Metal Organic Framework Porous Liquids for Integrated CO <sub>2</sub> Capture and Conversion
Integrated selective capture and conversion of CO<sub>2</sub> to high-value products is a highly energy-efficient and realistic strategy toward a carbon-neutral future. Inspired by nature, we have rationally designed type-III Porous Liquids (PLs) using carbonic anhydrase (CA) mimicking ZIF-8 and Good's buffer-based ionic liquid (IL) for highly efficient integrated selective capture and conversion of CO<sub>2</sub> under practical conditions. The PLs exhibit remarkable selectivity and uptake capacity for CO<sub>2</sub>, among the highest reported for ZIF-8 based type-III PLs. The superior capture performance is ascribed to the molecular sieving effect and retention of high porosity in PL, further aided by the fluid media enabling both physi- and chemisorption storage pathways and high mass transport. The PLs catalyse CO<sub>2</sub> hydration, and the pore-encapsulated CO<sub>2</sub> and bicarbonate are in dynamic equilibrium. The captured CO<sub>2</sub> is subsequently converted to CaCO<sub>3</sub> in high yield. As against CA, the PLs are more tolerant to reaction conditions and showed better performance. Remarkably, PLs selectively capture and convert CO<sub>2</sub> from simulated flue gas (15% CO<sub>2</sub>) and ambient air (0.04% CO<sub>2</sub>), a highly desirable yet unexplored application. The study demonstrates PLs as a modular material for integrated CO<sub>2</sub> capture and catalytic conversion under practical conditions for a sustainable closed loop carbon economy.
Authors
- Sanjog S. Nagarkar (ORCID: https://orcid.org/0000-0001-5487-6225)
- Raj Kumar (ORCID: https://orcid.org/0009-0003-1226-3924)
- Rishabh Dubey
- Himani Goyal
- Kamendra P. Sharma
- Akshay Kulshrestha
Institutions
- Indian Institute of Technology Bombay (IN)
Publication Details
- Journal
- Small
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1002/smll.202514343
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00