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Träfflista för sökning "WFRF:(Dolbin Alexander V.) "

Sökning: WFRF:(Dolbin Alexander V.)

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1.
  • Bagatskii, M.I., et al. (författare)
  • Low-temperature dynamics of matrix isolated methane molecules in fullerite C60 : the heat capacity, isotope effects
  • 2014
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 40:8, s. 678-684
  • Tidskriftsartikel (refereegranskat)abstract
    • The heat capacity of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4–120 K. The contribution of CH4 molecules to the heat capacity of the solution has been separated. The contributions of CH4 and CD4 molecules to the heat capacity of the solutions (CH4)0.40C60 and (CD4)0.40C60 have been compared. It is found that above 90 K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14–35 K the heat capacities of CH4 and CD4 molecules are satisfactorily described by contributions of the translational and libration vibrations, as well as the tunnel rotation for the equilibrium distribution of the nuclear spin species. The isotope effect is due to mainly the difference in the frequencies of local translational and libration vibrations of molecules CH4 and CD4. The contribution of the tunnel rotation of the CH4 and CD4 molecules to the heat capacity is dominant below 8 K. The isotopic effect is caused by the difference between both the conversion rates and the rotational spectra of the nuclear spin species of CH4 and CD4 molecules. The conversion rate of CH4 molecules is several times lower than that of CD4 ones. Weak features observed in the curves of temperature dependencies of the heat capacity of CH4 and CD4 molecules near 6 and 8 K, respectively, are most likely a manifestation of first-order polyamorphic phase transitions in the orientational glasses of these solutions.
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2.
  • Dolbin, Alexander V, et al. (författare)
  • Radial thermal expansion of single-walled carbon nanotube bundles at low temperatures.
  • 2008
  • Ingår i: Fizika Nizkikh Temperatur. - : AIP Publishing. - 0132-6414. ; 34:8, s. 860-862
  • Tidskriftsartikel (refereegranskat)abstract
    • For the first time, the linear coefficient of radial thermal expansion is measured on a system of carbon single-walled nanotube (SWNT) bundles at low temperatures (2.2–120 K). The measurements are performed using a dilatometer with a sensitivity of 2×10−9 cm. A cylindrical sample 7 mm high and 10 mm in diameter was obtained by compressing powder. The resulting bundles of nanotubes are oriented perpendicular to the sample axis. The starting powder consisted of over 90% SWNTs with outer diameter 1.1 nm, the length varying in the range 5–30 µm. A change of sign of the radial thermal expansion coefficient at 5.5 K is observed.
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3.
  • Dolbin, Alexander V., et al. (författare)
  • Specific features of thermal expansion and polyamorphism in CH4 – C60 solutions at low temperatures
  • 2007
  • Ingår i: Low Temperature Physics. - : AIP Publishing. - 1063-777X .- 1090-6517. ; 33:12, s. 1068-1072
  • Tidskriftsartikel (refereegranskat)abstract
    • The temperature dependence of the linear thermal expansion coefficient alpha(T) is investigated in the temperature range of 2.5 to 23 K for two different CH4-C-60 solutions in which CH4 molecules occupy 24 and 50% of the octahedral interstitial sites of the C-60 lattice. In both cases, alpha(T) exhibits hysteresis, suggesting the existence of two types of orientational glass associated with these solutions. The temperature of the first-order phase transition between these two glasses is estimated, and the behavior of these two glasses is compared. The characteristic times of thermalization tau(1), reorientation of the C-60 molecules tau(2), and of the phase transformation between the glasses tau('), are estimated for these solutions. Both the temperature dependence of alpha(T) and the characteristic thermalization time tau(1) are found to have features near the phase transition temperature, and an explanation is put forward to explain these observed features.
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4.
  • Dolbin, Alexander V., et al. (författare)
  • The effect of the noncentral impurity-matrix interaction upon the thermal expansion and polyamorphism of solid CO-C60 solutions at low temperatures
  • 2008
  • Ingår i: Fizika Nizkikh Temperatur. - : AIP Publishing. - 0132-6414. ; 34:6, s. 592-598
  • Tidskriftsartikel (refereegranskat)abstract
    • Orientational glasses with CO molecules occupying 26 and 90% of the octahedral interstitial sites in the C60 lattice have been investigated by the dilatometric method in a temperature interval of 2.5–22 K. At temperatures 4–6 K the glasses undergo a first-order phase transition which is evident from the hysteresis of the thermal expansion and the maxima in the temperature dependences of the linear thermal expansion coefficients a(T), and the thermalization times t1(T) of the samples. The effect of the noncentral CO–C60 interaction upon the thermal expansion and the phase transition in these glasses was clarified by comparing the behavior of the properties of the CO–C60 and N2–C60 solutions.
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5.
  • Dolbin, Alexander V., et al. (författare)
  • Thermal expansion of solutions of deuteromethane in fullerite C60 at low temperature : Isotopic effect
  • 2009
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics. - 1063-777X .- 1090-6517. ; 35:3, s. 226-231
  • Tidskriftsartikel (refereegranskat)abstract
    • The thermal expansion of CD4 solutions in the orientational glass C60 with molar concentration of deuteromethane 20 and 50% has been investigated in the temperature range 2.5–23 K. The orientational glass CD4–C60 undergoes a first-order phase transition in the temperature interval 4.5–55 K. This transition is manifested as hysteresis of the linear thermal expansion coefficient alpha as well as maxima in the temperature dependences alpha(T) and tau1(T), where tau1 is the characteristic thermalization time of the experimental samples. The characteristic re-orientation times of the C60 molecules and the characteristic phase transformations occurring in the experimental solutions are determined. The results of the present study are compared with the results of a similar study of the solution CH4–C60. It is concluded that tunneling rotation of the CH4 and CD4 molecules occupying interstitial positions in the fullerite C60 lattice occurs.
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6.
  • Manzhelii, V.G., et al. (författare)
  • Thermal expansion and polyamorphism of N2 – C60 solutions
  • 2006
  • Ingår i: Low Temperature Physics. - : AIP Publishing. - 1063-777X .- 1090-6517. ; 32:7, s. 695-699
  • Tidskriftsartikel (refereegranskat)abstract
    • The linear coefficients alpha(T) of N-2-C-60 solutions with 9.9% and 100% of the C-60 lattice thermal expansion interstitials filled with N-2 are investigated in the interval 2.2-24 K. The dependence alpha(T) has a hysteresis suggesting co-existence of two types of orientational glasses in these solutions. The features of the glasses are compared. The characteristic times of phase transformations in the solutions and reorientation of C-60 molecules are estimated.
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7.
  • Bagatskii, M. I., et al. (författare)
  • Low-temperature heat capacity of fullerite C-60 doped with deuteromethane
  • 2012
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - Melville, NY : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 38:1, s. 67-73
  • Tidskriftsartikel (refereegranskat)abstract
    • The heat capacity C of fullerite doped with deuteromethane (CD4)(0.4)(C-60) has been investigated in the temperature interval 1.2-120K. The contribution Delta C-CD4 of the CD4 molecules to the heat capacity C has been isolated. It is shown that at T approximate to 120K the rotational motion of CD4 molecules in the octahedral voids of the C-60 lattice is weakly hindered. When the temperature is lowered to 80K, the rotational motion of the CD4 molecules changes from weakly hindered rotation to libration. In the range T = 1.2-30 K, Delta C-CD4 is described quite accurately by the sum of contributions from the translational and librational vibrations and tunneling rotation of CD4 molecules. The contribution of tunneling rotation to the heat capacity Delta C-CD4(T) is dominant below 5K. The effect of nuclear-spin conversion of the CD4 molecules on the heat capacity has been observed and the characteristic times for nuclear spin conversion between the lowest levels of the A- and T-species of CD4 molecules at T < 5K have been estimated. A feature observed in Delta C-CD4(T) near T = 5.5K is most likely a manifestation of a first-order phase transition in the orientational glass form of the solution. (C) 2012 American Institute of Physics. [doi: 10.1063/1.3677237]
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8.
  • Bagatskii, M.I., et al. (författare)
  • The low-temperature heat capacity of fullerite C60
  • 2015
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 41:8, s. 630-636
  • Tidskriftsartikel (refereegranskat)abstract
    • The heat capacity at constant pressure of fullerite C60 has been investigated using an adiabatic calorimeter in a temperature range from 1.2 to 120 K. Our results and literature data have been analyzed in a temperature interval from 0.2 to 300 K. The contributions of the intramolecular and lattice vibrations into the heat capacity of C60 have been separated. The contribution of the intramolecular vibration becomes significant above 50 K. Below 2.3K the experimental temperature dependence of the heat capacity of C60 is described by the linear and cubic terms. The limiting Debye temperature at T → 0 K has been estimated (Θ0=84.4 K). In the interval from 1.2 to 30K the experimental curve of the heat capacity of C60 describes the contributions of rotational tunnel levels, translational vibrations (in the Debye model with Θ0=84.4 K), and librations (in the Einstein model with ΘE,lib=32.5 K). It is shown that the experimental temperature dependences of heat capacity and thermal expansion are proportional in the region from 5 to 60K. The contribution of the cooperative processes of orientational disordering becomes appreciable above 180 K. In the high-temperature phase the lattice heat capacity at constant volume is close to 4.5 R, which corresponds to the high-temperature limit of translational vibrations (3 R) and the near-free rotational motion of C60 molecules (1.5 R).
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9.
  • Bagatskii, M.I., et al. (författare)
  • The specific heat and the radial thermal expansion of bundles of single-walled carbon nanotubes
  • 2012
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 38:6, s. 523-528
  • Tidskriftsartikel (refereegranskat)abstract
    • The specific heat at constant pressure C(T) of bundles of single-walled carbon nanotubes (SWNTs) closed at their ends has been investigated in the temperature interval of 2–120 K. It is found that the curve C(T) has features near 5, 36, 80, and 100 K. The experimental results on the C(T) and the radial thermal expansion coefficient αR(T) of bundles of SWNTs oriented perpendicular to the sample axis have been compared. It is found that the curves C(T) and αR(T) exhibit a similar temperature behavior at T > 10 K. The temperature dependence of the Grüneisen coefficient γ(T) has been calculated. The curve γ(T) also has a feature near 36 K. Above 36 K the Grüneisen coefficient is practically independent of temperature (γ ≈ 4). Below 36 K, γ(T) decreases monotonically with lowering temperature and becomes negative at T < 6 K.
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10.
  • Dolbin, Alexander V., et al. (författare)
  • Low-temperature radial thermal expansion of single-walled carbon nanotube bundles saturated with nitrogen
  • 2010
  • Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : AIP Publishing. - 1063-777X .- 1090-6517. ; 36:5, s. 365-369
  • Tidskriftsartikel (refereegranskat)abstract
    • The effect of a N2 impurity on the radial thermal expansion coefficient αr of single-walled carbon nanotube bundles has been investigated in the temperature interval 2.2–43 K by the dilatometric method. Saturation of nanotube bundles with N2 caused a sharp increase in the positive magnitudes of αr in the whole temperature range used and a very high and wide maximum in the thermal expansion coefficient αr(T) at T ~ 28 K. The low temperature desorption of the impurity from the N2-saturated powder of bundles of single-walled carbon nanotubes with open and closed ends has been investigated.
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