Carbon molecular sieves (CMS) with a tunable pore structure hold significant promise for efficient CH/CH separation. However, understanding the relationship between a precursor's carbon framework and the microstructure of carbonized products is still ambiguous and requires further investigation. Herein, a relative aliphaticity/aromaticity regulated strategy was proposed to tailor the carbon skeleton of the polyamide precursor, aiming to fine tune the CMS pore size between the kinetic diameter of CH (4.
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