CO2 Capture by Hybrid Ultramicroporous TIFSIX-3-Ni under Humid Conditions Using Non-Equilibrium Cycling

Although pyrazine-linked hybrid ultramicroporous materials (HUMs, pore size <7 angstrom) are benchmark physisorbents for trace carbon dioxide (CO2) capture under dry conditions, their affinity for water (H2O) mitigates their carbon capture performance in humid conditions. Herein, we report on the co-adsorption of H2O and CO2 by TIFSIX-3-Ni-a high CO2 affinity HUM-and find that slow H2O sorption kinetics can enable CO2 uptake and release using shortened adsorption cycles with retention of ca. 90 % of dry CO2 uptake. Insight into co-adsorption is provided by in situ infrared spectroscopy and ab initio calculations. The binding sites and sorption mechanisms reveal that both CO2 and H2O molecules occupy the same ultramicropore through favorable interactions between CO2 and H2O at low water loading. An energetically favored water network displaces CO2 molecules at higher loading. Our results offer bottom-up design principles and insight into co-adsorption of CO2 and H2O that is likely to be relevant across the full spectrum of carbon capture sorbents to better understand and address the challenge posed by humidity to gas capture.

Automated summary

This study investigates the co-adsorption of water and carbon dioxide by a high CO2 affinity ultramicroporous material. It is found that slow water sorption kinetics enable shortened adsorption cycles with retention of approximately 90% of dry CO2 uptake. In situ infrared spectroscopy and ab initio calculations provide insight into the binding sites and sorption mechanisms of CO2 and H2O molecules in the ultramicropore.