High yield nitrogen-doped carbon monolith with rich ultramicropores prepared by in-situ activation for high performance of selective CO2 capture.

Constrained by the unsatisfactory physical adsorption capacity and the low carbon yield from chemical activation, practical utilization of carbon materials for CO 2 capture and separation (CCS) remains a huge challenge. Herein, we proposed a novel in-situ activation methodology to prepare a category of porous carbon monoliths in which the potassium ion activation sites are evenly introduced through acid-base reaction, contributing to the high carbon yield, abundant ultramicropores as well as rich nitrogen content. Tested at adsorption temperatures of 0, 25 and 40 °C, the as-prepared carbon monoliths display remarkable static CO 2 uptake (7.1, 5.0 and 3.7 mmol/g, respectively) and excellent selective adsorption ability in dynamic breakthrough experiment with a binary mixture of CO 2 /N 2 (68, 63 and 67, respectively). Along with the experiments, the CO 2 adsorption mechanism was determined by calculating the adsorption density and adsorption energy on slit pore with various pore sizes and surface functionalities using grand canonical Monte Carlo (GCMC) simulation. The narrow micropores can significantly and effectively increase the CO 2 adsorption capacity, while the functional groups played the second role. [Display omitted] [ABSTRACT FROM AUTHOR]