Abstract
The glass-to-liquid transition of water, particularly in high-density water (HDW), has long been a controversial topic due to challenges posed by inevitable crystallization. In this study, we addressed this issue by creating homogeneous high-density glass from a dilute glycerol aqueous solution under high pressure. Using dielectric spectroscopy, we explored the glass transition of HDW in glycerol solutions across the full concentration range under high pressures. HDW was found to exhibit two distinct relaxation modes: one linked to cooperative motion and the other to noncooperative local motion. The fragility index classification of HDW, derived from the cooperative motion of water, suggests that HDW behaves as a "fragile" liquid, contradicting previous suggestions. Extrapolation to pure HDW indicates that the dielectric relaxation observed in pure HDW originates from noncooperative local water motion.
Published Version
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