This framework demonstrates effective CO2 capture and enhanced selectivity in flue gas and biogas, suggesting its potential application.
The development of porous materials for the selective capture of CO2 from flue gas and biogas is crucial for ecological conservation and clean energy advancement. Herein, a novel three-dimensional copper-based metal-organic framework (Cu-MOF) was solvothermally synthesized by using a multifunctional ligand abundant in carboxyl and triazole groups. Inorganic secondary building units (SBUs) feature two types of square-planar mononuclear copper SBUs: a highly polar cis configuration and a symmetric trans configuration. This dual-SBU design maximizes the density of open-metal sites (OMSs) (2.84 per nm3) while simultaneously enhancing both polarity and structural stability. The ligand contains an abundance of uncoordinated N and O atoms, which furnish densely populated Lewis-base sites (LBSs) throughout the pores. The dual-site distribution of OMSs and LBSs present in two distinct polar channels results in a relatively high BET specific surface area, a substantial CO2 uptake capacity, and a CO2/N2 selectivity of 112. Breakthrough experiments reveal a dynamic CO2 uptake of 2.42 mmol g-1 per cycle with well-maintained recyclability. Grand-canonical Monte Carlo and DFT calculations reveal the synergistic binding of CO2 to both OMSs and LBSs, underscoring the practical potential for low-energy CO2 separation from flue gas and biogas.
No takes yet. Share an insight, caveat, or question.
Zhang et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: