Nanomeshes with Sub-10 nm Pores by Glycerol-Triggered 2D Assembly in Liquid Phases for Fast and Selective Membranes.

ABSTRACT

Nanomeshes having ultrathin thicknesses and penetrating nanopores promise fast diffusion and precise selectivity and are highly desired in diffusion-involved processes such as separation. Herein, we report a liquid-phase two-dimensional (2D) assembly strategy to synthesize phenolic and carbonaceous nanomeshes with sub-10 nm pores and thicknesses. The synthesis is enabled simply by introducing glycerol in the thermopolymerization of resol/polyether micelles dispersed in ethanol. Experimental and simulation results reveal that glycerol's strong ability to form hydrogen bonds constrain the motion of the micelles, directing them to pack and merge exclusively in the lateral direction. Upon removal of polyether, we obtain phenolic nanomeshes with lateral sizes up to hundreds of micrometers, which can be further converted to carbonaceous nanomeshes. As a proof of concept, we use stacked phenolic and carbonaceous nanomeshes as separation membranes. They show superior permselectivity to nanosized solutes with permeance ∼2-110 times higher than that of other membranes.