Abstract
Metal-organic framework (MOF)-derived nanoscale porous materials are widely deployed in carbon capture, but the CO2 capacity is varied by different post-treatments, and its mechanism is still unclear. Herein, we prepared UiO-66 and treated it with methanol solvent and thermal activation approaches, which showed ∼3 times enhanced CO2 capacities from 15.1 to 45.0 mg/g and excellent recyclability of 10 cycles. The methanol treatment efficiently removes the residual guest molecules, including N,N-dimethylformamide, dangling organic linkers, and their derivatives, in the micropores (∼0.8 nm) of UiO-66 and improves the surface area, pore volume, and void fraction to enhance the CO2 capacity close to the ideal UiO-66 materials. The molecular dynamics simulation also proved a good linear relationship between the surface areas, void fraction, and CO2 capacity. This work provides a deep understanding of the MOF’s activation mechanism and its applications in CO2 capture.
Original language | English |
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Pages (from-to) | 12159-12167 |
Number of pages | 9 |
Journal | ACS Applied Nano Materials |
Volume | 6 |
Issue number | 13 |
DOIs | |
State | Published - Jul 14 2023 |
Funding
This research was supported financially by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, US Department of Energy (award no. DE-SC0022273).
Funders | Funder number |
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U.S. Department of Energy | DE-SC0022273 |
Basic Energy Sciences | |
Chemical Sciences, Geosciences, and Biosciences Division |
Keywords
- CO capture
- UiO-66
- metal−organic frameworks
- methanol activation
- solvent-exchange