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1.


   
    Two-dimensional-layered perovskite ALaTa2O7:Bi3+ (A = K and Na) phosphors with versatile structures and tunable photoluminescence / G. J. Zhou [et al.] // ACS Appl. Mater. Interfaces. - 2018. - Vol. 10, Is. 29. - P. 24648-24655, DOI 10.1021/acsami.8b08129. - Cited References: 48. - The authors acknowledge the support from the National Natural Science Foundation of China (Nos. 51722202, 91622125, and 51572023) and the Natural Science Foundations of Beijing (2172036) and RFBR (17-52-53031). . - ISSN 1944-8244
   Перевод заглавия: 2D-слоистые перовскитоподобные люминофоры ALaTa2O7:Bi3+ (A = K and Na) с разнообразными структурами и управляемой люминесценцией.
РУБ Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
GENERALIZED GRADIENT APPROXIMATION
   YELLOW-EMITTING PHOSPHOR

Кл.слова (ненормированные):
2D-layered perovskite -- Bi3+ emission -- ion exchange -- photoluminescence tuning -- white light LEDs
Аннотация: Topological chemical reaction methods are indispensable for fabricating new materials or optimizing their functional properties, which is particularly important for two-dimensional (2D)-layered compounds with versatile structures. Herein, we demonstrate a low-temperature (∼350 °C) ion exchange approach to prefabricate metastable phosphors ALa1–xTa2O7:xBi3+ (A = K and Na) with RbLa1–xTa2O7:xBi3+ serving as precursors. The as-prepared ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) share the same Dion–Jacobson type 2D-layered perovskite phase, and photoluminescence analyses show that ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) phosphors exhibit broad emission bands peaking at 540, 550, and 510 nm, respectively, which are attributed to the nonradiative transition of Bi3+ from excited state 3P1 or 3P0 to ground state 1S0. The various Bi3+ local environments at the crystallographic sites enable the different distributions of emission and excitation spectra, and the photoluminescence tuning of ALa0.98Ta2O7:0.02 Bi3+ (A = Rb, K, and Na) phosphors are realized through alkali metal ion exchange. Notably, the combination of superior trivalent bismuth emission and low-temperature ion exchange synthesis leads to a novel yellow-emitting K(La0.98Bi0.02)Ta2O7 phosphor which is successfully applied in a white LED device based on a commercially available 365 nm LED chip. Our realizable cases of this low-temperature ion exchange strategy could promote exploration into metastable phosphors with intriguing properties.

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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.
Chinese Acad Sci, Tech Inst Phys & Chem, Beijing 100190, Peoples R China.
Univ Chinese Acad Sci, Beijing 100049, Peoples R China.
SB RAS, KSC, Fed Res Ctr, 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.

Доп.точки доступа:
Zhou, Guojun; Jiang, Xingxing; Zhao, Jing; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lin, Zheshuai; Liu, Quanlin; Xia, Zhiguo
}
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2.


   
    Tuning the peak effect in the Y1−xNdxBa2Cu3O7−δ compound / D. M. Gokhfeld [et al.] // Ceram. Int. - 2017. - Vol. 43, Is. 13. - P. 9985-9991, DOI 10.1016/j.ceramint.2017.05.011. - Cited References: 37. - This work was supported by the Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Region Science and Technology Support Fund to the research project no. 16-48-243018 and the Russian Foundation for Basic Research, project no. 16-38-00400. . - ISSN 0272-8842
   Перевод заглавия: Управление пик-эффектом в соединении Y1−xNdxBa2Cu3O7−δ
Кл.слова (ненормированные):
Peak effect -- Bulk superconductors -- Critical current -- Pinning -- Characterization -- YBCO
Аннотация: Polycrystalline Y1−xNdxBa2Cu3O7−δ (x=0.02, 0.11, and 0.25) superconductors are synthesized. Nd atoms are uniformly distributed over grains. The magnetization loops of the samples have a pronounced second peak in a wide temperature range. The magnetization data are analyzed using the extended critical state model. It is found that the order-disorder transition of the vortex lattice is affected by doping with neodymium and temperature; the second-peak field and width decrease monotonically with increasing x value. The undoped polycrystalline YBa2Cu3O7−δ compound is assumed to exhibit the peak effect in higher magnetic fields.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Gokhfeld, D. M.; Гохфельд, Денис Михайлович; Balaev, D. A.; Балаев, Дмитрий Александрович; Yakimov, I. S.; Petrov, M. I.; Петров, Михаил Иванович; Semenov, S. V.; Семёнов, Сергей Васильевич
}
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3.


   
    Tuning the peak effect by in Y1-xNdxBa2Cu3O7-δ compound by Nd doping / S. V. Semenov [et al.] // Moscow International Symposium on Magnetism (MISM-2017) : 1-7 July 2017 : book of abstracts. - 2017. - Ст. 3PO-I-19. - P. 576. - Библиогр.: 4

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Доп.точки доступа:
Semenov, S. V.; Семёнов, Сергей Васильевич; Gokhfeld, D. M.; Гохфельд, Денис Михайлович; Balaev, D. A.; Балаев, Дмитрий Александрович; Yakimov, I. S.; Petrov, M. I.; Петров, Михаил Иванович; Moscow International Symposium on Magnetism(7 ; 2017 ; Jul. ; Moscow); Московский государственный университет им. М.В. Ломоносова; Российский фонд фундаментальных исследований
}
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4.


   
    Tuning the magnetic, transport and optical properties of FeSi2 nanocrystals / A. S. Tarasov [et al.] // Fourth Asian school-conference on physics and technology of nanostructured materials (ASCO-NANOMAT 2018) : proceedings. - Vladivostok : Dalnauka, 2018. - P. 143
   Перевод заглавия: Регулирование магнитных, транспортных и оптических свойств нанокристаллов FeSi2

Материалы конференции

Доп.точки доступа:
Tarasov, A. S.; Тарасов, Антон Сергеевич; Visotin, M. A.; Высотин, Максим Александрович; Volochaev, M. N.; Волочаев, Михаил Николаевич; Solovyov, L. A.; Соловьев, Леонид Александрович; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Rautskii, M. V.; Рауцкий, Михаил Владимирович; Zhandun, V. S.; Жандун, Вячеслав Сергеевич; Yakovlev, I. A.; Яковлев, Иван Александрович; Nemtsev, I. V.; Немцев, Иван Васильевич; Varnakov, S. N.; Варнаков, Сергей Николаевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Asian School-Conference on Physics and Technology of Nanostructured Materials(4 ; 2018 ; Sept. ; 23-28 ; Vladivostok); Азиатская школа-конференция по физике и технологии наноструктурированных материалов(4 ; 2018 ; сент. ; 23-28 ; Владивосток); Институт автоматики и процессов управления ДВО РАН; Дальневосточный федеральный университет
}
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5.


   
    Tuning terahertz vibrations to control flexibility in soft porous crystals / A. E. J. Hoffman, J. Wieme, I. Senkovska [et al.] // 4th European conference on metal organic frameworks and porous polymers : Programme and book of abstracts. - 2021. - Ст. P-74 (S3P15). - Cited References: 7 . - ISBN 978-83-951195-7-6
   Перевод заглавия: Настройка терагерцовых колебаний для контроля гибкости мягких пористых кристаллов

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Доп.точки доступа:
Hoffman, A. E. J.; Wieme, J.; Senkovska, I.; Krylov, A. S.; Крылов, Александр Сергеевич; Rogge, S. M. J.; Kaskel, S.; Speybroeck, V. V.; European conference on metal organic frameworks and porous polymers(4 ; 2021 ; Sept. 13-15 ; Kraków, Poland (virtual))
}
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6.


   
    Tuning Q-factor and perfect absorption using coupled Tamm states on polarization-preserving metasurface / N. V. Rudakova, R. G. Bikbaev, L. E. Tyryshkina [et al.] // Photonics. - 2023. - Vol. 10, Is. 12. - Ст. 1391, DOI 10.3390/photonics10121391. - Cited References: 58 . - ISSN 2304-6732
   Перевод заглавия: Управление добротностью и идеальным поглощением с помощью связанных оптических таммовских состояний на сохраняющей поляризацию метаповерхности
Кл.слова (ненормированные):
bound state in the continuum -- optical Tamm state -- coupled modes -- cholesteric liquid crystal -- polarization-preserving metasurface
Аннотация: The circular polarization of light flips its handedness after a conventional metallic mirror reflection. Therefore, a polarization-preserving metasurface is a crucially important element in a series of chiral photonic structures. They include tunable cholesteric LCs and anisotropic photonic crystals. Chiral structures are rich in interfacial localized modes including Tamm states. In this report, coupled modes formed as a result of the interaction between two chiral optical Tamm states or a chiral optical Tamm state and a chiral Tamm plasmon polariton are analytically and numerically investigated. It is shown that the effective control of coupled modes can be carried out by changing the pitch of the cholesteric and the angle between the optical axis of the cholesteric and the polarization-preserving anisotropic mirror. The influence of the metasurface period on the spectral characteristics of coupled modes is investigated. The possibility of realizing a bound state in the continuum of the Friedrich–Wintgen type, resulting from the destructive interference of coupled modes, which leads to the collapse of the resonance line corresponding to the chiral optical Tamm state, has been demonstrated.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Siberian Federal University, Krasnoyarsk 660041, Russia

Доп.точки доступа:
Rudakova, N. V.; Рудакова, Наталья Викторовна; Bikbaev, R. G.; Бикбаев, Рашид Гельмединович; Tyryshkina, L. E.; Тырышкина, Лариса Е.; Vetrov, S. Ya.; Ветров, Степан Яковлевич; Timofeev, I. V.; Тимофеев, Иван Владимирович
}
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7.


   
    Tuning of the interparticle interactions in ultrafine ferrihydrite nanoparticles / Y. V. Knyazev, D. A. Balaev, R. N. Yaroslavtsev [et al.] // Adv. Nano Res. - 2022. - Vol. 12, Is. 6. - P. 605-616, DOI 10.12989/anr.2022.12.6.605. - Cited References: 73. - This study was supported by the Russian Science Foundation, project no. 21-72-00025 “Tuning the Magnetic Properties of Ultrafine Biocompatible Ferrihydrite Nanoparticles through Interparticle Interactions” (https://rscf.ru/project/21-72-00025/) . - ISSN 2287-237X
Кл.слова (ненормированные):
ferrihydrite ultrafine nanoparticles -- hyperfine structure -- interparticle interactions -- iron oxyhydroxide -- superparamagnetic relaxation -- surface coatings
Аннотация: We prepared two samples of ultrafine ferrihydrite (FH) nanoparticle ensembles of quite a different origin. First is the biosynthesized sample (as a product of the vital activity of bacteria Klebsiella oxytoca (hereinafter marked as FH-bact) with a natural organic coating and negligible magnetic interparticle interactions. And the second one is the chemically synthesized ferrihydrite (hereinafter FH-chem) without any coating and high level of the interparticle interactions. The interparticle magnetic interactions have been tuned by modifying the nanoparticle surface in both samples. The coating of the FH-bact sample has been partially removed by annealing at 150℃ for 24 h (hereinafter FH-annealed). The FH-chem sample, vice versa, has been coated (1.0 g) with biocompatible polysaccharide (arabinogalactan) in an ultrasonic bath for 10 min (hereinafter FH-coated). The changes in the surface properties of nanoparticles have been controlled by XPS. According to the electron microscopy data, the modification of the nanoparticle surface does not drastically change the particle shape and size. A change in the average nanoparticle size in sample FH-annealed to 3.3 nm relative to the value in the other samples (2.6 nm) has only been observed. The estimated particle coating thickness is about 0.2-0.3 nm for samples FH-bact and FH-coated and 0.1 nm for sample FH-annealed. Mössbauer and magnetization measurements are definitely shown that the drastic change in the blocking temperature is caused by the interparticle interactions. The experimental temperature dependences of the hyperfine field hf>(T) for samples FH-bact and FH-coated have not revealed the effect of interparticle interactions. Otherwise, the interparticle interaction energy Eint estimated from the hf>(T) for samples FH-chem and FH-annealed has been found to be 121kB and 259kB, respectively.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Knyazev, Yu. V.; Князев, Юрий Владимирович; Balaev, D. A.; Балаев, Дмитрий Александрович; Yaroslavtsev, R. N.; Ярославцев, Роман Николаевич; Krasikov, A. A.; Красиков, Александр Александрович; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Mikhlin, Y. L.; Volochaev, M. N.; Волочаев, Михаил Николаевич; Bayukov, O. A.; Баюков, Олег Артемьевич; Stolyar, S. V.; Столяр, Сергей Викторович; Iskhakov, R. S.; Исхаков, Рауф Садыкович
}
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8.


   
    Tuning of the coordination and emission properties of 4-amino-2,1,3-benzothiadiazole by introduction of diphenylphosphine group / T. S. Sukhikh, R. M. Khisamov, D. A. Bashirov [et al.] // Cryst. Growth Des. - 2020. - Vol. 20, Is. 9. - P. 5796-5807, DOI 10.1021/acs.cgd.0c00406. - Cited References: 58. - This work is supported by the Russian Science Foundation (project no. 19-73-00030) and partly by RFBR (viz., powder XRD data processing and determination of the structure of 1. CINF7/INFHINF8/INF using powder XRD) according to the research project no. 19-52-80003. We acknowledge the European Synchrotron Radiation Facility for provision of synchrotron radiation facilities and thank Prof. Andrew N. Fitch. We are grateful to Siberian Supercomputer Centre of Institute of Computational Mathematics and Mathematical Geophysics for computational capability and thank the technical staff of the Institute for the assistance . - ISSN 1528-7483. - ISSN 1528-7505
   Перевод заглавия: Настройка координационных и эмиссионных свойств 4-амино-2,1,3-бензотиадиазола путем введения дифенилфосфиновой группы
РУБ Chemistry, Multidisciplinary + Crystallography + Materials Science, Multidisciplinary
Рубрики:
COMPLEXES
   BENZOTHIADIAZOLE

   CHEMISTRY

   SUBSTITUENTS

   LIGANDS

   PROGRAM

Аннотация: A novel amino-benzothiadiazole bearing diphenylphosphine groups (L) was designed and synthesized. A number of its coordination compounds of Cu(I) (1·0.75C7H8, 2a,b), Pd(II) (4), and Pt(II) (5) were prepared demonstrating the coordination of L ligand via N and/or P atoms. The reaction with strong Lewis acid Zn(II) resulted in the rearrangement of P—N—P to P–P–N moiety and formation of complex 3. The structures of L, 2–5 were determined by single crystal X-ray (XRD) diffraction, while that of 1·0.75C7H8 was determined by powder XRD analysis. Intermolecular secondary bonding of S···S interactions in the compounds, unusual for benzothiadiazoles, was discussed supported by quantum chemical calculations. Differences in the structures of the compounds cause significant changes of photophysical properties. In particular, the position of the electronic absorption band is featured by the conformation of L, viz., the dihedral angle between the benzothiadiazole unit and the P—N—P moiety, as proved by TD-DFT calculations performed on model molecules. The photophysical properties of the compounds also strongly depend on the coordination mode of L: the presence of a bond between the metal and the N atom of the thiadiazole unit plays an essential role in defining the position of the absorption and emission bands as well as emission lifetime of these compounds. The thermally activated delayed fluorescence and phosphorescence mechanisms in a thermal equilibrium were determined for 1·0.75C7H8. Complex 5 features a broad emission band spanning the entire visible region; moreover, it shows an unusual clear-white luminescence, which remains visible even in the daylight.

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Держатели документа:
Russian Acad Sci, Nikolaev Inst Inorgan Chem, Siberian Branch, Novosibirsk 630090, Russia.
Russian Acad Sci, Kirensky Inst Phys, Siberian Branch, Krasnoyarsk 660036, Russia.
Novosibirsk State Univ, Natl Res Univ, Dept Nat Sci, Novosibirsk 630090, Russia.
Shihexi Univ, Dept Chem, Shihezi 832000, Xinjiang, Peoples R China.

Доп.точки доступа:
Sukhikh, Taisiya S.; Khisamov, Radmir M.; Bashirov, D. A.; Komarov, Vladislav Yu; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ryadun, Alexey A.; Benassi, E.; Konchenko, Sergey N.; Russian Science FoundationRussian Science Foundation (RSF) [19-73-00030]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]
}
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9.


   
    Tuning of photoluminescence by cation nanosegregation in the (CaMg)x(NaSc)1-xSi2O6 solid solution / Z. Xia [et al.] // J. Am. Chem. Soc. - 2016. - Vol. 138, Is. 4. - P. 1158-1161, DOI 10.1021/jacs.5b12788. - Cited References: 23. - Work performed by Z.X. and Q.L. was supported by the National Natural Science Foundation of China (51272242 and 51572023), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), and the Beijing Nova Program (Z131103000413047). Work performed by G.L., J.W., Z.M., M.B., and D.J.M. at Argonne National Laboratory was supported by the Office of Basic Energy Sciences of the U.S. Department of Energy (DOE) through Grant DE-AC02-06CH11357 for research on heavy elements chemistry and materials sciences. TEM was accomplished in part at the Center for Nanoscale Materials, a DOE Office of Science User Facility under Contract DE-AC02-06CH11357. Sector 20 operations at APS are supported by DOE and the Canadian Light Source, with additional support from the University of Washington. G.L. acknowledges travel support from the CAS/SAFEA International Partnership Program for Creative Research Teams. K.R.P. gratefully acknowledges support from the National Science Foundation (DMR-1307698). . - ISSN 0002-7863
   Перевод заглавия: Управление люминесценцией за счет наносегрегации катионов в твердом растворе (CaMg)x(NaSc)1-xSi2O6
РУБ Chemistry, Multidisciplinary
Рубрики:
SPINODAL DECOMPOSITION
   ENERGY-TRANSFER

   EXSOLUTION

   CLINOPYROXEN

   NANOCRYSTALS

   SEGREGATION

   MECHANISMS

   PYROXENESS

   JERVISITE

   PHOSPHORS

Аннотация: Controlled photoluminescence tuning is important for the optimization and modification of phosphor materials. Herein we report an isostructural solid solution of (CaMg)x(NaSc)1-xSi2O6 (0 < x < 1) in which cation nanosegregation leads to the presence of two dilute Eu2+ centers. The distinct nanodomains of isostructural (CaMg)Si2O6 and (NaSc)Si2O6 contain a proportional number of Eu2+ ions with unique, independent spectroscopic signatures. Density functional theory calculations provided a theoretical understanding of the nanosegregation and indicated that the homogeneous solid solution is energetically unstable. It is shown that nanosegregation allows predictive control of color rendering and therefore provides a new method of phosphor development. © 2016 American Chemical Society.

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Держатели документа:
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Chemical Sciences and Engineering Division, Argonne, IL, United States
Center for Nanoscale Materials, Nanoscience and Technology Division, Argonne, IL, United States
Nuclear Engineering Division, Argonne, IL, United States
X-ray Science Division, Argonne National Laboratory, Argonne, IL, United States
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 National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, China
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL, United States

Доп.точки доступа:
Xia, Z.; Liu, G.; Wen, J.; Mei, Z.; Balasubramanian, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Peng, L.; Gu, L.; Miller, D. J.; Liu, Q.; Poeppelmeier, K. R.
}
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10.


   
    Tuning of photoluminescence and local structures of substituted cations in xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7:Eu2+ phosphors / M. Chen [et al.] // Chem. Mater. - 2017. - Vol. 29, Is. 3. - P. 1430-1438, DOI 10.1021/acs.chemmater.7b00006. - Cited References: 37. - The present work was supported by the National Natural Science Foundation of China (Grants 91622125 and 51572023), Natural Science Foundations of Beijing (2172036), and Fundamental Research Funds for the Central Universities (FRF-TP-15-003A2). . - ISSN 0897-4756
   Перевод заглавия: Управляемая люминесценция и локальная структура замещаемых катионов в люминофоре xSr2Ca(PO4)2-(1-x)Ca10Li(PO4)7:Eu2+
Кл.слова (ненормированные):
Calcium -- Energy transfer -- Europium -- Light emission -- Lithium -- Luminescence -- Phosphors -- Photoionization -- Photoluminescence -- Single crystals -- Composition ranges -- Crystal-field splitting -- Luminescence measurements -- Non-linear variation -- Photoionization process -- Polyhedra distortion -- Rare earth doped solids -- Temperature dependent -- Solid solutions
Аннотация: Local structure modification in solid solution is an essential part of photoluminescence tuning of rare earth doped solid state phosphors. Herein we report a new solid solution phosphor of Eu2+-doped xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7 (0 ≤ x ≤ 1), which share the same β-Ca3(PO4)2 type structure in the full composition range. Depending on the x parameter variation in xSr2Ca(PO4)2-(1 - x)Ca10Li(PO4)7:Eu2+, the vacancies generated in the M(4) site enable the nonlinear variation of cell parameters and volume, and this increases the magnitude of M(4)O6 polyhedra distortion. The local structure modulation around the Eu2+ ions causes different luminescent behaviors of the two-peak emission and induces the photoluminescence tuning. The shift of the emission peaks in the solid solution phosphors with different compositions has been discussed. It remains invariable at x ≤ 0.5, but the red-shift is observed at x > 0.5 which is attributed to combined effect of the crystal field splitting, Stokes shift, and energy transfer between Eu2+ ions. The temperature-dependent luminescence measurements are also performed, and it is shown that the photoionization process is responsible for the quenching effect.

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Держатели документа:
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
State Key Laboratory of Tribology, Tsinghua University, Beijing, China

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