Nitrogen-Doping Chemical Behavior of Graphene Materials with Assistance of Defluorination

摘要： Heteroatom-doping reactions are essential to achieve advanced graphene-based materials for energy and biological areas. Unfortunately, considerably less is known regarding the detailed reaction pathways up to now. Here, we focus on investigating the nitrogen (N) doping process of fluorinated graphene (FG) under the assistance of defluorination based on modified in situ fourier transform infrared spectroscopy. It was demonstrated FG possesses a higher and more effective reactivity with ammonia in comparison with other graphene derivatives, which enable N-doping to proceed efficiently with assistance of defluorination even at a lower temperature (16.8 at % of N at 300 °C, 19.9 at % of N at 400 °C). Combining with Density functional theory, it was proved that, at the initial reaction step of N-doping, ammonia molecule attacked and substituted the C-F of FG by the new C-NH2. Sequentially, amino group was cyclized to the three-membered ring of ethylenimine. More importantly, the dissociation and migration of C-F bonds facilitates the dissociating of C-C bonds and the recombining of C-N bonds, thus significantly promoting the N atom in ethylenimine ring to transform to the pyridinic-N or graphitic-N in graphene skeleton.