The chemical identity, state and structure of catalytically active centers during the electrochemical CO(2) reduction on porous Fe–nitrogen–carbon (Fe–N–C) materials

We report novel structure–activity relationships and explore the chemical state and structure of catalytically active sites under operando conditions during the electrochemical CO(2) reduction reaction (CO(2)RR) catalyzed by a series of porous iron–nitrogen–carbon (FeNC) catalysts. The FeNC catalysts were synthesized from different nitrogen precursors and, as a result of this, exhibited quite distinct physical properties, such as BET surface areas and distinct chemical N-functionalities in varying ratios. The chemical diversity of the FeNC catalysts was harnessed to set up correlations between the catalytic CO(2)RR activity and their chemical nitrogen-functionalities, which provided a deeper understanding between catalyst chemistry and function. XPS measurements revealed a dominant role of porphyrin-like Fe–N(x) motifs and pyridinic nitrogen species in catalyzing the overall reaction process. Operando EXAFS measurements revealed an unexpected change in the Fe oxidation state and associated coordination from Fe(2+) to Fe(1+). This redox change coincides with the onset of catalytic CH(4) production around –0.9 V(RHE). The ability of the solid state coordinative Fe(1+)–N(x) moiety to form hydrocarbons from CO(2) is remarkable, as it represents the solid-state analogue to molecular Fe(1+) coordination compounds with the same catalytic capability under homogeneous catalytic environments. This finding highlights a conceptual bridge between heterogeneous and homogenous catalysis and contributes significantly to our fundamental understanding of the FeNC catalyst function in the CO(2)RR.