Regulating coordination environment around transition metal (Fe, Co) single atom catalysts for efficient Hg0 adsorption

Abstract

Elemental mercury (Hg0) is one of the main pollutants released during coal combustion, which is difficult to remove due to its hydrophobicity and volatility, resulting in serious environmental pollution. Therefore, it is urgent to develop a low-cost and high-performance catalyst to remove Hg0. In this work, using first-principles study, the effect of nonmetal (NM = B, C and O) coordination environment on the charge distribution of graphene-supported transition metal single atom catalysts (TM-N4-SAC) has been investigated. It is found that regulating the TM-N4-SAC with NM coordination atoms with fewer valence electrons than N atom can cause TM atoms to lose more electrons, and the charge distribution in the active center to be locally deviated. Moreover, in-depth analysis of the adsorption configuration, charge density difference, charge transfer, adsorption energy and density of state of Hg0 adsorption on NM modified TM-N4-SAC confirmed that the adsorption of Hg0 can be effectively enhanced only when TM atoms lose more electrons. Thus, Fe-N3B- and Co-N3B-SAC have the strongest ability to adsorb Hg0 because they have the most negative adsorption energy of −1.13 and −0.49 eV. This work provides theoretical guidance for the design of SAC for efficient adsorption of Hg0.