| 1. |
- Aleksandrovskii, A. N., et al.
(författare)
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Effect of argon on the thermal expansion of fullerite C60 at helium temperatures
- 2001
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Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics. - 1063-777X .- 1090-6517. ; 27:3, s. 245-246
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Tidskriftsartikel (refereegranskat)abstract
- The linear thermal expansion of compacted Ar-doped fullerite C60(ArxC60) is investigated at 2–12 K using a dilatometric method. The thermal expansion of ArxC60 is also studied after partial desaturation of argon from fullerite. It is revealed that argon doping resulted in a considerable change of the temperature dependence of the thermal expansion of fullerite. An explanation of the observed effects is proposed.
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| 2. |
- Aleksandrovskii, A. N., et al.
(författare)
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Low-temperature thermal expansion of pure and inert gas-doped fullerite C60
- 2003
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Ingår i: Fizika Nizkikh Temperatur (Kharkov). - : AIP Publishing. - 0132-6414 .- 1816-0328. ; 29:4, s. 432-442
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Tidskriftsartikel (refereegranskat)abstract
- The low temperature (2–24 K) thermal expansion of pure (single-crystal and polycrystalline) C60 and polycrystalline C60 intercalated with He, Ne, Ar, and Kr has been investigated using the high-resolution capacitance dilatometer. The investigation of the time dependence of the sample length variations deltaL(t) on heating by deltaT shows that the thermal expansion is determined by the sum of positive and negative contributions, which have different relaxation times. The negative thermal expansion usually prevails at helium temperatures. The positive expansion is connected with the phonon thermalization of the system. The negative expansion is caused by reorientation of the C60 molecules. It is assumed that the reorientation is of a quantum character. The inert gas impurities affect the reorientation of the C60 molecules very strongly, especially at liquid helium temperatures. A temperature hysteresis of the thermal expansion coefficient of Kr– and He–C60 solutions has been revealed. The hysteresis is attributed to orientational polyamorphous transformation in these systems.
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| 3. |
- Aleksandrovskii, A.N., et al.
(författare)
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On the polyamorphism of fullerite-based orientational glasses.
- 2005
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Ingår i: Low Temperature Physics. - : AIP Publishing. - 1063-777X .- 1090-6517. ; 31:5, s. 429-444
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Tidskriftsartikel (refereegranskat)abstract
- The dilatometric investigation in the temperature range of 2–28 K shows that a first-orderpolyamorphous transition occurs in the orientational glasses based on C60 doped with H2, D2 andXe. A polyamorphous transition was also detected in C60 doped with Kr and He. It is observed thatthe hysteresis of thermal expansion caused by the polyamorphous transition (and, hence, the transitiontemperature) is essentially dependent on the type of doping gas. Both positive and negativecontributions to the thermal expansion were observed in the low-temperature phase of the glasses.The relaxation time of the negative contribution occurs to be much longer than that of the positivecontribution. The positive contribution is found to be due to phonon and libron modes, whilst thenegative contribution is attributed to tunneling states of the C60 molecules. The characteristictime of the phase transformation from the low-T phase to the high-T phase has been found for theC60–H2 system at 12 K. A theoretical model is proposed to interpret these observed phenomena.The theoretical model proposed, includes a consideration of the nature of polyamorphism inglasses, as well as the thermodynamics and kinetics of the transition. A model of noninteractingtunneling states is used to explain the negative contribution to the thermal expansion. The experimentaldata obtained is considered within the framework of the theoretical model. From the theoreticalmodel the order of magnitude of the polyamorphous transition temperature has been estimated.It is found that the late stage of the polyamorphous transformation is described well by theKolmogorov law with an exponent of n = 1. At this stage of the transformation, the two-dimensionalphase boundary moves along the normal, and the nucleation is not important.
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| 4. |
- Aleksandrovskii, A.N., et al.
(författare)
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Thermal expansion of fullerite C60 alloyed with argon and neon
- 2001
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Ingår i: Low temperature physics (Woodbury, N.Y., Print). - Woodbury : American Institute of Physics. - 1063-777X .- 1090-6517. ; 27:12, s. 1033-1036
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Tidskriftsartikel (refereegranskat)abstract
- The linear thermal expansion of compacted fullerite C60 alloyed with argon (ArxC60) and neon (NexC60) are investigated by a dilatometric method. The experimental temperature is 2–12 K. In the same temperature interval the thermal expansion of ArxC60 and NexC60 are examined after partial desaturation of the gases from fullerite. It is found that Ar and Ne alloying affects the temperature dependence of the thermal expansion coefficient of C60 quite appreciably. The libration and translation contributions to the thermal expansion of pure C60 are separated. The experimental results on the thermal expansion are used to obtain the Debye temperature of pure C60. The effects observed are tentatively interpreted.
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| 5. |
- Aleksandrovskii, A. N., et al.
(författare)
-
Thermal expansion of single-crystal fullerite C60 at helium temperatures
- 2000
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Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : AIP Publishing. - 1063-777X .- 1090-6517. ; 26:1, s. 75-80
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Tidskriftsartikel (refereegranskat)abstract
- The thermal expansion of single-crystal fullerite C60 has been studied in the range of liquid-helium temperatures (2–10 K). At temperatures below ~4.5 K the thermal expansion of fullerite C60 becomes negative, in agreement with the previous results on polycrystalline materials. A qualitative explanation of the results is proposed.
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| 6. |
- Bagatskii, M.I., et al.
(författare)
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Low-temperature dynamics of matrix isolated methane molecules in fullerite C60 : the heat capacity, isotope effects
- 2014
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Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics (AIP). - 1063-777X .- 1090-6517. ; 40:8, s. 678-684
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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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| 7. |
- Dolbin, Alexander V, et al.
(författare)
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Radial thermal expansion of single-walled carbon nanotube bundles at low temperatures.
- 2008
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Ingår i: Fizika Nizkikh Temperatur. - : AIP Publishing. - 0132-6414. ; 34:8, s. 860-862
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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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| 8. |
- Dolbin, Alexander V., et al.
(författare)
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Specific features of thermal expansion and polyamorphism in CH4 – C60 solutions at low temperatures
- 2007
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Ingår i: Low Temperature Physics. - : AIP Publishing. - 1063-777X .- 1090-6517. ; 33:12, s. 1068-1072
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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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| 9. |
- Dolbin, Alexander V., et al.
(författare)
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The effect of the noncentral impurity-matrix interaction upon the thermal expansion and polyamorphism of solid CO-C60 solutions at low temperatures
- 2008
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Ingår i: Fizika Nizkikh Temperatur. - : AIP Publishing. - 0132-6414. ; 34:6, s. 592-598
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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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| 10. |
- Dolbin, Alexander V., et al.
(författare)
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Thermal expansion of solutions of deuteromethane in fullerite C60 at low temperature : Isotopic effect
- 2009
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Ingår i: Low temperature physics (Woodbury, N.Y., Print). - : American Institute of Physics. - 1063-777X .- 1090-6517. ; 35:3, s. 226-231
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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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