Apr 24, 2024
5:00pm - 7:00pm
Flex Hall C, Level 2, Summit
Nageh Allam1
American University in Cairo1
<br/>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 potential applicability in the large spectrum of electrocatalytic applications.