Abstract
New phase diagrams for water confined in graphene nanocapillaries and single-walled carbon nanotubes (CNTs) are proposed, identifying ice structures, their melting points and revealing the presence of a solid-liquid critical point. For quasi-2D water in nanocapillaries, we show through molecular-dynamics simulations that AA stacking in multilayer quasi-2D ice arises from interlayer hydrogen-bonding and is stable up to three layers, thereby explaining recent experimental observations. Detailed structural and energetic analyses show that quasi-2D water can freeze discontinuously through a first-order phase transition or continuously with a critical point. The first-order transition line extends to a continuous transition line, defined by a sharp transition in diffusivity between solid-like and liquid-like regimes. For quasi-1D water, confined in CNTs, we observe the existence of a similar critical point at intermediate densities. In addition, an end point is identified on the continuous-transition line, above which the solid and liquid phases deform continuously. The solid-liquid phase transition temperatures in CNTs are shown to be substantially higher than 273 K, confirming recent Raman spectroscopy measurements. We observe ultrafast proton and hydroxyl transport in quasi-1D and -2D ice at 300 K, exceeding those of bulk water up to a factor of five, thereby providing possible applications to fuel-cells and electrolyzers.
Highlights
Water molecules confined in nanometer-sized pores or adsorbed at interfaces exhibit unusual phase behavior that deviates significantly from bulk water due to confinement effects[1,2,3,4,5,6]
The initial structures were obtained from grand canonical Monte Carlo (GCMC) simulations[45], which were performed at a constant external chemical potential of liquid water
We extend our simulations to denser trigonal (n = 3) ice nanotubes and expand our understanding of the phase behavior of nanoconfined water by identifying different phase transition regimes characterized by the behavior of thermodynamic, structural and dynamic properties along the solid-liquid phase transition line
Summary
Water molecules confined in nanometer-sized pores or adsorbed at interfaces exhibit unusual phase behavior that deviates significantly from bulk water due to confinement effects[1,2,3,4,5,6]. Recent MD studies by Jiao et al.[48] report a similar behavior for monolayer square ice confined in graphene channels, where the 2D structure factor exhibits a continuous change on melting, over temperatures ranging from 310 K to 325 K.
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