Carbon dioxide (CO2) capture and storage is
a fundamental
global environmental issue that has driven researchers to develop
ingenious strategies to overcome this issue. Herein, N-enriched nanoporous
carbon fibers were prepared from commercially available polyacrylonitrile
fiber through a one-pot simultaneous carbonization/activation strategy.
The effect of the amount of the activating agent and carbonization
temperature on the nanoporous/surface chemical properties of carbons
and the consequent CO2 adsorption performance was fully
investigated. This direct activating strategy protected the fiber
morphology of the resulting nanoporous carbons, while also resulting
in a well-developed porous structure. The as-prepared nanoporous carbon
fiber shows the maximum Brunauer–Emmett–Teller surface
area and total pore volume of 2330 m2 g–1 and 1.25 cm3 g–1, respectively, together
with a nitrogen content of up to 14.36 wt %. The optimal nanoporous
carbon fiber exhibited CO2 uptakes of 6.16 and 4.03 mmol
g–1 at 1 bar and 0 and 25 °C, respectively,
with an acceptable CO2/N2 selectivity of 23.
Besides, the optimal sample depicts a dynamic CO2 capture
capacity of 0.84 mmol g–1 and only a 3% CO2 uptake capacity loss after five adsorption–desorption cycles.
Overall, the combined effect of narrow microporosity and nitrogen
functionalities determined the CO2 uptake of this series
of N-doped nanoporous carbon fibers.