Authors: R.J. Mashl, S. Joseph, N.R. Aluru and E. Jakobsson
Affilation: University of Illinois, United States
Pages: 152 - 153
Keywords: nanotubes, water dynamics, order disorder transition, proton conduction
Molecular dynamics (MD) simulations suggest that water readily enters carbon nanotubes. This is also suggested by the fact that fluorescence in nanotubes is affected by the pH of external electrolyte. Distinctive symmetrical water structures emerge when water is energy minimized within nanotubes. In this paper we report on MD simulations in which we observe the formation of hexagonal ice at 300 K in a nanotube of critical diameter. Simulations, Observations, and Analysis. The simulation systems consisted of single-walled, open-ended carbon nanotubes 40 Å long and of various diameters (eight different diameters altogether), embedded in a hydrophobic slab and bathed in SPC/E water at 300K. All of the tubes filled with water and remained filled for the entire 2 ns of simulated time. We used the GROMACS simulation package and particle-mesh Ewald sums for the electrostatic interactions. After equilibration of each system, the state of the water in the lumen of the nanotube was analyzed by fluctuation-correlation analysis. Diffusion coefficients for the water inside the nanotubes as a function of channel diameter were computed. The diffusion coefficient is somewhat reduced from the bulk value in all sizes of nanotubes, with an anomalous reduction at a diameter of 12.2 Å (carbon atom center-to-center, or about 8.4 Å based on van der Waals surfaces) where the longitudinal motion is effectively eliminated. Rotational autocorrelation functions based on the water molecules dipole moments for the same simulations show that the water in the 12.2-Å diameter tube is anomalously immobilized rotationally as well. By comparing snapshots of the systems, it is seen that the water in the critical size tube is in a much more ordered regular array than in either smaller or larger tubes. A cross-section through the critical size tube in Fig. 4 shows that the water assumes a regular hexagonal pattern. By virtue of the translational and rotational immobilization and the hexagonal symmetry, we conclude that confinement of water in a nanotube of particular dimensions induces 300K water to form hexagonal ice. Significance. In considering charge carriers for nanoscale semiconductors, electrons have the disadvantage of tunneling distances of nanometers, rendering distinction between on and off states problematic. Protons in ice tunnel between adjacent water molecules over the length of a few Ångstroms. Proton-ice conduction might be switched off by a perturbation that disorders the water, dramatically reducing proton mobility. We suggest that protons tunneling through ice created by confinement in nanotubes be considered further as a possible conduction mechanism for nanoscale semiconductors.