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| 1. 
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Zinenko, V. I.
Lattice dynamics and phase transitions in a crystal Ba2ZnTeO6 / V. I. Zinenko, A. S. Shinkorenko // Phys. Solid State. - 2022. - Vol. 64, Is. 12. - P. 1986-1992, DOI 10.21883/PSS.2022.12.54395.445. - Cited References: 12. - The calculations were performed using the computer resources ”Integrated simulation and processing of data of mega-class scientific research units” of National Research Centre” Kurchatov Institute“ (http://ckp.urcki.ru)
. - ISSN 1063-7834. - ISSN 1090-6460
Кл.слова (ненормированные):
lattice dynamics -- phase transitions -- double perovskites
Аннотация: The lattice dynamics of Ba2ZnTeO6 double perovskite in three phases has been studied. Vibrational spectra and dynamic charges are calculated. In the rhomobohedral phase R3¯m, soft modes were found; after their condensation, the C2/m phase was obtained, which agrees with the experiment. An assessment was made of the dependence of the enthalpy of different phases on pressure; it showed that the monoclinic phase is more favorable at 0 pressure, but as the pressure increases to 2.9 GPa, the cubic phase Fm3¯m becomes advantageous.
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Публикация на русском языке Зиненко, Виктор Иванович. Динамика решетки и фазовые переходы в кристалле Ba2ZnTeO6 [Текст] / В. И. Зиненко, А. С. Шинкоренко // Физ. тверд. тела. - 2022. - Т. 64 Вып. 12. - С. 2021-2027
Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB, Russian Academy of Sciences, Krasnoyarsk, Russia
Доп.точки доступа:
Shinkorenko, A. S.; Шинкоренко, Алексей Сергеевич; Зиненко, Виктор Иванович
}
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| 2.
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Gavrichkov, V. A.
Magnetic interaction in doped 2D perovskites with nanoscale inhomogenety: lattice nonlocal effects vs superexchange / V. A. Gavrichkov, S. I. Polukeev // XIX Конференция "Сильно коррелированные электронные системы и квантовые критические явления" : сборник тезисов / чл. прогр. ком. С. Г. Овчинников и др. - Москва, 2022. - P. 194-196. - Библиогр.: 1
. - ISBN 978-5-4344-0954-4
,
Материалы конференции
Доп.точки доступа:
Овчинников, Сергей Геннадьевич \чл. прогр. ком.\; Ovchinnikov, S. G.; Polukeev, S. I.; Гавричков, Владимир Александрович; "Сильно коррелированные электронные системы и квантовые критические явления", конференция(19 ; 2022 ; 26 мая ; Москва); Российская академия наук; Физический институт им. П.Н. Лебедева РАН
}
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| 3.
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Temperature phase transitions in Rb2KRe3+F6 elpasolites / A. N. Vtyurin, A. S. Krylov, S. N. Krylova [и др.] // Perovskites and other framework structure crystalline materials: 2d-perovskites, aurivillius, ruddlesden-popper, dion-jacobson phases, tungsten bronzes, clays, and others : Collaborating Academics, 2021. - P. 309-326. - (Artificially created materials and applications ; Vol. 1)
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Держатели документа:
Библиотека Института физики им. Л. В. Киренского СО РАН
Доп.точки доступа:
Vtyurin, A. N.; Втюрин, Александр Николаевич; Krylov, A. S.; Крылов, Александр Сергеевич; Krylova, S. N.; Крылова, Светлана Николаевна; Gerasimova, J. V.; Герасимова, Юлия Валентиновна; Ivanenko, A. A.; Иваненко, Александр Анатольевич; Voronov, V. N.; Воронов, Владимир Николаевич
}
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| 4.
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Broadband light emitting zero-dimensional antimony and bismuth-based hybrid halides with diverse structures / C. K. Deng, S. Q. Hao, K. J. Liu [et al.] // J. Mater. Chem. C. - 2021. - Vol. 9, Is. 44. - P. 15942-15948, DOI 10.1039/d1tc04198c. - Cited References: 52. - This work was supported by Beijing Municipal Natural Science Foundation (2182080) and the National Natural Science Foundation of China (51972021 and 51702329). The work was partly supported by the Fundamental Research Funds for the Central Universities (FRF-IDRY-19-005) and by the RFBR according to the research project No. 19-52-80003. S. H. and C. W. (DFT calculations) acknowledge support from the Department of Energy, Office of Science Basic Energy Sciences under Grant DE-SC0014520. Access to QUEST, the supercomputing resources facilities at Northwestern University, is also acknowledged
. - ISSN 2050-7526. - ISSN 2050-7534
Перевод заглавия: Широкополосное излучение от нульмерных гибридных галогенидов на основе сурьмы и висмута с разнообразной структуройРУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
CRYSTAL-STRUCTURE
LONE-PAIR
EMISSION
PEROVSKITES
TIN
LUMINESCENCE
Аннотация: Low-dimensional organic–inorganic metal halides have recently attracted extensive attention because of their various structures and distinguished photoelectric properties. Herein, we report a series of new zero-dimensional organic–inorganic hybrid metal halides: (TMEDA)3Bi2Cl12·H2O, (TMEDA)3Bi2Br12·H2O, (TMEDA)3Sb2Br12·H2O, and (TMEDA)5Sb6Cl28·2H2O [TMEDA = N,N,N′·trimethylethylenediamine]. (TMEDA)3M2X12·H2O (M = Bi or Sb, X = Cl or Br) crystallizes in the monoclinic space group P21/n, and (TMEDA)5Sb6Cl28·2H2O crystallizes in the orthorhombic space group Pnma. (TMEDA)3M2X12 possesses a zero-dimensional structure with the metal halide ions of [MBr6]3− isolated by the organic TMEDA2+ cations. Interestingly, the (TMEDA)5Sb6Cl28·2H2O structure consists of a combination of corner-connected octahedra [Sb4Cl18]6− and edge-shared [Sb2Cl10]4−, which is quite rare. The light emission of all these compounds was measured, and (TMEDA)3Sb2Br12·H2O exhibits the most intense luminescence. Upon 400 nm ultraviolet light excitation, (TMEDA)3Sb2Br12·H2O exhibited strong broadband yellow emission centered at 625 nm with a full-width at half-maximum of ∼150 nm originating from self-trapped excitons. This work suggests the possibility of new types of hybrid halides by introducing different metal centers and probing the structural evolution and photoluminescent properties, serving as a reference for the relationship between structure and luminescent performance and demonstrating their potential use as phosphors in light-emitting diodes.
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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.
Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Shanxi Normal Univ, Sch Chem & Mat Sci, Key Lab Magnet Mol & Magnet Informat Mat, Minist Educ, Linfen 041004, Shanxi, Peoples R China.
Доп.точки доступа:
Deng, Chenkai; Hao, Shiqiang; Liu, Kunjie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wolverton, Christopher; Fan, Liubing; Zhou, Guojun; Chen, D.a.; Zhao, Jing; Liu, Quanlin; Beijing Municipal Natural Science FoundationBeijing Natural Science Foundation [2182080]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [51972021, 51702329]; Fundamental Research Funds for the Central UniversitiesFundamental Research Funds for the Central Universities [FRF-IDRY-19-005]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]; Department of Energy, Office of Science Basic Energy SciencesUnited States Department of Energy (DOE) [DE-SC0014520]
}
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| 5.
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Solvatochromic photoluminescent effects in all-inorganic manganese(II)-based perovskites by highly selective solvent-induced crystal-to-crystal phase transformations / H. Xiao, P. Dang, X. Yun [et al.] // Angew. Chem. - 2021. - Vol. 133, Is. 7. - P. 3743-3751, DOI 10.1002/ange.202012383. - Cited References: 73. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018)
. - ISSN 1521-3757
Перевод заглавия: Сольватохромные фотолюминесцентные эффекты в полностью неорганическом перовските на основе марганца (II), вызванные высокоселективными фазовыми превращениями кристалла-кристалл, индуцированными растворителем
Кл.слова (ненормированные):
lead-free materials -- low-dimensional perovskites -- luminescence -- manganese -- phase transitions
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.
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Держатели документа:
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun, 130022 China
University of Science and Technology of China, Hefei, 230026 China
Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, 430074 China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Siberian Federal University, 660041 Krasnoyarsk, Russia
Department of Physics, Far Eastern State Transport University, 680021 Khabarovsk, Russia
Доп.точки доступа:
Xiao, Hui; Dang, Peipei; Yun, Xiaohan; Li, Guogang; Wei, Yi; Xiao, Xiao; Zhao, Yajie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cheng, Ziyong; Lin, Jun
}
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| 6.
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Solvatochromic Photoluminescent Effects in All-Inorganic Manganese(II)-Based Perovskites by Highly Selective Solvent-Induced Crystal-to-Crystal Phase Transformations / H. Xiao, P. P. Dang, X. H. Yun [et al.] // Angew. Chem. Int. Edit. - 2021. - Vol. 60, Is. 7. - P. 3699-3707, DOI 10.1002/anie.202012383. - Cited References: 85. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018)
. - ISSN 1433-7851. - ISSN 1521-3773РУБ Chemistry, Multidisciplinary
Рубрики:
LEAD-FREE
HALIDE PEROVSKITE
NANOCRYSTALS
MN2+
LUMINESCENCE
Кл.слова (ненормированные):
lead-free materials -- low-dimensional perovskites -- luminescence -- manganese -- phase transitions
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.
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WOS
Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, 5625 Renmin St, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Hefei 230026, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, Wuhan 430074, Peoples R China.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr,KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Доп.точки доступа:
Xiao, Hui; Dang, Peipei; Yun, Xiaohan; Li, Guogang; Wei, Y.i.; Xiao, Xiao; Zhao, Yajie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cheng, Ziyong; Lin, Jun
}
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| 7.
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Magnetic transitions in exotic perovskites stabilized by chemical and physical pressure / Y. L. Ma, M. S. Molokeev, C. H. Zhu [et al.] // J. Mater. Chem. C. - 2020. - Vol. 8, Is. 15. - P. 5082-5091, DOI 10.1039/c9tc06976c. - Cited References: 79. - This work was financially supported by the National Science Foundation of China (NSFC-21801253, 11804404 and 21875287) and the National Science Foundation (NSF) Grant No. DMR-1809931. Structural analysis of exotic materials in this study was partly supported by the Research Grant No. 075-15-2019-1886 from the Government of the Russian Federation. The XANES work at the Brookhaven National Laboratory, NSLS-II, was supported by the DOEBES (DE-SC0012704). The NSLS-II work was performed on beamline 7-BM and the authors gratefully acknowledge the invaluable help of the beamline scientists Steven Ehrlich and Syed Khalid.
. - ISSN 2050-7526. - ISSN 2050-7534
Перевод заглавия: Магнитный переход в экзотических перовскитах, стабилизированных химическим и физическим давлениемРУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
COLOSSAL MAGNETORESISTANCE
CATION ORDER
RMN3O6 R
T-C
TEMPERATURE
Аннотация: Exotic perovskites significantly enrich materials for multiferroic and magnetoelectric applications. However, their design and synthesis is a challenge due to the mostly required recipe conditions at extremely high pressure. Herein, we presented the Ca2−xMnxMnTaO6 (0 ≤ x ≤ 1.0) solid solutions stabilized by chemical pressure assisted with intermediate physical pressure up to 7 GPa. The incorporation of Mn2+ into the A-site neither drives any cationic ordering nor modifies the orthorhombic Pbnm structure, namely written as (Ca1−x/2Mnx/2)(Mn1/2Ta1/2)O3 with disordered A and B site cationic arrangements. The increment of x is accompanied by a ferromagnetic to antiferromagnetic transition around x = 0.2, which is attributed to the double-exchange interactions between A-site Mn2+ and B-site Mn3+. Partial charge disproportionation of the B-site Mn3+ into Mn2+ and Mn4+ occurs for x above 0.8 samples as manifested by X-ray spectrum and magnetic behaviors. The coexistence of B-site Mn3+ (Jahn–Teller distortion ion) and B′-site Ta5+ (second-order Jahn–Teller distortion ion) could be energetically responsible for the absence of A-site columnar ordering as observed in other quadruple perovskites with half of the A-sites occupied by small transition-metal cations. These exceptional findings indicate that exotic perovskites can be successfully stabilized at chemical and intermediate physical pressure, and the presence of Jahn–Teller distortion cations at the same lattice should be avoided to enable cationic ordering.
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Держатели документа:
Sun Yat Sen Univ, Sch Chem, Minist Educ, Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Peoples R China.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
New Jersey Inst Technol, Dept Phys, Newark, NJ 07102 USA.
Rutgers State Univ, Dept Phys & Astron, 136 Frelinghuysen Rd, Piscataway, NJ 08854 USA.
Доп.точки доступа:
Ma, Yalin; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhu, Chuanhui; Zhao, Shuang; Han, Yifeng; Wu, Meixia; Liu, Sizhan; Tyson, Trevor A.; Croft, Mark; Li, Man-Rong
}
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| 8.
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Structural, magnetic, electronic, and dilatation properties of the ordered solid solutions Ln0.2Sr0.8CoO3-δ (Ln = Sm, Gd, Dy) with the same oxygen nonstoichiometry index δ / V. A. Dudnikov, Y. S. Orlov, M. V. Bushinsky [et al.] // J. Alloy. Compd. - 2020. - Vol. 830. - Ст. 154629, DOI 10.1016/j.jallcom.2020.154629. - Cited References: 44. - The work was financially supported by Russian Foundation for Basic Research (grant No. 19-03-00017); RFBR and BRFFR as a part of scientific project No. 18-52-00017 and project F18R-119; Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science to the research project: "New thermoelectric materials based on multi-scale spatially inhomogeneous substituted rare-earth cobalt oxides and the Ruddlesden-Popper phases " project No. 18-42-243004, Project of Basic Research SB RAS V.45.3.3.
. - ISSN 0925-8388. - ISSN 1873-4669РУБ Chemistry, Physical + Materials Science, Multidisciplinary + Metallurgy & Metallurgical Engineering
Рубрики:
LN(1-X)SR(X)COO(3-DELTA) LN
COBALTATE PEROVSKITES
Кл.слова (ненормированные):
Rare earth cobalt oxide solid solutions -- Layered perovskite-type cobalt oxides -- Structural -- Magnetic -- Electronic -- Dilatation properties
Аннотация: Single-phase samples of the layered perovskite-like cobalt oxides Ln0.2Sr0.8CoO3-δ (Ln = Sm, Gd, Dy) with the same oxygen nonstoichiometry index δ = 0.37 ± 0.01 were synthesized. All samples are characterized by a tetragonal unit cell with the space group I4/mmm. The structural, magnetic, electric transport and dilatation properties of the obtained samples are investigated. The studied samples are characterized by two anomalies in magnetic properties, a high-temperature maximum near Тm = 350 К with magnetic field hysteresis below Tm, and a diffuse peak in the intermediate temperature range, which shifts with ionic radius decrease of the rare-earth element to higher temperatures. The high-temperature maxima of the magnetic susceptibility correlate with anomalies in thermal expansion, heat capacity and the features in the temperature dependences of the electrical resistivity, pointing to a strong relationship between the structural, magnetic and electronic degrees of freedom. The given comparative analysis of the experimental data of various substituting rare-earth elements with the same oxygen nonstoichiometry has been carried out for the first time.
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Держатели документа:
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
RAS, Fed Res Ctr KSC SB, Inst Chem & Chem Technol, Krasnoyarsk 660036, Russia.
Lebedev Phys Inst, Moscow 119991, Russia.
NAS Belarus, Sci Pract Mat Res Ctr, Minsk 220072, BELARUS.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Ioffe Inst, St Petersburg 194021, Russia.
Доп.точки доступа:
Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Bushinsky, M. V.; Solovyov, L. A.; Vereshchagin, S. N.; Gavrilkin, S. Yu; Tsvetkov, A. Yu; Gorev, M. V.; Горев, Михаил Васильевич; Novikov, S. V.; Mantytskaya, O. S.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [19-03-00017]; RFBRRussian Foundation for Basic Research (RFBR) [18-52-00017, F18R-119]; BRFFR [18-52-00017, F18R-119]; Russian Foundation for Basic Research, Government of Krasnoyarsk Territory [18-42-243004, SB RAS V.45.3.3]
}
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| 9.
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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 хромофоровРУБ 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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| 10.
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Tunable photoluminescence in Sb3+-doped zero-dimensional hybrid metal halides with intrinsic and extrinsic self-trapped excitons / J. Zhou, M. Z. Li, M. S. Molokeev [et al.] // J. Mater. Chem. C. - 2020. - Vol. 8, Is. 15. - P. 5058-5063, DOI 10.1039/d0tc00391c. - Cited References: 33. - This work is supported by the National Natural Science Foundation of China (No. 51722202, 51961145101, 51972118, 21576002 and 61705003), Fundamental Research Funds for the Central Universities (D2190980), the Guangdong Provincial Science & Technology Project (2018A050506004), and Beijing Technology and Business University Research Team Construction Project (No. PXM2019_014213_000007). This work was also funded by RFBR according to the Research Project No. 19-52-80003.
. - ISSN 2050-7526. - ISSN 2050-7534
Перевод заглавия: Перестраиваемая фотолюминесценция в нульмерных гибридных металлогалогенидах, легированных Sb3 +, с внутренними и внешними автолокализованными экситонамиРУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
WHITE-LIGHT EMISSION
LUMINESCENCE
PEROVSKITES
CS2NASCCL6
CS2NAYCL6
Аннотация: Dopants in luminescent metal halides provide an alternative way for photoluminescence tuning towards versatile optical applications. Here we report a trivalent antimony (Sb3+)-doped single crystalline 0D metal halide with the composition of (C9NH20)9[Pb3Cl11](ZnCl4)2:Sb3+. This compound possessed the coexistence of two emission centers including intrinsic and extrinsic self-trapped excitons (STEs), which are ascribed to [Pb3Cl11]5− clusters and triplet STEs formed by the 3P1–1S0 transition of Sb3+. By regulating the Sb3+ concentration, the emission can be tuned from green to yellow and finally to orange, which would help to develop optically pumped white light-emitting diodes (WLEDs) with different photometric characteristics. Moreover, this dopant-induced extrinsic STE approach presents a new direction towards tuning the luminescence properties of 0D metal halides, and may find application in environmentally-friendly, high-performance metal halide light emitters.
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Держатели документа:
Beijing Technol & Business Univ, Sch Sci, Beijing 100048, Peoples R China.
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
RAS, SB, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Peoples R China.
Доп.точки доступа:
Zhou, Jun; Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Sun, Jiayue; Xu, Denghui; Xia, Zhiguo
}
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| 11.
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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 выходаРУБ 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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| 12.
|
Su, Binbin.
Unveiling Mn2+ dopant states in two-dimensional halide perovskite toward highly efficient photoluminescence / B. B. Su, M. S. Molokeev, Z. G. Xia // J. Phys. Chem. Lett. - 2020. - Vol. 11, Is. 7. - P. 2510-2517, DOI 10.1021/acs.jpclett.0c00593. - Cited References: 49. - This work is supported by the National Natural Science Foundation of China (51961145101, 51972118, and 51722202), Fundamental Research Funds for the Central Universities (D2190980), the Guangdong Provincial Science & Technology Project (2018A050506004), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project no. 19-52-80003.
. - ISSN 1948-7185
Перевод заглавия: Открытие легирующих состояний Mn2 + в двумерном галоидном перовските для высокоэффективной фотолюминесценцииРУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Atomic, Molecular & Chemical
Рубрики:
LEAD BROMIDE PEROVSKITES
ENERGY-TRANSFER
EXCITON DYNAMICS
DOPING MN2+
Аннотация: Doping is able to create novel optoelectronic properties of halide perovskites, and the involved mechanism of efficient emission is still a challenge. Herein Mn2+ substitution into 2D layered perovskites (C8H20N2)PbBr4 was investigated, demonstrating broad-band orange-red emission originating from the 4T1 → 6A1 transition of Mn2+ dopant. The photoluminescence quantum yield (PLQY) of Mn2+ emission is up to 60.8% related to the energy transfer in coupled states. We verify that an actual Mn2+ dopant as low as 0.476% reaches a high PLQY, whereas the nominal adding amount is 0.8 as the Mn2+/Pb2+ ratio. The small activation energy (∼6.72 meV) between the Mn2+ d state and the trap state accounts for this highly efficient energy transfer and photoluminescence. The proposed luminescence mechanism in Mn2+-doped 2D halide perovskites would provide unique insights into the doping design toward high-performance luminescence materials.
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Держатели документа:
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Technol, Guangzhou 510640, Guangdong, 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.
Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo
}
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| 13.
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Hybrid Metal Halides with Multiple Photoluminescence Centers / M. Z. Li [et al.] // Angew. Chem. Int. Edit. - 2019. - Vol. 58, Is. 51. - P. 18670-18675, DOI 10.1002/anie.201911419. - Cited References: 42. - This work is supported by the National Natural Science Foundation of China (Nos. 51722202 and 51972118), Fundamental Research Funds for the Central Universities (D2190980), the Guangdong Provincial Science & Technology Project (2018A050506004) and by European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement No. [819740], project SCALE-HALO).
. - ISSN 1433-7851. - ISSN 1521-3773
Перевод заглавия: Гибридные галогениды металлов с несколькими центрами фотолюминесценцииРУБ Chemistry, Multidisciplinary
Рубрики:
LIGHT EMISSION
PEROVSKITES
BR
Кл.слова (ненормированные):
light-emitting diodes -- manganese -- metal halides -- photoluminescence -- 0D materials
Аннотация: Very little is known about the realm of solid‐state metal halide compounds comprising two or more halometalate anions. Such compounds would be of great interest if their optical and electronic properties could be rationally designed. Herein, we report a new example of metal halide cluster‐assembled compound (C9NH20)9[Pb3Br11](MnBr4)2, featuring distinctly different anionic polyhedra, namely, a rare lead halide cluster [Pb3Br11]5− and [MnBr4]2−. In accordance with its multinary zero‐dimensional (0D) structure, this compound is found to contain two distinct emission centers, 565 nm and 528 nm, resulting from the formation of self‐trapped excitons and 4T1‐6A1 transition of Mn2+ ions, respectively. Based on the high durability of (C9NH20)9[Pb3Br11](MnBr4)2 upon light and heat, as well as high photoluminescence quantum yield (PLQY) of 49.8 % under 450 nm blue light excitation, white light‐emitting diodes (WLEDs) are fabricated, showcasing its potential in backlight application.
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Держатели документа:
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, 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, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China.
Swiss Fed Inst Technol, Lab Inorgan Chem, Dept Chem & Appl Biosci, Vladimir Prelog Weg 1, CH-8093 Zurich, Switzerland.
Empa Swiss Fed Labs Mat Sci & Technol, Lab Thin Films & Photovolta, Oberlandstr 129, CH-8600 Dubendorf, Switzerland.
Доп.точки доступа:
Li, Mingze; Zhou, Jun; Zhou, Guojun; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Morad, Viktoriia; Kovalenko, Maksym, V; Xia, Zhiguo
}
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| 14.
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Single-Component White-Light Emission in 2D Hybrid Perovskites with Hybridized Halogen Atoms / G. Zhou [et al.] // Adv. Opt. Mater. - 2019. - Vol. 7, Is. 24. - Ст. 1901335, DOI 10.1002/adom.201901335. - Cited References: 35. - G.J.Z. and M.Z.L. contributed equally to this work. The present work was supported by the National Natural Science Foundations of China (Grant Nos. 51722202 and 51972118), the Fundamental Research Funds for the Central Universities (D2190980), and the Guangdong Provincial Science & Technology Project (No. 2018A050506004).
. - ISSN 2195-1071
Перевод заглавия: Однокомпонентное вещество, излучающее белый свет, из ряда двумерных гибридных перовскитов с гибридизованными атомами галогенов
Кл.слова (ненормированные):
2D halide perovskites -- photoluminescence -- white-light emission
Аннотация: With single-component photoinduced white-light (WL) emission, low-dimensional hybrid halide perovskites have emerged as a new generation of luminescent materials; however, the effect of halogens on the intrinsic light emissions and the corresponding mechanisms is still unknown. Herein, the investigation of a family of two-dimensional (2D) hybrid perovskites R2PbBr4−xClx (R = BA+, PMA+, PEA+; x = 0, 1, 2, 3, 4) highlights the influence of halogens on intrinsic emission to reveal the dependence of the photoluminescence on the nature and contribution of the halogens. Ultrabroad emissions covering the entire visible‐light region are achieved in the halogen hybrid systems with the stoichiometry of R2PbBr2Cl2 (R = BA+, PMA+, PEA+), showing their potential as single‐component WL phosphors in solid‐state lighting devices. The origin of the WL emissions is the synergistic recombination emission of free excitons and self‐trapped excitons. The ratio of halogens (Br/Cl) is confirmed to be a critical factor to fine‐tune the intrinsic emission properties. This work provides a feasible strategy to achieve single‐component WL emission in 2D hybrid perovskites, and proposes a method for regulating halogen contents for optimizing luminescent properties.
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Держатели документа:
The Beijing Municipal Key Laboratory of New Energy Materials and Technologies School of Materials Sciences and Engineering University of Science and Technology Beijing, Beijing 100083, P. R. China
Laboratory of Crystal Physics Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Department of Engineering Physics and Radioelectronics Siberian Federal University, Krasnoyarsk 660041, Russia
Department of Physics Far Eastern State Transport University, Khabarovsk 680021, Russia
State Key Laboratory of Luminescent Materials and Devices and Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques South China University of Technology, Guangzhou 510641, P. R. China
Доп.точки доступа:
Zhou, Guojun; Li, Mingze; Zhao, Jing; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo
}
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| 15.
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Role of Halogen Atoms on High-Efficiency Mn2+ Emission in Two-Dimensional Hybrid Perovskites / G. J. Zhou [et al.] // J. Phys. Chem. Lett. - 2019. - Vol. 10, Is. 16. - P. 4706-4712, DOI 10.1021/acs.jpclett.9b01996. - Cited References: 37. - This work is supported by the National Natural Science Foundation of China (No. 51722202 and 51572023), the Natural Science Foundations of Beijing (2172036), the Fundamental Research Funds for the Central Universities (FRF-TP-18-002C1), and the Guangdong Provincial Science & Technology Project (No. 2018A050506004).
. - ISSN 1948-7185
Перевод заглавия: Роль атомов галогенов в высокоэффективном излучении Mn2 + в двумерном гибридном перовскитеРУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Atomic, Molecular & Chemical
Рубрики:
ENERGY-TRANSFER
LIGHT-EMISSION
DOPING MN2+
LEAD-FREE
NANOCRYSTALS
Аннотация: Doped halide pervoskites as highly efficient light emitters have recently fascinated the research community, while the influence of halogen atoms X (X = Cl, Br, I) on the hybrid energy levels and photoluminescence properties remains a challenge. Here, the role of X compositions in the two-dimensional hybrid perovskite BA2PbX4 (BA = C4H9NH3) on the doped Mn2+ emission is identified, wherein Mn2+ reveals a strong luminescence dependence on the nature of the halogen, and optimum Mn2+ emission with a record quantum yield of 60.1% has been achieved in BA2PbBr4. Density functional theory calculations show that BA2PbBr4 holds low Br vacancy concentration and unique coupled states of the Mn-3d level and Pb-6p level at the conduction band minimum, leading to efficient energy transfer from the host to Mn2+. Our work sheds new light on the methods to realize strong exciton–dopant exchange coupling for achieving high-efficiency dopant luminescence.
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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.
Beihang Univ, Sch Phys, Minist Educ, Key Lab Micronano Measurement Manipulat & Phys, Beijing 100191, Peoples R China.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China.
Доп.точки доступа:
Zhou, Guojun; Jia, Xiaofang; Guo, Shaoqiang; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhang, Junying; Xia, Zhiguo
}
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| 16.
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Manipulation of Bi3+/In3+ Transmutation and Mn2+-Doping Effect on the Structure and Optical Properties of Double Perovskite Cs2NaBi1-xInxCl6 / J. Zhou [et al.] // Adv. Opt. Mater. - 2019. - Vol. 7, Is. 8. - Ст. 1801435, DOI 10.1002/adom.201801435. - Cited References: 51. - J.Z. and X.M.R. contributed equally to this work. The present work was supported by the National Natural Science Foundation of China (Grant Nos. 51722202, 51572023, and 91622125) and Natural Science Foundations of Beijing (2172036). X.W.Z. acknowledges the support from National Key R&D Program of China (Grant No. 2016YFB0700700).
. - ISSN 2195-1071
Перевод заглавия: Влияние перестановок Bi3+/In3+ и Mn2+ -допирования на структуру и оптические свойства двойного перовскита Cs2NaBi1-xInxCl6РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
HALIDE DOUBLE PEROVSKITE
LEAD-FREE
ENERGY-TRANSFER
NANOCRYSTALS
BR
Кл.слова (ненормированные):
band gap engineering -- halide double perovskites -- Mn2+ doping
Аннотация: The halide double perovskite family represented by A2(B+,B3+)X6 can overcome the lead toxicity and enable generally large band gap engineering via B/B sites' transmutation or exotic dopants to fulfill the emerging applications in the optoelectronic fields. Herein, the design and the experimental synthesis of a new family of Mn2+‐doped Cs2NaBi1‐xInxCl6 crystals with an intense orange‐yellow emission band are reported, and the phase formation stability is discussed via a combined experimental–theoretical approach. Depending on the manipulation of Bi3+/In3+ combination, the band gap increases with In3+ content, and a subsequent evolution from indirect to direct band gap is verified. First‐principles calculations and parity analyses indicate a parity forbidden effect on Cs2NaInCl6, and a combination effect of absorption on Cs2NaBi1‐xInxCl6 from both Cs2NaBiCl6 and Cs2NaInCl6. The associated Mn2+‐doped photoluminescence depending on the Bi3+/In3+ substitution is also addressed from the variation of the different Mn–Cl environment and neighboring‐cation effect.
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Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China.
Shenzhen Univ, Coll Phys & Optoelect Engn, Shenzhen Key Lab Flexible Memory Mat & Devices, Shenzhen 518060, Peoples R China.
Shenzhen Univ, Coll Optoelect Engn, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Peoples R China.
KSC SB RAS, Fed Res Ctr, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China.
Доп.точки доступа:
Zhou, Jun; Rong, Ximing; Zhang, Peng; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wei, Peijia; Liu, Quanlin; Zhang, Xiuwen; Xia, Zhiguo
}
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| 17.
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Calculation and Comparison of Electronic, Vibrational, Polarization, and Magnetic Properties of Double Perovskites CaMnTi2O6 and CaFeTi2O6 / N. D. Andryushin, V. I. Zinenko, M. S. Pavlovskii, A. S. Shinkorenko // J. Exp. Theor. Phys. - 2019. - Vol. 129, Is. 6. - P. 1036-1044, DOI 10.1134/S1063776119110013. - Cited References: 18. - This work was supported by the Russian Foundation for Basic Research (project no. 18-02-00130-a)
. - ISSN 1063-7761
Кл.слова (ненормированные):
Antiferromagnetism -- Crystal lattices -- Density functional theory -- Electronic properties -- Ferroelectricity -- Ground state -- Iron compounds -- Perovskite -- Spin polarization
Аннотация: Vibrational, polarization, magnetic, and electronic properties of double perovskites CaMnTi2O6 and CaFeTi2O6 with a rare type of “column” ordering of divalent metal cations have been calculated based on the density functional theory. Analysis of the crystal lattice dynamics for paraelectric phase P42/nmc of both compounds has revealed that ferroelectric instability exists only in CaMnTi2O6. It is found that the structure distortion of the paraphrase of CaMnTi2O6 in the eigenvector of the unstable polar mode leads to a structure with the P42/nmc space group. The calculated spontaneous polarization for the ferroelectric phase of CaMnTi2O6 is Ps = 25 μC/cm2. The spin-polarization calculations have shown that the ground state is ferromagnetic in the CaFeTi2O6 crystal and antiferromagnetic in the CaMnTi2O6 crystal. The exchange interaction constants have been calculated using the Heisenberg model and the mean field approximation; the phase transition temperature for each compound has been estimated.
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Публикация на русском языке Расчет и сравнение электронных, колебательных, поляризационных и магнитных свойств двойных перовскитов CaMnTi2O6 и CaFeTi2O6 [Текст] / Н. Д. Андрюшин [и др.] // Журн. эксперим. и теор. физ. - 2019. - Т. 156 Вып. 6. - С. 1137-1146
Держатели документа:
Kirensky Institute of Physics, Federal Research Center “Krasnoyarsk Scientific Center,” Siberian Branch,Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Доп.точки доступа:
Andryushin, N. D.; Андрюшин, Никита Дмитриевич; Zinenko, V. I.; Зиненко, Виктор Иванович; Pavlovskii, M. S.; Павловский, Максим Сергеевич; Shinkorenko, A. S.; Шинкоренко, Алексей Сергеевич
}
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| 18.
|
Ferromagnet-antiferromagnet transition in layered perovskites of Sr3YCo4O10.5 type / I. O. Troyanchuk [et al.] // Mater. Res. Express. - 2019. - Vol. 6, Is. 2. - Ст. 026105, DOI 10.1088/2053-1591/aaef21. - Cited References: 30. - This work was supported by the Belarussian Foundation for Basic Research (project F18R-159) and Russian Foundation Basic Research (contract no. 18-52-00020). Yu S Orlov and SG Ovchinnikov are grateful Russian Foundation Basic Research (contracts no. 18-52-00017 Bel_a, 16-02-00507) and Council on grants of the President of the Russian Federation (SP-1844.2016.1) for the support.
. - ISSN 2053-1591РУБ Materials Science, Multidisciplinary
Рубрики:
SPIN
NANOWIRES
Кл.слова (ненормированные):
neutron diffraction -- orbital ordering -- spin state
Аннотация: Sr1−xYxCoO2.65 (x = 0.2) with layered perovskite structure was studied by neutron diffraction, synchrotron x-ray and magnetometry methods. It is shown that in the 90–375 K temperature range the crystal structure can be described by the monoclinic space group A2/m with the superstructure 4√2a p × 2√2a p × 4a p (with a p corresponding to the unit cell parameter of the primitive cell) while basic diffraction peaks are well indexed in the space group I4/mmm (2a p × 2a p × 4a p ) shows an almost standard magnetization. The basic magnetic structure is G-type antiferromagnetic with average magnetic moments of 2.7 μ B/Co and 1.7 μ B/Co in anion-deficient CoO4+γ and stoichiometric CoO6 layers, respectively. A ferromagnetic component of about 0.27 μ B/Co is determined from the magnetization measurements at 8 K. Sr0.8Y0.2CoO2.65 shows an almost standard magnetization versus temperature dependence whereas Sr0.75Y0.25CoO2.65 exhibits an antiferromagnet-ferromagnet transition accompanied by a structural transformation. There is practically no spontaneous magnetization in x = 0.3. The type of the magnetic structure and the high value of TN suggest that the Co3+ ions are in both structural layers predominantly in the low-spin (LS)/high-spin (HS) state mixture. It is proposed that the ferromagnetic component is due to the orbital ordering occurring at TN in the CoO5 pyramids and the concomitant appearance of ferromagnetic coupling between the Co3+(HS) ions located in these CoO5 pyramids in the anion-deficient CoO4+γ layer.
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Держатели документа:
Natl Acad Sci Belarus Mat Sci, Sci & Pract Ctr, Minsk, BELARUS.
Joint Inst Nucl Res, Dubna, Russia.
Inst Laue Langevin, Grenoble, France.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk 660074, Russia.
Доп.точки доступа:
Troyanchuk, I. O.; Bushinsky, M. V.; Tereshko, N. V.; Lanovsky, R. A.; Sikolenko, V. V.; Ritter, C.; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Belarussian Foundation for Basic Research [F18R-159]; Russian Foundation Basic Research [18-52-00017 Bel_a, 16-02-00507, 18-52-00020]; Council on grants of the President of the Russian Federation [SP-1844.2016.1]
}
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| 19.
|
Thermal expansion and polarization of (1-x)PNN-xPT solid solutions / M. V. Gorev [et al.] // Integr. Ferroelectr. - 2019. - Vol. 196, Is. 1. - P. 60-63, DOI 10.1080/10584587.2019.1591957. - Cited References: 6
. - ISSN 1058-4587. - ISSN 1607-8489
Перевод заглавия: Тепловое расширение и поляризация твердых растворов (1-x)PNN-xPTРУБ Engineering, Electrical & Electronic + Physics, Applied + Physics, Condensed Matter
Рубрики:
BEHAVIOR
Кл.слова (ненормированные):
thermal expansion -- polarization -- relaxors -- perovskites
Аннотация: The paper presents the results of detailed studies of the thermal expansion of (1-x)he paper presents the results of detailed studies of the thermal expansion of (1-x)PbNi1/3Nb2/3O3-xPbTiO3 solid solutions with x = 0-0.8. The anomalous and lattice contributions to deformation and the thermal expansion coefficient are analyzed and the mean square polarization Pd is determined. The results obtained are discussed within the framework of the thermodynamic theory and the Landau 2-4-6 coefficients for solid solutions are estimated.
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Держатели документа:
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk, Russia.
Siberian Fed Univ, Inst Phys & Radioelect, Krasnoyarsk, Russia.
Univ Latvia, Inst Solid State Phys, LV-1063 Riga, Latvia.
Доп.точки доступа:
Gorev, M. V.; Горев, Михаил Васильевич; Flerov, I. N.; Флёров, Игорь Николаевич; Bormanis, K.; Kalvane, A.; International Scientific Conference on Functional Materials and Nanotechnologies(12 ; 2018 ; Oct. 02-05 ; Riga, Latvia)
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Broad-Band Emission in a Zero-Dimensional Hybrid Organic [PbBr6] Trimer with Intrinsic Vacancies / J. Zhou [et al.] // J. Phys. Chem. Lett. - 2019. - Vol. 10, Is. 6. - P. 1337-1341, DOI 10.1021/acs.jpclett.9b00238. - Cited References: 28. - This work was supported by the National Natural Science Foundation of China (Grant Nos. 51722202, 91622125, 51572023, 11574003, 21833009, and 21533010) and the Natural Science Foundation of Beijing (2172036). We were grateful to Prof. Keli Han for his support to supply the femtosecond transient absorption spectroscopy device.
. - ISSN 1948-7185
Перевод заглавия: Широкополосная эмиссия в нульмерном гибридном органическом тримере [PbBr6] с внутренними вакансиямиРУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Atomic, Molecular & Chemical
Рубрики:
WHITE-LIGHT EMISSION
HALIDE PEROVSKITES
LUMINESCENCE
Аннотация: The understanding of broad-band emission mechanisms on low-dimensional metal halides is an urgent need for the design principle of these materials and their photoluminescence tuning. Herein, a new zero-dimensional (0D) organic–inorganic hybrid material (C9NH20)6Pb3Br12 has been discovered, in which face-sharing PbBr6 trimer clusters crystallize with organic cations (C9NH20+), forming periodic structure with 0D blocks. Broad-band green emission peaking at about 522 nm was observed for this material, with a full width at half-maximum (fwhm) of 134 nm. The emission was attributed to excitons trapped at controlled intrinsic vacancies, and this is the new example in 0D metal halides, also confirmed by spectroscopy analysis and first-principles calculations. Discovery of the single-crystalline hybrid material and observation of defect-induced luminescence extend the scope of bulk 0D materials and understanding of photophysical properties for optoelectronic applications.
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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.
Anhui Normal Univ, Minist Educ, Key Lab Funct Mol Solids, Anhui Key Lab Optoelect Mat Sci & Technol, Wuhu 241000, Anhui, Peoples R China.
Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116000, Peoples R China.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China.
South China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China.
Доп.точки доступа:
Zhou, Jun; Li, Mingze; Ning, Lixin; Zhang, Ruiling; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Yang, Songqiu; Han, Keli; Xia, Zhiguo
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 Стандартный Расширенный Профессиональный Распределенный По словарю ГРНТИ-навигатор УДК-навигатор Тематический навигатор
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