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Low-temperature thermal expansion of pure and inert gas-doped fullerite C₆₀

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 variatio...

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Bibliographic Details
Main Authors: Aleksandrovskii, A.N., Bakai, A.S., Dolbin, A.V., Esel`son, V.B., Gadd, G.E., Gavrilko, V.G., Manzhelii, V.G., Moricca, S., Sundqvist, B., Udovidchenko, B.G.
Format: Article
Language:English
Published: Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України 2003
Series:Физика низких температур
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Online Access:http://dspace.nbuv.gov.ua/handle/123456789/128827
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Summary: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 ΔL(t) on heating by ΔT 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.