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Unusual magnetic transitions and nature of magnetic resonance spectra in oxide glasses containing gadolinium / J. . Kliava [et al.] // Phys. Rev. B. - 2005. - Vol. 71, Is. 10. - Ст. 104406, DOI 10.1103/PhysRevB.71.104406. - Cited References: 40 . - ISSN 1098-0121

РУБ Physics, Condensed Matter
Рубрики:
ELECTRON-PARAMAGNETIC-RESONANCE
   BORATE GLASSES
   IONS
   BEHAVIOR
   GD3+
   SPECTROSCOPY
   SYSTEMS
   GD-3+
   FIELD
   SHAPE
Кл.слова (ненормированные):
gadolinium -- glass -- lanthanide -- oxide -- anisotropy -- article -- chemical structure -- concentration response -- electron spin resonance -- energy -- magnetism -- molecular physics -- nanoparticle -- phase transition -- refraction index -- temperature sensitivity
Аннотация: Magnetic susceptibility, electron paramagnetic resonance (EPR), and optical properties have been studied in a glass system {20La(2)O(3)-22Al(2)O(3)-23B(2)O(3)-35(SiO2+GeO2)} with a part of La2O3 substituted by Gd2O3 in different concentrations. Positive Weiss constants have been found in the more heavily doped glasses and ascribed to clustering of Gd3+ ions. Two magnetic phase transitions at 55 and 12 K were detected and ascribed, respectively, to ferromagnetic and antiferromagnetic clusters containing Gd ions. The overall shape of the EPR spectra shows the presence of clustering at the higher Gd contents. At low temperatures the cluster-related resonance signal is altered in shape, indicating an onset of magnetic anisotropy field. This signal is convincingly fitted to superparamagnetic resonance arising from ferromagnetic nanoparticles. The clustering, depending on the Gd concentration, correlates with a significant shift to lower energies of the strong optical absorption band edge, ascribed to a charge transfer transition between Gd ions. A nonmonotonous change of refractive index with the increase of the Gd content indicates changes in the glass matrix and in Gd cluster structure.

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Держатели документа:
Univ Bordeaux 1, CNRS, UMR 5798, CPMOH, F-33405 Talence, France
Bar Ilan Univ, Dept Chem, IL-52900 Ramat Gan, Israel
RAS, SB, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
SI Vavilov State Opt Inst, St Petersburg 199034, Russia
Bar Ilan Univ, Dept Phys, IL-52900 Ramat Gan, Israel
ИФ СО РАН
CPMOH, UMR 5798, CNRS-Universite Bordeaux-I, 33405 Talence Cedex, France
Department of Chemistry, Bar-Ilan University, Ramat-Gan 52900, Israel
L. V. Kirensky Institute of Physics SB RAS, Krasnoyarsk 660036, Russian Federation
S. V. Vavilov State Optical Institute, St. Petersburg 199034, Russian Federation
Department of Physics, Bar-Ilan University, Ramat-Gan 52900, Israel

Доп.точки доступа:
Kliava, J.; Malakhovskii, A. V.; Малаховский, Александр Валентинович; Edelman, I. S.; Эдельман, Ирина Самсоновна; Potseluyko, A. M.; Petrakovskaja, E. A.; Петраковская, Элеонора Анатольевна; Melnikova, S.V.; Мельникова, Светлана Владимировна; Zarubina, T. V.; Petrovskii, G.; Bruckental, Y.; Yeshurun, Y.
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Upconversion luminescence of CsScF4 crystals doped with erbium and ytterbium / D. A. Ikonnikov [et al.] // Opt. Mater. - 2016. - Vol. 60. - P. 584-589, DOI 10.1016/j.optmat.2016.09.016. - Cited References:33. - The authors are grateful to D. L. Chertkova for excellent technical assistance. The work was partially supported by the Russian Foundation for Basic Research Grant 15-52-53080, by the Russian President Grant SS-7612.2016.2, and by Project No0358-2015-0012 of SB RAS Program NoII.2P. . - ISSN 0925-3467. - ISSN 1873-1252

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
MODULATED STRUCTURE
   LANTHANIDE
   NANOCRYSTALS
   PHOSPHORS
Кл.слова (ненормированные):
Fluoride crystals -- Erbium -- Ytterbium -- Up-conversion -- Luminescence -- Crystal structure -- Power dependence -- Pump wavelength dependence
Аннотация: Tetragonal CsScF4 crystals doped with (5 at.%) Er and Er/Yb (0.5 at.%/5 at.%) are grown and their crystal structure is determined to belong to Pmmn space group. Er and Yb ions are shown to occupy distorted octahedral Sc sites with the center of inversion. Bright visible upconversion luminescence was observed under 970-980 nm pumping with red (4F9/2), yellow (4S3/2) and green (2H11/2) bands of comparable intensity. UCL tuning curves maximize at 972 nm (CSF:Er) and at 969.7 nm (CSF:Er,Yb) pumping wavelengths. Different ratios between yellow-green and red luminescence intensities in CSF:Er and CSF:Er, Yb are explained by contribution of cross-relaxation in CSF:Er UCL UC in CSF:Er is a three stage process while UC in CSF:Er, Yb is a two stage process. The peculiarities of power dependences are explained by the power-dependent repopulation between starting levels of UC. (C) 2016 Elsevier B.V. All rights reserved.

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Держатели документа:
Siberian Fed Univ, Krasnoyarsk, Russia.
LV Kirenskii Inst Phys, Krasnoyarsk, Russia.
Far Eastern State Transport Univ, Khabarovsk, Russia.

Доп.точки доступа:
Ikonnikov, D. A.; Voronov, V. N.; Воронов, Владимир Николаевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Russian Foundation for Basic Research [15-52-53080]; Russian President [SS-7612.2016.2, 0358-2015-0012, II.2P]
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    Hydrothermal crystallization of a Ln2(OH)4SO4·nH2O layered compound for a wide range of Ln (Ln = La-Dy), thermolysis, and facile transformation into oxysulfate and oxysulfide phosphors / X. Wang [et al.] // RSC Adv. - 2017. - Vol. 7, Is. 22. - P. 13331-13339, DOI 10.1039/c7ra00645d. - Cited References: 54. - This work was partly supported by the National Natural Science Foundation of China (Grants No. 51672039, 51172038, and 51302032), the Fundamental Research Fund for the Central Universities (Grant No. N140204002), the Grants-in-Aid for Scientific Research (KAKENHI No. 26420686), and the Russian Foundation for Basic Research (15-52-53080). Xuejiao Wang acknowledges the financial support received from the China Scholarship Council for her overseas Ph. D. study at the National Institute of Materials Science (Contract No. 201406080035). . - ISSN 2046-2069
   Перевод заглавия: Гидротермальная кристаллизация слоистых соединений Ln2(OH)4SO4·nH2O с широким диапазоном Ln (Ln = La-Dy), термолиз и плавный переход в оксисульфатные и оксисульфидные люминофоры
Кл.слова (ненормированные):
Dysprosium -- Hydrothermal synthesis -- Light emission -- Phase structure -- Phosphors -- Rare earth elements -- Acceleration voltages -- Chemical compositions -- Electron beam irradiation -- Hydrothermal conditions -- Hydrothermal crystallization -- Lanthanide contraction -- Photoluminescence properties -- Structure refinements -- Dysprosium compounds
Аннотация: The synthesis of a layered Ln2(OH)4SO4·nH2O material (Ln-241) with a smaller lanthanide ion (Dy3+) was successfully achieved through the optimization of the hydrothermal conditions, and the effect of lanthanide contraction on the chemical composition, phase structure, and crystallite/particle morphology of the products was investigated and discussed. Structure refinement showed that the lattice parameters (a, b, and c), cell volume, and axis angle across the series (Ln = La-Dy) monotonously decrease as the size of Ln3+ decreases. Comparative TG/DTA analysis in air indicated that the dehydroxylation temperature of Ln-241 tends to increase, whereas the dehydration and desulfurization temperatures decrease as the size of Ln3+ decreases, thus narrowing the stable temperature range for Ln2O2SO4. Taking advantage of the fact that Ln-241 has exactly the same Ln/S molar ratio as Ln2O2SO4 and Ln2O2S, the latter two groups of important compounds (excluding Ce) were facilely transformed from the former via the removal of water by calcination. The photoluminescence properties of Eu3+ and Tb3+, in terms of excitation, emission, fluorescence decay, quantum yield, and emission color, were investigated and compared for the two hosts Gd2O2S and Gd2O2SO4, and the (Gd0.99Tb0.01)2O2S phosphor was shown to be stable under electron beam irradiation in the studied range and exhibited an increasingly higher emission brightness as the acceleration voltage (up to 7 kV) or beam current (up to 50 μA) increased.

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Держатели документа:
Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang, Liaoning, China
Institute of Ceramics and Powder Metallurgy, School of Materials Science and Engineering, Northeastern University, Shenyang, Liaoning, China
Research Centre for Functional Materials, National Institute for Materials Science, Tsukuba, Ibaraki, Japan
College of New Energy, Bohai University, Jinzhou, Liaoning, 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
School of Physics and Electronic Engineering, Jiangsu Normal University, Xuzhou, Jiangsu, China
World Premier International Centre for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Tsukuba, Ibaraki, Japan

Доп.точки доступа:
Wang, X.; Li, J. -G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, W.; Zhu, Q.; Tanaka, H.; Suzuta, K.; Kim, B. -N.; Sakka, Y.
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Malakhovskii, A. V.
Origin of the giant circular dichroism of vibronic f-f transitions / A. V. Malakhovskii // Mol. Phys. - 2017. - Vol. 115, Is. 14. - P. 1687-1690, DOI 10.1080/00268976.2017.1317113. - Cited References:24. - Russian Foundation for Basic Researches [grant number 16-02-00273]; the President of Russia [grant number Nsh-7559.2016.2]. . - ISSN 0026-8976. - ISSN 1362-3028

РУБ Chemistry, Physical + Physics, Atomic, Molecular & Chemical
Рубрики:
D-3 LANTHANIDE(III) COMPLEXES
   RARE-EARTH IONS
   OPTICAL-ACTIVITY
   LINE STRENGTHS
Кл.слова (ненормированные):
Natural circular dichroism -- f-f transitions
Аннотация: Taking into account the space inhomogeneity of the light electromagnetic wave, a new quantum mechanical expression for the natural optical activity (NOA) of electron transitions has been obtained, which is consistent with the phenomenological theory. It is shown that properties of the NOA of parity forbidden f–f transitions substantially differ from those of allowed transitions. The experimentally observed large NOA of the f–f transitions and extremely large (close to unity) NOA of vibrational repetitions of the f–f transitions are qualitatively explained on the basis of the obtained theoretical expression.

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Держатели документа:
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Малаховский, Александр Валентинович; Russian Foundation for Basic Researches [16-02-00273]; [Nsh-7559.2016.2]
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    Pure red upconversion luminescence and optical thermometry of Er3+ doped sensitizer-rich SrYbInO4 phosphors / N. Z. Zhang [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 27. - P. 7361-7366, DOI 10.1039/c8tc02565g. - Cited References:34. - The present work was supported by the National Natural Science Foundation of China (Grant 91622125, 51722202 and 51572023) and the Natural Science Foundations of Beijing (2172036), and M. Molokeev acknowledges support of the Russian Foundation for Basic Research (17-52-53031). . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Чистая красная апконверсионная люминесценция и оптическая термометрия люминофора SrYbInO4 допированного Er3+

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
TEMPERATURE-SENSING BEHAVIOR
   EMISSION
   NANOCRYSTALS
   LANTHANIDE
Аннотация: Er3+ doped sensitizer-rich SrYbInO4 upconversion phosphors with an orthorhombic structure (Pnma) were synthesized by using a high temperature solid state reaction and their phase structure, site occupation and microstructure have been analyzed. Interestingly, upon the excitation from 980 nm pulsed laser diodes, the SrYbInO4:Er3+ phosphor emitted a nearly pure red emission on account of the 4F9/2 → 4I15/2 transition of Er3+. Additionally, based on the pump power dependence of the upconversion intensity and the schematic diagram of the energy levels, the upconversion mechanism in this system was verified in a two-photon process. The temperature-dependent behaviors of the as-synthesized sample demonstrated the potential for applications in optical thermometry.

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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.

Доп.точки доступа:
Zhang, Ningzi; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, Quanlin; Xia, Zhiguo
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Golovnev, N. N.
Structure and Thermal Decomposition of Nd(III), Gd(III) and Tb(III) 2-Thiobarbiturates / N. N. Golovnev, M. S. Molokeev, I. V. Sterkhova // Russ. J. Inorg. Chem. - 2019. - Vol. 64, Is. 9. - P. 1146-1151, DOI 10.1134/S0036023619090134. - Cited References: 21. - The work was performed as part of the State Assignment of the Ministry of Education and Science of the Russian Federation to the Siberian Federal University in 2017-2019. (4.7666.2017/BCh). The powder X-ray diffraction studies were performed using the equipment at the Baikal and Krasnoyarsk Centers for Collective Use of the Siberian Branch of the Russian Academy of Sciences. . - ISSN 0036-0236. - ISSN 1531-8613

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
CRYSTAL-STRUCTURE
TRANSFORMATION
Кл.слова (ненормированные):
lanthanide(III) 2-thiobarbiturates -- structure -- thermal stability
Аннотация: Complexes [Ln2(H2O)6(μ2-Htba−O,O')4(Htba−O)2]n (Ln = Tb (I), Gd (II), Nd (III); and H2tba is thiobarbituric acid) have been synthesized. According to single-crystal X-ray diffraction, monoclinic crystals of I–III are isostructural. They contain three independent Htba– ions (one terminal and two bridging) and two independent Ln3+ ions. Six Htba– ligands (two terminal and four O,O'-bridging) and two water molecules are coordinated to one Ln3+ ion, and four O,O'-bridging Htba– ions and four water molecules are coordinated to the other Ln3+ ion to form square antiprisms. The antiprisms are bound by Htba– bridging ions into layers. Numerous hydrogen bonds and π–π interactions stabilize the structures of the compounds. Thermal decomposition of complexes I and II performed in air results in mixtures of oxides and oxysulfates, whereas complex III forms Nd2O2SO4.

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Публикация на русском языке Головнев Н. Н. Структура и термическое разложение 2-тиобарбитуратов Nd(III), Gd(III) и Tb(III) [Текст] / Н. Н. Головнев, М. С. Молокеев, И. В. Стерхова // Журн. неорг. химии. - 2019. - Т. 64 № 9. - С. 965-970

Держатели документа:
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Kirensky Inst Phys, Siberian Branch, Krasnoyarsk 660036, Russia.
Far Eastern State Transport Univ, Khabarovsk 680021, Russia.
Russian Acad Sci, Favorsky Inst Chem, Siberian Branch, Irkutsk 664033, Russia.

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Sterkhova, I., V; Ministry of Education and Science of the Russian FederationMinistry of Education and Science, Russian Federation [4.7666.2017/BCh]
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    Incorporating rare-earth terbium(III) Ions into Cs2AgInCl6:Bi nanocrystals toward tunable photoluminescence / Y. Liu, X. M. Rong, M. Z. Li [et al.] // Angew. Chem. - Int. Edit. - 2020. - Vol. 59, Is. 28. - P. 11634-11640, DOI 10.1002/anie.202004562. - Cited References: 43. - This work is supported by the National Natural Science Foundation of China (51961145101, 51972118 and 51722202), Fundamental Research Funds for the Central Universities (FRFTP-18-002C1), 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 1433-7851. - ISSN 1521-3773
   Перевод заглавия: Включение редкоземельного тербия (III) в нанокристаллы Cs2AgInCl6: Bi для перестраиваемой фотолюминесценции

РУБ Chemistry, Multidisciplinary
Рубрики:
HALIDE DOUBLE PEROVSKITE
   LEAD-FREE
   LANTHANIDE
   STABILITY
   EMISSION
Кл.слова (ненормированные):
doping -- energy transfer -- perovskite nanocrystals -- photoluminescence -- terbium
Аннотация: The incorporation of impurity ions or doping is a promising method for controlling the electronic and optical properties and the structural stability of halide perovskite nanocrystals (NCs). Herein, we establish relationships between rare‐earth ions doping and intrinsic emission of lead‐free double perovskite Cs2AgInCl6 NCs to impart and tune the optical performances in the visible light region. Tb3+ ions were incorporated into Cs2AgInCl6 NCs and occupied In3+ sites as verified by both crystallographic analyses and first‐principles calculations. Trace amounts of Bi doping endowed the characteristic emission (5D4→7F6‐3) of Tb3+ ions with a new excitation peak at 368 nm rather than the single characteristic excitation at 290 nm of Tb3+. By controlling Tb3+ ions concentration, the emission colors of Bi‐doped Cs2Ag(In1−x Tbx )Cl6 NCs could be continuously tuned from green to orange, through the efficient energy‐transfer channel from self‐trapped excitons to Tb3+ ions. Our study provides the salient features of the material design of lead‐free perovskite NCs and to expand their luminescence applications.

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Держатели документа:
Univ Sci & Technol Beijing, Beijing Municipal Key Lab New Energy Mat & Techno, Sch Mat Sci & Engn, Beijing 100083, Peoples R China.
Shenzhen Univ, Shenzhen Key Lab Special Funct Mat, Shenzhen Engn Lab Adv Technol Ceram, Guangdong Res Ctr Interfacial Engn Funct Mat,Coll, Shenzhen 518060, Peoples R China.
Fed Res Ctr KSC SB RASs, Lab Crystal Phys, Kirensky Inst 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 & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Technol, Guangzhou 510641, Peoples R China.

Доп.точки доступа:
Liu, Ying; Rong, Ximing; Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Xia, Zhiguo
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Hydrates of lanthanide(III) 2-thiobarbiturates: synthesis, structure, and thermal decomposition / N. N. Golovnev, M. S. Molokeev, M. K. Lesnikov, A. S. Samoilo // Russ. J. Inorg. Chem. - 2020. - Vol. 65, Is. 7. - P. 999-1005, DOI 10.1134/S0036023620070098. - Cited References: 22. - This study was financially supported by the Russian Foundation for Basic Research within scientific project no. 19-52-80003 . - ISSN 0036-0236
Кл.слова (ненормированные):
lanthanides(III) -- thiobarbiturates -- hydrates -- structure -- stability
Аннотация: The hydrates Ln(Htba)3 ∙ 3H2O (Ln = Yb (I), Er (II), Ho (III); Н2tba = 2-thiobarbituric acid), Ln(Htba)3 ∙ 2H2O and Ln(Htba)3 ∙ 8H2O were crystallized from aqueous solutions. According to single-crystal X-ray diffraction analysis data, the structure of monoclinic crystals of isostructural complexes I–III was [Ln2(H2O)6(μ2-Htba-О,O')4(Htba-О)2]n. The formation of isostructural Ln(Htba) ∙ 2H2O (Ln = La, Ce, Eu, Yb, Lu), Ln(Htba)3 ∙ 8H2O (Ln = Eu, Tb, Ho, Yb) and Y(Htba)3 ∙ nH2O (n = 2, 8) was confirmed by the comparison of X-ray diffraction patterns, and their composition was determined by elemental and thermal analyses. The stability of crystal hydrates under heating in an air atmosphere and in contact with their saturated solutions was studied.

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Публикация на русском языке Гидраты 2-тиобарбитуратов лантаноидов(III): синтез, структура и термическое разложение [Текст] / Н. Н. Головнев, М. С. Молокеев, М. К. Лесников, А. С. Самойло // Журн. неорг. химии. - 2020. - Т. 65 № 7. - С. 915-921

Держатели документа:
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Kirenskii Institute of Physics, Federal Research Center “Krasnoyarsk Scientific Center,” Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Golovnev, N. N.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lesnikov, M. K.; Samoilo, A. S.
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Incorporating rare-earth terbium(III) ions into Cs2AgInCl6:Bi nanocrystals toward tunable photoluminescence / Y. Liu, X. M. Rong, M. Z. Li [et al.] // Angew. Chem. - 2020. - Vol. 132, Is. 28. - P. 11731-11737, DOI 10.1002/ange.202004562. - Cited References: 43 . - ISSN 1521-3757

РУБ Chemistry, Multidisciplinary
Рубрики:
HALIDE DOUBLE PEROVSKITE
   LEAD-FREE
   LANTHANIDE
   STABILITY
   EMISSION
Кл.слова (ненормированные):
doping -- energy transfer -- perovskite nanocrystals -- photoluminescence -- terbium
Аннотация: The incorporation of impurity ions or doping is a promising method for controlling the electronic and optical properties and the structural stability of halide perovskite nanocrystals (NCs). Herein, we establish relationships between rare‐earth ions doping and intrinsic emission of lead‐free double perovskite Cs2AgInCl6 NCs to impart and tune the optical performances in the visible light region. Tb3+ ions were incorporated into Cs2AgInCl6 NCs and occupied In3+ sites as verified by both crystallographic analyses and first‐principles calculations. Trace amounts of Bi doping endowed the characteristic emission (5D4→7F6‐3) of Tb3+ ions with a new excitation peak at 368 nm rather than the single characteristic excitation at 290 nm of Tb3+. By controlling Tb3+ ions concentration, the emission colors of Bi‐doped Cs2Ag(In1−xTbx)Cl6 NCs could be continuously tuned from green to orange, through the efficient energy‐transfer channel from self‐trapped excitons to Tb3+ ions. Our study provides the salient features of the material design of lead‐free perovskite NCs and to expand their luminescence applications.

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Держатели документа:
Univ Sci, Sch Materials Sciences, Beijing Municipal Key Lab New Energy Materials, Technology Beijing,Technologies,Engn, Beijing, P. R. China.
Shenzhen Univ, Coll Materials Sci, Guangdong Res Ctr Interfacial Engn Functional Mat, Shenzhen Key Lab Special Functional Materials, Shenzhen, P. R. China.
Kirensky Inst Phys, Fed Res Ctr KSC SB RASs, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys, Radioelectronics, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
S China Univ Technology, Sch Materials Sci, State Key Lab Luminescent Materials, Guangdong Prov Key Lab Fiber Laser Materials, Guangzhou, P. R. China.

Доп.точки доступа:
Liu, Ying; Rong, Ximing; Li, Mingze; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhao, Jing; Xia, Zhiguo
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10.

    Liu, Ying.
    Lattice doping of lanthanide ions in Cs2AgInCl6 nanocrystals enabling tunable photoluminescence / Y. Liu, M. S. Molokeev, Zh. Xia // Energy Mater. Adv. - 2021. - Vol. 2021. - Ст. 2585274, DOI 10.34133/2021/2585274. - Cited References: 42. - This work was supported by the National Natural Science Foundation of China (grant numbers 51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (grant number FRFTP-18-002C1), the Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (grant number 2017BT01X137). This work was also funded by RFBR according to the research project no. 19-52-80003 . - ISSN 2692-7640
   Перевод заглавия: Решеточное легирование ионами лантаноидов в нанокристаллах Cs2AgInCl6, обеспечивающее перестраиваемую фотолюминесценцию
Аннотация: Lead-free halide double perovskite Cs2AgInCl6 has become the research hotspot in the optoelectronic fields. It is a challenge to utilize the lattice doping by different lanthanide ions with rich and unique photoluminescence (PL) emissions for emerging photonic applications. Here, we successfully incorporated Dy3+, Sm3+, and Tb3+ ions into Cs2AgInCl6 nanocrystals (NCs) by the hot-injection method, bringing diverse PL emissions of yellowish, orange, and green light in Cs2AgInCl6:Ln3+ (Ln3+ = Dy3+, Sm3+, Tb3+). Moreover, benefiting from the energy transfer process, Sm3+ and Tb3+ ion-codoped Cs2AgInCl6 NCs achieved tunable emission from green to yellow orange and a fluorescent pattern from the as-prepared NC-hexane inks by spray coating was made to show its potential application in fluorescent signs and anticounterfeiting technology. This work indicates that lanthanide ions could endow Cs2AgInCl6 NCs the unique and tunable PL properties and stimulate the development of lead-free halide perovskite materials for new optoelectronic applications.

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Держатели документа:
The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology, Beijing, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RASs, Russia
Department of Engineering Physics and Radioelectronics, Siberian Federal University, Russia
Department of Physics, Far Eastern State Transport University, Russia
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Engineering, South China University of Technology, China

Доп.точки доступа:
Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo
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