摘要
Ultrathin and defect-free MOF membranes are actively pursued to realize high-performance hydrogen purification and carbon capture, which are of great significance for energy conservation and environmental sustainability. Zeolitic imidazolate framework-67 (ZIF-67) possesses exceptional pore apertures for sieving hydrogen from other larger gases. However, the preferential heterogeneous nucleation and growth of ZIF-67 crystals greatly challenge the synthesis of ZIF-67 membranes. In this work, a tunable-reaction-zone contra-diffusion synthesis is proposed to effectively assemble ZIF-67 nanocrystals into ultrathin GO laminates. The contra-diffusion-match growth of ZIF-67 constructs a compact ZIF-67@GO hybrid structure with superior H 2 /CO 2 separation factor of 140.8 and H 2 permeance of 1.7 × 10 −7 mol m −2 s −1 Pa −1 , transcending the state-of-art upper bounds. The excellent separation performance is attributed to the collaborative effect of the size-sieving and the selective attraction of the ZIF-67@GO hybrid structure. Long-term operation also reveals the superior stability of the ZIF-67@GO hybrid membrane for H 2 /CO 2 separation. The rational-design approach grants a novel way to fabricate ultrathin and defect-free ZIF-67 crystalline membranes for high-performance gas separation.
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