Библиотека института физики им. Л.В. Киренского СО РАН

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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Jing Y., Liu Y., Jiang X., Molokeev M. S., Lin Z., Xia Z.
Заглавие : Sb3+dopant and halogen substitution triggered highly efficient and tunable emission in lead-free metal halide single crystals
Место публикации : Chem. Mater. - 2020. - Vol. 32, Is. 12. - P.5327-5334. - ISSN 08974756 (ISSN), DOI 10.1021/acs.chemmater.0c01708
Примечания : Cited References: 46. - 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), Guangzhou Science & Technology Project (202007020005), 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
Аннотация: Rational doping and compositional control remain significant challenges in designing luminescent metal halides to achieve highly efficient and tunable emission. Here, the air-stable lead-free Cs2InCl5·H2O crystal with a zero-dimensional structure was investigated as a pristine compound to design new luminescence materials. Sb3+-doping in Cs2InCl5·H2O:Sb3+ enabled broadband yellow emission with a photoluminescence quantum yield up to 95.5%. The emission colors can be expanded into the orange-red region by halogen compositional substitution for Cs2InX5·H2O:Sb3+ (X = Cl/Br/I). The optical characterizations along with the theoretical calculations demonstrate that the characteristic singlet and triplet self-trapped exciton emissions of ns2-metal-halide centers account for the tunable luminescence. Moreover, the admirable stability against air and heat pave way for its further applications in white light-emitting diodes and high-resolution fluorescent signs in anticounterfeiting technology. Our achievement in the case of Sb3+-doped Cs2InCl5·H2O represents a successful strategy for developing stable lead-free metal halides with highly efficient emission for versatile optical applications.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Plotnikova A. A., Bragin V. I., Knyazev Yu. V.
Заглавие : Structural Characteristics and Processability of Sphalerite in Lead-Zinc Ore of the Gorevka Deposit
Место публикации : J. Min. Sci. - 2019. - Vol. 55, Is. 6. - P.995-1006. - ISSN 1062-7391, DOI 10.1134/S1062739119066381. - ISSN 1573-8736(eISSN)
Примечания : Cited References: 33
Аннотация: The theoretical and experimental substantiation of the behavior of ferrous sphalerite in magnetic separation is given in terms of the Gorevka deposit ore. In sphalerite of this deposit, the content of isomorphous iron ranges as 4-9%. The Mossbauer spectroscopy showed the singlet and two doublet lines of iron, demonstrating separate arrays of iron atoms in sphalerite lattice, with formation of Fe-Fe pairs and clusters of three or more iron atoms. It is found that distribution of iron in sphalerite into three forms coincides for magnetic and nonmagnetic products of zinc concentrate separation. It is determined that magnetic separation undivides sphalerite grains by the isomorphous iron content but is governed by the genetic features of the deposit formation-association of sphalerite with magnetic minerals (pyrrhotine and siderite) and the absence of such associations in galena.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Ying, Rong, Ximing, Li, Mingze, Molokeev M. S., Zhao, Jing, Xia, Zhiguo
Заглавие : Incorporating rare-earth terbium(III) ions into Cs2AgInCl6:Bi nanocrystals toward tunable photoluminescence
Место публикации : Angew. Chem. - 2020. - Vol. 132, Is. 28. - P.11731-11737. - ISSN 1521-3757(eISSN), DOI 10.1002/ange.202004562
Примечания : Cited References: 43
Предметные рубрики: HALIDE DOUBLE PEROVSKITE
LEAD-FREE
LANTHANIDE
STABILITY
EMISSION
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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Coondoo I., Panwar N., Krylova S. N., Krylov A. S., Alikin D., Jakka S. K., Turygin A., Shur V. Y., Kholkin A. L.
Заглавие : Temperature-dependent Raman spectroscopy, domain morphology and photoluminescence studies in lead-free BCZT ceramic
Место публикации : Ceram. Int. - 2021. - Vol. 47, Is. 2. - P.2828-2838. - ISSN 02728842 (ISSN), DOI 10.1016/j.ceramint.2020.09.137
Примечания : Cited References: 65. - I.C. would like to thank financial assistance by national funds (OE), through FCT – Fundação para a Ciência e a Tecnologia, I.P., in the scope of the framework contract foreseen in the numbers 4, 5 and 6 of the article 23, of the Decree-Law 57/2016, of August 29, changed by Law 57/2017, of July 19. This work was developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020 & UIDP/50011/2020, financed by national funds through the Portuguese Foundation for Science and Technology / MCTES . The authors would also like to acknowledge the Ural Center for Shared Use “Modern nanotechnology”, Ural Federal University, Russia and the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS”. The authors would like to thank Dr. E. Venkata Ramana, Department of Physics, University of Aveiro for the dielectric measurements. The work was supported by Government of the Russian Federation (Act 211, 440 Agreement 02.A03.21.0006)
Аннотация: Present work focuses on detailed temperature-dependent X-ray diffraction, Raman scattering, domain configuration, and photoluminescence (PL) studies in the (Ba0·85Ca0.15) (Zr0·10Ti0.90)O3 (BCZT) ceramics. The comprehensive Raman spectroscopy analysis in the present work not only validates the presence of the intermediate orthorhombic phase in BCZT, but also provides evidence of another transition: rhombohedral R3c phase to R3m at low temperature. Temperature behaviour of the lowest frequency transverse optical mode (soft E (TO) phonon) and hard modes was studied. Temperature dependence of peak positions, intensities, and linewidths of Raman phonon modes signalled the presence of phase transitions near −50 ± 5 °C, 0±5 °C, 35±5 °C and 110 ± 10 °C. Evolution of domain morphology occurring at phase transitions above room temperature was studied by piezoresponse force microscopy technique. Analysis of PL spectra revealed disorder/heterogeneity in the sample and indicated the existence of self-trapped excitons. PL spectra are composed of four distinct colour components (~2.55eV:blue, ~2.32eV:green, ~2.08eV:orange and ~1.78eV:red).
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Denisova L. T., Molokeev M. S., Denisov V. M., Golubeva E. O., Galiakhmetova N. A.
Заглавие : Synthesis, Structure, and Thermophysical Properties of Pb10 – xBix(GeO4)2 + xVO4)4 – x (x = 0–3) in the Temperature Range of 350–950 K
Место публикации : Phys. Solid State. - 2020. - Vol. 62, Is. 11. - P.2045-2051. - ISSN 10637834 (ISSN), DOI 10.1134/S1063783420110116
Примечания : Cited References: 26. - The study was carried out under the state assignment for science for the Siberian Federal University, project no. FSRZ-2020-0013
Аннотация: The Pb10 – xBix(GeO4)2 + x(VO4)4 – x (x = 0–3) compounds with an apatite structure have been obtained for the first time from the initial PbO, Bi2O3, GeO2, and V2O5 oxides by the solid-state synthesis in the temperature range of 773–1073 K. The structure of the compounds has been determined by X-ray diffraction analysis. The effect of temperature on specific heat of the synthesized compounds has been investigated by differential scanning calorimetry. The thermodynamic properties of the compounds have been calculated from the experimental Cp = f(T) data.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Ying, Rong, Ximing, Li, Mingze, Molokeev M. S., Zhao, Jing, Xia, Zhiguo
Заглавие : Incorporating rare-earth terbium(III) Ions into Cs2AgInCl6:Bi nanocrystals toward tunable photoluminescence
Место публикации : Angew. Chem. - Int. Edit. - 2020. - Vol. 59, Is. 28. - P.11634-11640. - ISSN 1433-7851, DOI 10.1002/anie.202004562. - ISSN 1521-3773(eISSN)
Примечания : 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.
Предметные рубрики: HALIDE DOUBLE PEROVSKITE
LEAD-FREE
LANTHANIDE
STABILITY
EMISSION
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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Vorobyev S. A., Saikova S. V., Novikova S. A., Fetisova O. Y., Zharkov S. M., Krylov A. S., Likhatski M. N., Mikhlin Y. L.
Заглавие : Colloidal and immobilized nanoparticles of lead xanthates
Место публикации : ACS Omega. - 2019. - Vol. 4, Is. 7. - P.11472-11480. - ISSN 24701343 (ISSN), DOI 10.1021/acsomega.9b00841
Примечания : Cited References: 56. - This research was supported by Russian Science Foundation, project 18-17-00135.
Аннотация: Although nanoparticles of heavy metal xanthates and their hydrosols can play important roles in froth flotation, environmental issues, analytics, and manufacturing of metal sulfide nanocomposites, they have received little attention. We studied colloidal solutions and immobilized particles prepared via interaction of aqueous lead nitrate with alkyl xanthates applying UV−vis absorption spectroscopy, dynamic light scattering, zeta potential measurement, thermogravimetry analysis, Fourier transform infrared spectroscopy, Raman scattering, X-ray photoelectron spectroscopy, atomic force microscopy, and transmission electron microscopy. The hydrodynamic diameter of colloidal particles of Pb(SSCOR)2 decreased from 500 to 50 nm with an increase in the alkyl radical length and the initial xanthate to lead ratio (X/Pb); the zeta potential magnitude varied similarly, although it remained negative. The effect of pH in the range of 4.5−11 was minor, but the colloids produced using excess of Pb2+ in alkaline media were close to PbX and decomposed much easier than PbX2. The uptake of lead xanthates on supports was generally low because of negative charges of the colloids; however, 50−100 nm thick PbX2 films were deposited on PbS and SiO2 from the media of X/Pb 2 and pH 9 because of preadsorption of Pb2+, while nanorods formed on highly oriented pyrolytic graphite.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhou J., Luo J., Rong X., Wei P., Molokeev M. S., Huang Y., Zhao J., Liu Q., Zhang X., Tang J., Xia Z.
Заглавие : Lead-Free Perovskite Derivative Cs2SnCl6−xBrx Single Crystals for Narrowband Photodetectors
Место публикации : Adv. Opt. Mater. - 2019. - Vol. 7, Is. 10. - Ст.1900139. - ISSN 21951071 (ISSN), DOI 10.1002/adom.201900139
Примечания : Cited References: 26. - J.Z., J.J.L., X.M.R. contributed equally to this work. The present work was supported by the National Natural Science Foundation of China (Grants 51722202, 91622125, 51572023, and 11774239), Natural Science Foundations of Beijing (2172036), and National Key R&D Program of China (grant no. 2016YFB0700700).
Ключевые слова (''Своб.индексиров.''): band structure--cs2snbr6--cs2sncl6--lead-free perovskite derivatives--narrowband photodetection
Аннотация: Lead-free and stable Sn halide perovskites demonstrate tremendous potential in the field of optoelectronic devices. Here, the structure and optical properties of the “defect” perovskites Cs2SnCl6−xBrx are reported, as well as their use as photodetector materials. Millimeter‐sized Cs2SnCl6−xBrx single crystals are grown by the hydrothermal method, with the body color continuously changing from transparent to yellow and finally to dark red. Narrowband single‐crystal photodetectors using Cs2SnCl6−xBrx crystals are presented, which show a high detectivity of ≈2.71 × 1010 Jones, with narrowband photodetection (full‐width at half‐maximum ≈45 nm) and high ion diffusion barriers. Moreover, the response spectra are continuously tuned from near violet to orange depending on the variation of the bandgap of the single crystals by changing the halide compositions. The strong surface charge recombination of the excess carriers near the crystal surfaces produced by short wavelength light elucidates the narrowband photodetection behavior. This work provides a new paradigm in the design of lead‐free, stable, and high‐performance perovskite derivatives for optoelectronics applications.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhou, Guojun, Jia, Xiaofang, Guo, Shaoqiang, Molokeev M. S., Zhang, Junying, Xia, Zhiguo
Заглавие : Role of Halogen Atoms on High-Efficiency Mn2+ Emission in Two-Dimensional Hybrid Perovskites
Место публикации : J. Phys. Chem. Lett. - 2019. - Vol. 10, Is. 16. - P.4706-4712. - ISSN 1948-7185, DOI 10.1021/acs.jpclett.9b01996
Примечания : 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).
Предметные 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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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Su, Binbin, Molokeev M. S., Xia, Zhiguo
Заглавие : Unveiling Mn2+ dopant states in two-dimensional halide perovskite toward highly efficient photoluminescence
Место публикации : J. Phys. Chem. Lett. - 2020. - Vol. 11, Is. 7. - P.2510-2517. - ISSN 1948-7185, DOI 10.1021/acs.jpclett.0c00593
Примечания : 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.
Предметные 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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11.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Li M., Zhou J., Molokeev M. S., Jiang X., Lin Z., Zhao J., Xia Z.
Заглавие : Lead-Free Hybrid Metal Halides with a Green-Emissive [MnBr4] Unit as a Selective Turn-On Fluorescent Sensor for Acetone
Место публикации : Inorg. Chem. - 2019. - Vol. 58, Is. 19. - P.13464-13470. - ISSN 00201669 (ISSN) , DOI 10.1021/acs.inorgchem.9b02374
Примечания : Cited References: 38. - This work is supported by the National Natural Science Foundation of China (Nos. 51722202 and 51972118), 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).
Аннотация: Organic-inorganic hybrid metal halides with zero-dimensional (0D) structure has emerged as a new class of light-emitting materials. Herein, a new lead-free compound (C9NH20)2MnBr4 has been discovered and a temperature-dependent phase transition has been identified for two phases (space group P21/c and C2/c) in which individual [MnBr4]2- anions connect with organic cations, (C9NH20 +) (1-buty-1-methylpyrrolidinium+), forming periodic structure with 0D blocks. A green emission band, peaking at 528 nm with a high photoluminescence quantum efficiency (PLQE) of 81.08%, has been observed at room temperature, which is originated from the 4T1(G) to 6A1 transition of tetrahedrally coordinated Mn2+ ions, as also elaborated by density functional theory calculation. Accordingly, a fast, switchable, and highly selective fluorescent sensor platform for different organic solvents based on the luminescence of (C9NH20)2MnBr4 has been developed. We believe that the hybrid metal halides with high PLQE and the exploration of these as a fluorescence sensor will expand the applications scope of bulk 0D materials for future development.
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12.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xiao, Hui, Dang, Peipei, Yun, Xiaohan, Li, Guogang, Wei, Yi, Wei, Yi, Xiao, Xiao, Zhao, Yajie, Molokeev M. S., Cheng, Ziyong, Lin, Jun
Заглавие : Solvatochromic photoluminescent effects in all-inorganic manganese(II)-based perovskites by highly selective solvent-induced crystal-to-crystal phase transformations
Место публикации : Angew. Chem. - 2021. - Vol. 133, Is. 7. - P.3743-3751. - ISSN 1521-3757 (eISSN), DOI 10.1002/ange.202012383
Примечания : 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)
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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13.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Shaikhutdinov K. A., Popkov S. I., Semenov S. V., Balaev D. A., Dubrovskiy A. A., Sablina K. A., Volkov N. V.
Заглавие : Low-temperature resistivity of polycrystalline (La0.5Eu 0.5)0.7Pb0.3MnO3 in a magnetic fields
Место публикации : J. Phys. Conf. Ser. - 2010. - Vol. 200, Is. SECTION 5. - ISSN 17426588 (ISSN) , DOI 10.1088/1742-6596/200/5/052025
Ключевые слова (''Своб.индексиров.''): antiferromagnetic grains--comparative analysis--ferromagnetic grain--low temperatures--polycrystalline--specific heat measurement--spin dependent tunneling--transport and magnetic properties--antiferromagnetism--electric resistance--europium--grain boundaries--grain size and shape--lanthanum compounds--lead--magnetic field effects--magnetic properties--magnetoresistance--manganese oxide--single crystals--thermal variables measurement--lanthanum
Аннотация: The effect of grain boundaries on magnetoresistance (MR) of manganites have been investigated by the comparative analysis of the properties of single-crystal and polycrystalline (La0.5Eu0.5) 0.7Pb0.3MnO3. While MR of the single crystal is maximum near the Curie temperature and vanishes in the low-temperature region, the polycrystalline (La0.5Eu0.5)0.7Pb 0.3MnO3 sample exhibits high MR in the low-temperature region. In order to clarify the origin of the low-temperature MR, the transport and magnetic properties of the polycrystalline (La0.5Eu 0.5)0.7Pb0.3MnO3 in magnetic fields have been supplemented by study of magnetic properties and specific heat measurements. The results obtained could be attributed to spin-dependent tunneling between ferromagnetic grains through insulating antiferromagnetic grain boundaries. © 2010 IOP Publishing Ltd.
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14.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kartashev A. V., Flerov I. N., Volkov N. V., Sablina K. A.
Заглавие : Heat capacity and magnetocaloric effect in manganites (La1-yEuy)(0.7)Pb0.3MnO3 (y:0.2; 0.6)
Место публикации : J. Magn. Magn. Mater. - 2010. - Vol. 322, Is. 6. - P.622-627. - MAR. - ISSN 0304-8853, DOI 10.1016/j.jmmm.2009.10.026
Примечания : Cited Reference Count: 17. - Гранты: This work was supported by the Krasnoyarsk's regional sciences foundation and RFBR in the framework of project "Siberia''(Grant no. 09-02-98001), by Integrational project of Siberian and Far Eastern Departments of RAS(no. 101) and by Council on Grants from the President of the Russian Federation for Support of Leading Scientific Schools(Projectno. NSh-1011.2008.2). Dr Maxim S. Molokeev is acknowledged for the X-raycharacterization of the samples.Финансирующая организация: Krasnoyarsk's regional sciences foundation [09-02-98001]; Siberian and Far Eastern Departments [101]; Russian Federation [NSh-1011.2008.2]
Предметные рубрики:
Ключевые слова (''Своб.индексиров.''): manganites--magnetic phase transition--heat capacity--magnetocaloric effect--heat capacity--magnetic phase transition--magnetocaloric effect--manganites--adiabatic calorimeters--heat capacities--magnetic phase transitions--magneto-caloric effects--magnetocaloric effect--multi-element--nonmagnetics--relative cooling power--temperature range--europium--lead--manganese compounds--oxide minerals--specific heat--phase transitions
Аннотация: Heat capacity and intensive magnetocaloric effect (MCE) in manganites (La1-yEuy)(0.7)Pb0.3MnO3[y=0.2; 0.6] (LEPM) were investigated by means of adiabatic calorimeter. The heat capacity anomaly as well as the values of both the intensive (Delta T-AD) and the extensive (Delta S-MCE) MCE were found to decrease upon increased replacement of La with nonmagnetic Eu. However, because of widening of the MCE peaks, the LEPM compounds show the relative cooling power, RCP/Delta H, comparable to other solid solutions of manganites. Owing to strong effect of Eu - La substitution on the Curie temperature, LEPM might have potential as the solid state refrigerants in multi-element cooling apparatus operating in a wide temperature range. (C) 2009 Elsevier B.V. All rights reserved.
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15.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Fokina V. D., Bondarev V. S., Pogoreltsev E. I., Flerov I. N.
Заглавие : Efficiency of energy harvesting and storage using a multilayer capacitor based on BaTi0.86Sn0.14O3 ferroelectric lead-free ceramics
Место публикации : Ceram. Int. - 2022. - Vol. 48, Is. 22. - P.32966-32972. - ISSN 02728842 (ISSN), DOI 10.1016/j.ceramint.2022.07.227
Примечания : Cited References: 45
Аннотация: The study of the parameters of energy harvesting and storage in the lead-free solid solution BaTi0.86Sn0.14O3 (BTSnO) was performed. The permittivity shows the behavior similar to a diffuse phase transition with the critical exponent γ = 1.84, which is close to the value characteristic of relaxors. Large values of the recoverable energy density, Wrec=(5.8–7.0)∙104 J/m3, and the energy storage efficiency coefficient, η=(82–94) %, are implemented in a wide temperature range, 30–87°С, at a low electric field, E = 18.5 kV/cm. For the first time, the analysis of the Olsen cycle was performed using two phase diagrams: polarization – electric field and entropy – temperature. A fairly good agreement was found between the values of the energy conversion density, ND ≈ 0.15 J/cm3, which was determined using two approaches. A universal parameter is proposed for comparing the energy harvesting density for the materials studied in different ranges of temperature and electric fields.
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16.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhou G., Wang Y., Mao Y., Guo C., Zhang J., Molokeev M. S., Xia Z., Zhang X.-M.
Заглавие : Temperature/component-dependent luminescence in lead-free hybrid metal halides for temperature sensor and anti-counterfeiting
Колич.характеристики :9 с
Место публикации : Adv. Funct. Mater. - 2024. - Ст.2401860. - Article in press. - ISSN 1616301X (ISSN), DOI 10.1002/adfm.202401860. - ISSN 16163028 (eISSN)
Примечания : Cited References: 89. - G.J.Z. and Y.T.W. contributed equally to this work. This work was supported by the National Natural Science Foundation of China (No.52202177, 22271211), Fundamental Research Program of Shanxi Province (No.20210302124054), Science and Technology Innovation Project of Colleges and Universities in Shanxi Province (No.2021L262), 1331 Project of Shanxi Province, Postgraduate Innovation Project of Shanxi Province (No.2023KY462), and supported by the Ministry of Science and High Education of Russian Federation (No.FSRZ-2023-0006). The authors would like to thank Prof. Haijun Jiao, Leibniz-Institut für Katalyse e.V., Germany, for the theoretical support on the electron-transition mechanism
Аннотация: Hybrid metal halides (HMHs) have emerged as a promising platform for optically functional crystalline materials, but it is extremely challenging to thoroughly elucidate the electron transition coupled to additional ligand emission. Herein, to discover sequences of lead-free HMHs with distinct optically active metal cations are aimed, that is, Sb3+ (5s2) with the lone-pair electron configuration and In3+ (4d10) with the fully-filled electron configuration. (Me2NH2)4MCl6·Cl (Me = −CH3, M = Sb, In) exhibits the superior temperature/component-dependent luminescence behaviors resulting from the competition transition between triplet-states (Tn-S0) self-trapped excitons (STEs) of inorganic units and singlet-state (S1-S0) of organic cations, which is manipulated by the optical activity levels of [SbCl6]3− and [InCl6]3−. The bonding differences between Sb3+/In3+ and Cl− in terms of electronic excitation and hybridization are emphasized, and the different electron-transition mechanisms are established according to the PL spectra at the extreme temperature of 5 to 305 K and theoretical calculations. By fine-tuning the B-site Sb3+/In3+ alloying, the photoluminescence quantum yield (PLQY = 81.5%) and stability are optimized at 20% alloying of Sb3+. This research sheds light on the rules governing PL behaviors of HMHs, as well as exploring the optical-functional application of aviation temperature sensors and access-control systems.
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17.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Denisova L. T., Molokeev M. S., Golubeva E. O., Belousova N. V., Denisov V. M.
Заглавие : Synthesis, crystal structure and thermodynamic properties of apatite Pb3Bi2(GeO4)3
Место публикации : Phys. Solid State. - 2022. - Vol. 64, Is. 7. - P.889-893. - ISSN 10637834 (ISSN), DOI 10.21883/PSS.2022.07.54599.312. - ISSN 10906460 (eISSN)
Примечания : Cited References: 30. - This work was partially supported within the scope of the state assignment for science of FSAEI HE ”Siberian Federal University“, project number FSRZ-2020-0013
Аннотация: Apatite Pb3Bi2(GeO4)3 was obtained by the solid-phase method from the initial oxides of PbO, Bi2O3 and GeO2 by sequential firing in air at temperatures of 773–1003 K. Its crystal structure has been refined by X-ray diffraction. The high-temperature heat capacity (350–1000 K) of this compound was measured by differential scanning calorimetry. Based on these data, the main thermodynamic functions are calculated.
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18.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Денисова Л. Т., Молокеев, Максим Сергеевич, Голубева Е. О., Галиахметова Н. А.
Заглавие : Синтез, кристаллическая структура и термодинамические свойства апатитоподобных ванадато-германатов свинца гадолиния
Коллективы : Siberian Federal University [FSRZ-2020-0013]
Место публикации : Журн. СФУ. Химия. - 2022. - Т. 15, № 1. - Ст.128-136. - ISSN 1998-2836, DOI 10.17516/1998-2836-0277; J. Sib. Fed. Univ. Chem. - 2022. - ISSN 2313-6049(eISSN)
Примечания : Библиогр.: 25. - Авторы выражают благодарность Красноярскому региональному центру коллективного пользования ФИЦ КНЦ СО РАН. Работа выполнена при частичной финансовой поддержке в рамках государственного задания на науку ФГАОУ ВО «Сибирский федеральный университет», номер проекта FSRZ‑2020–0013
Аннотация: Методом твердофазных реакций обжигом на воздухе стехиометрических смесей PbO, Gd2O3, GeO2 и V2O5 в интервале температур 773–1073 K синтезированы апатиты Pb10-xGdx(GeO4)2+x(VO4)4-x (x = 0.5, 1.0). С использованием рентгеноструктурного анализа определена их кристаллическая структура. Методом дифференциальной сканирующей калориметрии измерена высокотемпературная теплоемкость (350–1000 K). По экспериментальным данным Cp = f(T) рассчитаны термодинамические свойства апатитов.The Pb10-xGdx(GeO4)2+x(VO4)4-x (x = 0.5, 1.0) apatites were synthesized by the solid-phase synthesis by roasting stoichiometric mixtures of PbO, Gd2O3, GeO2, and V2O5 in air at temperatures of 773–1073 K. Their crystal structure was determined using X‑ray diffraction analysis. The high-temperature heat capacity (350–1000 K) was measured by differential scanning calorimetry. The experimental data Cp = f (T) were used to calculate the thermodynamic properties of apatites.
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19.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Golovnev N. N., Aleksandrovsky A. S., Gerasimova M. A., Tomilin F. N., Mironov V. A., Demina A. V., Xia Z., Molokeev M. S.
Заглавие : Luminescent zero-dimensional hybrid lead thiohalide nanostructures for high quantum yield and broadband excitation
Место публикации : ACS Appl. Nano Mat. - 2021. - Vol. 4, Is. 4. - P.3654-3663. - ISSN 25740970 (ISSN), DOI 10.1021/acsanm.1c00162
Примечания : Cited References: 55. - This work is supported by the RFBR according to the research project No. 19-52-80003. This work is also supported by the National Natural Science Foundation of China (51961145101). V.M. thanks Russian Foundation for Basic Research (project number 19-03-00043) for funding. The use of equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” is acknowledged. The authors thank JSCC RAS for providing computational resources
Аннотация: Luminescent trans-[Pb(DMTU-S)4Cl2] (DMTU: N,N′-dimethylthiourea) was designed and prepared via either mechanochemical or solvothermal methods, and the structures of DMTU and trans-[Pb(DMTU-S)4Cl2] have been resolved using X-ray single-crystal diffraction. Upon excitation over broadband covering the range from 450 to 250 nm, trans-[Pb(DMTU-S)4Cl2] shows yellow-green emission peaking at 549 nm with a spectral width of 110 nm, which is assigned to the triplet–singlet transition of Pb2+ ions within distorted heterogeneous S4Cl2 octahedra. The broadband excitation comprised singlet–singlet transitions of Pb2+ ions and energy transfer from orbitals involving those of organic ligands. Simultaneous analysis of the luminescent bandwidth and Stokes shift gives for Pb2+ ions in S4Cl2 octahedra the value of the Huang–Rhys parameter S = 4.25 and the energy of phonon involved in the formation of the luminescence spectrum of the order of 90 meV. Quantum yield as high as 91% is detected for excitation at 365 nm. This high quantum yield indicates the absence of noticeable concentration quenching at an average distance of 9.4 Å between the Pb2+ ions within the structure of trans-[Pb(DMTU)4Cl2]. The weak spin–orbit intersystem crossing is deduced from a high photoluminescence quantum yield (PLQY) value. Time dependent-density functional theory (TD-DFT) calculations of the nanocluster indicate the red shift of absorption bands in Pb(DMTU)4Cl2 with respect to parent DMTU. The high-performance photoluminescence and stability demonstrated promising applications in photonics.
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20.

Вид документа : Статья из журнала
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Автор(ы) : Xiao, Hui, Dang, Peipei, Yun, Xiaohan, Li, Guogang, Wei, Y.i., Xiao, Xiao, Zhao, Yajie, Molokeev M. S., Cheng, Ziyong, Lin, Jun
Заглавие : Solvatochromic Photoluminescent Effects in All-Inorganic Manganese(II)-Based Perovskites by Highly Selective Solvent-Induced Crystal-to-Crystal Phase Transformations
Место публикации : Angew. Chem. Int. Edit. - 2021. - Vol. 60, Is. 7. - P.3699-3707. - ISSN 1433-7851, DOI 10.1002/anie.202012383. - ISSN 1521-3773(eISSN)
Примечания : 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)
Предметные рубрики: LEAD-FREE
HALIDE PEROVSKITE
NANOCRYSTALS
MN2+
LUMINESCENCE
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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