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Каталог книг и брошюр библиотеки ИФ СО РАН

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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Yang, Zhiyu, Zhou, Yayun, Qiao, Jianwei, Molokeev M. S., Xia, Zhiguo
Заглавие : Rapid synthesis of red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors and the tunable photoluminescence via Sr/Ba substitution
Место публикации : Adv. Opt. Mater. - 2021. - Vol. 9. Is. 16. - Ст.2100131. - ISSN 2195-1071, DOI 10.1002/adom.202100131
Примечания : Cited References: 44. - Z.Y. and Y.Z. contributed equally to this work. This research was supported by the National Natural Science Foundations of China (Grant Nos. 51972118 and 51961145101), International Cooperation Project of National Key Research and Development Program of China (No. 2021YFE0105700), Guangzhou Science & Technology Project (No. 202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (No. 2017BT01x137). This work was also funded by RFBR according to the research Project No. 19-52-80003
Предметные рубрики: LUMINESCENCE PROPERTIES
THERMAL-STABILITY
EU2+
GREEN
EU3+
SR
Аннотация: Discovering new Eu2+-doped red-emitting phosphors in oxide-based materials is a challenge for white light-emitting diode (WLED) applications. Herein, a highly efficient high-frequency induction heating method is employed to rapidly prepare the red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors peaking at 614 nm and exhibiting a high photoluminescence quantum yield of 78.4% under the excitation of 440 nm. The structural and spectral analyses suggest that Eu2+ ions tend to enter the [Sc1/Ga1O6] and [Ga2O6] polyhedrons with small coordination numbers, leading to the broadband red emission originated from large crystal field splitting of Eu2+ 5d level. The chemical substitution of Ba in the Sr site enhances the thermal stability and helps to the photoluminescence tuning from 614 to 728 nm in SrBaSc0.5Ga1.5O5:Eu2+. The WLED device fabricated by blending the red Sr1.7Ba0.3Sc0.5Ga1.5O5:Eu2+ and yellow Y3(Al, Ga)5O12:Ce3+ phosphors shows a high color-rendering index (Ra = 91.1), and low color-correlated temperature (CCT = 4750 K). This study aims to provide a new synthesis method and design principle for guiding the development of Eu2+-doped oxide-based red phosphors with low preparation cost; moreover, the photoluminescence tuning strategy via cation substitutions is essential to achieve tunable emission, even the near-infrared luminescence.
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Olshevskaya J., Shubin A., Kovaleva A., Tomilin F. N.
Заглавие : The effect of iron substitution on the structure and electronic properties of Cr2SiC by theoretical method
Коллективы : International workshop on functional MAX-materials, Kirensky Institute of Physics, Siberian Federal Univercity
Место публикации : International workshop on the properties of functional MAX-materials (2nd FunMax): book of abstracts/ org. com. M. Farle [et al.]. - 2021. - P.42
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu G., Hu T., Molokeev M. S., Xia Z.
Заглавие : Li/Na substitution and Yb3+ co-doping enabling tunable near-infrared emission in LiIn2SbO6:Cr3+ phosphors for light-emitting diodes
Место публикации : iScience. - 2021. - Vol. 24, Is. 4. - Ст.102250. - ISSN 25890042 (ISSN), DOI 10.1016/j.isci.2021.102250
Примечания : Cited References: 45. - The present work was supported by the National Natural Science Foundation of China of China (Grant Nos. 51972118 and 51961145101), the Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science & Technology Project (202007020005), the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Pro-gram (2017BT01X137), and RFBR according to the research project No. 19-52-80003
Аннотация: Near-infrared (NIR) phosphor-converted light-emitting diode (pc-LED) has great potential in non-invasive detection, while the discovery of tunable broadband NIR phosphor still remains a challenge. Here, we report that Cr3+-activated LiIn2SbO6 exhibits a broad emission band ranging from 780 to 1400 nm with a full width at half maximum (FWHM) of 225 nm upon 492 nm excitation. The emission peaks are tuned from 970 to 1020 nm together with considerable broadening of FWHM (∼285 nm) via Li/Na substitution. Depending on Yb3+ co-doping, a stronger NIR fluorescence peak of Yb3+ appears with improved thermal resistance, which is ascribed to efficient energy transfer from Cr3+ to Yb3+. An NIR pc-LED package has been finally designed and demonstrated a remarkable ability to penetrate pork tissues (∼2 cm) so that the insertion depth of a needle can be observed, indicating that the phosphor can be applied in non-destructive monitoring.
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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) : Arauzo A., Bartolome J., Luzon J., Drokina T. V., Petrakovskii G. A., Molokeev M. S.
Заглавие : Effect of R substitution in spin glass RFeTi2O7 compounds
Место публикации : J. Magn. Magn. Mater. - 2020. - Vol. 515. - Ст.167273. - ISSN 03048853 (ISSN), DOI 10.1016/j.jmmm.2020.167273
Примечания : Cited References: 38. - This study has been financed by MECOM Project MAT2014-53921-R, MICINN Project MAT2017-83468-R and Gobierno de Aragón RASMIA E12_17R. Authors would like to acknowledge the use of Servicio General de Apoyo a la Investigación-SAI, Universidad de Zaragoza
Аннотация: Zirconolite oxides R3+Fe3+Ti2O7 (R rare earth element) are known to exhibit spin glass behaviour at low temperatures. Here we present a detailed study of these compounds for R = Eu, Gd, Dy, Ho, and Er, together with reviewed previous measurements on Sm, Tb, Tm, Yb and Lu, with the scope of determining the role played by the rare earth on their magnetic properties. They have been investigated using X-ray powder diffraction, and further characterized by magnetization, frequency dependent ac susceptibility and heat capacity measurements. RFeTi2O7 compounds are all isostructural showing orthorhombic structure, space group Pcnb at 300 K. Disorder of the magnetic ions in the RFeTi2O7 lattice induces spin glass behaviour at low temperatures, mainly due to the Fe sublattice. We show that magnetic rare earth ions participate in the spin glass state tuning its properties. The single ion anisotropy of the R3+ ions, excluding exchange interaction with other magnetic ions, has been calculated by ab initio methods, and expressed in terms of the g tensor of the ground doublet or quasi-doublet in Kramers (Sm, Dy, Er, Yb) and non-Kramers (Tb, Ho) ions, respectively, in an effective spin S* = 1/2 model. In the case of R with a singlet ground state (Eu, Tm) or a multiplet state (Gd), the ion is isotropic. We show that the relative increase in the spin-glass temperature ΔTSGR/TSGFe with respect to the LuFeTi2O7, where Lu is non-magnetic, correlates qualitatively with the product of the ratio gz/gJ (R = Tb, Dy, Ho, and Er), or g⊥/gJ (R = Sm), times the ratio of exchange interactions JR,Fe/JFe,Fe determined from the paramagnetic room temperature susceptibility measurements. Besides, for increasing anisotropy the spin glass transition dynamics slows down to values typical of cluster glass. The coercive field below the transition is increased in the same trend. This paper explains the effect of the R-Fe exchange interaction and R single ion anisotropy on the spin-glass behaviour of these compounds.
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Удод, Любовь Викторовна, Романова, Оксана Борисовна
Заглавие : Влияние катионного замещения на магнитные свойства и электрическую поляризацию в системе Bi2(Sn0.9Ме0.1)2O7, Ме =Cr3+, Fe3
Коллективы : "Новое в магнетизме и магнитных материалах", международная конференция, Научный совет по физике конденсированных сред РАН, МИРЭА - Российский технологический университет, Московский государственный университет им. М.В. Ломоносова, Магнитное общество России
Место публикации : Новое в магнетизме и магнитных материалах: сборник трудов XXIV международной конференции/ прогр. ком.: Р. С. Исхаков, С. Г. Овчинников [и др.]. - 2021. - Секция 1: Новые магнитные и родственные им материалы: синтез и физические свойства. - С. 98-101
Примечания : Библиогр.: 13. - Исследование выполнено при финансовой поддержке программы No 3.5743.2021/6.7
Аннотация: Исследовано влияние гетерогенного замещения ионами Cr3+и Fe3+ на магнитные свойства и электрическую поляризацию пиростанната висмута.Установлена зависимость магнитных свойств от степени заполнения электронных оболочек ионов хрома и железа. Найден гистерезис поляризации в Bi2(Sn0.9Cr0.1)2O7.The effect of heterogeneous substitution by Cr3+ and Fe3+ ions on the magnetic properties and electric polarization of bismuth pyrostannate is investigated. The dependence of the magnetic properties on the degree of filling of the electron shells of chromium and iron ions has been established. The hysteresis of polarization was found in Bi2(Sn0.9Cr0.1)2O7.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Lim, Chang-Sung, Aleksandrovsky A. S., Molokeev M. S., Oreshonkov A. S., Atuchin V. V.
Заглавие : Structural and spectroscopic effects of Li+ substitution for Na+ in LixNa1-xCaGd0.5Ho0.05Yb0.45(MoO4)3 scheelite-type upconversion phosphors
Место публикации : Molecules. - 2021. - Vol. 26, Is. 23. - Ст.7357. - ISSN 1420-3049 (eISSN), DOI 10.3390/molecules26237357
Примечания : Cited References: 77. - This study was supported by the Research Program through the Campus Research Foundation funded by Hanseo University in 2021 (211Yunghap06)
Аннотация: A set of new triple molybdates, LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45, was successfully manufactured by the microwave-accompanied sol–gel-based process (MAS). Yellow molybdate phosphors LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45 with variation of the LixNa1-x (x = 0, 0.05, 0.1, 0.2, 0.3) ratio under constant doping amounts of Ho3+ = 0.05 and Yb3+ = 0.45 were obtained, and the effect of Li+ on their spectroscopic features was investigated. The crystal structures of LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45 (x = 0, 0.05, 0.1, 0.2, 0.3) at room temperature were determined in space group I41/a by Rietveld analysis. Pure NaCaGd0.5Ho0.05Yb0.45(MoO4)3 has a scheelite-type structure with cell parameters a = 5.2077 (2) and c = 11.3657 (5) Å, V = 308.24 (3) Å3, Z = 4. In Li-doped samples, big cation sites are occupied by a mixture of (Li,Na,Gd,Ho,Yb) ions, and this provides a linear cell volume decrease with increasing Li doping level. The evaluated upconversion (UC) behavior and Raman spectroscopic results of the phosphors are discussed in detail. Under excitation at 980 nm, the phosphors provide yellow color emission based on the 5S2/5F4 → 5I8 green emission and the 5F5 → 5I8 red emission. The incorporated Li+ ions gave rise to local symmetry distortion (LSD) around the cations in the substituted crystalline structure by the Ho3+ and Yb3+ ions, and they further affected the UC transition probabilities in triple molybdates LixNa1-xCaGd0.5(MoO4)3:Ho3+0.05/Yb3+0.45. The complex UC intensity dependence on the Li content is explained by the specificity of unit cell distortion in a disordered large ion system within the scheelite crystal structure. The Raman spectra of LixNa1-xCaGd0.5(MoO4)3 doped with Ho3+ and Yb3+ ions were totally superimposed with the luminescence signal of Ho3+ ions in the range of Mo–O stretching vibrations, and increasing the Li+ content resulted in a change in the Ho3+ multiplet intensity. The individual chromaticity points (ICP) for the LiNaCaGd(MoO4)3:Ho3+,Yb3+ phosphors correspond to the equal-energy point in the standard CIE (Commission Internationale de L’Eclairage) coordinates.
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Aplesnin S., Romanova O., Eremin E., Ryabinkina L., Demidenko O., Makovetskii G., Yanushkevich K.
Заглавие : The Influence Of Anionic Substitution With Structural And Electrical Properties Of Mn - Se - Те Chalkogenides
Коллективы : Moscow International Symposium on Magnetism
Место публикации : Moscow Int. Symp. on Magnet. (MISM-2011): Book of abstracts. - 2011. - Ст.24PO-I2-27. - P.693
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhang S., Gai S., Zhang X., Xia M., Zhou Z., Cheng X., Yao M., Molokeev M. S., Feng Q.
Заглавие : Enhanced luminescence properties of Li2MgTiO4: Mn4+, Ge4+ phosphor via single cation substitution for indoor plant cultivation
Место публикации : Ceram. Int. - 2022. - Vol. 48. Is. 3. - P.3070-3080. - ISSN 02728842 (ISSN), DOI 10.1016/j.ceramint.2021.10.082
Примечания : Cited References: 41. - The authors would like to gratefully acknowledge funds from National Natural Science Foundation of China (Grant No. 51974123), the Distinguished Youth Foundation of Hunan Province (Grant No. 2020JJ2018), Key R & D projects in Hunan Province (2020WK2016 & 2020SK2032), Hunan High Level Talent Gathering Project (2019RS1077 & 2020RC5007), the Natural Sciences Foundation of Hunan Agricultural University (19QN11), Hunan Provincial Key Laboratory of Crop Germplasm Innovation and Resource Utilization Science Foundation (19KFXM12), Changsha Science and technology plan (KH2005114), and the Scientific Research Fund of Hunan Provincial Education Department (19C0903)
Аннотация: Red and far-red emitting phosphors have been widely used in phosphor-converted light emitting diode (pc-LED) devices to provide lighting for indoor plant growth, thus achieving desired product qualities. Among the many ways to optimize phosphors’ optical performance, cationic substitution is one of the most effective methods. In this study, red phosphors (Li2MgTi1-x-yO4: xMn4+, yGe4+) were synthesized by high temperature solid state method and the optical performance of phosphors were improved with increasing Ge4+ constituents. In particular, luminescence intensity of Li2MgTiO4: 0.002Mn4+, 0.1Ge4+ increased by 152% under 468 nm excitation, and the thermostability of emission intensity increases from 22% (y = 0) to 43% (y = 0.1), which is about twice as much. Finally, pc-LED device was fabricated via the red phosphor Li2MgTiO4: 0.002Mn4+,0.1Ge4+ coated on a 470 nm ultraviolet chip. By changing the proportion of the phosphor, the electroluminescence spectra of pc-LED device could match well with the absorption regions of plant pigments. Therefore, Li2MgTiO4: 0.002Mn4+, 0.1Ge4+ phosphor has potential application in plant lighting. Furthermore, this work can offer some helpful references for improving luminescent efficiency by simply modulating the chemical composition.
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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Yang, Zhiyu, Zhao, Yifei, Zhou, Yayun, Qiao, Jianwei, Chuang, Yu-Chun, Molokeev M. S., Xia, Zhiguo
Заглавие : Giant red-shifted emission in (Sr,Ba)Y2O4:Eu2+ phosphor toward broadband near-infrared luminescence
Коллективы : International Cooperation Project of National Key Research and Development Program of China [2021YFE0105700]; National Natural Science Foundations of ChinaNational Natural Science Foundation of China (NSFC) [51972118, 51961145101]; Guangzhou Science & Technology Project [202007020005]; Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01X137]; RFBRRussian Foundation for Basic Research (RFBR) [19-52-80003]
Место публикации : Adv. Funct. Mater. - 2022. - Vol. 32, Is. 1. - Ст.2103927. - ISSN 1616-301X, DOI 10.1002/adfm.202103927. - ISSN 1616-3028(eISSN)
Примечания : Cited References: 60. - This research was supported by the International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), National Natural Science Foundations of China (Grant No. 51972118 and 51961145101), Guangzhou Science & Technology Project (202007020005), 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: LIGHT-SOURCES
PHOTOLUMINESCENCE
TRANSITION
CE3+
BLUE
SUBSTITUTION
Аннотация: Near-infrared (NIR) light-emitting diodes (LEDs) light sources are desirable in photonic, optoelectronic, and biological applications. However, developing broadband red and NIR-emitting phosphors with good thermal stability is always a challenge. Herein, the synthesis of Eu2+-activated SrY2O4 red phosphor with high photoluminescence quantum efficiency and broad emission band ranging from 540 to 770 nm and peaking at 620 nm under 450 nm excitation is designed. Sr/Ba substitution in SrY2O4:Eu2+ has been further utilized to achieve tunable emission by modifying the local environment, which facilitates the giant red-shifted emission from 620 to 773 nm while maintaining the outstanding thermal stability of SrY2O4:Eu2+. The NIR emission is attributed to the enhanced Stokes shift and crystal field strength originated from the local structural distortions of [Y1/Eu1O6] and [Y2/Eu2O6]. The investigation in charge distribution around Y/Eu provides additional insight into increasing covalency to tune the emission toward the NIR region. As-fabricated NIR phosphor-converted LEDs demonstration shows its potential in night-vision technologies. This study reveals the NIR luminescence mechanism of Eu2+ in oxide-based hosts and provides a design principle for exploiting Eu2+-doped NIR phosphors with good thermal stability.
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