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Catalyzed M–C coupling reactions in the synthesis of σ-(pyridylethynyl)dicarbonylcyclopentadienyliron complexes / V. V. Verpekin, O. V. Semeikin, A. D. Vasiliev [et al.] // RSC Adv. - 2020. - Vol. 10, Is. 29. - P. 17014-17025, DOI 10.1039/d0ra02333g. - Cited References: 86. - This research was funded by a grant from the Russian Science Foundation (project No. 18-73-00150). . - ISSN 2046-2069

РУБ Chemistry, Multidisciplinary
Рубрики:
NONLINEAR-OPTICAL PROPERTIES
METAL ALKYNYL COMPLEXES
CARBON BOND FORMATION
Аннотация: The reactions between terminal ethynylpyridines, (trimethylsilyl)ethynylpyridines and cyclopentadienyliron dicarbonyl iodide were studied under Pd/Cu-catalyzed conditions to develop a synthetic approach to the σ-alkynyl iron complexes Cp(CO)2Fe–C≡C–R (R = ortho-, meta-, para-pyridyl). Depending on the catalyst and reagents used, the yields of the desired σ-pyridylethynyl complexes varied from 40 to 95%. In some cases the reactions with ortho-ethynylpyridine gave as byproduct the unexpected binuclear FePd μ-pyridylvinylidene complex [Cp(CO)Fe{μ2-η1(Cα):η1(Cα)-κ1(N)-Cα=Cβ(H)(o-C5H4N)}(μ-CO)PdI]. The conditions, catalysts, and reagents that provide the highest yields of the desired σ-pyridylethynyl iron compounds were determined. The methods developed allowed the synthesis of the corresponding σ-4-benzothiadiazolylethynyl complex Cp(CO)2Fe–C≡C–(4-C6H3N2S) as well. Eventually, synthetic approaches to σ-alkynyl iron complexes of the type Cp(CO)2Fe–C≡C–R (R = ortho-, meta-, para-pyridyl, 4-benzothiadiazol-2,1,3-yl) based on the Pd/Cu-catalyzed cross-coupling reactions were elaborated.

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Держатели документа:
Russian Acad Sci, Krasnoyarsk Res Ctr, Siberian Branch, Inst Chem & Chem Technol, Akademgorodok 50-24, Krasnoyarsk 660036, Russia.
Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Ul Vavilova 28, Moscow 119991, Russia.
Russian Acad Sci, Siberian Branch, Krasnoyarsk Res Ctr, Inst Phys, Akademgorodok 50-38, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sobodny Prospect 79, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Verpekin, Victor V.; Semeikin, Oleg, V; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Kondrasenko, Alexander A.; Belousov, Yu. A.; Ustynyuk, Nikolai A.; Russian Science FoundationRussian Science Foundation (RSF) [18-73-00150]
}
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    Halogen substitution in zero-dimensional mixed metal halides toward photoluminescence modulation and enhanced quantum yield / M. Z. Li, Y. W. Li, M. S. Molokeev [et al.] // Adv. Opt. Mater. - 2020. - Vol. 8, Is. 16. - Ст. 2000418, DOI 10.1002/adom.202000418. - Cited References: 34. - M.L., Y.L. contributed equaly to this work. This work was supported by the National Natural Science Foundation of China (51961145101, 51972118, and 51722202), Fundamental Research Funds for the Central Universities (FRFTP-18-002C1), the Guangdong Provincial Science &Technology Project (2018A050506004), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01 x 137). This work was also funded by RFBR according to the research project No. 19-52-80003. The work at Jilin University is supported by the National Natural Science Foundation of China (Grant No. 61722403 and 11674121) and Jilin Province Science and Technology Development Program (Grant No. 20190201016JC). Calculations were performed in part at the high performance computing center of Jilin University. . - ISSN 2195-1071
   Перевод заглавия: Замена галогена в смешанных галогенидах металлов с нулевой размерностью для модуляции фотолюминесценции и увеличения квантового выхода

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
WHITE-LIGHT EMISSION
PEROVSKITES
EXCITONS
Кл.слова (ненормированные):
halogen substitution -- hybrid metal halides -- photoluminescene quantum yield
Аннотация: Zero‐dimensional (0D) organic−inorganic hybrid metal halides haveunprecedented degrees of freedom for structural tunability and photoluminescence modulation. Here, the 0D isomorphic hybrid metal mixed halides (C9NH20)9Pb3Zn2Br19(1−x )Cl19x (x = 0–1) with continuous halogen contents control, exhibiting tunable emission and enhancement of photoluminescence quantum yield (PLQY) are reported. The competitive bromine to chlorine substitution process in (C9NH20)9Pb3Zn2Br19(1−x )Cl19x occurs first in [ZnBr4−x Clx ]2− tetrahedron before the [Pb3Br11−x Clx ]5− trimer. The increasing Cl content in samples from x = 0 to 1 results in an expected blue shift of emission peak from 565 to 516 nm, and meanwhile a strikingly room temperature PL quantum yield increase from 8% to 91%. Combined experimental characterizations and theoretical calculations indicate that the blue shift of interband transition energy is responsible for the emission peak shift. Moreover, with the increasing Cl content, the enhanced electron−phonon interaction and the weakened thermal‐assisted nonradiative recombination result in more efficient radiative transition channels and ultimately enhanced PLQY. The impact of halogen substitution on electronic structures and optical properties in 0D hybrid metal halides is emphasized in this work as a new strategy to promote the future development of new luminescent materials.

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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.
Jilin Univ, Coll Mat Sci & Engn, Key Lab Automobile Mat MOE, State Key Lab Integrated Optoelect, Changchun 130012, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, Inst Opt Commun Mat, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China.

Доп.точки доступа:
Li, Mingze; Li, Yawen; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Na, Guangren; Zhang, Lijun; Xia, Zhiguo
}
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    Luminescence of monoclinic Y2O3:Eu nanophosphor produced via laser vaporization / A. I. Kostyukov, V. N. Snytnikov, V. N. Snytnikov [et al.] // Opt. Mater. - 2020. - Vol. 104. - Ст. 109843, DOI 10.1016/j.optmat.2020.109843. - Cited References: 19. - This work is financially supported by the Russian Foundation for Basic Research № 19-32-60027 . - ISSN 0925-3467
   Перевод заглавия: Люминесценция моноклинного Y2O3:Eu нанолюминофора, полученного испарением лазером
Кл.слова (ненормированные):
Photoluminescence of Eu3+ -- Monoclinic Y2O3:Eu nanophosphor -- Laser vaporization
Аннотация: Europium doped Y2O3spherical nanoparticles with the diameter ~10 nmobtained via cw laser vaporization are shown to crystallize in monoclinic symmetry class (C2/m space group). The size of nanoparticles established via HRTEM coincides with coherent scattering region established by XRD. Luminescence spectrum in the vicinity of ultranarrow transition demonstrates three peaks consistent with three inequivalent positions of Eu3+ ion in monoclinic Y2O3 lattice. Hypersensitive transition dominates in the spectrum, admitting the lack of inversion symmetry at Cs sites occupied by Eu3+. The spectrum of hypersensitive transition is expanded to the red part of spectrum due intense transitions terminating at higher-lying components of crystal-field-split 7F2 energy level. Obtaining chromaticity coordinates (0.669, 0.331)and absolute quantum yield (~21%) is possible using red phosphor based on monoclinic Y2O3:Eu3+.

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Держатели документа:
Novosibirsk State University, Pirogova Str. 2, Novosibirsk, 630090, Russian Federation
Boreskov Institute of CatalysisSB RAS, Lavrentieva Ave. 5, Novosibirsk, 630090, Russian Federation
Nikolaev Institute of Inorganic Chemistry SB RAS, Akad. Lavrentiev Ave. 3, Novosibirsk, 630090, Russian Federation
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
Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Kostyukov, A. I.; Snytnikov, V. N.; Ishchenko, A. V.; Rakhmanova, M. I.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич
}
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Gardymova, Anna P..
Optical textures and orientational structures in cholesteric droplets with conical boundary conditions / A. P. Gardymova, M. N. Krakhalev, V. Y. Zyryanov // Molecules. - 2020. - Vol. 25, Is. 7. - Ст. 1740, DOI 10.3390/molecules25071740. - Cited References: 53. - The authors are grateful for the financial support by the Russian Science Foundation (grant No. 18-72-10036). . - ISSN 1420-3049

РУБ Biochemistry & Molecular Biology + Chemistry, Multidisciplinary
Рубрики:
DISPERSED LIQUID-CRYSTALS
CHIRAL NEMATIC DROPLETS
IONIC MODIFICATION
Кл.слова (ненормированные):
cholesteric liquid crystal -- droplet -- optical texture -- orientational structure -- conical surface anchoring -- topological defect
Аннотация: Cholesteric droplets dispersed in polymer with conical boundary conditions have been studied. The director configurations are identified by the polarising microscopy technique. The axisymmetric twisted axial-bipolar configuration with the surface circular defect at the droplet’s equator is formed at the relative chirality parameter N0≤2.9 . The intermediate director configuration with the deformed circular defect is realised at 2.9
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Держатели документа:
Siberian Fed Univ, Inst Engn Phys & Radio Elect, Krasnoyarsk 660041, Russia.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Krakhalev, M. N.; Крахалев, Михаил Николаевич; Zyryanov, V. Ya.; Зырянов, Виктор Яковлевич; Russian Science FoundationRussian Science Foundation (RSF) [18-72-10036]
}
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Optical properties of the HoGa3(BO3)4 crystal: experiment and ab initio calculation / S. N. Krylova, A. S. Aleksandrovsky, E. M. Roginskii [et al.] // Ferroelectrics. - 2020. - Vol. 559, Is. 1. - P. 135-140, DOI 10.1080/00150193.2020.1722015. - Cited References: 22. - This work was supported by the Russian Foundation for Basic Research (grant No 18-02-00754) . - ISSN 0015-0193
Кл.слова (ненормированные):
HoGa3(BO3)4 -- ab initio calculation -- absorption spectrum -- band structure
Аннотация: Single crystal of HoGa3(BO3)4 has been grown using solution-melt synthesis. The optical band gap determined from the measured absorption spectrum is due to direct allowed transition and equals to 4.14 eV. The optical properties of this crystal are calculated by the plane-wave pseudo-potential method based on density functional theory. The structure of the crystal has been optimized. The electronic structure of HoGa3(BO3)4 is calculated. The experimental and theoretical fundamental absorption spectra are compared. The calculated bandgap is in good agreement with the experimental data.

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Держатели документа:
Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Ioffe Institute, St. Petersburg, Russian Federation
St. Petersburg State University, St. Petersburg, Russian Federation
Moscow Institute of Physics and Technology, Dolgoprudny, Russian Federation

Доп.точки доступа:
Krylova, S. N.; Крылова, Светлана Николаевна; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Roginskii, E. M.; Krylov, A. A.; Gudim, I. A.; Гудим, Ирина Анатольевна; Vtyurin, A. N.; Втюрин, Александр Николаевич
}
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    Effect of composition on the optical and photocatalytic properties of visible light responsive materials Bi26-xMgxO40 / D. S. Shtarev, R. Kevorkyants, M. S. Molokeev, A. V. Shtareva // Inorg. Chem. - 2020. - Vol. 59, Is. 12. - P. 8173-8183, DOI 10.1021/acs.inorgchem.0c00486. - Cited References: 41. - This study was supported by a grant from the Russian Science Foundation (Project No 19-73-10013). The authors acknowledge the help of the Yu. A. Kosygin Institute of Tectonics and Geophysics FEB RAS in conducting the study and offering their research equipment. The authors also thank the Research Center on Nanophotonics, the Center for Physical Methods of Surface Investigation (Dr. Alexandra Koroleva), and the Computing Centre of the Saint-Petersburg State University. R.K. acknowledges financial support from a grant from the Saint-Petersburg State University (Pure ID 39054581) . - ISSN 0020-1669
   Перевод заглавия: Влияние состава на оптические и фотокаталитические свойства новых материалов Bi26-xMgxO40, реагирующих на видимый свет
Аннотация: We report the synthesis and the crystal and electronic structure as well as the optical and photocatalytic properties of novel photoactive materials of the general formula Bi26–xMgxO40. Two compounds with compositions of Bi24.28(3)Mg1.72(3)O40 and Bi24.05(3)Mg1.95(3)O40 are synthesized using the pyrolytic method. According to X-ray diffraction analysis, the materials are monocrystalline species. Their electronic bandgaps determined from Tauc plots are 2.41 eV [Bi24.28(3)Mg1.72(3)O40] and 2.69 eV [Bi24.05(3)Mg1.95(3)O40]. Keeping in mind that optical bandgaps are typically larger than their electronic counterparts, we find that the bismuthate bandgaps match well that of Bi24Mg2O40 (2.26 eV) predicted by density functional theory. Apparently, the synthesized bismuthates are indirect bandgap semiconductors just like Bi24Mg2O40. Both materials demonstrate nearly identical luminescence spectra. Their luminescence emission at 620 nm is most efficiently excited by 365 nm light. The materials’ photocatalytic properties are evaluated in a visible light-induced photocatalytic phenol degradation reaction. Rather low activity of both compounds is detected. However, Bi24.05(3)Mg1.95(3)O40 is ∼2 times more photocatalytically active than Bi24.28(3)Mg1.72(3)O40, which is associated with a higher Bi5+ content in the former.

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Держатели документа:
Yu. A. Kosygin Institute of Tectonics and Geophysics FEB RAS, Khabarovsk, 680000, Russian Federation
Saint-Petersburg State University, Laboratory Photoactive Nanocomposite Materials, St Petersburg, 199034, Russian Federation
Far Eastern State Transport University, Khabarovsk, 680000, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Shtarev, D. S.; Kevorkyants, R.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Shtareva, A. V.
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    Vetrov, S. Ya.
    Localized modes in chiral photonic structures / S. Y. Vetrov, I. V. Timofeev, V. F. Shabanov // Phys. Usp. - 2020. - Vol. 63, Is. 1. - P. 33-56, DOI 10.3367/UFNe.2018.11.038490. - Cited References: 251 . - ISSN 1063-7869. - ISSN 1468-4780
Рубрики:
CHOLESTERIC LIQUID-CRYSTAL
   CONTROLLED LIGHT-SCATTERING
   SCULPTURED THIN-FILMS
Кл.слова (ненормированные):
light localization -- photonic crystals -- chirality -- chiral nematic liquid crystal -- Pancharatnam-Berry geometric phase -- avoided crossing of coupled modes -- cholesteric liquid crystal -- optical Tamm states -- nanocomposite -- resonant frequency dispersion -- hybrid modes
Аннотация: We discuss chiral structures in self-organizing, artificial, and biological materials. A review of experimental studies and recent advances in the localization of light in chiral structures is given. The behavior of polarized resonant modes in such structures is examined using the example of a one-dimensional photonic crystal containing liquid crystal materials. The anomalous spectral shifts of transmission peaks are interpreted as the contribution of the geometric phase caused by the twisting of the layers of the liquid crystal. The optical Tamm state localized at the boundary between chiral and nonchiral mirrors in the form of a cholesteric layer and a polarization-preserving anisotropic mirror is analytically and numerically described. Considerable attention is paid to the presentation of the properties of localized optical modes in the cholesteric with a resonant metal-dielectric nanocomposite. New possibilities for controlling the properties of the photonic structure are noted, due to the combination of the dispersion of the resonant medium and the intrinsic dispersion of the cholesteric. Attention is focused on controlled hybrid modes in the cholesteric structure formed by the coupling of localized modes. Possible applications and further ways of developing the concept of chiral photonic structures are deliberated.

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Публикация на русском языке Ветров, Степан Яковлевич. Локализованные моды в хиральных фотонных структурах [Текст] / С. Я. Ветров, И. В. Тимофеев, В. Ф. Шабанов // Успехи физ. наук. - 2020. - Т. 190 № 1. - С. 37-62

Держатели документа:
Russian Acad Sci, Siberian Branch, FRC KSC, Kirensky Inst Phys, Akademgorodok 50,Str 38, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Pr Svobodnyi 79, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Timofeev, I. V.; Тимофеев, Иван Владимирович; Shabanov, V. F.; Шабанов, Василий Филиппович; Ветров, Степан Яковлевич
}
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    Аверьянов, Евгений Михайлович.
    Новые методы исследования ориентационного порядка одноосных молекулярных пленок на основе оптических данных / Е. М. Аверьянов // Жидк. кристаллы и их практич. использ. - 2020. - Т. 20, № 1. - С. 41-46 ; Liq. Cryst. Appl., DOI 10.18083/LCAppl.2020.1.41. - Библиогр.: 7 . - ISSN 1991-3966
   Перевод заглавия: New methods for studying the orientation order of uniaxial molecular films on the base of optical data
Кл.слова (ненормированные):
тонкие молекулярные пленки -- органические полупроводники -- PTCDA -- ориентационный порядок -- эффекты локального поля -- molecular thin films -- organic semiconductors -- PTCDA -- orientation order -- local-field effects
Аннотация: Установлена связь компонент ε(1,2)j(ω) диэлектрической функции εj(ω) = ε1j(ω) + iε2j(ω) для одноосной молекулярной пленки в области изолированной полосы поглощения света, поляризованного вдоль (j = ||) и нормально (j = ⊥) оптической оси пленки, с параметром ориентационного порядка S дипольных моментов молекулярных переходов, отвечающих данной полосе поглощения. Развиты новые методы определения S, подтвержденные для пленки органического полупроводника PTCDA нанометровой толщины с известными зависимостями ε(1,2)j(ω) в областях прозрачности и низкочастотного электронного поглощения. Показано влияние ориентационного порядка и анизотропии динамических диполь-дипольных межмолекулярных взаимодействий (эффектов локального поля) на положение максимумов полос ε2j(ω).
The components ε(1,2)j(ω) of the dielectric function εj(ω) = ε1j(ω) + iε2j(ω) for uniaxial molecular film in the region of an isolated absorption band of the light polarized along (j = ||) and across (j = ⊥) the film optical axis were considered. The connection of the components with the orientation order parameter S of the dipole moments of molecular transitions corresponding to a given absorption band was established. New methods for determining S are developed. They are confirmed for the organic semiconductor PTCDA film of nanoscale thickness with the known dependences ε(1,2)j(ω) in the transparency and low-frequency electron absorption regions. The effect of the orientation order and anisotropy of dynamic dipole-dipole intermolecular interactions (local-field effects) on the maxima position of the ε2j(ω) bands was shown.

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Держатели документа:
Институт физики им. Л. В. Киренского, ФИЦ КНЦ СО РАН, Академгородок, 50, строение № 38, 660036 Красноярск, Россия

Доп.точки доступа:
Aver'yanov, E. M.

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Mixed-valence hydrated iron fluoridotitanate: synthesis, optics and calorimetry / S. V. Mel'nikova, N. M. Laptash, M. V. Gorev, E. I. Pogoreltsev // J. Phys. Chem. Solids. - 2020. - Vol. 142. - Ст. 109444, DOI 10.1016/j.jpcs.2020.109444. - Cited References: 35 . - ISSN 0022-3697
Кл.слова (ненормированные):
Crystal growth -- Fluoridotitanate -- Mixed valence -- Phase transition -- Optical properties -- Heat capacity
Аннотация: Mixed-valence hydrated fluoridotitanate with idealized formula FeTiF6·6H2O is the main product of fluoride processing of natural mineral ilmenite with hydrofluoric acid. Its single crystals were grown and optical and calorimetric experiments were carried out in the temperature range 200–350 K. Charge re-distribution, Fe2+Ti4+ to Fe3+Ti3+, in the compound studied was evident in XPS spectra. A first order ferroelastic phase transition occurs at temperatures T0↓ = 271.5 K, T0↑ = 274 ÷ 275.5 K with the symmetry change P3‾↔ P1‾. The structural transformation is accompanied by the appearance of a very weak optical anisotropy in the slice (001), a small anomaly of the heat capacity (ΔS = 1.5 J/mol K = 0.2R), and positive baric coefficients dT0/dp ≈ 30 ± 10 K/GPa.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Institute of Chemistry, Far Eastern Branch of RAS, Vladivostok, 690022, Russian Federation
Siberian Federal University, Krasnoyarsk, 660074, Russian Federation

Доп.точки доступа:
Mel'nikova, S. V.; Мельникова, Светлана Владимировна; Laptash, N. M.; Gorev, M. V.; Горев, Михаил Васильевич; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич
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10.

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

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

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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Peoples R China.

Доп.точки доступа:
Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Xia, Zhiguo
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