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    Влияние реакционных условий на размер наночастиц серебра в концентрированных золях Carey Lea / С. А. Воробьев, М. Н. Лихацкий, А. С. Романченко [и др.] // Журн. СФУ. Химия. - 2020. - Т. 13, № 3. - С. 372-384 ; J. Sib. Fed. Univ. Chem., DOI 10.17516/1998-2836-0190. - Библиогр.: 34. - Работа выполнена при финансовой поддержке Российского научного фонда, грант No 18-73-00142 . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: The Influence of the Reaction Conditions on the Size of Silver Nanoparticles in Carey Lea's Concentrated Sols

РУБ Chemistry, Multidisciplinary
Рубрики:
AG NANOPARTICLES
   CITRATE
   AGGREGATION
   SURFACE
   STABILITY
   KINETICS
Кл.слова (ненормированные):
наночастицы серебра -- концентрированные золи -- влияние реакционных условий -- цитрат-ион -- silver nanoparticles -- concentrated sols -- influence of reaction conditions -- citrate ion
Аннотация: В данной работе был изучен процесс восстановления растворов Ag (I) цитратными комплексами Fe (II), который позволяет получать наночастицы серебра с высокой стабильностью и концентрацией более 60 г/л. В ходе работы было установлено влияние скорости введения, скорости перемешивания, концентрации реагентов, рН среды и некоторых постсинтетических операций на средний размер наночастиц. Показано, что снижение концентрации Ag (I) и повышение концентрации стабилизатора, доведение рН реакционной среды до 7 позволяют получать наиболее мелкие и однородные частицы. В результате были найдены оптимальные условия, которые дали возможность уменьшить размер частиц и вместе с тем снизить концентрацию реактивов на 33 %. По данным РФЭС, ПЭМ, DLS и ИК были получены наночастицы металлического серебра с размером 6.5±1.8 нм, стабилизированные продуктом частичного распада цитрат-иона.
The reaction of reduction solution of Ag (I) by Fe (II) citrate complex was studied herein. This allows you to receive silver nanoparticles with high stability with a concentration above 60 g/l. It was determined that the nanoparticles size depends on the injection rate, mixing rate, reagent concentration, pH and some post-synthetic operations on the average size of nanoparticles. It was shown that decreasing the concentration of Ag (I) and increasing the concentration of stabilizer also bringing pH to 7 lead to small and uniform particles. Optimal conditions were found that made it possible to reduce particle size and reduce the concentration of reagents by 33 % in the results. According to XPS, TEM, DLS and FTIR datas, nanoparticles of metallic silver with a size of 6.5±1.8 nm were obtained, which stabilized by the product of partial decay of the citrate ion.

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Держатели документа:
Институт химии и химической технологии ФИЦ «Красноярский научный центр СО РАН», Российская Федерация, Красноярск
Сибирский федеральный университет, Российская Федерация, Красноярск
Институт физики им. Киренского, КНЦ СО РАН, Российская Федерация, Красноярск
Сибирский государственный университет науки и технологий им. М.Ф. Решетнева, Российская Федерация, Красноярск

Доп.точки доступа:
Воробьев, С. А.; Лихацкий, М. Н.; Романченко, А. С.; Иваненко, Т. Ю.; Машарова, Д. А.; Волочаев, Михаил Николаевич; Volochaev, M. N.; Михлин, Ю. Л.; RUSSIAN SCIENCE FOUNDATIONRussian Science Foundation (RSF) [18-73-00142]

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    Thermokinetic study of intermetallic phase formation in an Al/Cu multilayer thin film system / E. T. Moiseenko, V. V. Yumashev, R. R. Altunin [et al.] // Materialia. - 2023. - Vol. 28. - Ст. 101747, DOI 10.1016/j.mtla.2023.101747. - Cited References: 53. - This work was supported by the Russian Science Foundation under grant # 22-13-00313 . - ISSN 2589-1529
   Перевод заглавия: Термокинетическое исследование образования интерметаллических фаз в многослойной тонкопленочной системе Al/Cu
Кл.слова (ненормированные):
Intermetallics -- Thin film -- Solid-state reaction -- Kinetics -- Differential scanning calorimetry -- Electron diffraction
Аннотация: The solid-state reaction process in a multilayer thin film system (Al/Cu)50 has experimentally been studied using the methods of simultaneous thermal analysis (STA) and in situ electron diffraction. A detailed kinetic analysis of the phase formation processes during the solid-state reaction has shown that the observed solid-state transformations can be described by a statistically significant kinetic model where each stage corresponds to the reaction of the n-th order with autocatalysis. The low-temperature stage has been demonstrated to be attributable to the formation of the θ-Al2Cu phase, with the medium-temperature and high-temperature ones corresponding to the α2-AlCu3 and γ1-Al4Cu9 phases, respectively. The kinetic parameters for the formation of the phases θ-Al2Cu, α2-AlCu3 and γ1-Al4Cu9 have been determined. It has been shown that the kinetic model describing the solid-state reaction in the Al–Cu multilayer thin film system is in best agreement with the experimental data in the case of a competition between the formation stages of the α2-AlCu3 and γ1-Al4Cu9 phases.

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Держатели документа:
Siberian Federal University, 660041 79 Svobodny ave., Krasnoyarsk, Russia
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, 660036 Krasnoyarsk, Russia

Доп.точки доступа:
Moiseenko, E. T.; Yumashev, V. V.; Altunin, R. R.; Solovyov, L. A.; Volochaev, M. N.; Волочаев, Михаил Николаевич; Belousov, O. V.; Zharkov, S. M.; Жарков, Сергей Михайлович
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    Thermokinetic study of aluminum-induced crystallization of a-Si: The effect of Al layer thickness / S. M. Zharkov, V. V. Yumashev, E. T. Moiseenko [et al.] // Nanomaterials. - 2023. - Vol. 13, Is. 22. - Ст. 2925, DOI 10.3390/nano13222925. - Cited References: 70. - This work was supported by the Russian Science Foundation under grant #22-13-00313 . - ISSN 2079-4991
   Перевод заглавия: Термокинетическое исследование кристаллизации a-Si, индуцированной алюминием: влияние толщины слоя Al
Кл.слова (ненормированные):
amorphous silicon -- Al/Si -- nanolayer -- multilayer film -- metal-induced crystallization -- aluminum-induced crystallization -- kinetics -- activation energy -- enthalpy -- simultaneous thermal analysis (STA)
Аннотация: The effect of the aluminum layer on the kinetics and mechanism of aluminum-induced crystallization (AIC) of amorphous silicon (a-Si) in (Al/a-Si)n multilayered films was studied using a complex of in situ methods (simultaneous thermal analysis, transmission electron microscopy, electron diffraction, and four-point probe resistance measurement) and ex situ methods (X-ray diffraction and optical microscopy). An increase in the thickness of the aluminum layer from 10 to 80 nm was found to result in a decrease in the value of the apparent activation energy Ea of silicon crystallization from 137 to 117 kJ/mol (as estimated by the Kissinger method) as well as an increase in the crystallization heat from 12.3 to 16.0 kJ/(mol Si). The detailed kinetic analysis showed that the change in the thickness of an individual Al layer could lead to a qualitative change in the mechanism of aluminum-induced silicon crystallization: with the thickness of Al ≤ 20 nm. The process followed two parallel routes described by the n-th order reaction equation with autocatalysis (Cn-X) and the Avrami–Erofeev equation (An): with an increase in the thickness of Al ≥ 40 nm, the process occurred in two consecutive steps. The first one can be described by the n-th order reaction equation with autocatalysis (Cn-X), and the second one can be described by the n-th order reaction equation (Fn). The change in the mechanism of amorphous silicon crystallization was assumed to be due to the influence of the degree of Al defects at the initial state on the kinetics of the crystallization process.

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Держатели документа:
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Laboratory of Electron Microscopy, Siberian Federal University, Krasnoyarsk 660041, Russia
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Zharkov, S. M.; Жарков, Сергей Михайлович; Yumashev, V. V.; Moiseenko, E. T.; Altunin, R. R.; Solovyov, L. A.; Volochaev, M. N.; Волочаев, Михаил Николаевич; Zeer, G. M.; Nikolaeva, N. S.; Belousov, O. V.
}
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Thermochemistry, structure, and optical properties of a new β-La2(SO4)3 polymorphic modification / S. A. Basova, M. S. Molokeev, A. S. Oreshonkov [et al.] // Inorganics. - 2023. - Vol. 11, Is. 11. - Ст. 434, DOI 10.3390/inorganics11110434. - Cited References: 58. - The work was partly carried out within the framework of the Strategic Academic Leadership Program “Priority-2030” for the Kazan Federal University and the state assignment of the Kirensky Institute of Physics. - We acknowledge Lisa-Marie Wagner (JLU Giessen) for help with X-ray powder diffractometry, and Svetlana Volkova and Irina Palamarchuk (UTMN) for help with IR- and UV-spectrometry. The use of equipment provided by the Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” is acknowledged . - ISSN 2304-6740
Кл.слова (ненормированные):
rare earths -- lanthanum -- sulfate -- crystal chemistry -- thermodynamics -- chemical kinetics -- dielectrics
Аннотация: A new polymorphic modification of lanthanum sulfate was obtained by thermal dehydration of the respective nonahydrate. According to powder X-ray diffraction, it was established that β-La2(SO4)3 crystallized in the C2/c space group of the monoclinic system with the KTh2(PO4)3 structure type (a = 17.6923(9), b = 6.9102(4), c = 8.3990(5) Å, β = 100.321(3)°, and V = 1010.22(9) Å3). Temperature dependency studies of the unit cell parameters indicated almost zero expansion along the a direction in the temperature range of 300–450 K. Presumably, this occurred due to stretching of the [LaO9]n chains along the c direction, which occurred without a significant alteration in the layer thickness over the a direction. A systematic study of the formation and destruction processes of the lanthanum sulfates under heating was carried out. In particular, the decisive impact of the chemical composition and formation energy of compounds on the thermodynamic and kinetic parameters of the processes was established. DFT calculations showed β-La2(SO4)3 to be a dielectric material with a bandgap of more than 6.4 eV. The processing of β-La2(SO4)3 with the Kubelka–Munk function exhibited low values below 6.4 eV, which indicated a fundamental absorption edge above this energy that was consistent with LDA calculations. The Raman and infrared measurements of β-La2(SO4)3 were in accordance with the calculated spectra, indicating that the obtained crystal parameters represented a reliable structure.

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Держатели документа:
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen 625003, Russia
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Laboratory of Theory and Optimization of Chemical and Technological Processes, Tyumen State University, Tyumen 625003, Russia
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
School of Engineering and Construction, Siberian Federal University, Krasnoyarsk 660041, Russia
A.M. Butlerov Chemistry Institute, Kazan Federal University, Kazan 420008, Russia
Institute of Inorganic and Analytical Chemistry, Justus-Liebig-University Giessen, 35392 Giessen, Germany
Laboratory of Coherent Optics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk 660036, Russia
Institute of Nanotechnology, Spectroscopy and Quantum Chemistry, Siberian Federal University, Krasnoyarsk 660041, Russia
Departement of Science and Innovation, Northern Trans-Ural Agricultural University, Tyumen 625003, Russia
School of Natural Sciences, Tyumen State University, Tyumen 625003, Russia
Center for Materials Research (LaMa), Justus-Liebig-University Giessen, 35392 Giessen, Germany
Construction Institute, Industrial University of Tyumen, Tyumen 625000, Russia

Доп.точки доступа:
Basova, S. A.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Zhernakov, M. A.; Khritokhin, N. A.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Krylov, A. S.; Крылов, Александр Сергеевич; Sal’nikova, E. I.; Azarapin, N. O.; Shelpakova, N. A.; Muller-Buschbaum, K.; Denisenko, Yu. G.
}
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Karpov, S. V.
The role of the electron tunneling effect in the coagulation kinetics of polydisperse metal nanocolloids / S. V. Karpov, P. N. Semina, A. P. Gavrilyuk // Colloid J. - 2012. - Vol. 74, Is. 3. - P. 305-312, DOI 10.1134/S1061933X12030052. - Cited References: 16. - Authors are thankful to G. A. Chiganova for discussions and helpful comments. Studies were carried out with the support of grants: the Presidium of RAS No 29 and No 31, OFN RAS III.9.5, IP SB RAS No 43, IP SB RAS (and SFU) No 101. . - ISSN 1061-933X

РУБ Chemistry, Physical
Рубрики:
PARTICLES
Аннотация: The energy of pair interactions between metal nanoparticles of different sizes is shown to be able to increase upon coagulation due to the additional electrostatic effect resulting from mutual heteropolar charging of the particles. The tunnel electron transfer occurring upon the collisions between particles of different sizes may be the reason for the charging. The transfer is caused by the dependence of the electron work function on the particle size. The electron transfer through the interparticle gap equalizes the Fermi levels in particles of different sizes and is associated with this dependence. Using the example of bimodal silver nanocolloids, it is shown that mutual heteropolar charging of particles with different sizes may accelerate the coagulation of polydisperse colloidal systems by an order of magnitude or more as compared with monodisperse systems, in which this effect is absent.

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Публикация на русском языке Карпов, Сергей Васильевич. Роль электронного туннельного эффекта в кинетике коагуляции полидисперсных наноколлоидов металлов [Текст] / С. В. Карпов, П. Н. Сёмина, А. П. Гаврилюк // Коллоид. журн. - М. : Наука, 2012. - Т. 74 № 3. - С. 329-336

Держатели документа:
[Karpov, S. V.
Semina, P. N.] Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia
[Karpov, S. V.] Siberian Fed Univ, Krasnoyarsk 660028, Russia
[Gavrilyuk, A. P.] Russian Acad Sci, Siberian Branch, Inst Computat Modeling, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Semina, P. N.; Семина, Полина Николаевна; Gavrilyuk, A. P.; Карпов, Сергей Васильевич
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The effect of electron density on the kinetics of fullerene formation in carbon plasma / K. L. Stepanov [et al.] // Tech. Phys. Lett. - 2003. - Vol. 29, Is. 11. - P. 927-929, DOI 10.1134/1.1631366. - Cited References: 10 . - ISSN 1063-7850

РУБ Physics, Applied
Рубрики:
C-60
Аннотация: The influence of the carbon cluster charge on their coagulation kinetics has been studied. The equations of kinetics have been solved and it is established that allowance for the cluster charging leads to an increase in the rate of fullerene formation under otherwise equal conditions. In connection with this, the role of minor impurities with a low ionization potential in carbon-containing plasma is discussed. (C) 2003 MAIK "Nauka/Interperiodica".

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Держатели документа:
Natl Acad Sci Belarus, Lykov Inst Heat & Mass Transfer, Minsk, Byelarus
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Div, Krasnoyarsk, Russia
ИФ СО РАН
Lykov Inst. of Heat/Mass Transfer, Natl. Academy of Sciences of Belarus, Minsk, Belarus
Kirensky Institute of Physics, Siberian Division, Russian Academy of Sciences, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Stepanov, K. L.; Stankevich, Y. A.; Stanchits, L. K.; Churilov, G. N.; Чурилов, Григорий Николаевич; Fedorov, A. S.; Федоров, Александр Семенович; Novikov, P. V.
}
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Temperature dependent elastic repulsion of colloidal nanoparticles with a polymer adsorption layer / A. P. Gavrilyuk [et al.] // Colloid Polym. Sci. - 2018. - Vol. 296, Is. 10. - P. 1689-1697, DOI 10.1007/s00396-018-4383-y. - Cited References: 49. - The reported research was funded by the Russian Foundation for Basic Research, the government of the Krasnoyarsk territory and Krasnoyarsk Regional Fund of Science, grant 18-42-243023, the RF Ministry of Science and Education, the State contract with Siberian Federal University for scientific research in 2017-2019, and SB RAS Program No II.2P (0358-2015-0010). . - ISSN 0303-402X. - ISSN 1435-1536

РУБ Chemistry, Physical + Polymer Science
Рубрики:
STERICALLY-STABILIZED PARTICLES
DEPLETION FLOCCULATION
AGGREGATION
Кл.слова (ненормированные):
Nanoparticle -- Adsorption layer -- Elastic deformation -- Coagulation -- kinetics -- Elasticity modulus
Аннотация: The model of pairwise elastic repulsion of contacting colloidal nanoparticles with a rigid core and deformable shell is discussed. A simple analytical equation is applied for the energy of elastic repulsion of nanoparticles with arbitrary sizes and the elasticity moduli of self-healing polymer adsorption layers. The model is based on the representation of the absorption layer as a continuous medium that is elastically deformed upon the contact of nanoparticles. The major characteristic of this medium is the elasticity modulus. The magnitude of the elasticity modulus is determined from the condition of balance of the van der Waals attractive forces of nanoparticles and the elastic repulsion of their adsorption layers in the contact area, taking into account the temperature variations. We employed the kinetic approach to describe the dependence of the elasticity modulus on both the temperature and the rate of its change.

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Держатели документа:
RAS, SB, Inst Computat Modeling, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Math & Comp Sci, Krasnoyarsk 660041, Russia.
Siberian Fed Univ, Lab Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
RAS, SB, Fed Res Ctr KSC, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian State Univ Sci & Technol, Krasnoyarsk 660014, Russia.

Доп.точки доступа:
Gavrilyuk, A. P.; Gerasimov, V. S.; Герасимов, Валерий Сергеевич; Ershov, A. E.; Ершов, Александр Евгеньевич; Karpov, S. V.; Карпов, Сергей Васильевич; Russian Foundation for Basic Research; government of the Krasnoyarsk territory and Krasnoyarsk Regional Fund of Science [18-42-243023]; RF Ministry of Science and Education,; State contract with Siberian Federal University for scientific research in 2017-2019; SB RAS Program [II.2P (0358-2015-0010)]
}
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Synthesis and catalytic hydrogenation activity of Pd and bimetallic Au–Pd nanoparticles supported on high-porosity carbon materials / O. V. Belousov [et al.] // React. Kinet. Mech. Catal. - 2019. - Vol. 127, Is. 1. - P. 25–39, DOI 10.1007/s11144-018-1430-0. - Cited References: 57 . - ISSN 1878-5190
Кл.слова (ненормированные):
MOCVD -- Hydrothermal synthesis -- Palladium nanoparticles -- Mesostructured carbon -- Bimetallic Pd–Au catalyst -- Furfural diethyl acetal -- Hydrogenation
Аннотация: The processes of palladium deposition on various high-porosity carbon matrices (Sibunit, CMK-3) have been studied. Mesostructured carbon material CMK-3 was synthesized using a silicate template of SBA-15 type. Pd nanoparticles were loaded onto carbon matrices by metalorganic chemical vapour deposition (MOCVD) method using palladium(II) acetylacetonate precursor. Bimetal Au–Pd systems were synthesized by autoclave reduction of gold(III) chloride complexes on Pd-containing carbon matrices. Structure of the obtained composite particles was studied by electron microscopy and X-ray diffraction. The average diameter of Pd particles on Sibunit is about 10, and 5–6 nm on CMK-3. The catalytic activity of the synthesized materials was studied in the reaction of furfural diethyl acetal (FDEA) hydrogenation, using gas–liquid chromatographic analysis. There is significant difference in catalytic activity of MOCVD-Pd/C compared to conventional impregnated Pd/C systems: the hydrogenation rate is 3–6 times higher with MOCVD-derived catalysts. Introducing Au into a MOCVD-Pd/C catalyst increases the hydrogenation rate threefold. Considerable difference in the composition of hydrogenation products was observed between these differently prepared catalysts.

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Держатели документа:
Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences - A Separate Division of FSC KSC SB RAS, 50/24, Akademgorodok, Krasnoyarsk, Russian Federation
Boreskov Institute of Catalysis, 5, Lavrentieva, Novosibirsk, Russian Federation
Kirensky Institute of Physics of the Siberian Branch of the Russian Academy of Sciences - A Separate Division of FSC KSC SB RAS, 50/38, Akademgorodok, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Belousov, O. V.; Tarabanko, V. E.; Borisov, R. V.; Simakova, I. L.; Zhyzhaev, A. M.; Tarabanko, N.; Isakova, V. G.; Исакова, Виктория Гавриловна; Parfenov, V. V.; Ponomarenko, I. V.
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    Solid-state reaction in Cu/a-Si nanolayers: A comparative study of STA and electron diffraction data / E. T. Moiseenko, V. V. Yumashev, R. R. Altunin [и др.] // Materials. - 2022. - Vol. 15, Is. 23. - Ст. 8457, DOI 10.3390/ma15238457. - Cited References: 45. - This work was supported by the Russian Science Foundation under grant # 22-13-00313 . - ISSN 1996-1944
   Перевод заглавия: Твердофазная реакция в нанослоях Cu/a-Si: сравнительное исследование данных, полученных методами СТА и дифракции электронов
Кл.слова (ненормированные):
copper silicide -- thin films -- nanolayer -- solid-state reaction -- phase formation -- kinetics -- activation energy -- enthalpy -- DSC -- electron diffraction
Аннотация: The kinetics of the solid-state reaction between nanolayers of polycrystalline copper and amorphous silicon (a-Si) has been studied in a Cu/a-Si thin-film system by the methods of electron diffraction and simultaneous thermal analysis (STA), including the methods of differential scanning calorimetry (DSC) and thermogravimetry (TG). It has been established that, in the solid-state reaction, two phases are formed in a sequence: Cu + Si → η″-Cu3Si → γ-Cu5Si. It has been shown that the estimated values of the kinetic parameters of the formation processes for the phases η″-Cu3Si and γ-Cu5Si, obtained using electron diffraction, are in good agreement with those obtained by DSC. The formation enthalpy of the phases η″-Cu3Si and γ-Cu5Si has been estimated to be: ΔHη″-Cu3Si = −12.4 ± 0.2 kJ/mol; ΔHγ-Cu5Si = −8.4 ± 0.4 kJ/mol. As a result of the model description of the thermo-analytical data, it has been found that the process of solid-state transformations in the Cu/a-Si thin-film system under study is best described by a four-stage kinetic model R3 → R3 → (Cn-X) → (Cn-X). The kinetic parameters of formation of the η″-Cu3Si phase are the following: Ea = 199.9 kJ/mol, log(A, s−1) = 20.5, n = 1.7; and for the γ-Cu5Si phase: Ea = 149.7 kJ/mol, log(A, s−1) = 10.4, n = 1.3, with the kinetic parameters of formation of the γ-Cu5Si phase being determined for the first time.

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Держатели документа:
Laboratory of Electron Microscopy, Siberian Federal University, 79 Svobodny Ave., 660041 Krasnoyarsk, Russia
Institute of Chemistry and Chemical Technology, Federal Research Center KSC SB RAS, Akademgorodok 50/24, 660036 Krasnoyarsk, Russia
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, 660036 Krasnoyarsk, Russia

Доп.точки доступа:
Moiseenko, E. T.; Yumashev, V. V.; Altunin, R. R.; Zeer, G. M.; Nikolaeva, N. S.; Belousov, O. V.; Zharkov, S. M.; Жарков, Сергей Михайлович
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10.

Solid-phase reactions and the order-disorder phase transition in thin films / V. G. Myagkov [et al.] // Tech. Phys. - 2001. - Vol. 46, Is. 6. - P. 743-748, DOI 10.1134/1.1379645. - Cited References: 28 . - ISSN 1063-7842

РУБ Physics, Applied
Рубрики:
HIGH-TEMPERATURE SYNTHESIS
   ALLOY-FILMS
   KINETICS
   MULTILAYERS
   SYSTEMS
   GROWTH
Аннотация: A comparative analysis was carried out of the initiation temperatures of solid-phase reactions in bilayer solid films and the Kurnakov temperatures of the phases forming in the reaction products. It has been shown that in superstructures where ordering is usually observed, the Kurnakov temperature coincides with the initiation temperature of the solid-phase reactions if no other solid-phase structural transformation precedes the order-disorder phase transition in the state diagram. A rule was proposed by which pairs of films capable of entering into solid-phase reactions and their initiation temperatures can be determined. (C) 2001 MAIK "Nauka/Interperiodica".

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Держатели документа:
Russian Acad Sci, Siberian Branch, Kirenskii Inst Phys, Krasnoyarsk 660036, Russia
ИФ СО РАН
Kirenskii Inst. of Physics, Russian Academy of Sciences, Siberian Branch, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Myagkov, V. G.; Мягков, Виктор Григорьевич; Bykova, L. E.; Быкова, Людмила Евгеньевна; Bondarenko, G. N.; Бондаренко, Галина Николаевна; Bondarenko, G. V.; Бондаренко, Геннадий Васильевич; Myagkov, F. V.
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