Some Anomalies in the Self-Diffusion of Water in Disordered Carbons

• Published in: Journal of physical chemistry. C Vol. 116; no. 5; pp. 3667 - 3676
• Main Authors: Nguyen, Thanh X, Bhatia, Suresh K
• Format: Journal Article
• Language: English
• Published: Columbus, OH American Chemical Society 09-02-2012
• Subjects: Condensed matter: structure, mechanical and thermal properties; Cross-disciplinary physics: materials science; rheology; Diffusion; interface formation; Exact sciences and technology; Materials science; Nanoscale materials and structures: fabrication and characterization; Nanotubes; Other topics in nanoscale materials and structures; Physics; Solid surfaces and solid-solid interfaces; Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties); Confinement; Digital simulation; Molecular dynamics method; Theoretical study; Carbon nanotubes; Nanostructures; Carbon; Time dependence; Carbon fibers; Monte Carlo methods; Monolayers; Diffusion; Nanostructured materials; Self-diffusion; Nanoporosity
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/jp2110727

The unusual dynamics of water under confinement is important to a number of conventional and emerging industrial processes and to life in general; nevertheless, our understanding of this critical area is still in an early stage. Nanoporous carbons have provided a key material through which to investigate this dynamics; however, existing simulations have been based on 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. We show here that the irregular structure of such carbons critically influences the dynamics and the mode of diffusion (single file, subdiffusion or Fickian). Our molecular dynamics simulations, using a realistic hydrophobic carbon model based on hybrid reverse Monte Carlo simulation of the structure of an activated carbon fiber, show 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 is found in this subdiffusion regime, with the fits of time-dependent mean square displacement to the power law of time (∝t α), revealing that the exponent α varies significantly with temperature, especially at low temperatures (273–350 K). It reaches a minimum value of 0.5 at 298 K corresponding to the single-file diffusion regime and approaches unity at 610 K, corresponding to the Fickian mode. It is demonstrated that confinement effects lead to the experimentally observed non-Arrhenius behavior of the water dynamics at low temperatures (<350 K), 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.