Coal tar pitch-derived nitrogen-doped carbon hosting iron for enhanced ammonia electrosynthesis
Abstract
Renewable electricity powered N2 electroreduction provides a clean strategy for sustainable NH3 production, of which the fabrication of electrocatalysts with excellent performance, stability, and cost-effectiveness are vital for its real applications. Herein, we for the first time confined Fe species to the coal tar pitch derived nitrogen-doped porous carbon (denoted as Fe2O3/FeNC) by pyrolyzing a uniform mixture of medium temperature coal tar pitch, FeCl3∙6H2O, urea and NaCl. The obtained Fe2O3/FeNC exhibits an excellent N2 electroreduction activity in neutral media, evidenced by an NH3 yield of 38.17 μg h-1 mgcat-1 at -0.5 V versus reversible hydrogen electrode (vs. RHE) in 0.1 M Na2SO4 with a Faradaic efficiency (FE) of 22.01 % (-0.3 V vs. RHE), surpassing most Fe-based N2 reduction electrocatalysts reported to date. The detailed electrochemical investigations indicate that the improved N2 electroreduction performances mainly due to the following reasons. One is the highly dispersed Fe species provide sufficient active sites for N2 electroreduction. Another is the existence of both pyridinic-N and pyrrolic-N species facilitates N2 adsorption. In addition, the interconnected porous carbon matrix accelerates the electron and mass transfer during the electrolysis. Importantly, the in-situ formation of Fe-N-C and Fe2O3 nanoparticles on carbon substrate prevents the aggregation and leaching of the Fe species and increase the stability of Fe2O3/FeNC. This work presents an ingenious strategy for the mass fabrication of metal-based electrocatalyst for N2 electroreduction, enabling the high value utilization of coal tar pitch.
Keywords
N2 electroreduction, iron, coal tar pitch, electrocatalysis, N doped carbon
Cite This Article
Sun Y, Fang Y, Wang Y, Yu J, Zhao Z, Liu J, Fu Y, Li H, Qiu J, Zhang W, Ma T. Coal tar pitch-derived nitrogen-doped carbon hosting iron for enhanced ammonia electrosynthesis. Chem Synth 2025;5:[Accept]. http://dx.doi.org/10.20517/cs.2025.17