The effect of O2 impurities on the low temperature radial thermal expansion of bundles of closed single-walled carbon nanotubes

The effect of oxygen impurities upon the radial thermal expansion (ar) of bundles of closed single-walled carbon nanotubes has been investigated in the temperature interval 2.2-48 K by the dilatometric method. Saturation of bundles of nanotubes with oxygen caused an increase in the positive ar-values in the whole interval of temperatures used. Also, several peaks appeared in the temperature dependence ar(T) above 20 K. The low temperature desorption of oxygen from powders consisting of bundles of single-walled nanotubes with open and closed ends has been investigatedComment: 7 pages, 3 figure

Quantum effects in the radial thermal expansion of bundles of single-walled carbon nanotubes doped with 4He

The radial thermal expansion (ar) of bundles of single-walled carbon nanotubes saturated with 4He impurities to the molar concentration 9.4% has been investigated in the interval 2.5-9.5 K using the dilatometric method. In the interval 2.1-3.7 K (ar) is negative and is several times higher than the negative (ar) for pure nanotube bundles. This most likely points to 4He atom tunneling between different positions in the nanotube bundle system. The excess expansion was reduced with decreasing 4He concentration.Comment: 4 pages, 1 figure, will be published in Fiz.Nizk Temp. #7, 201

Radial thermal expansion of single-walled carbon nanotube bundles at low temperatures

The linear coefficient of the radial thermal expansion has been measured on a system of SWNT bundles in an interval of 2.2 - 120K. The measurement was performed using a dilatometer with a sensitivity of 2*10-9 cm. The cylindrical sample 7 mm high and 10 mm in diameter was obtained by compressing powder. The resulting bundles of the nanotubes were oriented perpendicular to the sample axis. The starting powder contained over 90% of SWNTs with the outer diameter 1.1 nm, the length varying within 5-30 um.Comment: 4 pages, 1 figur

Kinetics of 4He gas sorption by fullerite C60. Quantum effects

The kinetics of helium gas sorption by a C60 powder and subsequent desorption of the 4He impurity from the saturated powder has been investigated in the temperature interval T = 2-292 K. Evidence is obtained that supports the existence of two stages in the temperature dependences of sorption and desorption. The stages account for the different times taken by helium to occupy the octahedral and tetrahedral interstices in the C60 lattice. The characteristic times of sorption and desorption coincide. It is found that the temperature dependences of the characteristic times of occupying the octahedral and tetrahedral interstices are nonmonotonic. As the temperature is lowered from 292 K to 79.3 K, the characteristic times increase, which indicates a predominance of thermally activated diffusion of helium in C60. On a further decrease to T = 10 K the characteristic times reduce over an order of magnitude. Below 8 K the characteristic times of sorption and desorption are temperature-independent. This suggests a tunnel character of 4He diffusion in C60.Comment: 6 pages, 2 figure

Linearized semiclassical initial value time correlation functions with maximum entropy analytic continuation

The maximum entropy analytic continuation (MEAC) method is used to extend the range of accuracy of the linearized semiclassical initial value representation (LSC-IVR)/classical Wigner approximation for real time correlation functions. The LSC-IVR provides a very effective 'prior' for the MEAC procedure since it is very good for short times, exact for all time and temperature for harmonic potentials (even for correlation functions of nonlinear operators), and becomes exact in the classical high temperature limit. This combined MEAC+LSC/IVR approach is applied here to two highly nonlinear dynamical systems, a pure quartic potential in one dimensional and liquid para-hydrogen at two thermal state points (25K and 14K under nearly zero external pressure). The former example shows the MEAC procedure to be a very significant enhancement of the LSC-IVR, for correlation functions of both linear and nonlinear operators, and especially at low temperature where semiclassical approximations are least accurate. For liquid para-hydrogen, the LSC-IVR is seen already to be excellent at T = 25K, but the MEAC procedure produces a significant correction at the lower temperature (T = 14K). Comparisons are also made to how the MEAC procedure is able to provide corrections for other trajectory-based dynamical approximations when used as priors

Low-Temperature Mobility of Surface Electrons and Ripplon-Phonon Interaction in Liquid Helium

The low-temperature dc mobility of the two-dimensional electron system localized above the surface of superfluid helium is determined by the slowest stage of the longitudinal momentum transfer to the bulk liquid, namely, by the interaction of surface and volume excitations of liquid helium, which rapidly decreases with temperature. Thus, the temperature dependence of the low-frequency mobility is \mu_{dc} = 8.4x10^{-11}n_e T^{-20/3} cm^4 K^{20/3}/(V s), where n_e is the surface electron density. The relation T^{20/3}E_\perp^{-3} << 2x10^{-7} between the pressing electric field (in kV/cm) and temperature (in K) and the value \omega < 10^8 T^5 K^{-5}s^{-1} of the driving-field frequency have been obtained, at which the above effect can be observed. In particular, E_\perp = 1 kV/cm corresponds to T < 70 mK and \omega/2\pi < 30 Hz.Comment: 4 pages, 1 figur

On the electric activity of superfluid systems

The Keldysh's theory of superfluidity of rarefied electron-hole gas is generalized to a case of possible pair polarizability. It was shown that inhomogeneity of the system leads to dipole moment which is proportional to the density gradient. The dipole moment appears also near boundaries of the system. It was determined that quantized vortices in a magnetic field carry a real electric charge. In He II at H=10 T and helium rotation velocity $10^2$ s$^{-1}$ the charge density is about $10^4e$ cm$^{-3}$, where $e$ is the electron charge.Comment: 5 pages V. 2: replaced incorrect g valu

Thermal expansion of solid solutions Kr-CH4 at temperatures of liquid helium

A negative contribution of the CH4 impurity to the thermal expansion of the solution has been revealed in dilatometric studies of solid Kr+0.76% CH4, Kr+5.25% CH4 and Kr+10.5% CH4 solutions at 1-23 K. It is shown that the negative contribution results from changes in the occupancy of the ground state of the A-modifications of isolated CH4 molecules. Assuming that the CH4 impurity singles and clusters contribute to the thermal expansion independently, we can estimate their contributions. The contribution of the singles to the thermal expansion of the solid solution is negative. The energies of the first excitational rotational states were determined for singles and two-body and three-body clusters of CH4 molecules.Comment: 10 pages, 7 figure

Specific features of thermal expansion and polyamorphism in CH4–C60 solutions at low temperatures

The temperature dependence of the linear thermal expansion coefficient α(T) has been investigated in the temperature range of 2.5 to 23 K for two different CH4–C60 solutions in which CH4 molecules occupied 24 and 50% of the octahedral interstitial sites of the C60 lattice. In both cases, α(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 was estimated and the behavior of these two glasses compared. The characteristic times of thermalization τ1, reorientation of the C60 molecules τ2, and of the phase transformation between the glasses τ', have been estimated for these solutions. Both the temperature dependence of α(T) and the characteristic thermalization time τ1are found to have features near the phase transition temperature and an explanation has been put forward to explain these observed features