arXiv subjects

V. G. Gavrilko

Publications and source records attributed to V. G. Gavrilko.

16 recordsLinked to original sources

arXiv2018

Thermal expansion of organic superconductor a-(BEDT-TTF)2 NH4Hg(SCN)4

The temperature dependence of the linear thermal expansion coefficients (LTEC) of a single crystal of a-(BEDT-TTF)2NH4Hg(SCN)4 where BEDT-TTF is bis(ethylenedithio)tetrathiafulvalene was studied by the method of precision capacitive dilatometry in the temperature range 2-250 K along the crystallographic direction b* (perpendicular to the crystal layers). Negative values of LTEC were found below 4 K. Probably it is due to charge fluctuations as the temperature approaches the temperature of transition to the superconducting state Tc. It has been suggested that the bends on temperature dependence of LTEC observed in the temperature range 25-45 K are related to order-disorder arrangement of NH4+ ions. Weak maximum of the LTEC, detected at a temperature of about 200-220 K, can be caused by the processes of charge redistribution and the associated intermolecular interaction fluctuations.

cond-mat.supr-con↗

arXiv2017

Thermal expansion of organic superconductor k-(D4-BEDT-TTF)2Cu{N(CN)2}Br. Isotopic effect

Linear thermal expansion coefficient (LTEC) of single crystal k-(D4-BEDT-TTF)2Cu[N(CN)2]Br was studied across the crystal layers in the temperature range 2-290 K using the method of precise capacitive dilatometry. Below Tc = 11,6 K the LTEC of the sample had a small negative value, which is apparently due to the transition from the paramagnetic metal in the superconducting state. There was a bend of temperature dependence of the LTEC, which shows broad peak around 40 K and can be attributed to the elastic lattice anomaly around the end-point of Mott boundary. A sharp jump in the LTEC values and hysteresis was observed in the area of Tg ~ 75-77 K, what is likely explained by the transition in a glass-like state. The isotope effect in the thermal expansion is discusses, which manifested itself in a shift of the phase transitions in comparison with fully deuterated BEDT-TTF sample.

cond-mat.mes-hall↗

arXiv2016

The effect of the thermal reduction on the kinetics of low temperature 4He sorption and the structural characteristics of graphene oxide

The kinetics of the sorption and the subsequent desorption of 4He by the starting graphite oxide (GtO) and the thermally reduced graphene oxide samples (TRGO, Treduction = 200, 300, 500, 700 and 900 C) have been investigated in the temperature interval 1.5 - 20 K. The effect of the annealing temperature on the structural characteristics of the samples was examined by the X-ray diffraction (XRD) technique. On lowering the temperature from 20 K to 11-12 K, the time of 4He sorption increased for all the samples, which is typically observed under the condition of thermally activated diffusion. Below 5 K the characteristic times of 4He sorption by the GtO and TRGO-200 samples were only weakly dependent on temperature, suggesting the dominance of the tunnel mechanism. In the same region (T<5 K) the characteristic times of the TRGOs reduced at higher temperatures (300, 500, 700 and 900 C) were growing with lowering temperature, presumably due to the defects generated in the carbon planes on removing the oxygen functional groups (oFGs). The estimates of the activation energy (Ea) of 4He diffusion show that in the TRGO-200 sample the Ea value is 2.9 times lower as compared to the parent GtO, which is accounted for by GtO exfoliation due to evaporation of the water intercalated in the interlayer space of carbon. The nonmonotonic dependences Ea vs T for the GtO samples treated above 200 C are determined by a competition between two processes - the recovery of the graphite carbon structure, which increases the activation energy, and the generation of defects, which decreases the activation energy by opening additional surface areas and ways for sorption. The dependence of the activation energy on treatment temperature correlates well with the contents of the crystalline phase in GtO varying with a rise of the annealing temperature.

cond-mat.mes-hall↗

arXiv2013

Sorption of 4He, H2, Ne, N2, CH4 and Kr impurities in graphene oxide at low temperatures. Quantum effects

Sorption and the subsequent desorption of 4He, H2,Ne, N2, CH4 and Kr gas impurities by graphene oxide (GO), glucose-reduced GO (RGO-Gl) and hydrazine-reduced GO (RGO-Hz) powders have been investigated in the temperature interval 2-290 K. It has been found that the sorptive capacity of the reduced sample RGO-Hz is three to six times higher than that of GO. The reduction of GO with glucose has only a slight effect on its sorptive properties. The temperature dependences of the diffusion coefficients of the GO, RGO-Gl and RGO-Hz samples have been obtained using the measured characteristic times of sorption. It is assumed that the temperature dependences of the diffusion coefficients are determined by the competition of the thermally activated and tunneling mechanisms, the tunneling contribution being dominant at low temperatures.

cond-mat.mes-hall↗

arXiv2012

The effect of the glass transition in fullerite C60 on Ar impurity diffusion

The kinetics of sorption and subsequent desorption of argon gas by a C60 powder has been investigated in the temperature interval 58-290 K. The temperature dependence of the coefficients of Ar diffusion in fullerite has been obtained using the measured characteristic times of sorption. The diffusion coefficients of Ar decrease monotonically with lowering temperature in the whole range of the investigated temperatures, which corresponds to the thermally activated diffusion of Ar atoms in fullerite. The glass transition in fullerite induces an order-of-magnitude decrease in the activation energy of Ar diffusion in fullerite. Most likely this is because new directions may appear due to the glass transition in which the barriers separating the interstitial voids in the C60 lattice are significantly lower

cond-mat.mes-hall↗

arXiv2011

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 investigated

cond-mat.mes-hall↗

arXiv2011

Quantum phenomena in the radial thermal expansion of bundles of single-walled carbon nanotubes doped with 3He. A giant isotope effect

The radial thermal expansion αr of bundles of single-walled carbon nanotubes saturated with 3He up to the molar concentration 9.4% has been investigated in the temperature interval 2.1-9.5 K by high-sensitivity capacitance dilatometry. In the interval 2.1-7 K a negative αr was observed, with a magnitude which exceeded the largest negative αr values of pure and 4He-saturated nanotubes by three and two orders of magnitude, respectively. The contributions of the two He isotope impurities to the negative thermal expansion of the nanotube bundles are most likely connected with the spatial redistribution of 4He and 3He atoms by tunneling at the surface and inside nanotube bundles. The isotope effect turned out to be huge, probably owing to the higher tunneling probability of 3He atoms.

cond-mat.mes-hall↗

arXiv2010

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.

cond-mat.mes-hall↗

arXiv2010

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.

cond-mat.mes-hall↗

arXiv2009

The effect of sorbed hydrogen on low temperature radial thermal expansion of single walled carbon nanotube bundles

The effect of a normal H2 impurity upon the radial thermal expansion (Ar) of SWNT bundles has been investigated in the interval T = 2.2-27 K using the dilatometric method. It is found that H2 saturation of SWNT bundles causes a shift of the temperature interval of the negative thermal expansion towards lower (as compared to pure CNTs) temperatures and a sharp increase in the magnitude of (Ar) in the whole range of temperatures investigated. The low temperature desorption of H2 from a powder consisting of bundles of SWNTs, open and closed at the ends, has been investigated.

cond-mat.mes-hall↗

arXiv2008

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.

cond-mat.mtrl-sci↗

arXiv2008

The effect of the noncentral impurity-matrix interaction upon the thermal expansion and polyamorphism of solid CO-C60 solutions at low temperatures

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 - 23 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, and the thermalization times 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.

cond-mat.dis-nn↗

arXiv2006

Thermal expansion and polyamorphism of N2 - C60 solutions

The linear thermal expansion coefficients a(T) of N2 - C60 solutions with 9.9% and 100% of the C60 lattice interstitials filled with N2 have been investigated in the interval 2.2 - 24 K. The dependence a(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 C60 molecules have been estimated.

cond-mat.mtrl-sci↗

arXiv2004

On the polyamorphism of fullerite-based orientational glasses

The dilatometric investigation in the temperature range of 2-28K shows that a first-order polyamorphous transition occurs in the orientational glasses based on C60 doped with H2, D2 and Xe. A polyamorphous transition was also detected in C60 doped with Kr and He. It is observed that the hysteresis of thermal expansion caused by the polyamorphous transition (and, hence, the transition temperature) is essentially dependent on the type of doping gas. Both positive and negative contributions 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 positive contribution. The positive contribution is found to be due to phonon and libron modes, whilst the negative contribution is attributed to tunneling states of the C60 molecules. The characteristic time of the phase transformation from the low-T phase to the high-T phase has been found for the C60-H2 system at 12K. A theoretical model is proposed to interpret these observed phenomena. The theoretical model proposed, includes a consideration of the nature of polyamorphism in glasses, as well as the thermodynamics and kinetics of the transition. A model of non-interacting tunneling states is used to explain the negative contribution to the thermal expansion. The experimental data obtained is considered within the framework of the theoretical model. From the theoretical model 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 the Kolmogorov law with an exponent of n=1. At this stage of the transformation, the two-dimensional phase boundary moves along the normal, and the nucleation is not important.

cond-mat.dis-nn↗

arXiv2002

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 high-resolution capacitance dilatometer. The investigation of the time dependence of the sample length variations on heating 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 quantum character. The inert gas impurities affect very strongly the reorientation of the C60 molecules 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.

cond-mat.mtrl-sci↗

arXiv2002

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.

cond-mat.mtrl-sci↗