Gas Transport Mechanisms through Molecular Thin Carbon Nanomembranes

Molecular thin carbon nanomembranes (CNMs) synthesized by electron irradiation induced cross-linking of aromatic self-assembled monolayers (SAMs) are promising 2D materials for the next generation of filtration technologies. Their unique properties including ultimately low thickness of approximate to 1 nm, sub-nanometer porosity, mechanical and chemical stability are attractive for the development of innovative filters with low energy consumption, improved selectivity, and robustness. However, the permeation mechanisms through CNMs resulting in, e.g., an approximate to 1000 times higher fluxes of water in comparison to helium have not been yet understood. Here, a study of the permeation of He, Ne, D-2, CO2, Ar, O-2 and D2O using mass spectrometry in the temperature range from room temperature to approximate to 120 degrees C is studied. As a model system, CNMs made from [1 '',4 ',1 ',1]-terphenyl-4-thiol SAMs are investigated. It is found out that all studied gases experience an activation energy barrier upon the permeation which scales with their kinetic diameters. Moreover, their permeation rates are dependent on the adsorption on the nanomembrane surface. These findings enable to rationalize the permeation mechanisms and establish a model, which paves the way toward the rational design not only of CNMs but also of other organic and inorganic 2D materials for energy-efficient and highly selective filtration applications.

Automated summary

Molecular thin carbon nanomembranes synthesized by electron irradiation induced cross-linking of aromatic self-assembled monolayers are promising 2D materials for filtration technologies. A study on the permeation of various gases through these nanomembranes reveals activation energy barriers and adsorption-dependent permeation rates. These findings contribute to the understanding of permeation mechanisms and the rational design of energy-efficient and highly selective filters.