Dec 4, 2024
4:30pm - 4:45pm
Hynes, Level 3, Room 305
Nageh Allam1,Ahmed Agour1
The American University in Cairo1
Nageh Allam1,Ahmed Agour1
The American University in Cairo1
Electrochemical nitrogen reduction reaction (NRR) has been established as a promising and sustainable alternative to the Haber–Bosch process, which requires intensive energy to produce ammonia. Unfortunately, NRR is constrained by the high adsorption/activation of the N<sub>2</sub> energy barrier and the competing hydrogen evolution reaction, resulting in low faradic efficiency. Herein, a well-dispersed iron single-atom catalyst was successfully immobilized on nitrogen-doped carbon nanosheets (Fe<sub>SAC</sub>-N-C) synthesized from pre-hydrothermally derived Fe-doped carbon quantum dots with an average particle size of 2.36 nm and used for efficient electrochemical N<sub>2</sub> fixation at ambient conditions. The as-synthesized Fe<sub>SAC</sub>-N-C catalyst records an onset potential of 0.12 V<sub>RHE</sub>, exhibiting a considerable faradic efficiency of 23.7% and an NH<sub>3</sub> yield rate of 3.47 μg h<sup>–1</sup> cm<sup>–2</sup> in aqueous 0.1 M KOH electrolyte at a potential of −0.1 V<sub>RHE</sub> under continuous N<sub>2</sub> feeding conditions. The control experiments assert that the produced NH<sub>3</sub> molecules only emerge from the dissolved N<sub>2</sub>-gas, reflecting the remarkable stability of the nitrogen–carbon framework during electrolysis. The DFT calculations showed the Fe<sub>SAC</sub>-N-C catalyst to demonstrate a lower energy barrier during the rate-limiting step of the NRR process, consistent with the observed high activity of the catalyst. This study highlights the exceptional potential of single-atom catalysts for electrochemical NRR and offers a comprehensive understanding of the catalytic mechanisms involved. Ultimately, this work provides a facile synthesis strategy of Fe<sub>SAC</sub>-N-C nano-sheets with high atomic-dispersion, creating a novel design avenue of Fe<sub>SAC</sub>-N-C that can vividly have a potential applicability in the large spectrum of electrocatalytic applications.