▎ 摘　　要

Among the carbon-based two-dimensional (2D) materials, graphene oxide (GO) has been attracting growing interest because of its ability to be utilized in the field of water remediation. Therefore, an atomistic understanding of the transport properties of water in layered GO is pivotal for the development of novel GO membranes. Surprisingly, the very issue of the 2D self-diffusion of water confined between two GO sheets appears to be controversial, and simulations showing either a slowdown or no effect have been reported. In any case, the formation of hydrogen bonds, i.e., among the confined water and between water and the GO functional groups, was identified to control diffusion. However, the results of molecular dynamics (MD) simulations heavily depend on the forces used. Density functional theory (DFT) and empirical force fields are opposite when it comes to accuracy and numerical costs. As a compromise in the present study, we performed MD simulations using a DFT-based tight-binding method to investigate the diffusion of water confined between GO sheets. Specifically, we considered six GO/water models, differing in the ordering of the epoxide and hydroxyl groups as well as in the thickness of the water layer. For these models having GO interlayer distances between 8 and 12 angstrom, we find a reduction of the diffusion coefficient by a factor between 2 and 3 compared with bulk water. One possible origin of this effect is the temporary trapping of water within hydrogen-bonded water bridges between the GO sheets. The proposed mechanism should be taken into account in the development of, for instance, GO membranes for water remediation or applications in the field of selective transport in separation membranes.