Polymerizing monomer precursors to form monolayer carbon nitrides with determined C/N stoichiometries and tailored properties is intimately related to an in-depth understanding of the reaction paths. However, fundamental details related to molecular-level mechanisms remain largely unexplored because of the challenges associated with real-space visualization of early-stage polymerization processes involving C/N/H activation, stabilization, and evolution of intermediate states. Herein, we characterize the multistep reactions of melamine in the presence of coadsorbed cobalt on Au(111), using bond-resolved scanning probe microscopy (SPM) combined with density functional theory (DFT) calculations. Step-by-step evolution of on-surface-generated intermediate states have been monitored in real space; i.e., the initial step involves the condensation of melamine monomers to afford s-triazine tetramers, which further transform into C–C-linked octamers and longer oligomers. Furthermore, we demonstrate how the formation of the Au–Co–N motif influences the coplanar and out-of-plane configurations of reaction intermediates, therefore affecting C–N cleavage and C–C coupling. Our findings provide mechanistic insights into the preparation of monolayer carbon nitrides with predictable structures.
Li et al. (Sat,) studied this question.
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