Constructing Hierarchically Porous N‑Doped Carbons Derived from Poly(ionic liquids) with the Multifunctional Fe-Based Template for CO2 Adsorption
Nitrogen-doped hierarchical porous carbons with a rich pore structure were prepared via direct carbonization of the poly(ionic liquid) (PIL)/potassium ferricyanide compound. Thereinto, the bisvinylimidazolium-based PIL was a desirable carbon source, and potassium ferricyanide as a multifunctional F...
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Veröffentlicht in: | ACS omega 2021-03, Vol.6 (10), p.7186-7198 |
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Sprache: | eng |
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Zusammenfassung: | Nitrogen-doped hierarchical porous carbons with a rich pore structure were prepared via direct carbonization of the poly(ionic liquid) (PIL)/potassium ferricyanide compound. Thereinto, the bisvinylimidazolium-based PIL was a desirable carbon source, and potassium ferricyanide as a multifunctional Fe-based template, could not only serve as the pore-forming agent, including metallic components (Fe and Fe3C), potassium ions (etching carbon framework during carbonization), and gas generated during the pyrolysis process, but also introduce the N atoms to porous carbons, which were in favor of CO2 capture. Moreover, the hierarchically porous carbon NDPC-1-800 (NDPC, nitrogen-doped porous carbon) had taken advantage of the highest specific surface area, exhibiting an excellent CO2 adsorption capacity and selectivity compared with NDC-800 (NDC, nitrogen-doped carbon) directly carbonized from the pure PIL. Furthermore, its hierarchical porous architectures played an important part in the process of CO2 capture, which was described briefly as follows: the synergistic effect of mesopores and micropores could accelerate the CO2 molecules’ transportation and storage. Meanwhile, the appropriate microporous size distribution of NDPC-1-800 was conducive to enhancing CO2/N2 selectivity. This study was intended to open up a new pathway for designing N-doped porous carbons combining both PILs and the multifunctional Fe-based template potassium ferricyanide with wonderful gas adsorption and separation performance. |
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ISSN: | 2470-1343 2470-1343 |
DOI: | 10.1021/acsomega.1c00419 |