Thermodynamic and dilatometric properties of the dimerized phase of a C60 fullerene

This paper reports on the results of complex investigations into the structural, thermodynamic, and dilatometric properties of the C60 dimerized phase prepared under compression of a C60 fullerite at a pressure up to 8 GPa and a temperature of 290 K. It is demonstrated that the dimerized phase has a face-centered cubic structure with a lattice parameter a=14.02±0.05 Å. The dimeric structure of the studied sample is confirmed by x-ray diffraction analysis. According to the dilatometric data, the volume jump observed in the vicinity of the orientational transition for the dimerized phase is estimated to be approximately 30 times less than that for the C60 fullerite. The temperature dependence of the heat capacity of the (C60)2 crystalline dimer is examined using precision adiabatic vacuum calorimetry under normal pressure in the temperature range from T → 0 K to 340 K. The results obtained are used in the calculations of thermodynamic functions, namely, the heat capacity Cp0 (T), the enthalpy H0(T)-H0(0), the entropy S0(T), and the Gibbs function G0(T)-H0(0). The fractal dimension D is determined as a function of the heat capacity. The standard entropy of the formation of the (C60)2 crystalline dimer from a simple compound (graphite) at T=298.15 K and normal pressure is calculated.