Accurate stacking engineering of MOF nanosheets as membranes for precise H<sub>2</sub> sieving.
basic_science · Level V
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- Record sourced from PubMed, PMID 39737921.
- Also identified by DOI 10.1038/s41467-024-54663-7 and PMC identifier 11685790.
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Abstract
Two-dimensional (2D) metal-organic framework (MOF) nanosheet membranes hold promise for exact molecular transfer due to their structural diversity and well-defined in-plane nanochannels. However, achieving precise regulation of stacking modes between neighboring nanosheets in membrane applications and understanding its influence on separation performance remains unrevealed and challenging. Here, we propose a strategy for accurately controlling the stacking modes of MOF nanosheets via linker polarity regulation. Both theoretical calculations and experimental results demonstrate that a high linker polarity promotes neighboring nanosheets to a maximum AB stacking due to steric hindrance effects, leading to a controlled effective pore size of the membrane and consequently to improved molecular sieving. Among series of CuBDC-based 2D MOFs with different linkers, the CuBDC-NO<sub>2</sub> nanosheet membranes exhibit a reduced effective stacking aperture of 0.372 nm, yielding H<sub>2</sub> permeance of 4.44 × 10<sup>-7</sup> mol m<sup>-2</sup> s<sup>-1</sup> Pa<sup>-1</sup> with a high H<sub>2</sub>/CO<sub>2</sub> and H<sub>2</sub>/CH<sub>4</sub> selectivity of 266 and 536, respectively. This work represents the in-depth investigation of the accurate tuning of MOF nanosheet stacking in the field of 2D materials, offering more perspectives for broader applications with universality for various 2D materials.