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

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Каталог книг и брошюр библиотеки ИФ СО РАН

Каталог журналов библиотеки ИФ СО РАН

Труды сотрудников ИФ СО РАН

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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kirillov V. L., Balaev D. A., Semenov S. V., Shaikhutdinov K. A., Martyanov O. N.
Заглавие : Size control in the formation of magnetite nanoparticles in the presence of citrate ions
Коллективы : Siberian Branch of the Russian Academy of Sciences
Место публикации : Mater. Chem. Phys.: Elsevier Science, 2014. - Vol. 145, Is. 1-2. - P.75-81. - ISSN 0254-0584, DOI 10.1016/j.matchemphys.2014.01.036. - ISSN 1879-3312
Примечания : Cited References: 46. - This work was supported by the Interdisciplinary Integration Project no. 45 of the Siberian Branch of the Russian Academy of Sciences for 2012-2014.
Предметные рубрики: OLEIC-ACID
CATALYST
HYPERTHERMIA
PARTICLES
OXIDATION
REMOVAL
CO
Ключевые слова (''Своб.индексиров.''): magnetic materials--magnetic properties--precipitation--electron paramagnetic resonance
Аннотация: A one-pot synthesis method for the controllable growth of magnetite nanoparticles directly during the process of co-precipitation using citrate ions was developed. The effects of the concentration of citrate ions and the solution pH on the characteristics of magnetite particles with sizes in the range of 4-10 nm synthesized by the method of co-precipitation were studied. The results showed that the specified concentration of citrate ions allowed the preparation of magnetite particles with a definite size that exhibited superparamagnetic behaviour in a particular temperature range. As the concentration ratio of citrate to iron ions was increased from 0 to 0.11, the average size of the prepared magnetite particles decreased from 10.5 to 4.4 nm. As a result, the superparamagnetic blocking temperature decreased from 300 to 20 K, the saturation magnetisation decreased from 50 to 20 emu g(-1), and the average magnetic moment decreased from 8000 mu(B) to 340 mu(B) (at T = 300 K). The obtained experimental data proved that the size effects of the magnetite nanoparticles can be attributed to the capping of the magnetite surface by adsorbed citrate ions. Thus, the suggested approach allows magnetite nanoparticles to be prepared with an optimum particle size around superparamagnetic threshold that prevents their irreversible agglomeration and simultaneously allows them to be removed from a solution at an acceptable rate. (C) 2014 Elsevier B.V. All rights reserved.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Myagkov V. G., Tambasov I. A., Bayukov O. A., Zhigalov V. S., Bykova L. E., Mikhlin Yu. L., Volochaev M. N., Bondarenko G. N.
Заглавие : Solid state synthesis and characterization of ferromagnetic nanocomposite Fe-In2O3 thin films
Место публикации : J. Alloys Compd.: Elsevier Science, 2014. - Vol. 612. - P.189-194. - ISSN 0925-8388, DOI 10.1016/j.jallcom.2014.05.176. - ISSN 1873-4669
Примечания : Cited References: 56
Предметные рубрики: HIGH-TEMPERATURE FERROMAGNETISM
PHASE-FORMATION
In2O
OXIDE
NANOPARTICLES
CO
SEMICONDUCTORS
NANOCRYSTALS
COMBUSTION
SYSTEMS
Ключевые слова (''Своб.индексиров.''): thermite reactions--reactive films--ferromagnetic nanocomposite films--transparent conducting oxides
Аннотация: We have successfully synthesized ferromagnetic Fe-In2O 3 nanocomposite thin films for the first time using the thermite reaction Fe2O3 + In = In2O3 + Fe. The initial In/Fe2O3 bilayers were obtained by the deposition of In layers on α-Fe2O3 films. The reaction occurs in a self-propagating mode in a homogeneous thermal film plane field at heating rates above 20 K/s and at temperatures above initiation temperature T[[d]]in[[/d]] ~ 180 °C. At heating rates lower than 20 K/s the mixing of the In and Fe2O3 layers occurs across the whole In/Fe2O3 interface and the synthesis of the ferromagnetic α-Fe phase starts above the initiation temperature T[[d]]in[[/d]] = 180 °C. X-ray diffraction, X-ray photoelectron spectroscopy, Mossbauer spectroscopy, transmission electron microscopy and magnetic measurements were used for phase identification and microstructure observation of the synthesized Fe-In2O3 samples. The reaction products contain (1 1 0) textured α-Fe nanocrystals with a diameter around 100 nm and surrounded by an In2O3 matrix. These results enable new efficient low-temperature methods for synthesizing ferromagnetic nanocomposite films containing ferromagnetic nanoclusters embedded in transparent conducting oxides. © 2014 Elsevier B.V. All rights reserved.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Vereshchagin S. N., Solov'ev L. A., Rabchevskii E. V., Dudnikov V. A., Ovchinnikov S. G., Anshits A. G.
Заглавие : New method for regulating the activity of ABO3 perovskite catalysts
Коллективы : Council of the President of the Russian Federation for Support of Young Scientists and Leading Scientific Schools [NSh-2886.2014.2]
Место публикации : Kinet. Catal.: MAIK Nauka-Interperiodica / Springer, 2015. - Vol. 56, Is. 5. - P.640-645. - ISSN 0023, DOI 10.1134/S0023158415040199. - ISSN 16083210(eISSN)
Примечания : Cited References:23. - This work was supported in part by the Council of the President of the Russian Federation for Support of Young Scientists and Leading Scientific Schools (grant no. NSh-2886.2014.2).
Предметные рубрики: MEMBRANE REACTORS
METHANE COMBUSTION
OXIDATION
OXIDES
OXYGEN
PERFORMANCE
FEATURES
PHASES
CO
Ключевые слова (''Своб.индексиров.''): perovskite--cobalt--methane--deep oxidation--oxidative condensation
Аннотация: A new possibility of changing the activity and selectivity of perovskite catalysts in the oxidative conversion of methane was demonstrated using the Sr x Gd1–x CoO3–δ (0.5 x 0.9) compounds as an example. It was established that, at the same chemical composition, the disordering of Sr2+/Gd3+ ions over the A positions of the crystal structure led to a significant increase in activity in the deep oxidation reaction of CH4, as compared with the samples with an ordered distribution of cations.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhandun V. S., Zinenko V. I.
Заглавие : The effect of structural ordering on the magnetic, electronic, and optical properties of the LaPbMnSbO6 double perovskite
Коллективы : Russian Foundation for Basic Research [15-02-00340-a]; Russian Federation [NSH-924.2014.2]
Место публикации : J. Alloys Compd.: Elsevier Science, 2016. - Vol. 671. - P.184-191. - ISSN 0925-8388, DOI 10.1016/j.jallcom.2016.02.085. - ISSN 1873-4669(eISSN)
Примечания : Cited References:32. - This work was supported by the Russian Foundation for Basic Research, project no. 15-02-00340-a and the Grant of the President of the Russian Federation for Support of Leading Scientific Schools no. NSH-924.2014.2.
Предметные рубрики: SYSTEMS
NI
CO
Ключевые слова (''Своб.индексиров.''): ab initio calculation--double perovskite--magnetic materials--optical--properties--electronic properties--magnetic properties--layer compound
Аннотация: The interplay between the magnetic, electronic, and optical properties and the cation structural ordering in the LaPbMnSbO6 double perovskite is studied using the Vienna Ab Initio Simulation Package (VASP). The layer and rock-salt cation ordering types are investigated. Both of them are of great importance. The rock-salt ordering of B-site cations is one of the most frequently met cation ordering types in double perovskites; the layer ordering of both cations, which can be considered as a heterostructure, is interesting for fundamental research and experimental synthesis. It was established that the properties of the two investigated structures are strongly different. The compound with the layered structure exhibits the behavior typical of a semimetal with the ferromagnetic configuration of magnetic moments, which is unusual for a double perovskite. The rock-salt structure behaves as an antiferromagnetic insulator. Another surprising feature of the structure with the layer ordering is the coexistence of a polar phase and the metal-type conductivity. The calculated optical characteristics of the two ordered structures are compared with the experimental dates. (C) 2016 Elsevier B.V. All rights reserved.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Galyas A. I., Demidenko O. F., Makovetskii G. I., Yanushkevich K. I., Ryabinkina L. I., Romanova O. B.
Заглавие : Crystal structure and electrical properties of Gd (x) Mn1-x S and Ti (x) Mn1-x Se solid solutions
Коллективы :
Разночтения заглавия :авие SCOPUS: Crystal structure and electrical properties of GdxMn1 - xS and TixMn1 - xSe solid solutions
Место публикации : Phys. Solid State: MAIK NAUKA/INTERPERIODICA/SPRINGER, 2010. - Vol. 52, Is. 4. - P687-690. - ISSN 1063-7834, DOI 10.1134/S1063783410040037
Примечания : 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).
Предметные 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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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Iskhakov R. S., Komogortsev S. V., Chekanova L. A., Balaev A. D., Yuzova V. A., Semenova O. V.
Заглавие : The magnetic structure of ferromagnetic filaments of a CoNi(P) alloy in a porous silicon matrix
Место публикации : Tech. Phys. Lett.: AMER INST PHYSICS, 2003. - Vol. 29, Is. 4. - P263-266. - ISSN 1063-7850, DOI 10.1134/1.1573285
Примечания : Cited References: 12
Предметные рубрики: RANDOM ANISOTROPY
NI NANOWIRES
NANOCRYSTALLINE
FILMS
CO
FE
Аннотация: The magnetic and resonance properties of CoNi(P) alloys, synthesized by chemical deposition as films on single crystal silicon substrates and as filaments in linear pores of porous silicon substrates, were studied by magnetization and ferromagnetic resonance measurements. It is established that CoNi(P) alloys of the same composition but different morphologies occur in states characterized by different degrees of nonequilibrium, which is manifested by different modes of the magnetization approach to saturation. (C) 2003 MAIK "Nauka / Interperiodica".
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhigalov V. S., Frolov G. I., Kveglis L. I.
Заглавие : Nanocrystalline cobalt films prepared under ultrafast condensation conditions
Место публикации : Phys. Solid State: MAIK NAUKA/INTERPERIODICA/SPRINGER, 1998. - Vol. 40, Is. 11. - P1878-1883. - ISSN 1063-7834, DOI 10.1134/1.1130677
Примечания : Cited References: 12
Предметные рубрики: IRON FILMS
SUPERLATTICES
GROWTH
FE
CO
Аннотация: The magnetic and electrical properties and the temperature dependence of these properties of cobalt films prepared at high condensation rates (10(5)-10(6) Angstrom/s) are investigated. Incremented annealing reveals several nonequilibrium states of cobalt in transition from the as-prepared metastable structure to the ordinary hcp structure. The anomalies of the properties are analyzed from the standpoint of the nanocrystalline state of the samples. Model concepts of microcluster formations in the investigated films are also discussed. (C) 1998 American Institute of Physics. [S1063-7834(98)02411-3].
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Ji-Cai, Savchenko, Viktoriia, Kimberg V., Gel'mukhanov F., Odelius, Michael
Заглавие : High-resolution x-ray spectra of carbon monoxide reveal ultrafast dynamics induced by long UV pulse
Коллективы : RFBRRussian Foundation for Basic Research (RFBR) [19-29-12015]; National Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [11974108, 11574082]; Fundamental Research Funds for the Central UniversitiesFundamental Research Funds for the Central Universities [2021MS046]; European UnionEuropean Commission [860553]; Carl Tryggers Foundation [CTS18:285]; Helmholtz Virtual Institute [VI419]; Swedish Research CouncilSwedish Research CouncilEuropean Commission [VR 2019-03470, 2018-05973]
Место публикации : New J. Phys. - 2021. - Vol. 23, Is. 6. - Ст.063030. - ISSN 1367-2630, DOI 10.1088/1367-2630/ac0198
Примечания : Cited References: 47. - The reported study was funded by RFBR, project number 19-29-12015. J-CL thanks the support by the National Science Foundation of China under Grant Nos. 11974108, 11574082, and the Fundamental Research Funds for the Central Universities (No. 2021MS046). MO acknowledges funding from the European Union's Horizon 2020 research and innovation programme under the Marie Skodowska-Curie Grant Agreement No. 860553 and the Carl Tryggers Foundation (contract CTS18:285). FG acknowledges also the support from the Helmholtz Virtual Institute VI419 'Dynamic Pathways in Multidimensional Landscapes'. VK acknowledges the Swedish Research Council (VR 2019-03470). The calculations were partially enabled by resources provided by the Swedish National Infrastructure for Computing (SNIC) partially funded by the Swedish Research Council through Grant Agreement No. 2018-05973
Предметные рубрики: VIBRATIONAL STRUCTURE
SCATTERING
RAMAN
CO
COLLAPSE
PROBE
Аннотация: In theoretical simulations of a UV + x-ray pump-probe (UVX-PP) setup, we show that frequency detuning of the pump UV pulse acts as a camera shutter by regulating the duration of the UVX-PP process. This two-photon absorption with long overlapping UV and x-ray pulses, allowing for high spectral resolution, thereby provides information about ultrafast dynamics of the nuclear wave packet without the requirement of ultrashort pulses and controlled delay times. In a case study of carbon monoxide, the calculated UVX-PP spectra of the O1s−12π1 and C1s−12π1 core-excited states show different vibrational profiles. The interference of intermediate vibrational states reveals details of nuclear dynamics in the UVX-PP process related to a variable duration time controlled by the UV detuning. Both O1s−12π1 and C1s−12π1 pump-probe channels display a splitting of the spectral profile, which however is associated with different physical mechanisms. At the O1s−12π1 resonance, the observed dispersive and non-dispersive spectral bands intersect and result in destructive interference.
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