The unusual dynamics of water under confinement was important to a number of conventional and emerging industrial processes and to life in general; nevertheless, understanding of this critical area was still in an early stage. Nanoporous carbons have provided a key material through which to investigate this dynamics; however, existing simulations were based upon the use of idealized slit pore carbons or carbon nanotubes with smooth energy landscapes and fail to capture the influence of structural disorder inherent to real carbons. It was shown here that the irregular structure of such carbons critically influences the dynamics and the mode of diffusion (single file, sub-diffusion or Fickian). These molecular dynamics simulations, using a realistic hydrophobic carbon model based upon hybrid reverse Monte Carlo simulation of the structure of an activated carbon fiber, showed the existence of a single-file diffusion mode between the ballistic and Fickian modes in the narrowest pore regions of this material, not seen in simulations using model 2-D slit pores. A rich variety of behavior was found in this sub-diffusion regime, with the fits of time-dependent mean square displacement to the power law of time (∝tα), revealing that the exponent α varies significantly with temperature, especially at low temperatures (273-350K). It reaches a minimum value of 0.5 at 298K corresponding to the single-file diffusion regime and approaches unity at 610K, corresponding to the Fickian mode. It was demonstrated that confinement effects lead to the experimentally observed non-Arrhenius behavior of the water dynamics at low temperatures (<350K), for both the realistic carbon model and an idealized 2-D slit pore model, due to the transport of the adsorbed water as a large cluster in a water monolayer.

Some Anomalies in the Self-Diffusion of Water in Disordered Carbons. Nguyen, T.X., Bhatia, S.K.: Journal of Physical Chemistry C, 2012, 116[5], 3667-76