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.