Sizable glass formers feature numerous unique properties and potential applications, but many questions regarding their glass transition dynamics have not been resolved yet. Here, we have analyzed structural relaxation times measured as a function of temperature and pressure in combination with the equation of state obtained from pressure-volume-temperature measurements. Despite evidence from previous dielectric studies indicating a remarkable sensitivity of supercooled dynamics to compression, and contrary to intuition, our results demonstrated the proof for the almost equivalent importance of thermal energy and free volume fluctuations in controlling reorientation dynamics of sizable molecules. The found scaling exponent γ = 3.0 and Ev/Ep ratio of 0.6 were typical for glass-forming materials with relaxation dynamics determined by both effects with a minor advantage of thermal fluctuations involvement. It shows that the high values of key parameters characterizing the sensitivity of the glass transition dynamics to pressure changes, i.e., activation volume ΔV and dTg/dP, are not a valid premise for a remarkable contribution of volume to glass transition dynamics.
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http://dx.doi.org/10.1063/5.0217660 | DOI Listing |
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