Theoretical verification on adsorptive removal of caffeine by carbon and nitrogen-based surfaces: Role of charge transfer, π electron occupancy, and temperature

Abstract

Eliminating an emerging water pollutant, caffeine molecules, from an aqueous solution using carbon and nitrogen-based adsorbents is of significant interest to public health. These adsorbents have been shown to have decent adsorption capacity toward caffeine due to their surface functionality. Therefore, screening various carbon and nitrogen-based surfaces can be a better option for high-performance adsorbents to remove caffeine efficiently from wastewater. Herein, we present combined first principles and molecular dynamics quantification of the adsorption enthalpies of caffeine molecules on the possible active sites of carbon and nitrogen-based adsorbents (graphene, phagraphene, graphdiyne, single-wall carbon nanotube, fullerene, and graphitic carbon nitride) with the incorporation of Van der Waals interactions. From the DFT calculations, N-doped carbon surfaces show the highest adsorption energies of single and dimer CAF compared to pristine carbon-based adsorbents. A charge density difference and Bader charge analysis display that high charge transfer occurs between the caffeine's oxygen and the surface's nitrogen atoms. An abundance of π-electrons from the nitrogen atoms, composed of large electron clouds of aromatic rings on the graphitic carbon surface, tends to favor extensive π-π interactions with the caffeine molecule. The high value of p_z electron occupancy (1.445) of N in the hexagonal ring of the graphitic surface transfers additional charge transfer, which leads to strong adsorption energy of CAF than pristine surfaces. Also, the g-C₃N₄ surface adsorbs the CAF molecule with higher adsorption than other N-doped carbon surfaces due to the high p_{z_eo} (1.5448) of N atoms on the surface. At 310 K, the water molecules' kinetics aids the single and dimer caffeine molecules to adsorb with the highest adsorption energies on the active sites of g-C₃N₄ surfaces than graphene adsorbent.

Keywords: Adsorption; Caffeine; Carbon and nitrogen-based surfaces; Density functional theory; Molecular dynamics.