▎ 摘　　要

Graphene membranes with nanometer-scale pores could exhibit an extremely high permeance and selectivity for the separation of gas mixtures. However, to date, no experimental measurements of gas mixture separation through nanoporous single-layer graphene (SLG) membranes have been reported. Herein, we report the first measurements of the temperature-dependent permeance of gas mixtures in an equimolar mixture feed containing H-2, He, CH4, CO(2 )and SF6 from 22 to 208 degrees C through SLG membranes containing nanopores formed spontaneously during graphene synthesis. Five membranes were fabricated by transfer of CVD graphene from catalytic Cu film onto channels framed in impermeable Ni. Two membranes exhibited gas permeances on the order of 10(-6) to 10(-5) mol m(-2) s(-1) Pa-1 as well as gas mixture selectivities higher than the Knudsen effusion selectivities predicted by the gas effusion mechanism. We show that a new stenc selectivity mechanism explains the permeance data and selectivities. This mechanism predicts a mean pore diameter of 2.5 nm and an areal pore density of 7.3 X 10(13) m(-2), which is validated by experimental observations. A third membrane exhibited selectivities lower than the Knudsen effusion selectivities, suggesting a combination of effusion and viscous flow. A fourth membrane exhibited increasing permeance values as functions of temperature from 27 to 200 degrees C, and a CO2/SF6 selectivity > 20 at 200 degrees C, suggestive of activated translocation through molecular-sized nanopores. A fifth membrane exhibited no measurable permeance of any gas above the detection limit of our technique, 2 X 10(-7) mol m(-2) s(-1) Pa-1, indicating essentially a molecularly impermeable barrier. Overall, these data demonstrate that SLG membranes can potentially provide a high mixture separation selectivity for gases, with CVD synthesis alone resulting in nanometer-scale pores useful for gas separation. This work also shows that temperature-dependent permeance measurements on SLG can be used to reveal underlying permeation mechanisms.