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Kondo effects in variable-valence manganese-substituted thulium selenide / O. B. Romanova, S. S. Aplesnin, M. N. Sitnikov [et al.] // Ceram. Int. - 2024, DOI 10.1016/j.ceramint.2024.06.171. - Cited References: 31 . - Article in press. - ISSN 0272-8842. - ISSN 1873-3956
Кл.слова (ненормированные):
Impedance -- Magnetic properties -- Thermopower -- Kondo effect
Аннотация: The MnXTm1‒XSe (0 ≤ Х ≤ 0.2) solid solutions have been first synthesized and their structural, magnetic, and transport properties have been studied in the temperature range of 80–1000 K and magnetic fields of up to 12 kOe. The surface morphology of the samples has been examined and the chemical analysis has been carried out. It is shown that the valence change with the increasing substitution concentration is accompanied by a change in the lattice parameter and a decrease in the magnetic moment of the samples. The Kondo temperatures caused by the manganese and thulium subsystem have been found in the low- and room-temperature regions. The temperature of localization of small-radius polarons has been determined. A drastic decrease in the relaxation time in the range of the manganese ion percolation through the lattice in the MnXTm1‒XSe system has been established. The change of the current carrier type upon variation in the temperature and substitution concentration was determined from the Seebeck coefficient. A high-temperature extremum of thermopower was revealed, which is explained within the framework of the Anderson model.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russia
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, Russia
Scientific-Practical Materials Research Center NAS, Minsk, Belarus

Доп.точки доступа:
Romanova, O. B.; Романова, Оксана Борисовна; Aplesnin, S. S.; Аплеснин, Сергей Степанович; Sitnikov, M.N.; Udod, L. V.; Удод, Любовь Викторовна; Shabanov, A. V.; Шабанов, Александр Васильевич; Goncharov, V.S.; Zhivulko, A.M.; Yanushkevich, K.I.
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Phase transitions, baro- and piezocaloric effects in single crystal and ceramics of ferroelectric NH4HSeO4 / V. S. Bondarev, E. A. Mikhaleva, M. V. Gorev [et al.] // Solid State Sci. - 2024. - Vol. 148. - Ст. 107440, DOI 10.1016/j.solidstatesciences.2024.107440. - Cited References: 45. - The study was supported by the grant of the Russian Science Foundation No. 23-22-10014, Krasnoyarsk Regional Science Foundation, https://rscf.ru/en/project/23-22-10014/ . - ISSN 1293-2558. - ISSN 1873-3085
Кл.слова (ненормированные):
Ferroelectrics -- Phase transition -- Thermal properties -- High pressure -- Caloric effects
Аннотация: A study of heat capacity, thermal dilatation and sensitivity to hydrostatic and uniaxial pressure was carried out on single-crystal and ceramic samples of NH4HSeO4. The main parameters of low-temperature successive phase transitions B2 (T1) ↔ incommensurate IC (T2) ↔ ferroelectric P1 (T3) ↔ non-ferroelectric did not depend on the type of samples. The behavior of the volumetric strain and the results of direct measurements of T3(p) contributed to the resolution of the longstanding problem associated with the ambiguity of the sign of the corresponding volumetric baric coefficient. The role of thermal expansion anisotropy in the formation of the piezocaloric effect (PCE) near the ferroelectric phase transition at T3 has been studied. Due to the strong difference in the linear baric coefficients, the main contribution to the barocaloric effect (BCE) comes from the inverse intensive and extensive PCE associated with the a-axis. Compared to a single crystal, ceramics demonstrate lower BCE values, which, however, exist in a wider temperature range, which leads to close values of integral caloric parameters. The strong decrease in both BCE and PCE at low-temperature transformations in NH4HSeO4 compared to the ferroelectrics NH4HSO4 and NH4NH4SO4 is associated with a small change in entropy during three low-temperature phase transitions, ΣΔSi = 2.52 J/mol∙K, which is a consequence of a high degree of structural ordering in selenate as a result of a high-temperature transformation at T0 between the superionic and B2 phases, accompanied by a giant change in entropy, ΔS0≈Rln21.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036, Krasnoyarsk, Russia
Siberian Federal University, 660074, Krasnoyarsk, Russia
Krasnoyarsk State Agrarian University, 660049, Krasnoyarsk, Russia

Доп.точки доступа:
Bondarev, V. S.; Бондарев, Виталий Сергеевич; Mikhaleva, E. A.; Михалева, Екатерина Андреевна; Gorev, M. V.; Горев, Михаил Васильевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Bogdanov, E. V.; Богданов, Евгений Витальевич; Cherepakhin, A. V.; Черепахин, Александр Владимирович; Flerov, I. N.; Флёров, Игорь Николаевич
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    Novel AMoO4:Eu3+ (A = Ca and Ba) optical thermometer: Investigation of effect of local ionic coordination environment on optical performance and temperature measurement sensitivity / H. Gao, M. S. Molokeev, Q. Chen [et al.] // Ceram. Int. - 2023. - Vol. 49, Is. 16. - P. 26803-26810, DOI 10.1016/j.ceramint.2023.05.217. - Cited References: 52. - The work was supported by the program of Science and Technology International Cooperation Project of Qinghai province (No. 2022-HZ-807) and the National Natural Science Foundation of China (Grant No. 51802172), and was carried out within the framework of the Strategic Academic Leadership Program “Priority-2030′′ for the Siberian Federal University . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Новый оптический термометр AMoO4:Eu3+ (A = Ca и Ba): исследование влияния локального ионного координационного окружения на оптические характеристики и чувствительность измерения температуры
Кл.слова (ненормированные):
Phosphor -- Optical thermometer -- Coordination environment -- Abnormal thermal quenching
Аннотация: A range of Eu3+-doped AMoO4 (A = Ca and Ba) phosphors were successfully synthetized, and their crystal structures, optical performance, and temperature measurement sensitivities were investigated in detail. Peak doping concentration of CaMoO4:Eu3+ phosphor was 0.18, while peak doping concentration of BaMoO4:Eu3+ phosphor may be greater than 0.18. Then, temperature-dependent photoluminescence emission spectra of representative CaMoO4:0.09Eu3+ and BaMoO4:0.03Eu3+ phosphors were recorded. CaMoO4:0.09Eu3+ phosphor exhibited abnormal thermal quenching, which was attributed to defects caused by heterovalent substitution of ions and increase in the temperature, and good thermal stability. Finally, the possibility of using both phosphors as optical thermometers was discussed, which exhibited good temperature sensitivity. However, CaMoO4:0.09Eu3+ phosphor exhibited two peak absolute (Sa, 1.28 %K−1 and 1.39 %K−1) and relative sensitivities (Sr, 1.21 %K−1 and 1.20 %K−1). In addition, variation trend of Sr value with temperature was considerably peculiar. Two optimum Sa and Sr values were attributed to abnormal thermal quenching of CaMoO4:0.09Eu3+ phosphor. Peak Sa and Sr values of BaMoO4:0.03Eu3+ phosphor was 12.39 %K−1 and 0.89 %K−1, respectively. In addition, Sa of AMoO4:Eu3+ phosphor was negatively related to Eu3+ central asymmetry, while peak Sr value was more inclined to appropriate ionic central asymmetry.

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Держатели документа:
School of Mechanical Engineering, Qinghai University, Xining, 810016, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Siberian Federal University, Krasnoyarsk, 660041, Russia
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russia
Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing), Beijing, 100083, China

Доп.точки доступа:
Gao, Huabo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Chen, Qi; Min, Xin; Ma, Bin
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Temperature phase transitions in silver niobate and lithium-tantal-modified silver niobate ceramics / A. S. Krylov, S. N. Krylova, A. N. Vtyurin [et al.] // Phys. Chem. Chem. Phys. - 2023. - Vol. 25, Is. 16. - P. 11410-11417, DOI 10.1039/D3CP00607G. - Cited References: 42. - The work was financially supported by the Russian Foundation for Basic Research and DFG project number No 21-52-12018. The temperature Raman experiments were performed in the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” . - ISSN 1463-9076. - ISSN 1463-9084
Аннотация: The temperature behaviour of the 0.955 AgNbO3--0.045 LiTaO3and AgNbO3 ceramics were studied in the range from 10 to 415 K by Raman spectroscopy. Ab initio calculations of the Raman spectra in the Pmc21 phase of AgNbO3 were carried out using three potentials (A-PZ, PBE, PBEsol) for spectra interpretation. The Raman spectra peculiarities in AgNbO3 ceramics is observed and explained. The differences in the spectra of the 0.955 AgNbO3--0.045 LiTaO3 and AgNbO3 ceramics are shown. The temperatures of structural changes in the 0.955 AgNbO3--0.45 LiTaO3 and AgNbO3 ceramics were discussed. The structural phase transition below 120 K have been observed in silver niobate. The phase transition has been observed at 310 K and below 150 K in 0.955 AgNbO3--0.045 LiTaO3.

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Держатели документа:
Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russia
Siberian Federal University, Kirenskogo str. 28, Krasnoyarsk, Russia
Ioffe Institute, Polytekhnicheskaya 26, 194021, St. Petersburg, Russia
Electronic Materials Research Laboratory, International Center for Dielectric Research, Xi’an Jiaotong University, Xi’an, 710049, China

Доп.точки доступа:
Krylov, A. S.; Крылов, Александр Сергеевич; Krylova, S. N.; Крылова, Светлана Николаевна; Vtyurin, A. N.; Втюрин, Александр Николаевич; Roginskii, Evgenii M.; Jin, Li; Tian, Ye; Wei, Xiaoyong
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Characterization and magnetic properties of sintered glass-ceramics from dispersed fly ash microspheres / E. V. Fomenko, G. V. Akimochkina, Yu. V. Knyazev [et al.] // Magnetochemistry. - 2023. - Vol. 9, Is. 7. - Ст. 177, DOI 10.3390/magnetochemistry9070177. - Cited References: 50. - Russian Science Foundation and the Krasnoyarsk Regional Science Foundation, grant number 22-27-20039, https://rscf.ru/project/22-27-20039/ (accessed on 15 March 2023) . - ISSN 2312-7481
Кл.слова (ненормированные):
sintering -- dispersed microspheres -- fly ash -- glass-ceramics -- soft magnetic materials -- characterization -- Mossbauer spectroscopy -- magnetic measurements
Аннотация: The recycling of hazardous industrial waste into high-tech materials with desired properties is of considerable interest since it provides optimal alternatives for its final disposal. Coal fly ash, the major waste generated by coal-fired power plants, contains significant quantities of dispersed microspheres with a diameter smaller than 10 μm, which are anthropogenic atmospheric pollutants PM10. Due to their composition and fine-grained powder morphology, they can be converted into sintered products. In this study, dispersed microspheres from class C fly ash were directly sintered without any additive to form high-strength glass-ceramics with magnetic properties. The optimum processing conditions were achieved at a temperature of 1200 °C, at which samples with a compressive strength of 100.6 MPa were obtained. Sintering reduces the quantity of the glass phase and promotes the formation of larnite, Fe-spinel, ye’elimite, and ternesite. Mössbauer measurements show that the relative concentration of the magnetic phase compared to the paramagnetic one rises almost in order. The sintered sample demonstrates a narrower distribution of the hyperfine magnetic field and a significantly lower value of the coercive field of 25 Oe, which allows proposing such materials as soft magnetic materials. The presented results demonstrate promising industrial applications of hazardous PM10 to minimize solid waste pollution.

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Держатели документа:
Institute of Chemistry and Chemical Technology, Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia
Kirensky Institute of Physics, Federal Research Center “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, 79 Svobodny Av., 660041 Krasnoyarsk, Russia
Laboratory of Electron Microscopy, Siberian Federal University, 79 Svobodny Av., 660041 Krasnoyarsk, Russia
Department of Chemistry, Siberian Federal University, Svobodny Av. 79, 660041 Krasnoyarsk, Russia

Доп.точки доступа:
Fomenko, E. V.; Akimochkina, G. V.; Knyazev, Yu. V.; Князев, Юрий Владимирович; Semenov, S. V.; Семёнов, Сергей Васильевич; Yumashev, V. V.; Solovyov, L. A.; Anshits, A. G.
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    Abnormal Bi3+ activated NIR phosphor toward multifunctional LED applications / Y. Li, S. Gai, H. Zhu [et al.] // Ceram. Int. - 2023. - Vol. 49, Is. 23, Pt. B. - P. 39671-39680, DOI 10.1016/j.ceramint.2023.09.322. - Cited References: 45. - This research was jointly supported by the National Natural Science Foundation of China (Grant No. 51974123 ), the Key R & D Projects in Hunan Province ( 2021SK2047 , 2022NK2044 ), the Natural Science Foundation of Hunan Province, China (Grant No. 2021JJ40261 ), Wangcheng Science and Technology Plan ( KJ221017 ), the Science and Technology Innovation Program of Hunan Province ( 2022WZ1022 ) and the Strategic Academic Leadership Program “Priority-2030” for the Siberian Federal University . - ISSN 0272-8842. - ISSN 1873-3956
   Перевод заглавия: Аномальный Bi3+-активированный БИК-люминофор для применения в многофункциональных светодиодах
Кл.слова (ненормированные):
Phosphor -- Luminescence -- Bi3+ -- NIR emission
Аннотация: Herein, the strategy of replacing Ge4+ with smaller Si4+ was adopted to realize the site-selective occupation of Bi3+ activator in the small ring and obtain a near-infrared light-emitting in Zn2(Ge,Si)O4. The designed phosphor exhibits a broad NIR emission with FWHM ≈104 nm in the 650−860 nm region, with a center emission wavelength of about 750 nm. Interestingly, the more sensitive four-member ring sites gradually replaced the six-member ring sites and realized a large-scope photoluminescence regulation from blue to NIR by just after the crystal field engineering. The possible reasons for this phenomenon can be interpreted by centroid shift (εc) and crystal field splitting (εcfs). This work not only provides new insights for the development of Bi3+-activated NIR-emitting phosphors, but also provides thoughts for revealing the potential NIR luminous mechanism of Bi3+.

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Держатели документа:
College of Bioscience and Biotechnology, Hunan Agricultural University, Hunan, Changsha, 410128, China
Hunan Provincial Engineering Technology Research Center for Optical Agriculture, Hunan Agricultural University, Changsha, 410128, China
School of Materials Science and Engineering, Hunan Agricultural University, Hunan, Changsha, 410128, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Li, Y.; Gai, S.; Zhu, H.; Yin, J.; Guo, W.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lu, X.; Xia, M.; Zhou, Z.
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    Low-temperature phase transitions in ANLT4.5 ceramics / A. N. Vtyurin, A. S. Krylov, S. N. Krylova [et al.] // Materials Science and Nanotechnology (MSN-2023) : abstract book of International conference / Ural Federal University; org. com. A. N. Vtyurin et al. - Ekaterinburg, 2023. - Ст. 117. - P. 28. - Cited References: 5 . - ISBN 978-5-9500624-6-9
   Перевод заглавия: Низкотемпературные фазовые переходы в керамике ANLT4.5

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Держатели документа:
Kirensky Institute of Physics SB RAS
Siberian Federal University
Ioffe Physical-Technical Institute RAS
Intl. Center for Dielectric Research, Xi'an Jiaotong University, 710049, Xi'an, China

Доп.точки доступа:
Vtyurin, A. N. \org. com.\; Втюрин, Александр Николаевич; Vtyurin, A. N.; Krylov, A. S.; Крылов, Александр Сергеевич; Krylova, S. N.; Крылова, Светлана Николаевна; Roginskii, E. M.; Li, J.; Tian, Y.; Wei, X.; Уральский Федеральный университет им. Первого Президента России Б.Н. Ельцина; Ural Federal University; "Materials science and nanotechnology", International conference(2023 ; Aug. 27-30 ; Ekaterinburg)
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    Магнетизм бериллиевой керамики со структурой перовскита BeTiO3 / А. В. Павлов, Л. И. Квеглис, А. В. Джес [и др.] // Фундамент. пробл. совр. материаловед. - 2022. - Т. 19, № 1. - С. 115-124 ; Basic Probl. Mater. Sci., DOI 10.25712/ASTU.1811-1416.2022.01.013. - Библиогр.: 24 . - ISSN 1811-1416
   Перевод заглавия: Magnetism of beryllium ceramics with the perovskite structure BeTiO3
Кл.слова (ненормированные):
бериллиевая керамика -- магнитный гистерезис -- электронная структура -- икосаэдрические кластеры -- martensitic transformations -- orientation relations -- Pitch deformation -- polar decomposition of the tensor -- martensite nanocrystals
Аннотация: Известно, что введение в ВеО-керамику добавки TiO2 после термообработки в восстановительной атмосфере сопровождается значительным увеличением электропроводности и способностью поглощать электромагнитное излучение в широком диапазоне частот. До сих пор механизм этого влияния до конца не установлен. С использованием методов Лоренцевой электронной микроскопии в сканирующем электронном микроскопе, а также вибрационного магнитометра, установлено проявление ферромагнетизма. Такая особенность бериллиевой керамики способствует поглощению электромагнитной энергии в объемных образцах, содержащих наночастицы TiO2. Установлено, что присутствие наночастиц способствует формированию структуры перовскита в зонах спекания BeO + TiO2. В структуре перовскита возможна поляризация молекул за счет формирования поляронов, что приводят к деформации решетки и смещению атомов. В результате такого смещения происходит изменение ближнего порядка в структуре перовскита и к образованию икосаэдрической фазы из исходной фазы со структурой кубоктаэдра. Малый размер атома бериллия позволяет организоваться тетраэдрической плотной упаковке в форме икосаэдра из атомов кислорода вокруг центрального атома бериллия. В результате повышается атомная плотность и плотность электронных состояний на уровне Ферми. Предлагаются модели для объяснения причины появления ферромагнетизма и электропроводности, которые обнаружены в бериллиевой керамике. С помощью метода спин-поляризованных электронов проведены расчеты электронной структуры нанокластеров с различным ближним порядком.
It is known that the introduction of TiO2 additives into BeO ceramics after heat treatment in a reducing atmosphere is accompanied by a significant increase in electrical conductivity and the ability to absorb electromagnetic radiation in a wide frequency range. Until now, the mechanism of this influence has not been fully established. Using the methods of Lorentzian electron microscopy in a scanning electron microscope, as well as a vibration magnetometer, the manifestation of ferromagnetism was established. This feature of beryllium ceramics promotes the absorption of electromagnetic energy in bulk samples containing TiO2 nanoparticles. It was found that the presence of nanoparticles promotes the formation of the perovskite structure in the BeO + TiO2 sintering zones. In the structure of perovskite, polarization of molecules is possible due to the formation of polarons, which leads to deformation of the lattice and displacement of atoms. As a result of this displacement, a change in the short-range order in the perovskite structure occurs and to the formation of an icosahedral phase from the initial phase with a cuboctahedral structure. The small size of the beryllium atom makes it possible to organize a tetrahedral close packing in the form of an icosahedron of oxygen atoms around the central beryllium atom. As a result, the atomic density and the density of electronic states at the Fermi level increase. Models are proposed to explain the reasons for the appearance of ferromagnetism and electrical conductivity found in beryllium ceramics. Using the spin-polarized electron method, the electronic structure of nanoclusters with different short-range orders has been calculated.

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Держатели документа:
Сибирский федеральный университет, пр. Свободный, 79, 660041, Красноярск, Россия
Восточно-Казахстанский университет им. С. Аманжолова, ул. 30-ой Гвардейской дивизии, 34, 070002, Усть-Каменогорск, Республика Казахстан
Восточно-Казахстанский технический университет им. Д. Серикбаева, ул. Протозанова, 69, 070004, Усть-Каменогорск, Республика Казахстан
Национальный исследовательский Томский государственный университет, пр. Ленина, 36, 634050, Томск, Россия
Институт физики им. Л.В. Киренского, Академгородок, 50, стр. 38, 660036, Красноярск, Россия

Доп.точки доступа:
Павлов, А. В.; Квеглис, Людмила Иосифовна; Kveglis L. I.; Джес, А. В.; Сапрыкин, Д. Н.; Насибуллин, Р. Т.; Великанов, Дмитрий Анатольевич; Velikanov, D. A.; Немцев, Иван Васильевич; Nemtsev, I. V.; Шалаев, П. О.

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Temperature dependent structural, dielectric, Raman, piezoresponse and photoluminescence investigations in sol-gel derived BCZT ceramics / I. Coondoo, A. Krylov, D. K. Sharma [et al.] // Mater. Chem. Phys. - 2022. - Vol. 277. - Ст. 125526, DOI 10.1016/j.matchemphys.2021.125526. - Cited References: 82. - I.C. and J.S.K would like to acknowledge 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 FCT/MCTES. This work was partially developed within the scope of the project i3N, UIDB/50025/2020 & UIDP/50025/2020, financed by national funds through the FCT/MEC. Part of this work (A.K.) was supported by the Ministry of Science and Higher Education of the Russian Federation (grant no. 075-15-2021-588). This research used resources of 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 thank Dr. Gonzalo Irurueta, Center for Mechanical Engineering and Automation, University of Aveiro, Portugal and Dr. E. Venkata Ramana, Department of Physics, University of Aveiro, Portugal . - ISSN 0254-0584
Кл.слова (ненормированные):
Lead-free piezoelectrics -- Sol-gel -- Phase transitions -- Raman spectroscopy -- PFM -- Photoluminescence
Аннотация: 0.5Ba(Ti0.8Zr0.2)O3-0.5(Ba0.7Ca0.3)TiO3 [50BZT-50BCT or BCZT] based compounds have been the focus of a lot of research, particularly motivated by their high piezoelectric effect. However, the literature lacks an elaborate investigation of the phase transition behavior in BCZT ceramics obtained by wet chemistry processing. Here, we present an in-depth study on the temperature dependence of x-ray diffraction (XRD), Raman scattering, dielectric properties, local piezoresponse and photoluminescence (PL) to investigate the sequence of phase transitions in the BCZT ceramic synthesized via a chemical route. Phase formation was determined by Rietveld analysis of XRD data, while compositional homogeneity and elemental quantification of the compound was validated using energy dispersive x-ray spectroscopy (EDX) and x-ray photoelectron spectroscopy (XPS) studies. Detailed fitting of XPS data indicated the existence of Ti3+ species (∼6%) in the prepared BCZT. Phase transitions were examined by analyzing the modifications in the XRD profile of Bragg reflection {200} and anomalies observed in the temperature variation of dielectric and Raman spectra studied over a wide temperature range starting from 10K to beyond Curie temperature. Crystallographic transformation temperatures obtained from dielectric measurement agreed well with those assessed from the temperature evolution of Raman spectra. In addition to other transitions, Raman scattering results revealed the existence of a transition from to phase near −175 °C, a transition that has not been interpreted in BCZT (and generally not observed in parent BaTiO3 compound). The luminescence response was studied by photoluminescence (PL) spectroscopy in the temperature range 15–300 K. The position of the PL peak was observed to shift with temperature and discontinuities in the wavelength shift were noted near phase transitions. Evolution of domain morphology with temperature was examined by piezoresponse force microscopy technique. Consolidated results assign the phase sequence in sol-gel derived BCZT as: R(R3c)→-175±10°CR(R3m)→-50±10°CO→40±10°CT→120±10°CC.

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Держатели документа:
Department of Physics & CICECO – Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
DEMaC & CICECO – Aveiro Institute of Materials, University of Aveiro, Aveiro, 3810-193, Portugal
School of Natural Sciences and Mathematics, Ural Federal University, Ekaterinburg, 620026, Russian Federation
I3N-Aveiro, Department of Physics, University of Aveiro, Aveiro, 3810-193, Portugal
Physical Materials Science and Composite Materials Centre, Research School of Chemistry & Applied Biomedical Sciences, National Research Tomsk Polytechnic University, Tomsk, 634050, Russian Federation

Доп.точки доступа:
Coondoo, I.; Krylov, A. S.; Крылов, Александр Сергеевич; Sharma, D. K.; Krylova, S. N.; Крылова, Светлана Николаевна; Alikin, D.; Kumar, J. S.; Mirzorakhimov, A.; Melnikova, N.; Soares, M. J.; Kholkin, A. L.
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10.

    Enhanced luminescence properties of Li2MgTiO4: Mn4+, Ge4+ phosphor via single cation substitution for indoor plant cultivation / S. Zhang, S. Gai, X. Zhang [et al.] // Ceram. Int. - 2022. - Vol. 48. Is. 3. - P. 3070-3080, DOI 10.1016/j.ceramint.2021.10.082. - 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) . - ISSN 0272-8842
   Перевод заглавия: Улучшение люминесцентных свойств люминофора Li2MgTiO4: Mn4+, Ge4+ путем замещения одного катиона при выращивании комнатных растений
Кл.слова (ненормированные):
Mn4+ -- Titanate -- Cationic substitution -- Indoor plant cultivation
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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School of Pharmaceutical Sciences, Jishou University, Jishou, 416000, China
School of Chemistry and Materials Science, Hunan Agricultural University, Changsha, 410128, China
Hunan Provincial Engineering Technology Research Center for Optical Agriculture, Hunan Agricultural University, Changsha, 410128, China
College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, 410128, China
Xiangfeng Tea Group Co. Ltd, No. 139 Tianhua North Road, Changsha, Hunan, China
Hunan Rare Earth Metal Material Research Institute Co. Ltd, No. 108 Longyuan 2nd Road, Longping High-tech Park, Changsha, Hunan, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Zhang, S.; Gai, S.; Zhang, X.; Xia, M.; Zhou, Z.; Cheng, X.; Yao, M.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Feng, Q.
}
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