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RESEARCH PRODUCT

Dynamics of supercooled confined water measured by deep inelastic neutron scattering

Antonio CupaneGiovanni RomanelliVincenzo De Michele

subject

liquid-liquid transitionMaterials sciencePhysics and Astronomy (miscellaneous)HydrogenThermodynamicschemistry.chemical_element02 engineering and technologyNeutron scatteringKinetic energy01 natural sciencesInelastic neutron scatteringMomentumchemistry.chemical_compoundsilica xerogelconfined water0103 physical sciences010306 general physicsSupercoolingliquid–liquid transitionSettore FIS/07021001 nanoscience & nanotechnologyconfined water; hydrogen mean kinetic energy; liquid–liquid transition; silica xerogel; Physics and Astronomy (miscellaneous)Settore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)chemistryhydrogen mean kinetic energyAlkoxideWater of crystallization0210 nano-technology

description

In this paper, we present the results of deep inelastic neutron scattering (DINS) measurements on supercooled water confined within the pores (average pore diameter ~ 20 Å) of a disordered hydrophilic silica matrix obtained through hydrolysis and polycondensation of the alkoxide precursor Tetra-Methyl-Ortho-Silicate via the sol-gel method. Experiments were performed at two temperatures (250 K and 210 K, i.e., before and after the putative liquid–liquid transition of supercooled confined water) on a “wet” sample with hydration h ~ 40% w/w, which is high enough to have water-filled pores but low enough to avoid water crystallization. A virtually “dry” sample at h ~ 7% was also investigated to measure the contribution of the silica matrix to the neutron scattering signal. As is well known, DINS measurements allow the determination of the mean kinetic energy and the momentum distribution of the hydrogen atoms in the system and therefore, allow researchers to probe the local structure of supercooled confined water. The main result obtained is that at 210 K the hydrogen mean kinetic energy is equal or even slightly higher than at 250 K. This is at odds with the predictions of a semiempirical harmonic model recently proposed to describe the temperature dependence of the kinetic energy of hydrogen in water. This is a new and very interesting result, which suggests that at 210 K, the water hydrogens experience a stiffer intermolecular potential than at 250 K. This is in agreement with the liquid–liquid transition hypothesis.

10.1007/s11467-017-0699-1http://hdl.handle.net/10447/267048