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1.


   
    Antiferromagnetism of the cation-ordered warwickite system Mn2-xMgxBO4 (x=0.5, 0.6 and 0.7) / N. V. Kazak, N. A. Belskaya, E. M. Moshkina [et al.] // J. Magn. Magn. Mater. - 2020. - Vol. 507. - Ст. 166820, DOI 10.1016/j.jmmm.2020.166820. - Cited References: 39. - The reported study was funded by the Russian Foundation for Basic Research (no. 20-02-00559), Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science to the research project. 18-42243007. . - ISSN 0304-8853. - ISSN 1873-4766
РУБ Materials Science, Multidisciplinary + Physics, Condensed Matter
Рубрики:
SPIN-GLASS BEHAVIOR
   CRYSTAL-STRUCTURES

   SINGLE-CRYSTALS

   INSIGHTS

   MGFEBO4

Кл.слова (ненормированные):
Warwickites -- Antiferromagnet -- Cation ordering -- Jahn-Teller distortions
Аннотация: X-ray diffraction, heat capacity and magnetic measurements are performed on single crystals of Mn2-xMgxBO4 (x = 0.5, 0.6 and 0.7) with the warwickite structure. The monoclinic symmetry is found for all samples with the space group P21/n. The M1 site is occupied by trivalent Mn ions while the M2 site is occupied by a mixture of divalent Mg and Mn ions. Regular cation and charge distributions are observed, which is unusual for heterometallic warwickites. The local octahedral distortions of M1O6 show the monotonic dependence on the Mg content and are in accordance with the Jahn-Teller distortion. All samples are found to undergo long-range antiferromagnetic ordering with rather low transition temperatures of TN = 16, 14 and 13 K for x = 0.5, 0.6, and 0.7, respectively. The ordering of local octahedral distortions, caused by the strong electron-phonon interaction of the trivalent Mn ions, is proposed to stabilise the cationic ordering and, as a result, the long-range magnetic ordering in the material.

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Держатели документа:
FRC SB RAS, Kirensky Inst Phys, Krasnoyarsk, Russia.
Reshetnev Siberian State Univ Sci & Technol, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.
RAS, Zavoisky Phys Tech Inst, FRC Kazan Sci Ctr, Kazan, Russia.
Kazan Volga Reg Fed Univ, Kazan, Russia.

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Belskaya, N. A.; Moshkina, E. M.; Мошкина, Евгения Михайловна; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Sofronova, S. N.; Софронова, Светлана Николаевна; Eremina, R. M.; Eremin, E. V.; Еремин, Евгений Владимирович; Muftakhutdinov, A. R.; Cherosov, M. A.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [20-02-00559]; Government of Krasnoyarsk Territory; Krasnoyarsk Regional Fund of Science to the research project [18-42243007]
}
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2.


    Aplesnin, S. S.
    Change in the magnetocapacity in the paramagnetic region in a cation-substituted manganese selenide / S. S. Aplesnin, M. N. Sitnikov, A. M. Zhivul'ko // Phys. Solid State. - 2018. - Vol. 60, Is. 4. - P. 673-680, DOI 10.1134/S1063783418040029. - Cited References:19. - This work is supported by the Russian Foundation for Basic Research (project no. 17-32-50080), grant no. 16-52-00045 Bel_a, and state task no. 3.5743.2017/6.7. . - ISSN 1063-7834. - ISSN 1090-6460
РУБ Physics, Condensed Matter
Рубрики:
MULTIFERROICS
Аннотация: The capacity and the dielectric loss tangent of a Gd x Mn1–xSe (x ≤ 0.2) solid solution have been measured in the frequency range 1–300 kHz without a magnetic field and in a magnetic field of 8 kOe in the temperature range 100–450 K, and the magnetic moment of the solid solution has been measured in a field of 8.6 kOe. The magnetocapacity effect and the change in the magnetocapacity sign have been observed in room temperature in the paramagnetic region. A correlation of the changes in the dielectric permittivity and the magnetic susceptibility with temperature has been revealed. The magnetocapacity is described using the model with orbital electron ordering and the Maxwell–Wagner model.

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Публикация на русском языке Аплеснин, Сергей Степанович. Смена знака магнитоемкости в парамагнитной области в катион-замещенном селениде марганца [Текст] / С. С. Аплеснин, М. Н. Ситников, А. М. Живулько // Физ. тверд. тела. - 2018. - Т. 60 Вып. 4. - С. 670-676

Держатели документа:
Reshetnev Siberian State Aerosp Univ, Krasnoyarsk 660014, Russia.
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Natl Acad Sci Belarus, Sci Pract Mat Res Ctr, Minsk 220072, Byelarus.

Доп.точки доступа:
Sitnikov, M. N.; Zhivul'ko, A. M.; Аплеснин, Сергей Степанович; Russian Foundation for Basic Research [17-32-50080, 16-52-00045 Bel_a, 3.5743.2017/6.7]
}
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3.


    Bayukov, O. A.
    The prognostication possibility of some magnetic-properties for dielectrics on the basis of covalency parameters of ligand cation bonds / O. A. Bayukov, A. F. Savitskii // Phys. Status Solidi B. - 1989. - Vol. 155, Is. 1. - P. 249-255, DOI 10.1002/pssb.2221550125. - Cited References: 27 . - ISSN 0370-1972
РУБ Physics, Condensed Matter


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Доп.точки доступа:
Savitskii, A. F.; Баюков, Олег Артемьевич
}
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4.


    Belyaev, B. A.
    Impedance spectroscopy study of the electrical properties of cation-substituted barium hexaaluminate ceramics / B. A. Belyaev, N. A. Drokin, V. A. Poluboyarov // Phys. Solid State. - 2018. - Vol. 60, Is. 2. - P. 274-280, DOI 10.1134/S1063783418020063. - Cited References:18 . - ISSN 1063-7834. - ISSN 1090-6460
РУБ Physics, Condensed Matter
Рубрики:
DIELECTRIC-RELAXATION
   LIQUID-CRYSTALS

   SPECTRA

Аннотация: We report on the behavior of frequency and temperature dependences of the impedance of a measuring cell in the form of a parallel-plate capacitor filled with barium hexaaluminate ceramics with four aluminum cations replaced by iron (BaO · 2Fe2O3 · 4Al2O3). The measurements have been performed in the frequency range of 0.5–108 Hz at temperatures of 20-375°C. A technique for determining the electrical properties of the investigated ceramics is proposed, which is based on an equivalent electric circuit allowing the recorded impedance spectra to be approximated with sufficiently high accuracy. The established spectral features are indicative of the presence of two electric relaxation times different from each other by three orders of magnitude. This fact is explained by the difference between the charge transport processes in the bulk of crystallites and thin intercrystallite spacers, for which the charge activation energies have been determined.

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Публикация на русском языке Беляев, Борис Афанасьевич. Исследование электрофизических характеристик катион-замещенной керамики гексаалюмината бария методом импедансной спектроскопии [Текст] / Б. А. Беляев, Н. А. Дрокин, В. А. Полубояров // Физ. тверд. тела. - 2018. - Т. 60 Вып. 2. - С. 269–275

Держатели документа:
Russian Acad Sci, Kirensky Inst Phys, Fed Res Ctr KSC SB RAS, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Siberian State Aerosp Univ, Krasnoyarsk 660014, Russia.
Russian Acad Sci, Inst Solid State Chem & Mechanochem, Siberian Branch, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Drokin, N. A.; Дрокин, Николай Александрович; Poluboyarov, V. A.; Беляев, Борис Афанасьевич
}
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5.


    Beznosikov, B. V.
    Prediction of pra-phases of layered perovskite-like structures with cation vacancies / B. V. Beznosikov, K. S. Aleksandrov // J. Struct. Chem. - 2002. - Vol. 43, Is. 1. - P. 172-175, DOI 10.1023/A:1016098521933 . - ISSN 0022-4766

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РИНЦ,
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Публикация на русском языке Безносиков, Борис Валерьевич. Прогноз прафаз слоистых перовскитоподобных структур с катионными вакансиями [Текст] / Б. В. Безносиков, К. С. Александров // Журн. структ. химии. - Новосибирск : Изд-во СО РАН, 2002. - Т. 43 № 1. - С. 184-187


Доп.точки доступа:
Aleksandrov, K. S.; Александров, Кирилл Сергеевич; Безносиков, Борис Валерьевич
}
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6.


   
    Blue-shift of Eu2+ emission in (Ba,Sr)3Lu(PO4)3:Eu2+ eulytite solid-solution phosphors resulting from release of neighbouring-cation-induced stress / Z. Y. Wang [et al.] // Dalton Trans. - 2014. - Vol. 43, Is. 44. - P. 16800-16804, DOI 10.1039/c4dt02319f. - Cited References: 16. - The present work was supported by the National Natural Science Foundations of China (grant no. 51002146, no. 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in the University of the Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635) and the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306). V.V.A. is partly supported by the Ministry of Education and Science of the Russian Federation. . - ISSN 1477-9226. - ISSN 1477-9234
   Перевод заглавия: Синее смещение излучения Eu2+ в твердых растворах (Ba,Sr)3Lu(PO4)3:Eu2 со структурой эулита, вызванное снятием напряжения, индуцированного соседними катионами
РУБ Chemistry, Inorganic & Nuclear
Рубрики:
TUNABLE COLOR TONE
   EXCITED WHITE LEDS

   CRYSTAL-STRUCTURE

   TEMPERATURE

   IONS

Аннотация: A series of iso-structural eulytite-type (Ba,Sr)(3)Lu(PO4)(3):Eu2+ solid-solution phosphors with different Sr/Ba ratios were synthesized by a solid-state reaction. Crystal structures of (Ba,Sr)(3)Lu(PO4)(3):Eu2+ were resolved by the Rietveld method, which shows an eulytite-type cubic Bi-4(SiO4)(3) structure with cations disordered in a single C-3 site while the oxygen atoms were distributed over two partially occupied sites. The emission peaks of Ba(3-x)SrxLu(PO4)(3):Eu2+ (0

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
SB RAS, Inst Semicond Phys, Lab Opt Mat & Struct, Novosibirsk 630090, Russia
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia
Novosibirsk State Univ, Lab Semicond & Dielect Mat, Novosibirsk 630090, Russia

Доп.точки доступа:
Wang, Z. Y.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Атучин, Виктор Валерьевич; Liu, Q. L.
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7.


   
    Cation Distribution in the Composite Materials of the CaFe2O4-α-Fe2O3 Series / Y. V. Knyazev [et al.] // J. Struct. Chem. - 2019. - Vol. 60, Is. 5. - P. 763-771, DOI 10.1134/S0022476619050081. - Cited References: 25. - The study was performed with the financial support of the Russian Foundation for Basic Research, the Government of the Krasnoyarsk Krai, the Krasnoyarsk Regional Science Foundation within the project No. 18-42-243011 "The effect of the composition and the defective structure of CaFe2O4 based "core-shell" composite materials on their electronic and catalytic properties" and the UMNIK program. . - ISSN 0022-4766. - ISSN 1573-8779
РУБ Chemistry, Inorganic & Nuclear + Chemistry, Physical
Рубрики:
PD/P-TYPE CAFE2O4
   OXYGEN

   CONDUCTIVITY

Кл.слова (ненормированные):
solid-phase synthesis -- scanning electron microscopy -- Mössbauer spectroscopy -- cation vacancies
Аннотация: Structured composite materials CaFe2O4-α-Fe2O3 (α-Fe2O3 content is 2–82 wt.%) are obtained with the method of solid-phase synthesis at 1000 °C. The phase composition of the samples is studied using powder X-ray diffraction. It is shown that the content of CaFe2O4 and α-Fe2O3 phases changes linearly, depending on the composition of the starting material. The scanning electron microscopy data indicate the formation of a two-phase system α-Fe2O3-CaFe2O4. The Mössbauer spectroscopy data at room temperature testify the formation of cationic iron vacancies in the CaFe2O4 crystal structure in the absence of α-Fe2O3 structural defects. Cationic vacancies can be formed during the synthesis in the atmosphere of air.

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Публикация на русском языке Особенности катионного распределения в композиционных материалах ряда СaFe2O4—α-Fe2O3 [Текст] / Ю. В. Князев [и др.] // Журн. структ. химии. - 2019. - Т. 60 № 5. - С. 796-805

Держатели документа:
Russian Acad Sci, Kirensky Inst Phys, Siberian Branch, Fed Krasnoyarsk Res Ctr, Krasnoyarsk, Russia.
Russian Acad Sci, Inst Chem & Chem Technol, Siberian Branch, Fed Krasnoyarsk Res Ctr, Krasnoyarsk, Russia.

Доп.точки доступа:
Knyazev, Yu. V.; Князев, Юрий Владимирович; Shishkina, N. N.; Bayukov, O. A.; Баюков, Олег Артемьевич; Kirik, N. P.; Solovyov, L. A.; Zhizhaev, A. M.; Rabchevsky, E. V.; Anshits, A. G.; Russian Foundation for Basic Research; Government of the Krasnoyarsk Krai; Krasnoyarsk Regional Science Foundation [18-42-243011]; UMNIK program
}
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8.


   
    Cation substitution dependent bimodal photoluminescence in whitlockite structural Ca3-xSrx(PO4)2:Eu2+ (0 ≤ x ≤ 2) solid solution phosphors / H. P. Ji [et al.] // Inorg. Chem. - 2014. - Vol. 53, Is. 20. - P. 11119-11124, DOI 10.1021/ic501679f. - Cited References: 37. - This work was supported by the National Natural Science Foundations of China (Grant Nos. 51032007, 51002146, 51272242), the Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20130022110006), the Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), and Beijing Youth Excellent Talent Program (YETP0635). V.V.A. acknowledges the Ministry of Education and Science of the Russian Federation for financial support. . - ISSN 0020-1669. - ISSN 1520-510X
   Перевод заглавия: Катион зависимая бимодальная люминесценция в твердом растворе Ca3-xSrx(PO4)2:Eu2+ (0 ˂ x ˂ 2) со структурой витлокита
РУБ Chemistry, Inorganic & Nuclear
Рубрики:
LIGHT-EMITTING-DIODES
   EFFICIENT ENERGY-TRANSFER

   EMISSION-TUNABLE PHOSPHOR

   EXCITED WHITE LEDS

   CRYSTAL-STRUCTURE

   LUMINESCENCE PROPERTIES

   Mn2+ PHOSPHOR

   COLOR TONE

   PHASE

   Eu2+

Аннотация: Cation substitution dependent tunable bimodal photoluminescence behavior was observed in the Ca3-xSrx(PO4)2:Eu2+ (0 ≤ x ≤ 2) solid solution phosphors. The Rietveld refinements verified the phase purity and whitlockite type crystal structure of the solid solutions. The tunable photoluminescence evolution was studied as a function of strontium content, over the composition range 0.1 ≤ x ≤ 2. In addition to the emission band peak at 416 nm in Ca3(PO4)2:Eu2+, the substitution of Ca2+ by Sr2+ induced the emerging broad-band peak at 493-532 nm. A dramatic red shift of the emission peak located in the green-yellow region was observed on an increase of x in the samples with 0.75 ≤ x ≤ 2.00. The two emission bands could be related to the EuOn-Ca9 and EuOn-Ca9-xSrx emitting blocks, respectively. The values for the two kinds of emitting blocks in the solid solutions can be fitted well with the observed intensity evolution of the two emission peaks.

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Держатели документа:
China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
SB RAS, LV Kirensky Phys Inst, Lab Crystal Phys, Krasnoyarsk 660036, Russia
SB RAS, Inst Semicond Phys, Lab Opt Mat & Struct, Novosibirsk 630090, Russia
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia
Novosibirsk State Univ, Lab Semicond & Dielect Mat, Novosibirsk 630090, Russia
Univ Auckland, Dept Chem & Mat Engn, Auckland 1142, New Zealand

Доп.точки доступа:
Ji, H. P.; Huang, Z. H.; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Атучин, Виктор Валерьевич; Huang, S. F.
}
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9.


   
    Cation-substituted TmXMn1-XS solid solutions with special magnetic and electrical properties / O. B. Romanova [et al.] // 20th Int. Conf. on Magnetism (ICM-2015) : book of abstracts. - 2015. - P. 241
Рубрики:
Semiconductor spintronics

Материалы конференции

Доп.точки доступа:
Romanova, O. B.; Романова, Оксана Борисовна; Aplesnin, S. S.; Аплеснин, Сергей Степанович; Galyas, A. I.; Галяс А. И.; Yanushkevich, K. I.; Янушкевич, Казимир Иосифович; Sokolov, V. V.; Соколов В. В.; International Conference on Magnetism(20 ; 2015 ; Jul ; 5-10 ; Barselona, Spain)
}
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10.


   
    Controllable two-dimensional luminescence tuning in Eu2+,Mn2+ doped (Ca,Sr)9Sc(PO4)7 based on crystal field regulation and energy transfer / S. S. Liang [et al.] // J. Mater. Chem. C. - 2018. - Vol. 6, Is. 25. - P. 6714-6725, DOI 10.1039/c8tc01825a. - Cited References: 63. - This work was financially supported by the National Natural Science Foundation of China (NSFC No. 51672265, 51672266, 21521092, 51750110511, 51672257, and 51672259), the Key Research Program of Frontier Sciences of CAS (Grant No. YZDY-SSW-JSC018), the National Basic Research Program of China (2014CB643803), the Scientific and Technological Department of Jilin Province (Grant No. 20150520029JH and 20170414003GH), Jiangmen Innovative Research Team Program (2017) and Major Program of Basic Research and Applied Research of Guangdong Province (2017KZDXM083), the Russian Science Foundation (Grant No. 17-12-01047), and the Distinguished Scientist Fellowship Program of King Saud University, as well as the Deanship of Scientific Research at King Saud University through research group no. (RG-1939-038). . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Контролируемое двухпараметрическое управление люминесценцией в допированном Eu2+,Mn2+ (Ca,Sr)9Sc(PO4)7, основанное на регуляции кристаллического поля и переноса энергии
РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
SOLID-SOLUTION PHOSPHORS
   LIGHT-EMITTING-DIODES

   CATION SUBSTITUTION

Аннотация: Currently, controllable luminescence tuning and the generation of single component white emission are viable strategies to modify and optimize the luminescence performances of phosphors, which offer appealing prospects for the w-LED lighting industry. In this paper, we designed two-dimensional (2D) tunable color coordinates on the CIE diagram in the Eu2+,Mn2+ doped (Ca,Sr)9xSc(PO4)7 system by a combination of crystal field regulation and the energy transfer method. X-ray powder diffraction (XRD) and Rietveld refinement were utilized to analyze the phase composition and structural variation of the studied phosphors. The transmission electron microscopy (TEM) and photoluminescence spectra were exploited to analyze the generation of nanosegregation. The effects of the schedule of cation substitutions and energy transfer on the photoluminescence properties were investigated in detail. The corresponding luminescence mechanisms of the red-shifted emission with Sr2+ → Ca2+ substitution and Eu2+ → Mn2+ energy transfer were deeply discussed and proposed. In addition, the temperature-dependent thermal quenching behavior and the electroluminescence (EL) performance of the fabricated w-LED devices were also investigated to characterize the prepared Ca9(1−0.03−x−y)Sr9xSc(PO4)7:0.27Eu2+,9yMn2+. Finally, a representative w-LED device composed of a 369 nm UV chip and Ca9(1−0.03−0.02−0.5)Sr4.5Sc(PO4)7:0.27Eu2+,0.18Mn2+ could present excellent EL performance with the parameters CRI = 88, CCT = 3122 K and color coordinate (0.45, 0.44), which could well meet the commercial standard of warm white light. Therefore, our results suggest that this two-step luminescence tuning method is feasible to be applied in other phosphor systems for obtaining efficient white emitting phosphors.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, 388 Lumo Rd, Wuhan 430074, Peoples R China.
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Qingdao Univ, Sch Chem & Chem Engn, Qingdao 266071, Peoples R China.
King Saud Univ, Coll Appl Med Sci, Dept Dent Hlth, Riyadh, Saudi Arabia.
Wuyi Univ, Sch Appl Phys & Mat, Jiangmen 529020, Guangdong, Peoples R China.

Доп.точки доступа:
Liang, S. S.; Dang, P. P.; Li, G. G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Wei, Y.; Lian, H. Z.; Shang, M. M.; Al Kheraiff, A. A.; Lin, J.
}
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11.


   
    Crystal growth and cation order of Ni3-xCoxB2O6 oxyborates / S. Sofronova, E. Moshkina, A. Chernyshev [et al.] // CrystEngComm. - 2024, DOI 10.1039/D4CE00091A. - Cited References: 28. - The research was funded by Russian Science Foundation and Krasnoyarsk Regional Fund of Science, project № 23-12-20012 (https://rscf.ru/en/project/23-12-20012/) . - Article in press. - ISSN 1466-8033
Аннотация: A series of single crystals of Ni3-xCoxB2O6 compounds with the kotoite structure and with different concentrations of transition metal ions (x = 0; 0,19; 0,6; 0,93; 2) were obtained. The lattice parameters and atomic coordinates were determined using X-ray diffraction. The theoretical calculations using the WIEN2k package predict that nickel ions tend to occupy the 4f crystallographic position, while cobalt ions tend to occupy the 2a crystallographic positions. The study of the diffuse scattering spectra and comparison of the Racah parameters for the compounds Ni3B2O6 and Co2NiB2O6 provides experimental evidence that the nickel ions occupy crystallographic position 4f.

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Держатели документа:
Kirensky Institute of Physics of the Federal Research Center "Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences", 660036 Krasnoyarsk, Russia
Institute of Chemistry and Chemical Technology SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Russia

Доп.точки доступа:
Sofronova, S. N.; Софронова, Светлана Николаевна; Moshkina, E. M.; Мошкина, Евгения Михайловна; Chernyshev, A.; Чернышев, Артем Валерьевич; Vasil'ev, A. D.; Васильев, Александр Дмитриевич; Maximov, N.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Andryushchenko, T.; Андрющенко, Татьяна Александровна; Shabanov, A. V.; Шабанов, Александр Васильевич
}
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12.


   
    Crystal structure of enrofloxacinium tetrabromidodichloridostannate(IV) monohydrate / N. N. Golovnev [et al.] // J. Struct. Chem. - 2013. - Vol. 54, Is. 2. - P. 377-382, DOI 10.1134/S0022476613020157. - Cited References: 17. - The work was supported by the grant of the President of the Russian Federation for the support of leading scientific schools of the Russian Federation (NSh-4828.2012.2) and the Federal Targeted Program "Scientific and Scientific Pedagogical Personnel of Innovative Russia, 2009-2013" (State contracts Nos. 02.740.11.0269 and 02.740.11.0629). . - ISSN 0022-4766
РУБ Chemistry, Inorganic & Nuclear + Chemistry, Physical
Рубрики:
COMPLEX
Кл.слова (ненормированные):
crystal structure -- enrofloxacinium cation -- tetrabromidodichloridostannate(IV) anion -- hydrogen bonds
Аннотация: A new compound EnrH(3)[SnBr3.46Cl2.54]center dot H2O, where EnrH (3) (2+) is the enrofloxacinium cation (C19H24FN3O (3) (2+) ), is synthesized and its crystal and molecular structure is determined. Crystallographic data for enrofloxacinium tetrabromidodichloridostannate(IV) monohydrate are as follows: a = 17.1262(19) , b = 10.3435(11) , c = 17.2582(19) , beta = 119.203(1)A degrees, V = 2640.5(4) (3), space group P2(1)/c, Z = 4. Hydrogen bonds form a branched three-dimensional network linking EnrH (3) (2+) , [SnBr3.46Cl2.54](2-), and water molecules. The structure is also stabilized by the pi-pi interaction of EnrH (3) (2+) aromatic rings.

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Публикация на русском языке Кристаллическая структура моногидрата тетрабромидодихлоридостанната(IV) энрофлоксациния // Журнал структурной химии. - 2013. - Т. 54, № 2. - С. 325-330

Держатели документа:
Siberian Fed Univ, Krasnoyarsk, Russia
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Div, Krasnoyarsk, Russia

Доп.точки доступа:
Golovnev, N. N.; Головнёв, Николай Николаевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Golovneva, I. I.; Головнева И.И.; Glushchenko, G. A.; Глущенко, Гарий Анатольевич
}
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13.


   
    Dielectric properties of a mixed-valence Pb3Mn7O15 manganese oxide / N. V. Volkov [et al.] // J. Phys.: Condens. Matter. - 2010. - Vol. 22, Is. 37. - Ст. 375901, DOI 10.1088/0953-8984/22/37/375901. - Cited References: 14. - This study was supported by the Russian Foundation for Basic Research 'Siberia', project No. 09-02-98003, and the Siberian Branch of the Russian Academy of Sciences, integration project No. 101. . - ISSN 0953-8984
РУБ Physics, Condensed Matter

Кл.слова (ненормированные):
cation -- lead -- manganese derivative -- oxide -- article -- chemical model -- chemistry -- crystallization -- electric conductivity -- electronics -- methodology -- temperature -- Cations -- Crystallization -- Electric Conductivity -- Electronics -- Lead -- Manganese Compounds -- Models, Chemical -- Oxides -- Temperature -- AC electric field -- Analysis of resistivity -- Carrier hopping -- Charge ordering -- Complex dielectric constant -- Crystal site -- Debye models -- Dielectric constants -- Dielectric spectra -- Frequency windows -- Lattice sites -- Low frequency -- Manganese ions -- Mixed valence -- Mixed valence state -- Relaxation behaviors -- Temperature range -- Electric fields -- Manganese -- Manganese oxide -- Permittivity -- Single crystals -- Crystal symmetry
Аннотация: We investigated the low-frequency dielectric properties of a Pb3Mn7O15 single crystal with manganese ions in the mixed-valence state (Mn3+/Mn4+). Dielectric relaxation was found in the frequency window from 20 to 100 kHz in the temperature range 110-180 K. The dielectric spectra of the crystal were analyzed using a Debye model. Estimations made within the model and analysis of resistivity data suggest that the relaxation behavior of the dielectric constant is related to polaronic charge carrier hopping. Around 250 K, charge ordering occurs in the crystal when the Mn3+ and Mn4+ ions are arranged in a specific order among the crystal sites. With a decrease in temperature, an ac electric field can induce a charge hop between the equivalent lattice sites available, related to crystal symmetry. This hopping is equivalent to the reorientation of an electric dipole that yields Debye-type behavior of the complex dielectric constant. The observed anisotropy in the behavior of the dielectric properties and resistivity can be attributed to a pronounced two-dimensional character of the crystal structure.

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Держатели документа:
[Volkov, N. V.
Eremin, E. V.
Sablina, K. A.
Sapronova, N. V.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
ИФ СО РАН
L V Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk, Russia.
L V Kirensky Institute of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Volkov, N. V.; Волков, Никита Валентинович; Eremin, E. V.; Еремин, Евгений Владимирович; Sablina, K. A.; Саблина, Клара Александровна; Sapronova, N. V.
}
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14.


   
    Discovery of new narrow-band phosphors with the UCr4C4-related type structure by alkali cation effect / M. Zhao [et al.] // Adv. Opt. Mater. - 2019. - Vol. 7, Is. 6. - Ст. 1801631, DOI 10.1002/adom.201801631. - Cited References: 29. - This work was supported by the National Natural Science Foundations of China (Grant Nos. 51722202, 91622125, and 51572023) and Natural Science Foundations of Beijing (2172036). M.S.M. acknowledges the support of the Russian Foundation for Basic Research (No. 17-52-53031). . - ISSN 2195-1071
   Перевод заглавия: Открытие новых узкополосных люминофоров со структурой типа UCr4C4 с помощью замещения щелочных катионов
Кл.слова (ненормированные):
narrow-band emission -- phosphors -- photoluminescence -- substitution strategy -- white light-emitting diodes
Аннотация: Narrow-band luminescence materials used in white light-emitting diodes (WLEDs) have demonstrated a great potential to increase the maximum accessible color gamut, improve the color rendition, or enhance the visual luminous efficacy for illumination and display devices. So far, the discovery of narrow-band rare earth doped phosphors for emerging applications remains challenging owing to the limited systems in use and the broadening effect of 4f–5d transition. Here, two narrow-band cyan-emitting phosphors with the UCr4C4-related type structure, RbNa2K(Li3SiO4)4:Eu2+ (RNKLSO:Eu2+) and CsNa2K(Li3SiO4)4:Eu2+ (CNKLSO:Eu2+), are reported. The narrow-band emission results from the highly condensed network and a cube-like site for the activator (Eu2+). The emission peak assignments are investigated, and the variations of luminescence behavior with compositional changes of alkali cations are elaborated in detail. RNKLSO:8% Eu2+ (95%@250 °C of the integrated emission intensity at 25 °C) shows better thermal stability than that of CNKLSO:8% Eu2+ (79%@250 °C), which can be explained by the thermally activated crossover process represented in the configurational coordinate diagram. The optical properties of the as-fabricated WLEDs are studied and demonstrate potential with tunable properties for the full spectrum phosphor-converted LEDs. These findings in UCr4C4-type phases help shedding light on new avenues for fabricating new and totally unexpected narrow-emitting phosphors with versatile applications.

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Держатели документа:
The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing, 100083, China
State Key Laboratory of Luminescent Materials and Devices and Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, South China University of Technology, Guangzhou, 510641, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Zhao, M.; Zhou, Y.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Zhang, Q.; Liu, Q.; Xia, Z.
}
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15.


   
    Discovery of new solid solution phosphors via cation substitution-dependent phase transition in M-3(PO4)2:Eu2+ (M =Ca/Sr/Ba) quasi-binary sets / H. P. Ji [et al.] // J. Phys. Chem. C. - 2015. - Vol. 119, Is. 4. - P. 2038-2045, DOI 10.1021/jp509743r. - Cited References:48. - This work was supported by the National Natural Science Foundations ofChina (Grant Nos. 51032007, 51002146, and 51272242), the Research Fundfor the Doctoral Program of Higher Education of China (Grant No.20130022110006), the Natural Science Foundations of Beijing (2132050),the Program for New Century Excellent Talents in University of Ministryof Education of China (NCET-12-0950), the Beijing Nova Program(Z131103000413047), and Beijing Youth Excellent Talent Program(YETP0635). V.V.A. acknowledges the Ministry of Education and Science ofthe Russian Federation for financial support. . - ISSN 1932-7447
   Перевод заглавия: Открытие новых твердых растворов люминофоров посредством фазовых переходов при замещении катионов в квазибинарных составах M3(PO4)2:Eu2+ (M = Ca/Sr/Ba)
РУБ Chemistry, Physical + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary
Рубрики:
LIGHT-EMITTING-DIODES
   LUMINESCENCE PROPERTIES

   ENERGY-TRANSFER

Аннотация: The cation substitution-dependent phase transition was used as a strategy to discover new solid solution phosphors and to efficiently tune the luminescence property of divalent europium (Eu2+) in the M3(PO4)2:Eu2+ (M = Ca/Sr/Ba) quasi-binary sets. Several new phosphors including the greenish-white SrCa2(PO4)2:Eu2+, the yellow Sr2Ca(PO4)2:Eu2+, and the cyan Ba2Ca(PO4)2:Eu2+ were reported, and the drastic red shift of the emission toward the phase transition point was discussed. Different behavior of luminescence evolution in response to structural variation was verified among the three M3(PO4)2:Eu2+ joins. Sr3(PO4)2 and Ba3(PO4)2 form a continuous isostructural solid solution set in which Eu2+ exhibits a similar symmetric narrow-band blue emission centered at 416 nm, whereas Sr2+ substituting Ca2+ in Ca3(PO4)2 induces a composition-dependent phase transition and the peaking emission gets red shifted to 527 nm approaching the phase transition point. In the Ca3?xBax(PO4)2:Eu2+ set, the validity of crystallochemical design of phosphor between the phase transition boundary was further verified. This cation substitution strategy may assist in developing new phosphors with controllably tuned optical properties based on the phase transition.

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Держатели документа:
China Univ Geosci, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Sch Mat Sci & Technol, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia
SB RAS, Inst Semicond Phys, Lab Opt Mat & Struct, Novosibirsk 630090, Russia
Tomsk State Univ, Funct Elect Lab, Tomsk 634050, Russia
Novosibirsk State Univ, Lab Semicond & Dielect Mat, Novosibirsk 630090, Russia

Доп.точки доступа:
Ji, Haipeng; Huang, Zhaohui; Xia, Zhiguo; Molokeev, M. S.; Молокеев, Максим Сергеевич; Atuchin, V. V.; Fang, Minghao; Liu, Yangai
}
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16.


   
    Effect of A-site cation ordering on the thermoelectric properties of the complex cobalt oxides Gd1-xSrxCoO3-δ (x = 0.8 and 0.9) / V. A. Dudnikov [et al.] // Ceram. Int. - 2018. - Vol. 44, Is. 9. - P. 10299-10305, DOI 10.1016/j.ceramint.2018.03.037. - Cited References: 38. - This work was supported by the Russian Science Foundation , project no. 16-13-00060. . - ISSN 0272-8842
Кл.слова (ненормированные):
Substituted rare earth cobalt oxides -- Thermoelectric oxide materials -- Ordered and disordered states
Аннотация: The effect of substitution of Sr2+ ions for Gd3+ ions on the phase composition, electrical resistivity, thermoelectricity, and thermal conductivity of rare-earth cobalt oxides Gd1-xSrxCoO3-δ (x = 0.8 and 0.9) has been investigated. It has been determined that at the investigated strontium concentrations, the single-phase disordered nonstoichiometric cubic perovskites and superstructures with ordered Sr2+/Gd3+ ions and anion vacancies can be formed. The influence of ordering/disordering of Gd and Sr cations over crystal-lattice A- sites on the thermoelectric figure of merit and sample stability at high temperatures has been studied. The thermoelectric figure of merit of the disordered samples was found to exceed by far the analogous parameter of the ordered samples, which allows us to consider the disordering as a way of improving the thermoelectric parameters. Two contributions to the conductivities are discussed: high-temperature thermoactivation and low-temperatures variable range hopping. The parameters of the Mott electronic structure, including DOS N(εF), hopping energy ε (the energy of hopping conductivity activation), and hopping length Rh, have been estimated.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Ioffe Physical-Technical Institute, Russian Academy of Sciences, St. Petersburg, Russian Federation
Lebedev Physical Institute, Russian Academy of Sciences, Moscow, Russian Federation

Доп.точки доступа:
Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Kazak, N. V.; Казак, Наталья Валерьевна; Fedorov, A. S.; Федоров, Александр Семенович; Solov'yov, L. A.; Vereshchagin, S. N.; Burkov, A. T.; Novikov, S. V.; Gavrilkin, S. Yu.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
}
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17.


   
    Effect of cation ordering on a-sites on the physical properties of substituted rare-earth cobaltite oxides GD1-XSRXCOO3-Δ / V. A. Dudnikov [et al.] // Moscow International Symposium on Magnetism (MISM-2017) : 1-7 July 2017 : book of abstracts. - 2017. - Ст. 4PO-I-48. - P. 878

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Доп.точки доступа:
Dudnikov, V. A.; Дудников, Вячеслав Анатольевич; Orlov, Yu. S.; Орлов, Юрий Сергеевич; Gavrilkin, S. Yu.; Kazak, N. V.; Казак, Наталья Валерьевна; Platunov, M. S.; Платунов, Михаил Сергеевич; Solovyov, L. A.; Соловьев, Леонид Александрович; Vereshchagin, S. N.; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Moscow International Symposium on Magnetism(7 ; 2017 ; Jul. ; Moscow); Московский государственный университет им. М.В. Ломоносова; Российский фонд фундаментальных исследований
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18.


   
    Effect of cation substitution in fluorine-oxygen molybdates (NH4)(2-x) A (x) MoO2F4 / E. V. Bogdanov [et al.] // Phys. Solid State. - 2011. - Vol. 53, Is. 2. - P. 303-308, DOI 10.1134/S1063783411020065. - Cited References: 11. - This study was supported by the Russian Foundation for Basic Research (project no. 09-02-00062) and the Council on Grants from the President of the Russian Federation for Support of Leading Scientific Schools of the Russian Federation (project no. NSh-1011.2008.2). . - ISSN 1063-7834
РУБ Physics, Condensed Matter
Рубрики:
PHASE-TRANSITIONS
   CRYSTALS

   (NH4)(2)WO2F4

   DIFFRACTION

   OXYFLUORIDE

   MECHANISM

   DISORDER

Аннотация: Thermophysical and structural studies of (NH4)(2 - x) A (x) MoO2F4 (A = Cs, Rb, K) solid solutions of oxyfluorides have been performed. The character of the influence of cation substitutions on the stability of the initial phase (space group Cmcm) and on the mechanism of phase transitions has been elucidated.

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Держатели документа:
[Bogdanov, E. V.
Vasil'ev, A. D.
Flerov, I. N.] Russian Acad Sci, LV Kirensky Phys Inst, Siberian Branch, Krasnoyarsk 660036, Russia
[Vasil'ev, A. D.
Flerov, I. N.] Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660074, Russia
[Laptash, N. M.] Russian Acad Sci, Inst Chem, Far Eastern Branch, Vladivostok 690022, Russia
ИФ СО РАН
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk 660036, Russian Federation
Institute of Engineering Physics and Radioelectronics, Siberian Federal University, ul. Kirenskogo 28, Krasnoyarsk 660074, Russian Federation
Institute of Chemistry, Far Eastern Branch, Russian Academy of Sciences, pr. Stoletiya Vladivostoka 159, Vladivostok 690022, Russian Federation

Доп.точки доступа:
Bogdanov, E. V.; Богданов, Евгений Витальевич; Vasil'ev, A. D.; Васильев, Александр Дмитриевич; Flerov, I. N.; Флёров, Игорь Николаевич; Laptash, N. M.
}
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19.


   
    Effect of central cation substitution on the properties and phase transitions in (NH4)3Me(O2)2F4 oxyfluorides [Text] / V. D. Fokina, I. N. Flerov [et al.] // The 6th International Seminar on Ferroelastics Physics (ISFP-6) : Voronezh, September 22–25, 2009. - P43


Доп.точки доступа:
Fokina, V.D.; Flerov, I.N.; Molokeev, M.S.; Pogoreltsev, E.I.; Bogdanov, E.V.; Laptash, N.M.; International Seminar on Ferroelastic Physics(6 ; 2009 ; Sept. ; 22-25 ; Voronezh)
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20.


   
    Effect of central cation substitutionon the properties and phase transitions in (NH4)3Me(O2)2F4 oxyfluorides / V. D. Fokina, I. N. Flerov, M. S. Molokeev [et al.] // The 6th International Seminar on Ferroelastic Physics : abstract book. - Voronezh, 2009. - P. 5

Материалы конференции

Доп.точки доступа:
Fokina, V. D.; Фокина, Валентина Дмитриевна; Flerov, I. N.; Флёров, Игорь Николаевич; Molokeev, M. S.; Молокеев, Максим Сергеевич; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич; Bogdanov, E. V.; Богданов, Евгений Витальевич; Laptev, Y. V.; Воронежский государственный технический университет; Российская академия наук; International Seminar on ferroelastic physics (6 ; 2009 ; Sept. 22-25 ; Voronezh); Международный семинар по физике сегнетоэластиков (6(11) ; 2009 ; 22-25 сент. ; Воронеж)
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