Single atom-based catalysts (SACs), due to their exceptional electrocatalytic behavior, have been explored for numerous applications such as the oxygen reduction reaction, thermo-catalytic CO2 reduction, and other catalytic activities. Ammonia is one of the most used chemical compounds, and its electrochemical synthesis is a promising alternative as it is simple and cost-effective and shows selective tunability towards the synthesis. Utilizing single-atom electrocatalysts with comparatively low metal mass loading yet exceptional activity could be a better approach to maximize ammonia production. Herein, we report a practically viable magnesium SAC (MgNxC) for the promising reduction of nitrate to ammonia. The catalyst was prepared using green leaf extracts of Spinacia oleracea via simple one-step pyrolysis. We optimized their synthesis temperature to scrutinize the effect of SAC formation and their variation on the catalysis efficacy. The MgNxC650 catalyst, anchored on a defective graphitic matrix, exhibits the best-optimized potential of −0.58 V vs. RHE, a faradaic efficiency of 81.5 ± 2.9% and a yield rate of 392.5 ± 41.2 μmol h−1 mg−1cat. with excellent repeatability. A comprehensive study of the nature of the heterojunction formed at the reactive interface of MgNxC catalysts was carried out by Mott–Schottky analysis to probe the band structure of the intrinsically induced metal–semiconductor junction in the MgNxC catalysts, followed by the analysis of parameters like flat band potential and carrier density correlation. DFT is employed to optimize the most stable reactive site and various reaction pathways for favorable nitrate reduction reaction with probable reaction intermediates were explored. Collectively, our work demonstrates a simple, cost-effective, and convenient way to synthesize SACs. Moreover, it provides clear evidence that chlorophyll moieties can be used as a template to prepare metal catalysts singly anchored on the graphitic carbon matrix.
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