Abstract
Although oxygen added to nonaqueous lithium-mediated electrochemical ammonia synthesis (LiMEAS) enhances Faradaic efficiency, its effect on chemical stability and byproducts requires understanding. Therefore, standardized high-resolution gas chromatography-mass spectrometry and nuclear magnetic resonance were employed. Different volatile degradation products have been qualitatively analyzed and quantified in tetrahydrofuran electrolyte by adding some oxygen to LiMEAS. Electrodeposited lithium and reduction/oxidation of the solvent on the electrodes produced organic byproducts to different extents, depending on the oxygen concentration, and resulted in less decomposition products after LiMEAS with oxygen. The main organic component in solid-electrolyte interphase was polytetrahydrofuran, which disappeared by adding an excess of oxygen (3 mol %) to LiMEAS. The total number of byproducts detected was 14, 9, and 8 with oxygen concentrations of 0, 0.8, and 3 mol %, respectively. The Faradaic efficiency and chemical stability of the LiMEAS have been greatly improved with addition of optimal 0.8 mol % oxygen at 20 bar total pressure.