MOF-in-COF molecular sieving membrane for selective hydrogen separation

Covalent organic frameworks (COFs) are promising materials for advanced molecular-separation membranes, but their wide nanometer-sized pores prevent selective gas separation through molecular sieving. Herein, we propose a MOF-in-COF concept for the confined growth of metal-organic framework (MOFs) inside a supported COF layer to prepare MOF-in-COF membranes. These membranes feature a unique MOF-in-COF micro/nanopore network, presumably due to the formation of MOFs as a pearl string-like chain of unit cells in the 1D channel of 2D COFs. The MOF-in-COF membranes exhibit an excellent hydrogen permeance (>3000 GPU) together with a significant enhancement of separation selectivity of hydrogen over other gases. The superior separation performance for H-2/CO2 and H-2/CH4 surpasses the Robeson upper bounds, benefiting from the synergy combining precise size sieving and fast molecular transport through the MOF-in-COF channels. The synthesis of different combinations of MOFs and COFs in robust MOF-in-COF membranes demonstrates the versatility of our design strategy. Covalent organic frameworks (COFs) are promising materials for separation membranes, but their wide pores prevent selective gas separation through molecular sieving. Here, the authors demonstrate a Metal-organic framework (MOF)-in-COF membrane with a significant enhancement of separation selectivity of hydrogen over other gases.

Automated summary

COFs are promising for separation membranes, but MOF-in-COF membranes show significant enhancement in hydrogen selectivity over other gases.