Phase transitions study of the liquid crystal DIO with a ferroelectric nematic, a nematic and an intermediate phase and of mixtures with the ferroelectric nematic compound RM734 by adiabatic scanning calorimetry

Abstract

Adiabatic scanning calorimetry (ASC) is capable of providing simultaneously the specific enthalpy h(T) and the specific heat capacity cp(T), and is an important tool to determine the order of transitions and to render high-resolution information on pretransitional thermal behavior. Here we report on ASC results on the compound DIO and on mixtures with RM734. Both compounds exhibit a low-temperature ferroelectric nematic phase (NF) and a high-temperature paraelectric nematic (N). In DIO these two phases are separated by an intermediate phase (Nx). Detailed data of h(T) and cp(T), indicated that the intermediate phase was present in all mixtures over the complete composition range, albeit with strongly decreasing temperature width with decreasing mole fraction of DIO (xDIO). The xDIO dependence of the two transitions could be well described by a quadratic function and both transitions were weakly first order. The true latent heat of the Nx-N transition of DIO was as low as 0.0075 +/- 0.0005 J/g and 0.23 +/- 0.03 J/g for the NF-Nx transition, about twice the previously reported value of 0.115 J/g for the NF-N transition in RM734. In the mixtures both transition latent heats decrease gradually with decreasing xDIO. At all the Nx-N transitions pretransition fluctuation effects are absent and these transitions are purely but very weakly first order. As in RM734 the transition from the NF to the higher temperature phase exhibits substantial pretransitional behaviour. Power law analysis of cp(T) resulted in an effective critical exponent of 0.88 +/- 0.10 for DIO and this value decreased in mixtures with decreasing xDIO towards 0.50 +/- 0.05 reported for RM734. Ideal mixture analysis of the phase diagram was consistent with ideal mixture behavior for the total transition enthalpy change