催化作用
电化学
氨生产
本体电解
碳纤维
化学
无机化学
吸附
氧化还原
水溶液
电解
氮气
化学工程
材料科学
电解质
电极
循环伏安法
有机化学
物理化学
复合材料
工程类
复合数
作者
Ahmed M. Agour,Esraa Elkersh,Ghada E. Khedr,Hisham G. El-Aqapa,Nageh K. Allam
标识
DOI:10.1021/acsanm.3c02948
摘要
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 N2 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 (FeSAC-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 N2 fixation at ambient conditions. The as-synthesized FeSAC-N-C catalyst records an onset potential of 0.12 VRHE, exhibiting a considerable faradic efficiency of 23.7% and an NH3 yield rate of 3.47 μg h–1 cm–2 in aqueous 0.1 M KOH electrolyte at a potential of −0.1 VRHE under continuous N2 feeding conditions. The control experiments assert that the produced NH3 molecules only emerge from the dissolved N2-gas, reflecting the remarkable stability of the nitrogen–carbon framework during electrolysis. The DFT calculations showed the FeSAC-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 FeSAC-N-C nano-sheets with high atomic-dispersion, creating a novel design avenue of FeSAC-N-C that can vividly have a potential applicability in the large spectrum of electrocatalytic applications.
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