Abstract
The CO(2) electrochemical reduction reaction (CO(2)RR) has been a promising conversion method for CO(2) utilization. Currently, the lack of electrocatalysts with favorable stability and high efficiency hindered the development of CO(2)RR. Nitrogen-doped graphene nanocarbons have great promise in replacing metal catalysts for catalyzing CO(2)RR. By using the density functional theory (DFT) method, the catalytic mechanism and activity of CO(2)RR on 11 types of nitrogen-doped graphene have been explored. The free energy analysis reveals that the zigzag pyridinic N- and zigzag graphitic N-doped graphene possess outstanding catalytic activity and selectivity for HCOOH production with an energy barrier of 0.38 and 0.39 eV, respectively. CO is a competitive product since its free energy lies only about 0.20 eV above HCOOH. The minor product is CH(3)OH and CH(4) for the zigzag pyridinic N-doped graphene and HCHO for zigzag graphitic N-doped graphene, respectively. However, for Z-pyN, CO(2)RR is passivated by too strong HER. Meanwhile, by modifying the pH value of the electrolyte, Z-GN could be selected as a promising nonmetal electrocatalyst for CO(2)RR in generating HCOOH.