Changho Lee

Ultimate Permeation Across Atomically Thin Porous Graphene

Thin and Selective Outpourings When using a membrane to separate materials, the efficiency of the separation is limited by how fast the gas or liquid passes through the membrane and by how selective it is. Thinner membranes usually allow for faster flow rates but are usually less selective. Attempting to maintain selectivity, Celebi et al. (p. 289) developed a sophisticated way to drill holes of controlled diameter in a graphene sheet about two layers thick. For such a thin membrane, the primary barriers to separation come from entrance and exit from the holes and not from the motion through the membrane. Atomically thin nanoporous graphene membranes can sustain ultimate permeation in mass transport. A two-dimensional (2D) porous layer can make an ideal membrane for separation of chemical mixtures because its infinitesimal thickness promises ultimate permeation. Graphene—with great mechanical strength, chemical stability, and inherent impermeability—offers a unique 2D system with which to realize this membrane and study the mass transport, if perforated precisely. We report highly efficient mass transfer across physically perforated double-layer graphene, having up to a few million pores with narrowly distributed diameters between less than 10 nanometers and 1 micrometer. The measured transport rates are in agreement with predictions of 2D transport theories. Attributed to its atomic thicknesses, these porous graphene membranes show permeances of gas, liquid, and water vapor far in excess of those shown by finite-thickness membranes, highlighting the ultimate permeation these 2D membranes can provide.

Oxygen Concentration Control of Dopamine-Induced High Uniformity Surface Coating Chemistry

Material surface engineering has attracted great interest in important applications, including electronics, biomedicine, and membranes. More recently, dopamine has been widely exploited in solution-based chemistry to direct facile surface modification. However, unsolved questions remain about the chemical identity of the final products, their deposition kinetics and their binding mechanism. In particular, the dopamine oxidation reaction kinetics is a key to improving surface modification efficiency. Here, we demonstrate that high O(2) concentrations in the dopamine solution lead to highly homogeneous, thin layer deposition on any material surfaces via accelerated reaction kinetics, elucidated by Le Chateliers principle toward dopamine oxidation steps in a Michael-addition reaction. As a result, highly uniform, ultra-smooth modified surfaces are achieved in much shorter deposition times. This finding provides new insights into the effect of reaction kinetics and molecular geometry on the uniformity of modifications for surface engineering techniques.