. - P772819-1–772819-8

Доп.точки доступа:
Aleksandrovsky, A.S.; Vyunishev, A.M.; Zaitsev, A.I.; Rovsky, V.E.; Slabko, V.V.; Cherepakhin., A.V.
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19.

Random quasi-phase-matched conversion of broadband radiation in a nonlinear photonic crystal / A. S. Aleksandrovsky [et al.] // Phys. Rev. A. - 2010. - Vol. 82, Is. 5, DOI 10.1103/PhysRevA.82.055806. - Cited Reference Count: 22. - Гранты: The work was supported by the Ministry of Education and Science of the Russian Federation (Contract 16.740.11.0150), Grant of the President of the Russian Federation for the support of leading scientific schools No. SS-4645.2010.2, Grant No. RNP.2.1.1.3455, Projects 2.5.2 and 3.9.1 of PSB RAS, and Projects No. 27.1 and No. 5 of SB RAS. A. M. Vyunishev is grateful for the support from Krasnoyarsk Regional Fund of Science and Technical Activity Support. - Финансирующая организация: Ministry of Education and Science of the Russian Federation [16.740.11.0150]; Russian Federation for the support of leading scientific schools [SS-4645.2010.2, RNP.2.1.1.3455]; PSB RAS [2.5.2, 3.9.1]; SB RAS [27.1, 5]; Krasnoyarsk Regional Fund of Science and Technical Activity . - ISSN 1050-2947
Кл.слова (ненормированные):
Broad spectrum -- Broadband radiation -- Femtosecond laser pulse -- Fundamental wave -- Nonlinear generation -- Nonlinear photonic crystals -- Quasi-phase-matched -- Quasi-phase-matched frequency doubling -- Red shift -- Shorter wavelength -- Tetraborate -- Tuning ranges -- Vacuum ultraviolets -- Band structure -- Crystal structure -- Strontium -- Ultrafast lasers -- Ultrashort pulses -- Photonic crystals
Аннотация: Radiation in the range 187.5-215 nm was generated via random quasi-phase-matched frequency doubling of femtosecond laser pulses in nonlinear photonic crystals of strontium tetraborate. Abroad spectrum of fundamental radiation favors the probing of the nonlinear photonic crystal band structure. The red shift of the band structure upon the fundamental wave-vector rotation was observed. No principal limitations of the tuning range at its shorter wavelength boundary from the nonlinear photonic crystal (NPC) material are found. Calculation shows that the NPC structure enables enhancement of nonlinear generation in the vacuum ultraviolet.

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Держатели документа:
LV Kirenskii Inst Phys, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660079, Russia

Доп.точки доступа:
Aleksandrovsky, A.S.; Vyunishev, A.M.; Zaitsev, A.I.; Slabko, V.V.
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20.

Nonlinear photonic crystals of strontium tetraborate: Properties and conversion of radiation / A. S. Aleksandrovsky [et al.] // Proceedings of SPIE - The International Society for Optical Engineering. - 2010. - Vol. 7728: Nonlinear Optics and Applications IV (12 April 2010 through 15 April 2010, Brussels, ) Conference code: 81010, DOI 10.1117/12.853713 . - ISBN 0277786X (ISSN); 9780819482013 (ISBN)
Кл.слова (ненормированные):
nonlinear photonic crystal -- second harmonic generation -- strontium tetraborate -- As-grown -- Average power -- Domain shape -- Efficiency enhancement -- Femtoseconds -- Fourth harmonics -- Nonlinear diffraction -- Nonlinear optical process -- Nonlinear photonic crystals -- Quasi-phase-matched -- Second harmonic generation -- Tetraborate -- Ti: Sapphire laser -- Ti:sapphire oscillators -- Ferroelectricity -- Harmonic analysis -- Nonlinear optics -- Optical materials -- Photonic crystals -- Sapphire -- Strontium -- Harmonic generation
Аннотация: Random nonlinear photonic crystal (NPC) structures formed by as-grown domains in a non-ferroelectric strontium tetraborate (SBO) are investigated. The domain shape and orientation are similar to those in ferroelectric KTP. Nonlinear diffraction is the simplest way to detect, evaluate and characterize these structures. Reciprocal superlattice vectors spectra of NPC in SBO are very wide and enable broadband efficiency enhancement of nonlinear optical processes. Second harmonic (SH) generation of femtosecond Ti:sapphire oscillator radiation with 1.9% efficiency is obtained using nonlinear diffraction geometry. Random quasi phase matched generation at the wavelengths of fourth harmonic of Ti:sapphire laser is obtained with average power up to 1 ?W. © 2010 Copyright SPIE - The International Society for Optical Engineering.

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Держатели документа:
Kirensky Institute of Physics, Akademgorodok 50/38, 660036, Krasnoyarsk, Russian Federation
Siberian Federal University, Svobodniy 79, 660041, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Aleksandrovsky, A. S.; Zaitsev, A. I.; Cherepakhin, A. V.; Черепахин, Александр Владимирович; Vyunishev, A. M.; Rovsky, V. E.; Slabko, V. V.
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