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A Challenge toward novel quaternary sulfides SrLnCuS3 (Ln = La, Nd, Tm): Unraveling synthetic pathways, structures and properties / A. V. Ruseikina, M. V. Grigoriev, L. A. Solovyov [et al.] // Int. J. Mol. Sci. - 2022. - Vol. 23, Is. 20. - Ст. 12438, DOI 10.3390/ijms232012438. - Cited References: 62. - The research was funded by the Tyumen Oblast Government, as part of the West-Siberian Interregional Science and Education Center’s project No. 89-DON (3). This work was supported by state assignment of the Ministry of Science and Higher Education of the Russian Federation (Project Reg. No. 720000Φ.99.1.Б385AA13000) . - ISSN 1422-0067
Кл.слова (ненормированные):
inorganic materials -- quaternary sulfide -- synthesis -- crystal structure -- ab initio calculations -- magnetic measurements -- spectroscopy
Аннотация: We report on the novel heterometallic quaternary sulfides SrLnCuS3 (Ln = La, Nd, Tm), obtained as both single crystals and powdered samples. The structures of both the single crystal and powdered samples of SrLaCuS3 and SrNdCuS3 belong to the orthorhombic space group Pnma but are of different structural types, while both samples of SrTmCuS3 crystallize in the orthorhombic space group Cmcm with the structural type KZrCuS3. Three-dimensional crystal structures of SrLaCuS3 and SrNdCuS3 are formed from the (Sr/Ln)S7 capped trigonal prisms and CuS4 tetrahedra. In SrLaCuS3, alternating 2D layers are stacked, while the main backbone of the structure of SrNdCuS3 is a polymeric 3D framework [(Sr/Ln)S7]n, strengthened by 1D polymeric chains (CuS4)n with 1D channels, filled by the other Sr2+/Ln3+ cations, which, in turn, form 1D dimeric ribbons. A 3D crystal structure of SrTmCuS3 is constructed from the SrS6 trigonal prisms, TmS6 octahedra and CuS4 tetrahedra. The latter two polyhedra are packed together into 2D layers, which are separated by 1D chains (SrS6)n and 1D free channels. In both crystal structures of SrLaCuS3 obtained in this work, the crystallographic positions of strontium and lanthanum were partially mixed, while only in the structure of SrNdCuS3, solved from the powder X-ray diffraction data, were the crystallographic positions of strontium and neodymium partially mixed. Band gaps of SrLnCuS3 (Ln = La, Nd, Tm) were found to be 1.86, 1.94 and 2.57 eV, respectively. Both SrNdCuS3 and SrTmCuS3 were found to be paramagnetic at 20-300 K, with the experimental magnetic characteristics being in good agreement with the corresponding calculated parameters.

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Держатели документа:
Laboratory of Theory and Optimization of Chemical and Technological Processes, University of Tyumen, Tyumen, 625003, Russian Federation
Federal Research Center KSC SB RAS, Institute of Chemistry and Chemical Technology, Krasnoyarsk, 660036, Russian Federation
Institute of Natural Sciences and Mathematics, Ural Federal University named after the First President of Russia B.N. Yeltsin, Mira Str. 19, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk, 660079, Russian Federation
Institute of Physics and Technology, University of Tyumen, Volodarskogo Str. 6, Tyumen, 625003, Russian Federation
Institute of Inorganic Chemistry, University of Stuttgart, Stuttgart, D-70569, Germany
Scientific and Educational and Innovation Center for Chemical and Pharmaceutical Technologies, Ural Federal University named after the First President of Russia B.N. Yeltsin, Mira Str. 19, Russian Federation
«Advanced Materials for Industry and Biomedicine» Laboratory, Kurgan State University, Sovetskaya Str. 63/4, Kurgan, 640020, Russian Federation
University of Tyumen, Volodarskogo Str. 6, Tyumen, 625003, Russian Federation

Доп.точки доступа:
Ruseikina, A. V.; Grigoriev, M. V.; Solovyov, L. A.; Chernyshev, V. A.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Krylova, S. N.; Крылова, Светлана Николаевна; Shestakov, N. P.; Шестаков, Николай Петрович; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Garmonov, A. A.; Matigorov, A. V.; Eberle, M. A.; Schleid, T.; Safin, D. A.
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    An effect of reduced S-rich fluids on diamond formation under mantle-slab interaction / Y. V. Bataleva [et al.] // Lithos. - 2019. - Vol. 336-337. - P. 27-39, DOI 10.1016/j.lithos.2019.03.027. - Cited References: 73. - This work was supported by the Russian Science Foundation under Grant No. 14-27-00054 and a state assignment of IGM SB RAS. The authors thank S. Ovchinnikov for his assistance in implementation of the Mossbauer spectroscopy measurements. . - ISSN 0024-4937
   Перевод заглавия: Влияние восстановленных S-обогащенных флюидов на образование алмаза при взаимодействии мантиевых плит
Кл.слова (ненормированные):
Sulfur-rich fluid -- Iron carbide -- Diamond -- Mantle sulfides -- High-pressure experiment
Аннотация: Experimental study, dedicated to understanding the effect of S-rich reduced fluids on the diamond-forming processes under subduction settings, was performed using a multi-anvil high-pressure split-sphere apparatus in Fe3C-(Mg,Ca)CO3-S and Fe0-(Mg,Ca)CO3-S systems at the pressure of 6.3 GPa, temperatures in the range of 900–1600 °C and run time of 18–60 h. At the temperatures of 900 and 1000 °C in the carbide-carbonate-sulfur system, extraction of carbon from cohenite through the interaction with S-rich reduced fluid, as well as C0-producing redox reactions of carbonate with carbide were realized. As a result, graphite formation in assemblage with magnesiowüstite, cohenite and pyrrhotite (±aragonite) was established. At higher temperatures (≥1100 °C) formation of assemblage of Fe3+-magnesiowüstite and graphite was accompanied by generation of fO2-contrasting melts - metal-sulfide with dissolved carbon (Fe-S-C) and sulfide-oxide (Fe-S-O). In the temperature range of 1400–1600 °C spontaneous diamond nucleation was found to occur via redox interactions of carbide or iron with carbonate. It was established, that interactions of Fe-S-C and Fe-S-O melts as well as of Fe-S-C melt and magnesiowüstite, were С0-forming processes, accompanied by disproportionation of Fe. These resulted in the crystallization of Fe3+-magnesiowüstite+graphite assemblage and growth of diamond. We show that a participation of sulfur in subduction-related elemental carbon-forming processes results in sharp decrease of partial melting temperatures (~300 °C), reducting the reactivity of the Fe-S-C melt relatively to FeC melt with respect to graphite and diamond crystallization and decrease of diamond growth rate.

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Держатели документа:
Sobolev Institute of Geology and Mineralogy, Mineralogy Siberian Branch of the Russian Academy of Sciences, Academican Koptyug Ave., 3, Novosibirsk, 630090, Russian Federation
Novosibirsk State University, Pirogova str., 2, Novosibirsk, 630090, Russian Federation
Kirensky Institute of Physics, Siberian Branch of Russian Academy of Sciences, Akademgorodok 50, bld. 38, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Bataleva, Y. V.; Palyanov, Y. N.; Borzdov, Y. M.; Novoselov, I. D.; Bayukov, O. A.; Баюков, Олег Артемьевич
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Antiferromagnet-ferromagnet transition in alpha-MnxS manganese sulfides / G. A. Petrakovskii [et al.] // Phys. Solid State. - 2001. - Vol. 43, Is. 3. - P. 493-495 ; Phys. Solid State. - 2001. - Vol. 43, Is. 3. - P. 493-495, DOI 10.1134/1.1356126. - Cited References: 7 . - ISSN 1063-7834. - Вариант Sopus

РУБ Physics, Condensed Matter

Аннотация: Off-stoichiometric manganese monosulfides alpha -MnxS (1 less than or equal to x less than or equal to 1.25) are synthesized, and their crystal structure and magnetic properties are studied in the 4.2- to 300-K range. The compounds have a NaCl fcc lattice. Increasing the manganese ion concentration x in the antiferromagnetic semiconductors alpha -MnxS is found to result in concentration- (x(c) similar to 1.05) and temperature-driven (T-c similar to 50 K) magnetic transitions from the antiferromagnetic to ferromagnetic state, with the cubic structure remaining unchanged. (C) 2001 MAIK "Nauka/Interperiodica".

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Держатели документа:
Russian Acad Sci, Siberian Div, Kirenskii Inst Phys, Krasnoyarsk 660036, Russia
Krasnoyarsk State Univ, Krasnoyarsk 660041, Russia
ИФ СО РАН
Kirenskii Inst. of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Krasnoyarsk State University, Krasnoyarsk, 660041, Russian Federation
Kirenskii Inst. of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Krasnoyarsk State University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Petrakovskii, G. A.; Петраковский, Герман Антонович; Ryabinkina, L. I.; Рябинкина, Людмила Ивановна; Abramova, G. M.; Абрамова, Галина Михайловна; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Bovina, A. F.; Бовина, Ася Федоровна

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Beznosikov, B. V.
Crystal chemistry and structure of expected compounds A2BX4. II. Oxides, selenides, and sulfides 061A2B6+X4 2- and 080A2 2+B4+X4 2-. / B. V. Beznosikov, K. S. Aleksandrov // Sov. Phys.: Crystallogr. - 1985. - Vol. 30, Is. 5. - P. 533-535 ; Crystallography Reports ; Kristallografiya
Аннотация: Predictions of A2BX4 compounds for compositions 071A2 +B6+X4 2- with type structures of K2MgF4, beta -K2SO4, spinel, olivine, thenardite, phenacite, Sr2PbO4, and Pb3O4 are presented. K2MgF4 type structures are known and probable only in oxides and sulphides with hexavalent uranium because their formation is limited by the size of the hexavalent B cation. Structures of the beta -K2SO4 type are stable in compounds with large A cations. Among the sulphides with 076A2 +B6+X4 2-, the spinel crystal structure is as yet unknown, but is most probable in compounds with A+ = Li, Na, Ag, and with B6+ = Mo, W, and U. The olivine type structure is known only in Ag2CrO4, and no new compounds with this structure are expected to be found. A phenacite structure is probable only in three new oxides and in some sulphides with Li as A+. A thenardite type structure is probable in oxides with B6+ = Fe and Mn, but sulphides are unlikely. For 076A2 2+B4+X4 2- compounds with large A2+ ions and B4+ ions with radii from 0.57 A to RB 0.48RA + 0.11, a K2MgF4 structure would exist. For even larger A ions, the Sr2PbO4 structure would exist. In oxides with cations A2+ = Pb and Sn, compounds with Pb3O4 type structures are probable.-D.F.P.

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Публикация на русском языке Безносиков, Борис Валерьевич. Кристаллохимия и структуры ожидаемых соединений A2BX4. II. Оксиды, сульфиды, селениды составов A2[+]B[6+]X4[2-],A2[2+]D[4+]X4[2-1] [Текст] / Б. В. Безносиков, К. С. Александров // Кристаллография. - 1985. - Т. 30 Вып. 5. - С. 919-922

Держатели документа:
Siberian Branch of the Academy of Sciences, USSR.

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

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Beznosikov, B. V.
Crystal chemistry and structure of expected compounds A2BX4. III. Oxides, sulfides, and selenides 076A2 3+B2+X4 2-. / B. V. Beznosikov, K. S. Aleksandrov // Sov. Phys.: Crystallogr. - 1985. - Vol. 30, Is. 5. - P. 535-536 ; Crystallography Reports ; Kristallografiya
Аннотация: Predictions are made for A2BX4 compounds with the composition 076A3+B2+X4 2- having the structural types of K2MgF4, spinel, olivine, phenacite, Th3P4 and Fe2CaO4. Of the >2000 new compounds possible for A2BX4, about 40% will have spinel-type structures, 14% will be of the phenacite type, 13% of the olivine type, 10% of the Fe2CaO4 type, 9% of the beta -K2SO4 type, and 8% of the K2MgF4 type.-D.F.P.

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Публикация на русском языке Безносиков, Борис Валерьевич. Кристаллохимия и структуры ожидаемых соединений A2BX4. III. Оксиды, сульфиды, селениды составов A2[3+]B[2+]X4[2-1] [Текст] / Б. В. Безносиков, К. С. Александров // Кристаллография. - 1985. - Т. 30 Вып. 5. - С. 923-926

Держатели документа:
Inst. of Physics, Siberian Branch of Academy of Sciences, USSR.

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

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Crystal structure and electrical properties of Gd (x) Mn1-x S and Ti (x) Mn1-x Se solid solutions / A. I. Galyas [et al.] // Phys. Solid State. - 2010. - Vol. 52, Is. 4. - P. 687-690, DOI 10.1134/S1063783410040037. - Cited References: 10. - This study was supported by the Belarussian Republican Foundation for Fundamental Research (project no. F04-182), the Russian Foundation for Basic Research-Belarussian Republican Foundation for Fundamental Research (project no. 08-02-90031), the Russian Foundation for Basic Research (project nos. 09-02-00554-a and 09-02-92001-NNS-a), and the Federal Agency for Education of the Russian Federation (the State Program "Development of the Scientific Potential of the Higher School," project no. 2.1.1/401). . - ISSN 1063-7834

РУБ Physics, Condensed Matter
Рубрики:
MNSE
SULFIDES
CO
Аннотация: Regions of the existence of sulfide Gd (x) Mn1 - x S and selenide Ti (x) Mn1 - x Se solid solutions have been identified. Their electrical and thermoelectric properties have been studied in the temperature range 80-900 K. It has been established that the substitution of Gd2+ and Ti2+ ions for Mn2+ cations initiates reversal of the type of charge carrier with respect to the starting compounds MnS and MnSe. The cation substitution in solid solutions brings about a change from the hole conduction (alpha 0) characteristic of the manganese monosulfide and monoselenide to the electronic conduction (alpha 0).

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Держатели документа:
[Galyas, A. I.
Demidenko, O. F.
Makovetskii, G. I.
Yanushkevich, K. I.] Natl Acad Sci Belarus, Sci Pract Mat Res Ctr, Minsk 220072, Byelarus
[Ryabinkina, L. I.
Romanova, O. B.] Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
[Ryabinkina, L. I.
Romanova, O. B.] Reshetnev Siberian State Aerosp Univ, Krasnoyarsk 660014, Russia
ИФ СО РАН
Scientific-Practical Materials Research Centre, National Academy of Sciences of Belarus, ul. P. Brovki 19, Minsk, 220072, Belarus
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Akademgorodok 50, Krasnoyarsk, 660036, Russian Federation
Reshetnev Siberian State Aerospace University, pr. im. Gazety Krasnoyarskii Rabochii 31, Krasnoyarsk, 660014, Russian Federation

Доп.точки доступа:
Galyas, A. I.; Demidenko, O. F.; Makovetskii, G. I.; Yanushkevich, K. I.; Ryabinkina, L. I.; Рябинкина, Людмила Ивановна; Romanova, O. B.; Романова, Оксана Борисовна
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Electrical Conductivity and Thermopower in CoxMn1-xS Sulfides / G. I. Makovetskii [et al.] // Phys. Solid State. - 2008. - Vol. 50, Is. 10. - P. 1826-1829, DOI 10.1134/S1063783408100065. - Cited References: 6. - This study was supported by the Russian-Belarussian Foundation for Basic Research within the framework of the joint programs RFFI-BRFFI ( project no. RFFI-BRFFI 04-02-81018-Bel-2004a and project no. BRFFI-RFFIF04R-025). . - ISSN 1063-7834

РУБ Physics, Condensed Matter

Аннотация: This paper reports on the results of investigations into the structural, electrical, and thermoelectrical properties of sulfides CoxMn1-xS (0 0), whereas the compound with x = 0.4 exhibits metallic conduction (alpha 0). It is found that the band gap E-g of the compounds under investigation varies in the range from 1.46 eV for alpha-MnS (x

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Держатели документа:
[Makovetskii, G. I.
Galyas, A. I.
Demidenko, O. F.
Yanushkevich, K. I.] Natl Acad Sci, Joint Inst Solid State & Semicond Phys, Minsk 220072, Byelarus
[Ryabinkina, L. I.
Romanova, O. B.] Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia
ИФ СО РАН
Joint Institute of Solid-State and Semiconductor Physics, National Academy of Sciences of Belarus, ul. Petrusya Brovki 19, Minsk 220072, Belarus
Kirensky Institute of Physics, Siberian Branch, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk 660036, Russian Federation

Доп.точки доступа:
Makovetskii, G. I.; Galyas, A. I.; Demidenko, O. F.; Yanushkevich, K. I.; Ryabinkina, L. I.; Рябинкина, Людмила Ивановна; Romanova, O. B.; Романова, Оксана Борисовна
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Evolution of structural, thermal, optical, and vibrational properties of Sc2S3, ScCuS2, and BaScCuS3 semiconductors / N. O. Azarapin, A. S. Oreshonkov, I. A. Razumkova [et al.] // Eur. J. Inorg. Chem. - 2021. - Vol. 2021, Is. 33. - P. 3355-3366, DOI 10.1002/ejic.202100292. - Cited References: 50. - The work was partially carried out using the resources of the Research Resource Center "Natural Resources Management and Physico-Chemical Research" (Tyumen University) with financial support from the Ministry of Science and Higher Education of the Russian Federation (contract No. 05.594.21.0019, UIN RFMEFI59420X0019). The Raman spectroscopic studies were carried out at the collaborative research center for vibrational spectroscopy at ISSC UB RAS (Ekaterinburg, Russia). I.I.L. would like to acknowledge the support from the Research Program No. AAAA-A19-119031890025-9 (ISSC UB RAS). The use of the equipment of Krasnoyarsk Regional Center of Research Equipment of the Federal Research Center "Krasnoyarsk Science Center SB RAS" is acknowledged." The authors are grateful to Dr. Elena V. Vladimirova (ISSC UB RAS) for technical assistance . - ISSN 1434-1948. - ISSN 1099-0682

РУБ Chemistry, Inorganic & Nuclear
Рубрики:
RARE-EARTH
QUATERNARY CHALCOGENIDES
CRYSTAL-STRUCTURES
Кл.слова (ненормированные):
Complex sulfides -- Density functional calculations -- DTA -- Polychalcogenides -- Rare earths
Аннотация: In the present work, we report on the synthesis of Sc2S3, ScCuS2 and BaScCuS3 powders using a method based on oxides sulfidation and modification of their properties. The crystal structures and morphology of samples are verified by XRD and SEM techniques. Thermal stability has been studied by DTA which has revealed that Sc2S3 decomposes to ScS through melting at 1877 K. ScCuS2 and BaScCuS3 melt incongruently at temperatures of 1618 K and 1535 K, respectively. The electronic structure calculations show that the investigated compounds are semiconductors with indirect band gap (Eg). According to the diffuse reflection spectroscopy, Sc2S3, ScCuS2 and BaScCuS3 are wide-bandgap semiconductors featured the Eg values of 2.53 eV, 2.05 eV and 2.06 eV, respectively. The band gap decreases with the introduction of copper (I) and barium cations into the crystal structure of the compounds. Variation of local structure has been verified by Raman and infrared spectroscopy. The calculated vibrational modes of ScCuS2 correspond to CuS4 and Sc−S layer vibrations, even though ScS6 octahedra-like structural units can be found in the structure.

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Держатели документа:
Tyumen State Univ, Dept Inorgan & Phys Chem, Tyumen 625003, Russia.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Lab Mol Spect, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Engn & Construct, Krasnoyarsk 660041, Russia.
RAS, Fed Res Ctr KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
RAS, Fed Res Ctr KSC SB, Inst Chem & Chem Technol, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Ural Branch, Inst Solid State Chem, Ekaterinburg 620990, Russia.

Доп.точки доступа:
Azarapin, N. O.; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Razumkova, I. A.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Maximov, N. G.; Leonidov, I. I.; Shestakov, N. P.; Шестаков, Николай Петрович; Andreev, O. V.; Ministry of Science and Higher Education of the Russian Federation [05.594.21.0019, UIN RFME-FI59420X0019]; ISSC UB RAS [AAAA-A19-119031890025-9]
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First-principles calculations to investigate optical, phonon and electronic properties of quaternary sulfides SrRECuS3 (RE = La, Nd, Tm) / V. A. Chernyshev, A. V. Ruseikina, M. V. Grigoriev [et al.] // Inorg. Chem. Commun. - 2024. - Vol. 165. - Ст. 112449, DOI 10.1016/j.inoche.2024.112449. - Cited References: 43. - This work was supported by The Ministry of Science and Higher Education of the Russian Federation (project No. FEUZ-2023-0017) . - ISSN 1387-7003. - ISSN 1879-0259
Кл.слова (ненормированные):
Rare-earth elements -- Quaternary sulfide -- Optical properties -- Ab initio calculations -- Spectroscopy
Аннотация: The structure and properties of three layered heterometallic quaternary sulfides SrLaCuS3, SrNdCuS3 and SrTmCuS3 were studied for the first time using first-principles calculations in the stoichiometric and nonstoichiometric approximations. The applied DFT-based computations were performed using a hybrid functional with the contribution of nonlocal exchange in the Hartree-Fock formalism. It was revealed that the nonstoichiometry of SrLaCuS3 and SrNdCuS3 must be considered for modeling phonon spectra, elastic properties and band gaps. The wavenumbers and types of the Raman and "silent" modes at the Г-point were determined. From the analysis of displacement vectors, the degree of participation of ions in each mode was determined. The elastic constants and elastic moduli of the reported sulfides were calculated.

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Держатели документа:
Institute of Natural Sciences and Mathematics, Ural Federal University named after the First President of Russia B.N. Yeltsin, Ekaterinburg 620002, Russian Federation
University of Tyumen, Tyumen 625003, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russian Federation
Scientific and Educational and Innovation Center for Chemical and Pharmaceutical Technologies, Ural Federal University named after the First President of Russia B.N. Yeltsin, Ekaterinburg 620002, Russian Federation

Доп.точки доступа:
Chernyshev, V. A.; Ruseikina, A. V.; Grigoriev, M. V.; Krylova, S. N.; Крылова, Светлана Николаевна; Safin, D. A.
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10.

Giant magnetoresistance of MexMn1-xS (Me = Fe, Cr) sulfides / G. A. Petrakovskii [et al.] // JETP Letters. - 2000. - Vol. 72, Is. 2. - P. 70-72, DOI 10.1134/1.1312014. - Cited References: 6 . - ISSN 0021-3640

РУБ Physics, Multidisciplinary

Аннотация: The structural, electrical, and magnetic properties, as well as the magnetoresistance of polycrystalline MexMn1-xS (Me = Fe and Cr) sulfides were investigated in longitudinal magnetic fields of up to 50 kOe over the temperature range 4.2-300 K. The ferromagnetic compound FexMn1-xS (x = 0.29) exhibits the giant magnetoresistance (GMR) effect with magnitude delta(H) = -450% in a field of 30 kOe at 50 K. Antiferromagnetic CrxMn1-xS (x = 0.5) sulfide undergoes a transition to the GMR state (delta(H) similar to -25% in a field of 30 kOe at 4.2 K) in the region of antiferromagnet-ferromagnet transition (T-c similar to 66 K). A mechanism of the GMR in these compounds is discussed. (C) 2000 MAIK "Nauka/Interperiodica".

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Держатели документа:
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Div, Krasnoyarsk 660036, Russia
Krasnoyarsk State Univ, Krasnoyarsk 660062, Russia
ИФ СО РАН

Доп.точки доступа:
Petrakovskii, G. A.; Петраковский, Герман Антонович; Ryabinkina, L. I.; Рябинкина, Людмила Ивановна; Abramova, G. M.; Абрамова, Галина Михайловна; Balaev, A. D.; Балаев, Александр Дмитриевич; Balaev, D. A.; Балаев, Дмитрий Александрович; Bovina, A. F.; Бовина, Ася Федоровна
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