Unravelling the selective transport of Co²⁺ and Hg²⁺ ions through functionalized graphene nanostructures from aqueous...

Molecular dynamics (MD) simulations were employed to unravel the atomistic mechanisms responsible for the selective permeation of cobalt (Co²⁺) and mercury (Hg²⁺) ions through chemically functionalized nanoporous graphene (GRA) membranes. The computational framework consisted of nanoporous GRA membranes functionalized with electronegative fluorine (-F) and chlorine (-Cl) moieties and immersed in mixed aqueous nitrate environments. An external electric field applied along the membrane normal induced directed ionic migration across the pores. Detailed structural and dynamical analyses reveal that ion transport is dictated by a delicate balance among hydration free energy, ion-pore electrostatic interactions, and interfacial polarization effects. The F-functionalized nanoporous GRA membranes have been shown to promote enhanced ion transport when subjected to an external electric field. Notably, Co²⁺ ions exhibit preferential permeation through F-functionalized pores, whereas Hg²⁺ ions demonstrate higher permeation efficiency in Cl-functionalized pores. These findings provide a fundamental molecular-level understanding of how functional group chemistry and applied electric fields modulate ion selectivity and transport energetics in GRA-based membranes with tailored pore diameters, offering predictive insights for the rational design of next-generation nanofiltration and electroseparation systems.