Low-temperature dynamics of matrix isolated methane molecules in fullerite C60

The heat capacity, isotope effects

M. I. Bagatskii, V. G. Manzhelii, V. V. Sumarokov, A. V. Dolbin, M. S. Barabashko, B. Sundqvist

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The heat capacity of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4-120K. 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)0.4C60 and (CH4)0.4C60 have been compared. It is found that above 90K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14-35K 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 8K. 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 8K, respectively, are most likely a manifestation of first-order polyamorphic phase transitions in the orientational glasses of these solutions.

Original languageEnglish
Pages (from-to)678-684
Number of pages7
JournalLow Temperature Physics
Volume40
Issue number8
DOIs
Publication statusPublished - 1 Jan 2014
Externally publishedYes

Fingerprint

isotope effect
methane
specific heat
matrices
molecules
libration
nuclear spin
tunnels
intervals
vibration
rotational spectra
interstitials
solid solutions
temperature
glass
curves

ASJC Scopus subject areas

  • Physics and Astronomy (miscellaneous)

Cite this

Low-temperature dynamics of matrix isolated methane molecules in fullerite C60 : The heat capacity, isotope effects. / Bagatskii, M. I.; Manzhelii, V. G.; Sumarokov, V. V.; Dolbin, A. V.; Barabashko, M. S.; Sundqvist, B.

In: Low Temperature Physics, Vol. 40, No. 8, 01.01.2014, p. 678-684.

Research output: Contribution to journalArticle

Bagatskii, M. I. ; Manzhelii, V. G. ; Sumarokov, V. V. ; Dolbin, A. V. ; Barabashko, M. S. ; Sundqvist, B. / Low-temperature dynamics of matrix isolated methane molecules in fullerite C60 : The heat capacity, isotope effects. In: Low Temperature Physics. 2014 ; Vol. 40, No. 8. pp. 678-684.
@article{585b172d354b45678c4b97bb0a891427,
title = "Low-temperature dynamics of matrix isolated methane molecules in fullerite C60: The heat capacity, isotope effects",
abstract = "The heat capacity of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4-120K. 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)0.4C60 and (CH4)0.4C60 have been compared. It is found that above 90K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14-35K 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 8K. 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 8K, respectively, are most likely a manifestation of first-order polyamorphic phase transitions in the orientational glasses of these solutions.",
author = "Bagatskii, {M. I.} and Manzhelii, {V. G.} and Sumarokov, {V. V.} and Dolbin, {A. V.} and Barabashko, {M. S.} and B. Sundqvist",
year = "2014",
month = "1",
day = "1",
doi = "10.1063/1.4892643",
language = "English",
volume = "40",
pages = "678--684",
journal = "Fizika Nizkikh Temperatur (Kiev)",
issn = "0430-6244",
publisher = "American Institute of Physics",
number = "8",

}

TY - JOUR

T1 - Low-temperature dynamics of matrix isolated methane molecules in fullerite C60

T2 - The heat capacity, isotope effects

AU - Bagatskii, M. I.

AU - Manzhelii, V. G.

AU - Sumarokov, V. V.

AU - Dolbin, A. V.

AU - Barabashko, M. S.

AU - Sundqvist, B.

PY - 2014/1/1

Y1 - 2014/1/1

N2 - The heat capacity of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4-120K. 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)0.4C60 and (CH4)0.4C60 have been compared. It is found that above 90K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14-35K 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 8K. 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 8K, respectively, are most likely a manifestation of first-order polyamorphic phase transitions in the orientational glasses of these solutions.

AB - The heat capacity of the interstitial solid solution (CH4)0.4C60 has been investigated in the temperature interval 1.4-120K. 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)0.4C60 and (CH4)0.4C60 have been compared. It is found that above 90K the character of the rotational motion of CH4 and CD4 molecules changes from libration to hindered rotation. In the interval 14-35K 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 8K. 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 8K, respectively, are most likely a manifestation of first-order polyamorphic phase transitions in the orientational glasses of these solutions.

UR - http://www.scopus.com/inward/record.url?scp=84929580858&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84929580858&partnerID=8YFLogxK

U2 - 10.1063/1.4892643

DO - 10.1063/1.4892643

M3 - Article

VL - 40

SP - 678

EP - 684

JO - Fizika Nizkikh Temperatur (Kiev)

JF - Fizika Nizkikh Temperatur (Kiev)

SN - 0430-6244

IS - 8

ER -